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Source: IRS Form 990 via ProPublica Nonprofit Explorer
Total Revenue
▼$434.7M
Total Contributions
$62.4M
Total Expenses
▼$415M
Total Assets
$1B
Total Liabilities
▼$386.4M
Net Assets
$661.9M
Officer Compensation
→$4.2M
Other Salaries
$141M
Investment Income
▼$9.1M
Fundraising
▼$117.5K
Source: USAspending.gov · Searched by organization name
VA/DoD Awards
$647.7K
VA/DoD Award Count
3
Funding from the Department of Veterans Affairs and/or Department of Defense.
Total Federal Funding
$127.8M
Awards Found
126
Department of Education
$15.2M
INSTITUTIONAL PORTION OF THE HIGHER EDUCATION EMERGENCY RELIEF FUND
Department of Education
$12.5M
CARES EMERGENCY STUDENT AID & SCHOLARSHIP
Department of Education
$9.1M
GEORGIA EDUCATORS NETWORKING TO REVOLUTIONIZE AND TRANSFORM EDUCATION:GENERATE
Department of Health and Human Services
$7.9M
HEALTHY START INITIATIVE-ELIMINATING RACIAL/ETHNIC DISPARITIES
Department of Health and Human Services
$4.8M
ESTABLISHING A CENTER OF EXCELLENCE ON HEALTH DISPARITIES IN RURAL POPULATIONS
Department of Health and Human Services
$3.3M
THE CHURCH-BASED DIABETES PREVENTION AND TRANSLATION STUDY-2 (CBDPT-2)
Department of Health and Human Services
$3.2M
NSL - BACCALAUREATE NURSING - OTHER ADMIN CHANGES
Department of Education
$2.9M
MERCER UNIVERSITY EDUCATIONAL OPPORTUNITY CENTER
Department of Health and Human Services
$1.9M
THE SOUTHEASTERN CONSORTIUM FOR SUBSTANCE ABUSE TRAINING (SECSAT)
Department of Health and Human Services
$1.5M
MECHANISM OF ACTION OF STEROIDOGENIC ACUTE REGULATORY PROTEIN (STAR)
National Science Foundation
$1.5M
DEVELOPING COMPUTER SCIENCE MASTER TEACHERS FOR GEORGIA RURAL SCHOOLS -THE PROJECT AIMS TO SERVE THE NATIONAL NEED OF DEVELOPING HIGHLY EFFECTIVE COMPUTER SCIENCE (CS) TEACHER LEADERS. THESE TEACHER LEADERS WILL BE PREPARED TO STRENGTHEN THE ABILITY OF RURAL SCHOOL SYSTEMS TO PROVIDE ACCESS TO HIGH-QUALITY CS INSTRUCTION FOR ALL STUDENTS. IN PREPARING CS TEACHER LEADERS, THE PROJECT SEEKS TO ADDRESS THE INSUFFICIENT LEVEL OF CS INSTRUCTION IN RURAL SCHOOLS, A SIGNIFICANT GAP IN THE STEM KNOWLEDGE PIPELINE. THE PROJECT WILL PREPARE 16 EXEMPLARY AND CERTIFIED GRADES 6-12 STEM TEACHER LEADERS IN SOUTHERN GEORGIA SCHOOLS. THE PREPARATION OF CS TEACHER LEADERS WILL ENCOURAGE CONTINUING CS EDUCATION IN PARTNERING SCHOOL DISTRICTS AND PROVIDE CS LEARNING EXPERIENCES FOR CURRENT AND FUTURE STUDENTS. PROJECT EFFORTS ARE ALIGNED WITH THE GEORGIA DEPARTMENT OF EDUCATION'S CS CAREER PATHWAYS AND OPPORTUNITIES TO PURSUE CAREERS IN A WELL-PAYING INDUSTRY WITH A SHORTAGE OF APPLICANTS. PARTNERSHIPS WITH AGRICULTURE, HEALTH CARE, AND THE MILITARY WILL PROVIDE PARTICIPATING TEACHERS WITH EXPOSURE TO PATHS FOR STUDENTS TO PURSUE CS CAREERS. PROVIDING STUDENTS WITH CS EDUCATIONAL EXPERIENCES THAT CAN LEAD TO WELL-COMPENSATED JOBS WILL PROVIDE ECONOMIC BENEFITS TO RURAL COMMUNITIES ACROSS THE ENTIRE REGION. THIS PROJECT AT MERCER UNIVERSITY INCLUDES PARTNERSHIPS WITH WIREGRASS GEORGIA TECHNICAL COLLEGE, THE COMPUTER SCIENCE FOR GEORGIA ACADEMIC PARTNERS NETWORK, AND GEORGIA HIGH-NEED SCHOOL DISTRICTS IN CLINCH COUNTY, COFFEE COUNTY, DUBLIN CITY, EVANS COUNTY, JEFF DAVIS COUNTY, TATTNALL COUNTY, TREUTLEN COUNTY, AND WHEELER COUNTY. UNIQUE TO THE PROPOSED PROJECT IS CS AS A NEW TEACHING AREA FOR EXPERIENCED STEM TEACHERS. THE PROJECT WILL IMPLEMENT AND INVESTIGATE A PROFESSIONAL DEVELOPMENT APPROACH TO INCREASE THE NUMBER AND DIVERSITY OF CS TEACHER LEADERS IN RURAL, HIGH-NEED SCHOOL SYSTEMS IN SOUTHERN GEORGIA. GUIDING THE PROJECT'S APPROACH AND EVALUATION IS A RESEARCH-BASED FRAMEWORK THAT EXTENDS THE WORK OF THE DEVELOPING MASTER TEACHERS THROUGH THE SOUTH CAROLINA SCIENCE AND MATHEMATICS TEACHER LEADERS PROGRAM, WHICH HIGHLIGHTS AREAS OF NEED FOR RURAL SCHOOL SYSTEMS AND THEIR TEACHERS, SPECIFIC TO CS TEACHING AND LEADERSHIP. THE PROJECT TEAM WILL EMPLOY RESEARCH-BASED STRATEGIES TO DEVELOP A NETWORK OF TEACHER LEADERS WITH CS CONTENT AND PEDAGOGICAL KNOWLEDGE, UNDERSTANDINGS OF INSTRUCTIONAL COACHING, AND AWARENESS OF CONTENT-SPECIFIC TEACHER LEADERSHIP. THE STRATEGIES WILL BE IMPLEMENTED THROUGH A 14-MONTH ONLINE EDUCATIONAL SPECIALIST IN TEACHER LEADERSHIP MASTER?S DEGREE PROGRAM, FOLLOWED BY ONLINE CS MINI-COURSES, IN-PERSON CS LEADERSHIP ASSEMBLIES, AND CS SYSTEM-LEVEL PLANNING EVENTS. EVALUATION AND ASSESSMENT DATA WILL BE USED TO INVESTIGATE HOW THE PROJECT APPROACH AFFECTS THE LEARNING, ACTIONS, AND DISPOSITIONS OF THE MASTER TEACHING FELLOWS (MTFS) AND SCHOOL AND SYSTEM-LEVEL FACTORS IMPACTING THE MTFS' SUCCESS AS CS TEACHER LEADERS. NONPROFIT AND INDUSTRY PARTNERS WILL PROVIDE THE MTFS WITH CS CAREER-FOCUSED LINKS WITHIN RURAL COMMUNITIES. PROJECT RESULTS WILL BE PRESENTED AT PROFESSIONAL CONFERENCES AND SUBMITTED FOR PUBLICATION. THIS TRACK 3: MASTER TEACHING FELLOWSHIP PROJECT IS SUPPORTED BY THE ROBERT NOYCE TEACHER SCHOLARSHIP PROGRAM (NOYCE). THE NOYCE PROGRAM SUPPORTS TALENTED STEM UNDERGRADUATE MAJORS AND PROFESSIONALS TO BECOME STEM MASTER TEACHERS IN HIGH-NEED SCHOOL DISTRICTS. IT ALSO SUPPORTS RESEARCH ON THE RETENTION AND EFFECTIVENESS OF K-12 TEACHERS IN HIGH-NEED SCHOOL DISTRICTS. THIS AWARD REFLECTS NSF'S STATUTORY MISSION AND HAS BEEN DEEMED WORTHY OF SUPPORT THROUGH EVALUATION USING THE FOUNDATION'S INTELLECTUAL MERIT AND BROADER IMPACTS REVIEW CRITERIA.
Department of Health and Human Services
$1.4M
NURSE FACULTY LOAN PROGRAM
Department of Education
$1.3M
MERCER UNIVERSITY STUDENT SUPPORT SERVICES-HENRY
Department of Education
$1.3M
MERCER UNIVERSITY STUDENT SUPPORT SERVICES PROGRAM-MACON
Department of Health and Human Services
$1.3M
GRADUATE PSYCHOLOGY EDUCATION PROGRAMS
Department of Health and Human Services
$1.3M
NURSE FACULTY LOAN PROGRAM
Department of Health and Human Services
$1.2M
ARTERIAL CONTRACTILITY AND BLOOD PRESSURE REGULATION BY STATINS - PROJECT SUMMARY: STATINS ARE USED BY OVER 200 MILLION PEOPLE WORLDWIDE FOR TREATING ATHEROSCLEROTIC CARDIOVASCULAR DISEASES SUCH AS HYPERTENSION, CORONARY ARTERY DISEASE, AND STROKE. PRE-CLINICAL AND CLINICAL DATA SUGGEST THAT STATINS PRODUCE BLOOD PRESSURE (BP)-LOWERING ACTION IN SOME SUBJECTS WHILE HAVING BP-NEUTRAL EFFECTS IN OTHERS. HOWEVER, THE UNDERLYING MECHANISM FOR SUCH CONTRASTING EFFECTS REMAINS UNCLEAR. THE CONVENTIONAL VIEW IS THAT LONG-TERM STATIN THERAPY PRODUCES A RANGE OF BENEFICIAL VASCULAR EFFECTS DUE TO THE INHIBITION OF MEVALONATE/CHOLESTEROL BIOSYNTHESIS AND RHO AND RHO-ASSOCIATED PROTEIN KINASE (ROCK) SIGNALING IN VASCULAR SMOOTH MUSCLE CELLS (SMCS) AND ENDOTHELIAL CELLS (ECS). HOWEVER, WHETHER STATINS CAN DIRECTLY ACT ON A VASCULAR TARGET TO REGULATE ARTERIAL CONTRACTILITY, INDEPENDENT OF THE CONVENTIONAL PATHWAYS, AND THE PATHOPHYSIOLOGICAL SIGNIFICANCE OF SUCH A TARGET OF DIRECT STATIN ACTION REMAIN UNCLEAR. DUE TO THE COEXISTENCE OF HYPERTENSION AND DYSLIPIDEMIA AND THE USE OF STATINS BY OVER 200 MILLION PEOPLE, IT IS CRITICALLY IMPORTANT TO DETERMINE WHETHER STATINS HAVE INHERENT BP-LOWERING ACTIONS SO THAT CLINICIANS CAN TAILOR ANTIHYPERTENSIVE THERAPY TO THE NEEDS OF INDIVIDUAL PATIENTS. IN THIS PROPOSAL, WE AIM TO INVESTIGATE THE DIRECT VASCULAR EFFECTS OF THE THREE MOST COMMONLY USED STATINS IN RESISTANCE MESENTERIC ARTERIES (RMAS) FROM WILD-TYPE AND TRANSGENIC NORMOTENSIVE AND HYPERTENSIVE ANIMALS TO DETERMINE THE MECHANISM OF DIFFERENTIAL BP REGULATION BY STATINS, BOTH ACUTELY AND IN THE LONG- TERM, AND PROPOSE A FRAMEWORK FOR HARNESSING THE BP-LOWERING ACTIONS OF STATINS THAT MAY POTENTIALLY BENEFIT MILLIONS. BASED ON OUR NOVEL PRELIMINARY DATA, THE CENTRAL HYPOTHESIS OF THIS PROPOSAL IS THAT STATINS STIMULATE RAPID RMA VASODILATION BY SELECTIVELY INHIBITING PHOSPHODIESTERASE 1A (PDE1A) IN SMCS, THEREBY ELEVATING [CGMP]I, LEADING TO PROTEIN KINASE G (PKG) ACTIVATION, VASODILATION, AND BP REDUCTION, AN EFFECT THAT IS ABOLISHED BY ENDOTHELIAL DYSFUNCTION THAT IMPAIRS UPSTREAM NO SIGNALING INTO SMCS. IN THIS PROPOSAL, WE WILL TO CHARACTERIZE THE ROLE OF THE NO- PDE1A/CGMP-PKG SIGNALING AXIS, WHICH MAY SHED LIGHT ON THE MECHANISMS BEHIND BP-LOWERING AND BP-NEUTRAL EFFECTS OF STATINS. OVERALL, THIS PROPOSAL COULD UNVEIL NOVEL CARDIOVASCULAR TARGETS AND THERAPEUTIC APPLICATIONS OF THE WORLD’S MOST PRESCRIBED DRUGS IN HYPERTENSION, AND SERVE AS THE GUIDE TO CLINICIANS TO TAILOR ANTIHYPERTENSIVE THERAPY TO THE INDIVIDUAL NEEDS OF PATIENTS WITH COEXISTING HYPERTENSION AND DYSLIPIDEMIA.
Department of Education
$1.2M
TO EDUCATE AND PROVIDE ACADEMIC SUPPORT TO STUDENTS SEEKING TO BECOME CERTIFIED REHABILITATION COUNSELORS TO ADDRESS THE PERSONNEL SHORTAGES AT STATE VOCATIONAL REHABILITATION OR QUALIFYING AGENCIES
Department of Health and Human Services
$1M
PRIMARY CARE TRAINING AND ENHANCEMENT
Department of Health and Human Services
$994.6K
NURSING WORKFORCE DIVERSITY
Department of Health and Human Services
$992.9K
RURAL COMMUNITIES OPIOID RESPONSE-IMPLEMENTATION
Department of Health and Human Services
$975.5K
NURSING WORKFORCE DIVERSITY
Department of Education
$954.9K
REHABILITATION LONG-TERM TRAINING - REHABILITATION COUNSELING
Department of Education
$944.8K
TRIO - EDUCATIONAL OPORTUNITY CENTERS - EDUCATIONAL OPPORTUNITY CENTERS PROGRAM
Department of Health and Human Services
$943.9K
SOUTHEAST CONSORTIUM ON SUBSTANCE ABUSE TRAINING
Department of Health and Human Services
$938.9K
SL - PHARMACY - LOAN GRANT WITH FUNDS FOR NEW BUDGET PERIOD
Department of Homeland Security
$938.3K
RESEARCH ON PERSONAL AREA NETWORK (PAN) INTERFERENCE & COMPATABILITY ISSUES FOR PUBLIC SAFETY PERSONAL PROTECTIVE EQUIPMENT
Department of Health and Human Services
$887.2K
THE ROLE OF ROS ON BETA-2-ADRENERGIC RECEPTOR FUNCTION IN HUMAN AIRWAY
Department of Health and Human Services
$872K
ACADEMIC ADMINISTRATIVE UNITS IN PRIMARY CARE
Department of Health and Human Services
$813.8K
NOREPINEPHRINE MODULATES MEDIAL PREFRONTAL CORTEX NEURAL ENSEMBLES THAT CONTROL COCAINE SEEKING BEHAVIOR - PROJECT SUMMARY/ABSTRACT THIS K01 APPLICATION AIMS TO PREPARE DR. ALI GHEIDI FOR AN INDEPENDENT FACULTY POSITION BY PROVIDING SPECIALIZED TRAINING IN RODENT MODELS OF DRUG SELF-ADMINISTRATION (IVSA), CHEMOGENIC MANIPULATION OF NEURONS AND TARGETED DELETION OF NEURONAL ENSEMBLES. THEREFORE, DR. GHEIDI WILL WORK WITH A CAREFULLY SELECTED TRAINING TEAM OF MENTORS. TRAINING FOR DR. GHEIDI WILL CONSIST OF COURSES, MEETING WITH MENTORS, WORKSHOPS, SCIENTIFIC MEETINGS, AND PERFORMING EXPERIMENTS. DR. GHEIDI’S SHORT TERM GOAL IS TO UNDERSTAND THE ROLE OF NOREPINEPHRINE (NE) IN REGULATING NEURONAL ENSEMBLES IN COCAINE SEEKING BEHAVIOR. HIS LONG-TERM GOAL IS TO GAIN AN INDEPENDENT POSITION AS A RESEARCHER-EDUCATOR, WHERE HE CAN STUDY NEUROMODULATORS' ROLE IN REGULATING NEURONAL ENSEMBLES TO DRUG ABUSE. IN ADDITION TO ADVANCING THE CAREER OF DR. GHEIDI, THIS PROPOSAL WILL INCREASE UNDERSTANDING OF SUBSTANCE ABUSE, IN GENERAL, AND COCAINE RELAPSE, IN PARTICULAR. OVER THE PAST DECADE, A PARADIGM SHIFT HAS OCCURRED IN NEUROBIOLOGY, INCLUDING WITHIN THE FIELD OF DRUG ADDICTION. IN THESE STUDIES, ONLY A SELECT, DISTRIBUTED, AND A SPARSE GROUP OF NEURONS, KNOWN AS A NEURONAL ENSEMBLE, THOUGHT TO CODE DRUG TAKING EVENTS IS ISOLATED AND STUDIED. THIS SELECTIVE APPROACH OFFERS NEW INSIGHTS OVER TRADITIONAL METHODS, WHERE DRUG-INDUCED PERTURBATIONS ARE USUALLY STUDIED IN THE WHOLE BRAIN AREA OR CELL TYPE. INSTRUMENTAL TO THIS TASK IS THE USE OF FOS BASED APPROACHES. THESE TECHNIQUES ALLOW THE DIRECT MANIPULATION OF FOS POSITIVE NEURONS, AND BY EXTENSION NEURONAL ENSEMBLES, WITHOUT AFFECTING ADJACENT AREAS OR CELL TYPES NOT INVOLVED IN THE BEHAVIOR. FOR EXAMPLE, USING THE DAUN02 NEURONAL ABLATION METHOD IN THIS K01, SCIENTISTS HAVE IDENTIFIED NEURONAL ENSEMBLES IN THE PREFRONTAL CORTEX AND NUCLEUS ACCUMBENS CRITICAL TO COCAINE, HEROIN, NICOTINE, AND ALCOHOL TAKING AND SEEKING BEHAVIORS. HOWEVER, MISSING FROM THIS UNDERSTANDING IS THE CONTRIBUTION OF THE BRAIN'S NEUROMODULATORS (E.G., NE) IN SCULPTING NEURONAL ENSEMBLES AND INDUCING RELAPSE TO DRUG TAKING. THUS, THIS GRANT PROPOSAL AIMS TO ELUCIDATE THE ROLE OF NE ON PREFRONTAL CORTICAL NEURONAL ENSEMBLES INVOLVED IN COCAINE SEEKING BEHAVIORS IN FEMALE AND MALE RATS. THE PROPOSED RESEARCH WILL UTILIZE STATE OF THE ART TECHNIQUES MENTIONED ABOVE. AIM 1 OF THIS K01 PROPOSAL WILL DETERMINE THE ROLE OF NE IN THE MEDIAL PREFRONTAL CORTEX (MPFC) ENSEMBLES CONTROL OF COCAINE SEEKING. AIM 2 WILL UTILIZE DREADDS TO INACTIVATE THE NE-CONTAINING LOCUS COERULEUS PROJECTIONS THAT SPECIFICALLY INNERVATE THE MPFC TO FURTHER EXPLORE THE ROLE OF NE IN COCAINE SEEKING. A BETTER UNDERSTANDING OF HOW THESE PROCESSES OPERATE IN COCAINE SEEKING SITUATIONS CAN INFORM BOTH CLINICAL AND BASIC SCIENCE AS WELL AS INFORM CLINICAL CARE. RESULTS WILL ALSO INFORM BASIC SCIENTISTS ON THE NEURONAL UNDERPINNINGS OF LEARNED MOTIVATED BEHAVIORS, AND RESEARCHERS MAY ALSO DEVISE CLINICAL STRATEGIES TO TARGET NEURONAL ENSEMBLES BY CONTROLLING NEUROMODULATORS, INCLUDING NE, IN THE HUMAN BRAIN THAT CAN EASE CONDITIONS THAT LEAD TO RELAPSE OF COCAINE USE.
Department of Health and Human Services
$743.5K
THE FUNCTION OF EBV LMP1 CTAR3 IN SUMOYLATION AND ONCOGENESIS
Department of Health and Human Services
$700K
ADVANCED EDUCATION NURSING TRAINEESHIP
Department of Health and Human Services
$571.1K
ARRA - NURSE FACULTY LOAN PROGRAM
Department of Health and Human Services
$492.3K
RECEPTOR PHARMACOLOGY AND TOXICOLOGY OF SECOND-GENERATION PYRROLIDINE "BATH SALT" CATHINONES
Department of Health and Human Services
$471K
PROXIMAL TUBULAR TRANSPORT OF MERCURY AND EFFECTS OF REDUCED RENAL MASS
Department of Health and Human Services
$470.7K
FUNCTIONALIZED MICELLAR NANOCARRIERS FOR TARGETED CANCER THERAPY
Department of Health and Human Services
$468.1K
NURSE FACULTY LOAN PROGRAM
Department of Health and Human Services
$458.4K
WHOLE CELL NEISSERIA GONORRHOEAE MICRO PARTICULATE VACCINE
Department of Health and Human Services
$455K
RECEPTOR-GUIDED TARGETED THERAPY FOR ASTHMA
Department of Health and Human Services
$440.1K
A NOVEL NEUROPEPTIDE BRAIN DELIVERY SYSTEM FOR EPILEPSY
Department of Health and Human Services
$429.5K
INVESTIGATION OF HUMAN GUT-DERIVED MESENCHYMAL STEM CELLS FOR CELLULAR THERAPY - PROJECT SUMMARY/ABSTRACT: CELL THERAPY IS AN INNOVATIVE AND NON-TOXIC REGENERATIVE APPROACH FOR THE TREATMENT OF INFLAMMATORY AND DEGENERATIVE DISORDERS. MESENCHYMAL STROMAL/STEM CELLS (MSCS) ARE WIDELY BEING TESTED AS CELLULAR AND REGENERATIVE THERAPY AND IN SOME COUNTRIES, IT IS ALREADY APPROVED AS STANDARD CLINICAL CARE FOR THE MANAGEMENT OF INFLAMMATORY BOWEL DISEASE ASSOCIATED COMPLICATIONS. SPECIFICALLY, PERIANAL FISTULA (PF) IS A SERIOUS COMPLICATION OF CROHN’S DISEASE (CD) WHICH SUBSTANTIALLY AFFECTS THE QUALITY OF LIFE OF THOSE PATIENTS. TREATMENT OPTIONS ARE LIMITED AND ARE NOT HIGHLY EFFECTIVE. MSCS DERIVED FROM ADIPOSE TISSUE HAS BEEN APPROVED IN EUROPE FOR THE TREATMENT OF COMPLEX PF IN PATIENTS WITH CD. ALTHOUGH THIS STEM CELL THERAPY IS SHOWING EFFICACY, SIDE EFFECTS SUCH AS ANAL ABSCESS, PROCTALGIA, AND VARIATIONS IN TREATMENT RESPONSES ARE COMMON WHICH COULD BE DUE TO THE ALLOGENEIC NATURE OF THIS CELL THERAPY. THE CURRENT UNMET IS THE DEVELOPMENT OF AN AUTOLOGOUS CELL THERAPY STRATEGY WITH ENHANCED POTENCY AND SAFETY FOR THE TREATMENT OF PF. WE HYPOTHESIZE THAT MSCS DERIVED FROM THE RECTUM OF PATIENTS WITH CD DISPLAY ROBUST IMMUNOSUPPRESSIVE AND REGENERATIVE PROPERTIES THAT CAN BE USED AS AN AUTOLOGOUS CELLULAR THERAPY. WE ALSO HYPOTHESIZE THAT RECTUM DERIVED MSCS’ POTENCY CAN BE FURTHER IMPROVED WITH APPROPRIATE INFLAMMATORY CUE MEDIATED PREACTIVATION, AND THUS THEY CAN FUNCTION AMIDST CONFOUNDING FACTORS. IN THE PRESENT PRECLINICAL RESEARCH PHASE, WE AIM TO CHARACTERIZE THE POTENCY OF RECTUM DERIVED MSCS FROM PATIENTS WITH CD. MERCER UNIVERSITY SCHOOL OF MEDICINE’S MISSION IS TO EDUCATE STUDENTS TO BECOME FUTURE PHYSICIANS AND SERVE RURAL AND UNDERSERVED REGIONS OF GEORGIA. INVOLVEMENT OF STUDENTS IN THIS RESEARCH ENHANCEMENT AWARD PROGRAM WILL BRING EXPOSURE AND HELP THEM TO APPLY CELLULAR THERAPY IN RURAL HEALTH CARE. THE RESULTS OF THIS STUDY CAN INFORM A SECOND-GENERATION CELL THERAPY APPROACH NOT ONLY FOR THE MANAGEMENT OF PF BUT ALSO FOR BOWEL INFLAMMATION.
Department of Health and Human Services
$424.5K
TARGETING SEROTONIN 5-HT1A AND 5-HT7 RECEPTORS TO PREVENT AUDIOGENIC SEIZURES AND CORRECT TRANSLATIONALLY VALID EEG PHENOTYPES IN A JUVENILE FMR1 KNOCK-OUT MOUSE MODEL OF FRAGILE X SYNDROME
Department of Health and Human Services
$421.8K
UPTAKE OF MERCURY AT THE BASOLATERAL MEMBRANE OF ISOLATED PROXIMAL TUBULES
Department of Health and Human Services
$420.8K
NOVEL MECHANISMS OF ARTERIAL CONTRACTILITY REGULATION BY STATINS - PROJECT SUMMARY/ABSTRACT: STATINS ARE CHOLESTEROL-LOWERING DRUGS THAT HAVE BEEN CLINICALLY USED FOR MORE THAN 30 YEARS FOR THE PREVENTION AND TREATMENT OF ATHEROSCLEROTIC CARDIOVASCULAR DISEASES INCLUDING CORONARY ARTERY DISEASE AND STROKE. THE CONVENTIONAL VIEW IS THAT THE VASCULAR EFFECTS OF STATINS ARE CHOLESTEROL LOWERING-DEPENDENT AND/OR -INDEPENDENT (OR PLEIOTROPIC), BOTH OF WHICH REQUIRE LONG-TERM TREATMENT. SURPRISINGLY, STUDIES TO PRECISELY DETERMINE DIRECT VASCULAR EFFECTS OF STATINS ARE LACKING AND THEIR CLINICAL SIGNIFICANCE OBSCURE, BECAUSE ALMOST ALL STUDIES THAT REPORTED VASCULAR EFFECTS OF STATINS WERE CONDUCTED A) USING SUPRATHERAPEUTIC CONCENTRATIONS (1000-FOLD OR HIGHER) OF THE DRUG, B) MOSTLY ON NON-RESISTANCE, CONDUIT ARTERIES THAT DO NOT CONTROL REGIONAL ORGAN BLOOD FLOW AND SYSTEMIC BLOOD PRESSURE, AND C) ON CULTURED ARTERIES AND SMOOTH MUSCLE CELLS THAT MAY HAVE UNDERGONE TRANSFORMATION FROM A CONTRACTILE TO A NON-CONTRACTILE, PROLIFERATIVE PHENOTYPE. OUR LONG-TERM GOAL IS TO UNDERSTAND DIRECT ARTERIAL CONTRACTILITY REGULATION BY THERAPEUTIC CONCENTRATIONS OF STATINS ON FRESH ISOLATED ARTERIES AND ISOLATED MYOCYTES. THE RATIONALE BEHIND THE PROPOSED RESEARCH IS THAT THE GAINED KNOWLEDGE WILL BE CRITICAL FOR ENHANCING OUR UNDERSTANDING OF VASCULAR ACTIONS OF STATINS AND FUTURE FORMULATION OF MORE EFFECTIVE, SAFER AND PERSONALIZED STATIN THERAPY. THE OBJECTIVE OF THIS APPLICATION IS TO UNDERSTAND MOLECULAR MECHANISMS OF DIRECT STATIN EFFECTS ON DIFFERENT VASCULATURES. OUR NOVEL PRELIMINARY DATA OBTAINED USING AN INTEGRATED APPROACH SUGGESTS THAT THERAPEUTIC CONCENTRATIONS (0.1-10NM) OF STATINS PRODUCE BOTH VASOCONSTRICTION AND VASODILATION DEPENDING ON VASCULAR MICROENVIRONMENT. IMPORTANTLY, WE FOUND THAT SUCH VASCULAR EFFECTS OCCUR AT NANOMOLAR CONCENTRATIONS, WITHIN 2-3 MINUTES OF DRUG APPLICATION AND ARE INDEPENDENT OF LIPID SYNTHESIS INHIBITION BY STATINS, SUGGESTING CELL-SURFACE CHANNEL OR RECEPTOR BASED MECHANISMS. INDEED, OUR DATA SHOWS THAT STATIN-MEDIATED VASOCONSTRICTION IS DEPENDENT ON SMOOTH MUSCLE CELL L-TYPE CA2+ CHANNEL OPENING AND CA2+ INFLUX, WHEREAS VASORELAXATION IS CONSISTENT WITH CGMP-BASED PHOSPHODIESTERASE (PDE) INHIBITION. THE CENTRAL HYPOTHESIS OF THIS PROPOSAL IS THAT STATINS HAVE DIVERSE VASCULAR EFFECTS THAT ARE, AT LEAST, MEDIATED BY THE ACTIVATION OF VOLTAGE-GATED CAV1.2 ION CHANNEL AND EXTRACELLULAR CA2+ INFLUX INTO ARTERIAL SMOOTH MUSCLE CELLS TO CAUSE VASOCONTRACTION, AND INHIBITION OF CGMP-DEPENDENT PDE IN SMOOTH MUSCLE CELLS LEADING TO VASODILATION. THE OBJECTIVE OF THE PROPOSED RESEARCH WILL BE ACHIEVED USING A COMBINATION OF BIOCHEMICAL, MOLECULAR, IMAGING, GENETIC, IN-VITRO, IN-SILICO AND FUNCTIONAL APPROACHES. WITH A COLLABORATIVE TEAM OF THREE PROMINENT SCIENTISTS, THE PROPOSED PROJECT WILL GREATLY ENHANCE OUR UNDERSTANDING OF NOVEL VASCULAR ACTIONS OF THE WORLD’S MOST PRESCRIBED CLASS OF LIPID-LOWERING MEDICATIONS. OUR PROPOSED ACTIVITY WILL ALSO ESTABLISH INFRASTRUCTURE FOR CARDIOVASCULAR RESEARCH AND EDUCATION AT THE MERCER UNIVERSITY COLLEGE OF PHARMACY, AND WILL GREATLY BENEFIT PHARMACY STUDENTS, GRADUATE STUDENTS AND VOLUNTEERS THROUGH KNOWLEDGE CREATION AND EXPOSURE TO A BROAD SPECTRUM OF LABORATORY AND DATA ANALYSIS TECHNIQUES.
Department of Health and Human Services
$394.7K
THE ROLE OF PHOSPHORYLATION IN REGULATING THE ANTIDIABETIC EFFECTS OF O3FAR-1
Department of Health and Human Services
$389.2K
THE ROLE OF PATCH COMPARTMENT NEURONS IN REWARD AND HABITUAL BEHAVIOR.
Department of Health and Human Services
$387.8K
MOLECULAR PHARMACOLOGY OF XYLAZINE AT ADRENOCEPTORS: RELATION TO NECROTIC SKIN LESIONS ASSOCIATED WITH CHRONIC INTRAVENOUS ADMINISTRATION - PROJECT SUMMARY/ABSTRACT THE Α2-ADRENERGIC RECEPTOR (Α2R) AGONIST XYLAZINE HAS BEEN USED IN VETERINARY MEDICINE FOR DECADES OWING TO ITS ANESTHETIC, MUSCLE RELAXANT, AND ANALGESIC PROPERTIES. SINCE THE MID-2000’S HOWEVER, ILLICIT USE OF XYLAZINE HAS GROWN DRAMATICALLY AND OVER THE LAST FEW YEARS ALONE, THE ILLICIT USE OF XYLAZINE- ADULTERATED OPIOIDS, INCLUDING FENTANYL, HAS INCREASED EXPONENTIALLY. XYLAZINE USE IN HUMANS IS LINKED TO WELL-DOCUMENTED ADVERSE EFFECTS INCLUDING RESPIRATORY DEPRESSION, HYPOTENSION, OR BRADYCARDIA, WHICH CAN ALL BE DIRECTLY COUPLED TO ITS MECHANISM AS AN Α2R AGONIST. SIGNIFICANTLY, REPEATED INTRAVENOUS INJECTION OF XYLAZINE IN HUMANS HAS BEEN ASSOCIATED WITH NECROTIZING SKIN ULCERATION THAT IS INDEPENDENT OF BACTERIAL ETIOLOGY AND IS XYLAZINE-SPECIFIC. DESPITE THE RECENT INCREASE IN ILLICIT XYLAZINE USE, THE MOLECULAR MECHANISMS RELATED TO XYLAZINE’S ACTION AT Α2RS REMAIN POORLY UNDERSTOOD, AS IS THE MECHANISM OF XYLAZINE-MEDIATED SKIN NECROSIS. THIS PROJECT IS DIRECTLY LINKED TO THE BASIC RESEARCH AREAS OF INTEREST IN THIS NOTICE OF SPECIAL INTEREST FROM NIDA. WE HYPOTHESIZE THAT XYLAZINE EXHIBITS UNIQUE AGONIST BINDING AND FUNCTIONAL PROFILES AT PERIPHERAL Α2 AND Α1RS AND THAT ITS ULCERATIVE EFFECTS ON THE SKIN ASSOCIATED WITH INTRAVENOUS INJECTION ARE DUE TO PERIPHERAL Α2/Α1R-MEDIATED VASOCONSTRICTION, WHICH CAUSES HYPOPERFUSION AND HYPOXIA UPON REPEATED EXPOSURE LEADING TO SKIN NECROSIS. WE PROPOSE THREE SPECIFIC AIMS TO ADDRESS THIS HYPOTHESIS. IN AIM 1, WE WILL ASSESS THE BINDING AFFINITY OF XYLAZINE COMPARED TO THE STRUCTURALLY DISTINCT ΑR AGONISTS CLONIDINE, MOXONIDINE, Α- METHYLNOREPINEPHRINE AND EPINEPHRINE AT AGONIST-OCCUPIED CONFORMATIONS OF EACH OF THE SIX Α2/Α1R SUBTYPES (Α1A, Α1B, Α1D, Α2A, 2B, 2C), EXPRESSED IN TRANSLATIONALLY-RELEVANT VENOUS AND ARTERIAL SMOOTH MUSCLE CELLS (VSMC). IN AIM 2, WE WILL UTILIZE NOVEL TRUPATH G PROTEIN-BIOSENSORS IN BOTH VENOUS AND ARTERIAL VSMC TO ASSESS THE FUNCTIONAL EFFECTS OF XYLAZINE COMPARED TO THE OTHER AGONISTS AT Α1A, Α1B, Α1D, Α2A, Α2B, AND Α2CRS ENGAGED WITH DIFFERING GΑΒΓ COMBINATIONS. THIS AIM WILL INFORM ON XYLAZINE-INDUCED Α1R/Α2R SIGNALING AND WILL GAUGE DISTINCT G PROTEIN BIAS THAT THE AGENT MAY POSSESS, COMPARED TO THE OTHER Α1R/Α2R AGONISTS. IN AIM 3, WE WILL DIRECTLY TEST THE HYPOTHESIS THAT IV XYLAZINE-INDUCED SKIN NECROSIS IN VIVO IS CAUSED BY A PERIPHERAL Α2R-MEDIATED MECHANISM ASSOCIATED WITH VASOCONSTRICTION AND RESULTING HYPOPERFUSION AND HYPOXIA. TOGETHER, THESE AIMS WILL FILL GAPS IN THE LITERATURE RELATED TO XYLAZINE BINDING AND FUNCTION IN BOTH VENOUS AND ARTERIAL VSMC AS WELL AS MECHANISMS OF IV XYLAZINE-INDUCED SKIN NECROSIS.
Department of Health and Human Services
$387.7K
DEVELOPMENT OF A NOVEL MODEL TO STUDY THE EFFECTS OF LINE-1 RETROTRANSPOSONS IN DISEASE AND NORMAL PHYSIOLOGY USING NANOBODIES - LINE-1 RETROTRANSPOSONS ENCODE A MULTICISTRONIC ENZYMATIC COMPLEX WITH THREE OPEN READING FRAMES. THOUSANDS OF COPIES OF LINE-1 ARE EMBEDDED THROUGHOUT THE GENOME, AND THE ENZYME ACTIVITY OF LINE-1 HAS GENERATED APPROXIMATELY ONE THIRD OF THE HUMAN GENOME VIA THE INSERTION OF LINE-1 AND SINES, ANOTHER TYPE OF RETROTRANSPOSON THAT DOES NOT ENCODE ITS OWN PROTEINS. ALTHOUGH LINE-1 IS LARGELY SILENCED IN MOST HEALTHY SOMATIC CELLS, IT IS REACTIVATED IN A LARGE NUMBER OF DISEASES WHERE IT IS HYPOTHESIZED TO PLAY A ROLE IN PATHOGENESIS AND DISEASE PROGRESSION, AND SOME RESEARCHERS HAVE SUGGESTED THE LINE-1 MAY ALSO HAVE A NECESSARY BIOLOGICAL ROLE. ALTHOUGH LINE-1 REACTIVATION CAN AFFECT CELLS THROUGH MULTIPLE MECHANISMS, INCLUDING MUTATION OF GENOMIC DNA, THE EFFECTS OF LINE-1-ENCODED PROTEINS ON LINE-1-ASSOCIATED DISEASES HAVE BEEN PARTICULARLY HARD TO DISSECT OWING TO A LACK OF RELIABLE KNOCK DOWN MODELS. THE LACK OF RELIABLE KNOCKDOWN MODELS ARISES FROM I) THE LARGE NUMBER OF LINE-1 COPIES IN THE GENOME, WHICH MAKES CONVENTIONAL GENE EDITING UNFEASIBLE, INCLUDING PRIME, AND II) THE COMPLEX AND POORLY UNDERSTOOD INTERACTIONS AND CROSSTALK BETWEEN LINE-1, RNAI, AND INTERFERON PATHWAYS, WHICH MAKES THE USE OF SHRNA OR SIRNA DIFFICULT TO INTERPRET. WE PROPOSE HEREIN TO ESTABLISH A NOVEL MODEL TO KNOCK DOWN LINE-1 PROTEINS USING INTRACELLULAR FUNCTIONALIZED NANOBODIES, ALSO KNOWN AS INTRABODIES. WE WILL USE PHAGE DISPLAY TO ISOLATE NANOBODIES WITH HIGH-AFFINITY TO LINE-1 PROTEINS FROM A SYNTHETIC NANOBODY LIBRARY. THESE NANOBODY SEQUENCES WILL THEN BE FUSED TO GFP OR FBOXES TO ENABLE LIVE-CELL TRACKING AND KINETIC EXPERIMENTS (GFP- NANOBODIES) OR KNOCK DOWN OF LINE-1 PROTEINS (FBOXES). NOTABLY, FBOX-NANOBODY FUSIONS HAVE ACHIEVED 100% KNOCKOUT OF TARGET PROTEINS VIA RAPID UBIQUITINATION THROUGH THE RECRUITMENT OF E3 UBIQUITIN LIGASE, RESULTING IN PROTEASOMAL DEGRADATION. WE WILL THEN TEST THE ABILITY OF THESE FUNCTIONALIZED, LINE-1-SPECIFIC NANOBODIES TO FACILITATE LIVE-CELL LOCALIZATION OF LINE-1 PROTEINS AND TO ELIMINATE LINE-1 PROTEINS. WE WILL ALSO PERFORM AN INITIAL PHENOTYPIC CHARACTERIZATION OF CELLS -/+ KNOCKDOWN OF THE LINE-1 PROTEIN ORF1P, THE MOST HIGHLY EXPRESSED LINE-1 PROTEIN. SUCCESSFUL COMPLETION OF THESE AIMS WILL ADVANCE THE LINE-1 FIELD AND ENABLE MORE ROBUST HYPOTHESIS-TESTING TO DETERMINE THE ROLES OF LINE-1 PROTEINS IN DISEASE AS WELL AS RIGOROUSLY TESTING THEIR PROPOSED ROLE IN MAMMALIAN DEVELOPMENT.
Department of Health and Human Services
$381.1K
THREE-DIMENSIONAL CARDIAC ACCELEROMETRY FOR CARDIAC MONITORING
Department of Health and Human Services
$380.9K
AUTISM SPECTRUM DISORDER IN RURAL GEORGIA: EDUCATION AND RESOURCES - PROJECT SUMMARY AUTISM SPECTRUM DISORDER (ASD) IS A CONDITION CHARACTERIZED BY ATYPICAL SOCIAL COMMUNICATION, RIGID THINKING, AND REPETITIVE BEHAVIOR THAT IS BECOMING INCREASINGLY PREVALENT, WITH 1 IN EVERY 54 CHILDREN MEETING THE DIAGNOSTIC CRITERIA. ASD SIGNS AND SYMPTOMS CAN VARY BROADLY IN THEIR PRESENTATION, FROM RELATIVELY MILD IMPAIRMENTS TO SYMPTOMS SEVERE ENOUGH THAT THEY PREVENT INDIVIDUALS WITH ASD FROM LIVING INDEPENDENTLY. SOCIAL SUPPORT AND EARLY INTERVENTION THERAPIES HOWEVER CAN SIGNIFICANTLY AMELIORATE THE SEVERITY OF SEVERAL ASD SYMPTOMS. NOTABLY, THE YOUNGER CHILDREN ARE WHEN THERAPIES AND INTERVENTIONS ARE BEGUN, THE MORE EFFECTIVE THEY WILL ULTIMATELY BE. WHILE CHILDREN CAN BE RELIABLY DIAGNOSED WITH ASD AT AS YOUNG AS 18 MONTHS, THE AVERAGE AGE AT TIME OF DIAGNOSIS IS 4.5 YEARS WHICH MEANS THAT CHILDREN WITH ASD OFTEN MISS THERAPEUTIC OPPORTUNITIES FOR LACK OF A DIAGNOSES. DELAYED DIAGNOSES ARE ESPECIALLY COMMON IN CHILDREN FROM RURAL COMMUNITIES. RESEARCH THAT INVESTIGATED POSSIBLE CAUSES FOR DELAYED ASD DIAGNOSES IN RURAL COMMUNITIES FOUND LACK OF PARENTAL KNOWLEDGE ABOUT ASD, HESITANCY AMONG CLINICIANS TO DIAGNOSE YOUNG CHILDREN WITH ASD, AND A LACK OF KNOWLEDGE REGARDING STEPS TO TAKE TO HAVE A CHILD TESTED FOR ASD TO BE SIGNIFICANT FACTORS. IN ORDER TO ADDRESS ASD-RELATED DISPARITIES IN RURAL COMMUNITIES, WE CREATED A WEBPAGE DEDICATED TO HELPING FAMILIES AND INDIVIDUALS EFFECTED BY ASD NAVIGATE THE DIAGNOSTIC PROCESS. OUR WEBPAGE DIRECTS USERS TO ASD “ON-BOARDING’ ORGANIZATIONS, AND ALSO HAS RESOURCES FOR FINDING EARLY INTERVENTION THERAPY CENTERS NEAR THEIR HOME COMMUNITIES, PROVIDES LINKS TO FINANCIAL RESOURCES, AND LINKS TO COMMUNITY BASED SUPPORT ORGANIZATIONS. WE WOULD LIKE TO EXPAND OUR WEBPAGE INTO AN ONLINE ASD TOOLKIT THAT WILL BE REVIEWED BY RURAL FAMILIES WHO HAVE A CHILD WITH ASD. OUR TOOLKIT WILL ALSO GIVE FAMILIES OPPORTUNITIES TO DIRECT CONTENT CREATION BY SOLICITING FAMILIES’ INPUT THROUGH USER FEEDBACK QUESTIONS AND FOCUS GROUPS. THE GOAL OF THE ASD TOOLKIT IS TO CREATE AN EASY TO USE GUIDE FOR LIVING WITH AND MANAGING ASD IN RURAL GEORGIA THAT HAS BEEN SHAPED INSIGHTS FROM FAMILIES AFFECTED BY ASD. WE WILL ALSO CREATE AN ONLINE COURSE ABOUT ASD DIAGNOSIS AND RESOURCES FOR RURAL PHYSICIANS THAT WILL BE INFORMED BY INPUT FROM FAMILIES AFFECTED BY ASD. WE WILL INVITE FEEDBACK FROM OUR TARGETED PHYSICIANS THOUGH USER FEEDBACK QUESTIONS AND AN ASD RESOURCES QUIZ. ULTIMATELY, WE WILL USE THE PHYSICIAN INPUT WE RECEIVE ON THE COURSE TO DEVELOP A CONTINUING MEDICAL EDUCATION (CME) PROGRAM THAT WILL BE AVAILABLE THROUGH PROJECT ECHO.
National Endowment for the Humanities
$380.2K
MERCER UNIVERSITY SOUTHERN STUDIES CENTER - NEH CHALLENGE GRANT
Department of Health and Human Services
$358.1K
ACE ENGINEERED MSCS AS A MULTIDRUG-DELIVERY PLATFORM FOR BREAST CANCER THERAPY
Department of Health and Human Services
$348.2K
NURSING WORKFORCE DIVERSITY
Department of Health and Human Services
$341.5K
MECHANISTIC ANALYSIS OF THE ROLE OF EXTRACHROMOSOMAL TELOMERIC CIRCLES IN THE ALT
Department of Health and Human Services
$339.6K
TARGETING THE STRUCTURALLY CONSERVED PORTAL PROTEIN AS A STRATEGY TO DEVELOP A FIRST-IN-CLASS BROAD-SPECTRUM HERPESVIRUS ANTIVIRAL DRUG, PORT 1 - THERE ARE NINE HUMAN HERPESVIRUS (HHV) PATHOGENS THAT CAUSE SIGNIFICANT WORLDWIDE MORBIDITY AND MORTALITY WITH TREATMENT COSTS IN THE BILLIONS OF DOLLARS ANNUALLY. THEIR UBIQUITOUS NATURE CONTRIBUTES TO PRIMARY INFECTION EARLY IN LIFE AND MOST ADULTS PERMANENTLY HARBOR ONE OR MORE LATENT HERPESVIRUS SPECIES. PRIMARY DISEASE RANGES FROM ASYMPTOMATIC TO SELF-LIMITING (HERPES LABIALIS) TO LIFE-THREATENING (CANCER). THE PI STUDIES A SERIES OF NON-TOXIC, NON-NUCLEOSIDE SMALL MOLECULE ANTIVIRAL DRUG CANDIDATES (PORT COMPOUNDS) WITH A UNIQUE MECHANISM OF ACTION: INHIBITION OF VIRAL DNA PACKAGING BY TARGETING THE VIRAL PORTAL PROTEIN. THE PROPOSED STUDIES SEEK TO EXPLOIT THE REMARKABLE STRUCTURAL AND FUNCTIONAL RELATEDNESS OF HERPESVIRUS PORTALS. DURING HERPESVIRUS GENOME REPLICATION, CONCATAMERS OF VIRAL DSDNA ARE CLEAVED INTO SINGLE LENGTH UNITS BY A VIRUS-ENCODED TERMINASE AND PACKAGED INTO PROCAPSIDS THROUGH A CHANNEL LOCATED AT A SINGLE CAPSID VERTEX - THE PORTAL. THE PORTAL IS ABSOLUTELY REQUIRED FOR VIRAL REPLICATION. IN ALL CASES, FUNCTION IS HIGHLY CONSERVED IN THAT PORTALS ARE ESSENTIAL FOR DNA PACKAGING AND PLAY A ROLE IN RELEASING VIRAL DNA DURING INFECTION. OUR RECENT FINDINGS, WHICH ARE THE BASIS OF THIS GRANT APPLICATION, SHOW THAT PORT 1 CAN PREVENT VIRAL REPLICATION IN HUMAN AND ANIMAL SPECIES IN ALL THREE HERPESVIRUS SUBFAMILIES (ALPHA, BETA AND GAMMA). THE REMARKABLE STRUCTURAL CONSERVATION OF THE PORTAL PROTEIN CORE FOR ALL HERPESVIRUS SPECIES ACROSS ALL THREE SUB- FAMILIES MAY PROVIDE AN OPPORTUNITY TO DEVELOP A BROAD-SPECTRUM HHV DRUG. FURTHERMORE, A DRUG WITH A COMPLETELY DIFFERENT MECHANISM THAN NUCLEOSIDE ANALOGS (E.G. ACYCLOVIR) WOULD HAVE GREAT CLINICAL VALUE FOR TREATING DRUG RESISTANT HERPESVIRUSES. A BROAD-SPECTRUM ANTI-HERPESVIRAL DRUG COULD BE USED TO TREAT MORE THAN ONE HERPESVIRUS INFECTION AT ONE TIME – PARTICULARLY IN IMMUNOCOMPROMISED CANCER AND TRANSPLANT PATIENTS, AND FILL THE NEED FOR ALTERNATIVE OR FIRST GENERATION THERAPIES FOR CERTAIN HERPESVIRUSES (EBV AND CMV). WE PROPOSE FOUR COMPLEMENTARY AIMS TO FURTHER THESE STUDIES. AIM 1 WILL INCLUDE SYNTHESIS AND TESTING OF PORT 1 IN VITRO ACTIVITY AGAINST ALPHA, BETA, AND GAMMA HERPESVIRUSES. PORT1 MECHANISM OF ACTION WILL BE CONFIRMED VIA TEM BY SHOWING THAT CELLS INFECTED BY A VIRUS FROM ANY HHV SUBFAMILY CONTAIN ONLY EMPTY CAPSIDS. AIMS 2-4 WERE CONCEPTUALIZED BASED ON THE HYPOTHESIS THAT PORT 1 EXHIBITS BROAD-SPECTRUM ACTIVITY AGAINST HUMAN AND ANIMAL HERPESVIRUSES. PRELIMINARY DATA ARE PROVIDED SHOWING THAT PORT 1 HAS SIGNIFICANT IN VITRO ACTIVITY AGAINST MURINE CYTOMEGALOVIRUS AND MURINE GAMMAHERPESVIRUS 68. THESE RESULTS WERE NOT UNEXPECTED BASED ON THE REMARKABLE STRUCTURAL AND FUNCTIONAL RELATEDNESS OF ALL HERPESVIRUS PORTALS. AIMS 2-4 WILL TEST THE IN VIVO EFFICACY OF THE LEAD BROAD SPECTRUM PORT 1 COMPOUND ACTIVITY AGAINST HERPES-VIRUSES FROM ALL THREE SUBFAMILIES. IN THE SPIRIT OF THE NIH REAP GRANT MECHANISM, THESE STUDIES WILL PROVIDE AN EXCITING, MENTORED LABORATORY EXPERIENCE FOR UNDERGRADUATE, GRADUATE AND MEDICAL STUDENT RESEARCHERS.
Department of Defense
$339K
ATOMIC AND MOLECULAR INVESTIGATION OF CORROSION FOR PREVENTION AND CONTROL
Department of Health and Human Services
$292.1K
DEVELOPMENT OF NOVEL MALARIA PRE-ERYTHROCYTIC VACCINE ANTIGENS TARGETING PLASMODIUM SPOROZOITE LIVER INFECTION - PREVIOUSLY, USING A PHAGE PEPTIDE DISPLAY LIBRARY, OUR GROUP HAS IDENTIFIED PLASMODIUM PARASITE LIGANDS AND CORRESPONDING HOST CELL RECEPTORS IMPORTANT FOR SPOROZOITE-KUPFFER CELL INTERACTION IN THE MAMMALIAN LIVER. USING A SIMILAR APPROACH, WE IDENTIFIED THE HP1 PEPTIDE, A STRUCTURAL MIMIC OF A LIGAND THAT THE SPOROZOITE USES TO INFECT HEPATOCYTES. IMMUNIZATION WITH THE HP1 PEPTIDE PROTECTS ~ 50 % MICE FROM P. BERGHEI CHALLENGE. USING AN ANTI-HP1 ANTIBODY, WE IDENTIFIED PLASMODIUM PHOSPHOLIPID SCRAMBLASE (PLS) AS THE SPOROZOITE LIGAND OF HEPATOCYTES AND A POTENTIAL VACCINE ANTIGEN. WE PROPOSE 1) TO IDENTIFY PLS PROTEIN EPITOPES THAT FUNCTION IN HEPATOCYTE RECOGNITION, FOR USE AS A VACCINE ANTIGEN; AND 2) TO DEVELOP A TRI- FUNCTIONAL VACCINE ANTIGEN CONTAINING I) A SPOROZOITE CIRCUMSPOROZOITE PROTEIN (CSP) EPITOPE, TARGETING LIVER SINUSOID BINDING, II) A SPOROZOITE GAPDH-RELATED EPITOPE, TARGETING SPOROZOITE EXIT FROM THE CIRCULATION VIA KUPFFER CELL TRAVERSAL, AND III) SPOROZOITE PLS EPITOPE, TARGETING HEPATOCYTE INFECTION. WE EXPECT THAT THIS APPROACH WILL LEAD TO ENHANCEMENT OF THE MODERATE PROTECTIVE EFFICACY OF THE MOST ADVANCED RTS,S/AS01 MALARIA VACCINE.
National Science Foundation
$275.6K
MODELING FOR UNDERSTANDING PHYSICAL PHENOMENA AND ENGAGING PRE-SERVICE TEACHERS IN SCIENCE -THIS PROJECT AIMS TO SERVE THE NATIONAL INTEREST BY PREPARING ELEMENTARY SCHOOL TEACHERS TO INTEGRATE MODEL-BASED INQUIRY INTO THE CURRICULUM TO ENHANCE STUDENT LEARNING OF SCIENCE. IN ELEMENTARY SCHOOLS, SCIENCE IS OFTEN TAUGHT UTILIZING ENGLISH LANGUAGE ARTS BEST PRACTICES. CHILDREN READ ABOUT AND MEMORIZE SCIENCE FACTS INSTEAD OF ENGAGING IN SCIENCE PRACTICES TO DEVELOP SCIENTIFIC KNOWLEDGE. IN EFFORTS TO BUILD PROSPECTIVE ELEMENTARY SCIENCE TEACHER UNDERSTANDING OF, ABILITY TO, AND PREPAREDNESS FOR TEACHING USING MODEL-BASED INQUIRY (MBI) THE PROJECT AIMS TO SITUATE MBI INTO A PHYSICAL SCIENCE COURSE. THE MODELING FOR UNDERSTANDING PHYSICAL PHENOMENA AND ENGAGING TEACHERS IN SCIENCE (MUPPETS) PROJECT WILL DEVELOP A PHYSICAL SCIENCE COURSE FOR PROSPECTIVE ELEMENTARY TEACHERS (TO BE TAKEN PRIOR TO THE SCIENCE EDUCATION METHODS COURSE) IN WHICH THE PRESERVICE TEACHERS ARE LEARNERS OF SCIENCE IN AN ENVIRONMENT THAT UTILIZES SCIENCE EDUCATION RESEARCH-BASED PEDAGOGICAL APPROACHES. PRE-SERVICE TEACHER GAIN EXPERIENCE LEARNING SCIENCE USING TECHNIQUES WELL SUITED FOR ELEMENTARY STUDENTS AND IN ACCORDANCE WITH THE NEXT GENERATION SCIENCE STANDARDS. WHEN PROSPECTIVE ELEMENTARY TEACHERS ENTER THE SCIENCE EDUCATION METHODS COURSE, THE PHYSICAL SCIENCE COURSE EXPERIENCE IS A FAMILIAR CONTEXT TO DRAW UPON, AN OPPORTUNITY NOT TYPICALLY FOUND IN ELEMENTARY EDUCATION TEACHER PREPARATION PROGRAMS. THE PURPOSE OF THE MUPPETS PROJECT IS TO DETERMINE HOW PROSPECTIVE ELEMENTARY TEACHERS ENGAGE WITH MODEL-BASED INQUIRY (MBI) THAT CENTERS ON GATHERING AND MAKING SENSE OF DATA AND PEER-TO-PEER DISCOURSE. MORE SPECIFICALLY, THIS PROJECT SEEKS TO UNDERSTAND HOW MAKING SENSE OF PHENOMENA THROUGH COLLABORATIVE DISCUSSIONS INFLUENCES THE COMPOSITION AND SUBSTANCE OF MODELS AND EXPLANATIONS ACROSS MODEL ITERATIONS TO ESTABLISH THE IMPACT ON THEIR UNDERSTANDING OF (1) PHYSICAL SCIENCE, SCIENCE, AND UNIVERSAL EPISTEMOLOGICAL VIEWS; (2) META-MODELING KNOWLEDGE; AND (3) MODELING PRACTICE. DATA IS ANALYZED USING A MIXED-METHODS APPROACH EMPLOYING A QUANTITATIVE ANALYSIS OF PRE-AND POST-SURVEY DATA TO ASSESS PROSPECTIVE ELEMENTARY TEACHERS? VIEWS OF KNOWLEDGE (EPISTEMOLOGY) AND META-MODELING KNOWLEDGE BEFORE AND AFTER ENGAGING IN MBI. THE QUALITATIVE DATA COMPONENT OF THE RESEARCH INCLUDES THE OBSERVED WRITTEN EXPLANATIONS AND THINK-ALOUD PROTOCOL TO CHARACTERIZE TYPES OF MODELING PRACTICE THAT PRE-SERVICE ELEMENTARY TEACHERS USE TO EXPLAIN PHENOMENA THROUGH THE VISUAL, WRITTEN, AND ORAL REPRESENTATIONS THEY CREATE ACROSS FIVE SETS OF ITERATIVE MODELS. THE NSF IUSE: EHR PROGRAM SUPPORTS RESEARCH AND DEVELOPMENT PROJECTS TO IMPROVE THE EFFECTIVENESS OF STEM EDUCATION FOR ALL STUDENTS. PARTIAL FUNDING IS FROM THE ROBERT NOYCE TEACHER SCHOLARSHIP PROGRAM. THROUGH THE ENGAGED STUDENT LEARNING TRACK, THE PROGRAM SUPPORTS THE CREATION, EXPLORATION, AND IMPLEMENTATION OF PROMISING PRACTICES AND TOOLS. THIS AWARD REFLECTS NSF'S STATUTORY MISSION AND HAS BEEN DEEMED WORTHY OF SUPPORT THROUGH EVALUATION USING THE FOUNDATION'S INTELLECTUAL MERIT AND BROADER IMPACTS REVIEW CRITERIA.- SUBAWARDS ARE NOT PLANNED FOR THIS AWARD.
Department of Education
$272.4K
MERCER UNIVERSITY STUDENT SUPPORT SERVICES-HENRY
Department of Education
$272.4K
MERCER UNIVERSITY STUDENT SUPPORT SERVICES-MACON
Department of Health and Human Services
$272.1K
RURAL RESIDENCY PLANNING AND DEVELOPMENT PROGRAM
Department of Defense
$268.7K
DEVELOPMENT NOVEL DRUGS TARGETING SEROTONIN RECEPTORS TREAT MOTOR, SOCIAL, COGNITIVE,SENSORY DOMAINS AUTISM SPECTRUM DISORDER USING MOUSE MODELS
Department of Health and Human Services
$253.6K
MANIPULATION OF THE SUMO MACHINERY BY EBV LMP1
Department of Health and Human Services
$238.9K
RURAL COMMUNITIES OPIOID RESPONSE PROGRAM-OVERDOSE RESPONSE - LYING AT THE SOUTHERN TIP OF THE APPALACHIAN MOUNTAINS IN NORTH GEORGIA, FANNIN, GILMER, GORDON, AND POLK COUNTIES ARE FOUR OF THE HARDEST-HIT COUNTIES IN THE STATE IN TERMS OF OPIOID OVERDOSE. THE REGION HAS A HIGHLY DISPROPORTIONATE BURDEN OF OPIOID OVERDOSE, WITH EACH COUNTY HAVING A 2018-2020 OPIOID OVERDOSE MORTALITY RATE HIGHER THAN THE STATE AVERAGE (FANNIN 18.9, GILMER 18.8, GORDON 0.0, AND POLK 18.7 PER 100,000 VS. 12.2 STATEWIDE). BETWEEN 2019 AND 2020, GEORGIA SAW A 35% INCREASE IN DRUG RELATED DEATHS. OF NOTE, FANNIN COUNTY HAS BEEN RANKED BY THE CDC IN THE TOP 5% AS ONE OF THE MOST VULNERABLE COUNTIES IN THE NATION FOR HIV AND/OR HEPATITIS C INFECTION AS A RESULT OF THE OPIOID EPIDEMIC. IN ADDITION, THE REGION EXHIBITS A 36% HIGHER OVERDOSE-RELATED ER VISIT RATE THAN THE REST OF THE STATE AND 120% HIGHER OVERDOSE-RELATED ER VISIT RATE THAN THE REST OF THE NATION. THE REGION’S POPULATION IS MORE LIKELY TO EXPERIENCE A HIGH UNINSURED ADULT POPULATION, IS GENERALLY OLDER, AND IS MORE LIKELY TO LIVE IN POVERTY THAN THE REST OF THE STATE AND THE NATION. ALTHOUGH THE NORTH GEORGIA OPEN PROGRAM HAS MADE STRIDES OVER THE PAST FOUR YEARS, THERE REMAINS COMPLICATIONS IN THE ACCESS TO ADEQUATE PREVENTION, TREATMENT, AND RECOVERY SERVICES THROUGHOUT THE FOUR-COUNTY REGION. AS AN EXAMPLE, DESPITE HAVING SOME OF THE HIGHEST OVERDOSE RATES IN THE STATE, OVER THE COURSE OF THE THREE-YEAR RCORP IMPLEMENTATION PROJECT, THE COLLABORATIVE WAS ABLE TO INCREASE DATA WAIVED MEDICATION?ASSISTED TREATMENT (MAT) FROM TWO TO THREE PROVIDERS. HOWEVER, THESE ARE THE ONLY THREE MAT PROVIDERS IN THE ENTIRE 4-COUNTY AREA (A RATIO OF MORE THAN 75,000 RESIDENTS PER MAT-WAIVED PROVIDER), AND THEY ARE UNABLE TO MEET THE DEMAND FOR THEIR SERVICES. THE OVERALL LACK OF SUBSTANCE USE DISORDER TREATMENT RESOURCES WITHIN THE AREA UNDERSCORES THE IMPORTANCE OF PREVENTION, BOTH OF OPIOID USE DISORDER ITSELF, AND OF OPIOID OVERDOSE. DEVELOPED DURING THE RCORP PLAN NING GRANT, THE VISION OF NORTH GEORGIA OPEN IS “A GEORGIA FREE OF OPIOID OVERDOSE AND MISUSE,” WITH A MISSION “TO CREATE AND SUSTAIN OPIOID PREVENTION, TREATMENT, AND RECOVERY INITIATIVES IN FANNIN, GILMER, GORDON, AND POLK COUNTIES.” TO ACHIEVE THIS VISION AND MISSION, NORTH GEORGIA OPEN ESTABLISHED 5 GOALS THAT WILL GUIDE OUR EFFORTS. THESE 5 GOALS ARE: - GOAL 1: IMPLEMENT EVIDENCE-BASED INITIATIVES TO PREVENT OPIOID USE DISORDER AND OPIOID OVERDOSE IN FANNIN, GILMER, GORDON, AND POLK COUNTIES. - GOAL 2: IMPLEMENT EVIDENCE-BASED INITIATIVES TO INCREASE ACCESS TO TREATMENT FOR OPIOID USE DISORDER IN FANNIN, GILMER, GORDON, AND POLK COUNTIES. - GOAL 3: IMPLEMENT EVIDENCE-BASED INITIATIVES TO SUPPORT AND EXPAND THE RECOVERY COMMUNITY WITHIN FANNIN, GILMER, GORDON, AND POLK COUNTIES. - GOAL 4: EVALUATE THE EFFECT OF NORTH GEORGIA OPEN ON OPIOID USE DISORDER AND OTHER SUBSTANCE USE DISORDERS IN FANNIN, GILMER, GORDON, AND POLK COUNTIES. - GOAL 5: ENACT A COMPREHENSIVE SUSTAINABILITY PLAN DESIGNED TO SUSTAIN THE PARTNERSHIPS ACROSS THE COMMUNITY AND TO IMPLEMENT FINANCIAL SUSTAINABILITY STRATEGIES.
Department of Health and Human Services
$227.8K
VARICELLA-ZOSTER VIRUS ENCAPSIDATION PROTEINS
Department of Health and Human Services
$226.8K
REACTIVE ALDEHYDE DNA DAMAGE IN MITOCHONDRIAL MUTAGENESIS AND DISEASE PATHOPHYSIO
Department of Health and Human Services
$226.8K
THE ROLE OF MU OPIOID RECEPTOR ACTIVATION IN PSYCHOSTIMULANT-INDUCED GENE EXPRESS
Department of Health and Human Services
$226.8K
BIOCHEMICAL MECHANISMS OF PBA AND CHK IN TUMORIGENIC CELLS
Department of Health and Human Services
$224.9K
PROGENITOR CELL MEDIATED BIOENGINEERING OF THE CEREBROVASCULATURE
Department of Agriculture
$224.5K
ARP ECONOMIC DEVELOPMENT GRANT FOR RURAL HEALTH CARE FACILITIES
Department of Health and Human Services
$219.3K
ORAL DELIVERY OF PROTEIN ANTIGENS AND THEIR STABILITY BY ALGINATE MICROSPHERES
National Endowment for the Humanities
$215.3K
COTTON CULTURE IN THE SOUTH FROM THE CIVIL WAR TO THE CIVIL RIGHTS MOVEMENT
Department of Health and Human Services
$208.2K
PRIMARY CARE TRAINING AND ENHANCEMENT
Department of Health and Human Services
$206.8K
ARRA - NURSE FACULTY LOAN PROGRAM
National Endowment for the Humanities
$185.3K
COTTON CULTURE IN THE SOUTH FROM THE CIVIL WAR TO THE CIVIL RIGHTS MOVEMENT
National Science Foundation
$174.5K
GOING FURTHER: AN INTEGRATIVE APPROACH TO A MORE RESEARCH-ORIENTED, EXPLORATORY JUNIOR-LEVEL LAB
Department of Health and Human Services
$171.7K
RURAL COMMUNITIES OPIOID RESPONSE (PLANNING)
Department of Health and Human Services
$160.7K
SCHOLARSHIPS FOR DISADVANTAGED STUDENTS
Department of Health and Human Services
$151.9K
SCHOLARSHIPS FOR DISADVANTAGED STUDENTS
National Endowment for the Humanities
$148.6K
INTEGRATING VOICES OF REFUGEES AND IMMIGRANTS: FACULTY AND CURRICULUM DEVELOPMENT [WE PROPOSE TO DEVELOP ADVANCED FRENCH AND SPANISH COURSES WITH HIGH-IMPACT PRACTICES AND HUMANITIES SOURCES THAT WILL PREPARE STUDENTS TO WORK WITH REFUGEES AND IMMIGRANTS?POPULATIONS IN WHICH OUR STUDENTS ARE SHOWING INTEREST. WE ALSO PROPOSE FACULTY DEVELOPMENT WORKSHOPS THAT WILL: TRAIN HUMANITIES FACULTY AND OTHERS TO INCORPORATE ORAL HISTORY PROJECTS INTO THEIR COURSES AND CREATE OPEN EDUCATIONAL RESOURCE (OER) TEXTBOOKS; EDUCATE THEM ON REFUGEES AND IMMIGRANTS IN THE U.S.; AND GUIDE THEM IN THE APPLICATION OF PLACE-BASED THEORIES. WE WILL DEVELOP A ROBUST CURRICULUM AND A COLLECTION OF PRIMARY DOCUMENTS (ORAL HISTORIES) FOR OUR SPANISH AND FRENCH COURSES THAT WILL BE USED BY MERCER FACULTY AND FREELY SHARED AS AN OER. WE WILL CLAIM A PLACE FOR THE HUMANITIES IN AN AREA OF STUDY THAT ALREADY ATTRACTS STUDENTS TO MAJORS IN GLOBAL HEALTH AND RELATED FIELDS.]
Department of Health and Human Services
$148.3K
FFAR4 AND NIGROSTRIATAL FUNCTION: A NOVEL TARGET FOR TREATMENT OF PD?
National Science Foundation
$137.1K
COLLABORATIVE RESEARCH: INTEGRATIVE ANALYSIS OF HOMINID FEEDING BIOMECHANICS
National Science Foundation
$134.2K
CREATING A GROW-YOUR-OWN PROGRAM FOR RECRUITING AND SUPPORTING COMPUTER SCIENCE TEACHER CANDIDATES IN RURAL GEORGIA -THE PROJECT AIMS TO SERVE THE NATIONAL NEED OF BUILDING CAPACITY TO PREPARE HIGH-QUALITY COMPUTER SCIENCE (CS) TEACHERS. THOUSANDS OF CS POSITIONS REMAIN UNFILLED, PARTLY DUE TO A SHORTAGE OF CS TEACHERS TO EDUCATE STUDENTS FOR FUTURE CS CAREERS. THIS PROJECT INTENDS TO RESPOND TO THE SHORTAGE BY CREATING A PATHWAY FOR HIGH SCHOOL STUDENTS TO BECOME CS TEACHERS, WITH SCHOLARSHIP FUNDS AS AN INCENTIVE. THE PROJECT TEAM PLANS TO DEVELOP A GROW-YOUR-OWN (GYO) MODEL FOR PROSPECTIVE CS TEACHERS, FOCUSED ON RURAL GEORGIA. THE AIM OF THE GYO MODEL WILL BE TO RECRUIT INTERESTED STUDENTS FROM HIGH SCHOOL WHO INTEND TO RETURN TO THEIR HOMETOWN TO TEACH CS. DUAL ENROLLMENT COURSES (FOR HIGH SCHOOL AND COLLEGE CREDIT), STIPENDS FOR TWO-YEAR COLLEGE COURSES, AND SCHOLARSHIP FUNDS FOR TWO YEARS AT MERCER WILL COMBINE TO PROVIDE A COLLEGE EDUCATION FOR PROSPECTIVE CS TEACHERS. THIS PROJECT AT MERCER UNIVERSITY INCLUDES PARTNERSHIPS WITH WIREGRASS GEORGIA TECHNICAL COLLEGE AND EIGHT RURAL GEORGIA HIGH-NEED SCHOOL DISTRICTS (CLINCH, COFFEE, DUBLIN, EVANS, JEFF DAVIS, TATTNALL, TREUTLEN, AND WHEELER). PROJECT GOALS INCLUDE IDENTIFYING AND ADDING NEW PARTNERS, DEVELOPING A GYO MODEL INCORPORATING DUAL ENROLLMENT AND COMMUNITY COLLEGE PATHWAYS; AND CREATING A RECRUITMENT PLAN. INFORMAL INTERVIEWS AND SURVEYS WITH DISTRICT LEADERS, TEACHERS, AND PROSPECTIVE CS TEACHERS WILL INFORM THE DEVELOPMENT OF A GYO MODEL THAT MEETS THE NEEDS OF THE COMMUNITY. ALTHOUGH THIS SPECIFIC PROJECT SEEKS TO ADDRESS THE SHORTAGE OF CS TEACHERS IN RURAL GEORGIA, THE PROJECT TEAM INTENDS TO SHARE EFFECTIVE STRATEGIES AT STATE AND NATIONAL CONFERENCES TO PROMOTE TRANSFER OF THE DEVELOPMENT PROCESS TO OTHER SETTINGS. AN EXTERNAL EVALUATOR AND AN ADVISORY BOARD WILL ALSO SUPPORT THE PROJECT. THIS CAPACITY BUILDING PROJECT IS SUPPORTED THROUGH THE ROBERT NOYCE TEACHER SCHOLARSHIP PROGRAM (NOYCE). THE NOYCE PROGRAM SUPPORTS TALENTED STEM UNDERGRADUATE MAJORS AND PROFESSIONALS TO BECOME EFFECTIVE K-12 STEM TEACHERS AND EXPERIENCED, EXEMPLARY K-12 TEACHERS TO BECOME STEM MASTER TEACHERS IN HIGH-NEED SCHOOL DISTRICTS. IT ALSO SUPPORTS RESEARCH ON THE EFFECTIVENESS AND RETENTION OF K-12 STEM TEACHERS IN HIGH-NEED SCHOOL DISTRICTS. THIS AWARD REFLECTS NSF'S STATUTORY MISSION AND HAS BEEN DEEMED WORTHY OF SUPPORT THROUGH EVALUATION USING THE FOUNDATION'S INTELLECTUAL MERIT AND BROADER IMPACTS REVIEW CRITERIA.- SUBAWARDS ARE NOT PLANNED FOR THIS AWARD.
National Science Foundation
$128.7K
COLLABORATIVE RESEARCH: FEEDING ONTOGENY AT THE INTERFACE OF BEHAVIOR AND MORPHOLOGY
National Science Foundation
$124.8K
BUILDING CAPACITY IN SUPPORT OF THE DEVELOPMENT OF COMPUTER SCIENCE MASTER TEACHERS FOR RURAL SOUTH GEORGIA
Department of Health and Human Services
$118.9K
LDS - PHARMACY - LOAN GRANT WITH FUNDS FOR NEW BUDGET PERIOD
National Science Foundation
$116.3K
MRI TRACK 1: ACQUISITION OF AN ULTRA-HIGH ACCURACY DIGITAL MICROSCOPE FOR ADVANCING RESEARCH AND EDUCATIONAL PROJECTS -THE ACQUISITION OF AN ULTRA-HIGH ACCURACY DIGITAL MICROSCOPE AT MERCER UNIVERSITY WILL SIGNIFICANTLY ADVANCE MULTIDISCIPLINARY RESEARCH IN DEVELOPING COATED MATERIALS WITH ANTIBACTERIAL AND ANTIFUNGAL PROPERTIES. THIS TOOL WILL ENABLE RESEARCHERS TO EVALUATE COATINGS ON VARIOUS SUBSTRATES, POTENTIALLY LEADING TO ALTERNATIVES TO TRADITIONAL ANTIBIOTICS. THE MICROSCOPE'S APPLICATIONS EXTEND TO INVESTIGATING SURFACES OF POLYMERS AND COMPOSITES USED IN MULTIPLE INDUSTRIES, AIDING IN THE DEVELOPMENT OF PROTECTIVE COATINGS TO ENHANCE MATERIAL PERFORMANCE AND LONGEVITY. IT WILL ALSO FACILITATE STUDIES OF WEAR AND EROSION, ADDRESSING CRITICAL CONCERNS IN AEROSPACE AND OIL AND GAS INDUSTRIES. THE GRANT WILL ENHANCE EXPERIMENTAL PARTICIPATION FOR FACULTY AND STUDENTS ACROSS VARIOUS ENGINEERING AND SCIENCE DISCIPLINES, PROVIDING VALUABLE TRAINING OPPORTUNITIES AND BROADENING THE PARTICIPATION OF UNDERREPRESENTED GROUPS. ADDITIONALLY, THE MICROSCOPE WILL SERVE EDUCATIONAL PURPOSES, ENRICHING THE CURRICULUM AND INTEGRATING RESEARCH WITH EDUCATION. THIS DUAL-USE APPROACH WILL PROVIDE STUDENTS WITH HANDS-ON EXPERIENCE USING CUTTING-EDGE TECHNOLOGY IN REAL-WORLD SCIENTIFIC INVESTIGATIONS, ULTIMATELY CONTRIBUTING TO ADVANCEMENTS IN NATIONAL HEALTH, ECONOMIC GROWTH, AND SOCIETAL WELFARE. THE RESEARCH ENABLED BY THIS INSTRUMENT INCLUDES EXPLORING THE BENEFITS OF USING THIN FILMS FOR ANTIBACTERIAL WATER TREATMENT AND ANTIFUNGAL ATTACHMENT TO POLYMERIC SURFACES AND SUBSEQUENT BIOFILM FORMATION. THE ULTRA-HIGH ACCURACY DIGITAL MICROSCOPE ENABLES STRUCTURES? ANALYSIS BEFORE AND AFTER THIN FILMS DEPOSITION AND AFTER EXPOSURE TO MICROBES, EXAMINING COATINGS? MORPHOLOGY AND PERFORMANCES. THIN FILMS ARE DEPOSITED ONTO SUBSTRATES USING THE DC HIGH VACUUM MAGNETRON SPUTTERING SYSTEM. THE DIGITAL MICROSCOPE IS ALSO FACILITATING STUDY OF SURFACE DEGRADATION FOR MATERIALS EXPOSED TO ACCELERATED WEATHERING CONDITIONS. IT IS SUPPORTING THE DEVELOPMENT AND OPTIMIZATION OF THIN FILMS CAPABLE OF PROTECTING POLYMERS, 3D PRINTED POLYMERS AND COMPOSITES AGAINST THE SYNERGISTIC EFFECTS OF ULTRAVIOLET RADIATION, MOISTURE AND TEMPERATURES. IT IS ENHANCING THE EXPERIMENTAL STUDY OF EROSION AND FURTHER DEVELOPMENT OF MODELS FOR PROTECTION AGAINST EROSION AND ABRASION. THE DIGITAL OPTICAL MICROSCOPY IS SUPPORTING THE FUNDAMENTAL RESEARCH BY ENSURING FAST 3D EVALUATION OF THE VOLUME LOSS AND SURFACE ROUGHNESS PERMITTING EXTENDED OPTIMIZATION STUDIES OF MATERIALS IN CONTACT. THIS AWARD REFLECTS NSF'S STATUTORY MISSION AND HAS BEEN DEEMED WORTHY OF SUPPORT THROUGH EVALUATION USING THE FOUNDATION'S INTELLECTUAL MERIT AND BROADER IMPACTS REVIEW CRITERIA.- SUBAWARDS ARE NOT PLANNED FOR THIS AWARD.
National Science Foundation
$101.4K
RIDIR COLLABORATIVE RESEARCH: BUILDING A DATABASE TO DETERMINE ENVIRONMENTAL AND FAMILIAL EFFECTS ON SOCIAL AND BIOLOGICAL FACTORS
National Aeronautics and Space Administration
$99.9K
ASSISTIVE TECHNOLOGY FOR VISUALLY IMPAIRED GLOBE PARTICIPANTS
Department of Health and Human Services
$98.6K
RURAL HEALTH NETWORK DEVELOPMENT PLANNING GRANT PROGRAM - THE SERVE HEALTH NETWORK (STRENGTHENING ESSENTIAL RESOURCES FOR VITAL AND EQUITABLE HEALTH NETWORK) PLANNING PROJECT AIMS TO ADDRESS CRITICAL HEALTH DISPARITIES IN NORTH GEORGIA'S RURAL COUNTIES OF FANNIN, GILMER, GORDON, AND POLK. THESE REGIONS, EMBLEMATIC OF NUMEROUS RURAL AREAS, GRAPPLE WITH MULTIFACETED CHALLENGES IN HEALTHCARE ACCESSIBILITY AND QUALITY OWING TO GEOGRAPHICAL ISOLATION, SOCIO-ECONOMIC FACTORS, AND A DEARTH OF HEALTHCARE PROFESSIONALS AND FACILITIES. OVER THE COURSE OF A ONE-YEAR PLANNING GRANT, LED BY PROJECT DIRECTOR, DR. ALLEN TINDOL OF MERCER UNIVERSITY SCHOOL OF MEDICINE, SERVE HEALTHCARE NETWORK (SERVE) AIMS TO ASSESS THE FEASIBILITY AND STRATEGIZE THE IMPLEMENTATION OF A GROUNDBREAKING INITIATIVE. THE FOCAL POINT OF THIS ENDEAVOR IS TO ESTABLISH A COMPREHENSIVE RURAL HEALTH NETWORK THAT HARNESSES THE CAPABILITIES OF RECOVERY COMMUNITY ORGANIZATIONS (RCOS) AS TELEHEALTH ORIGINATING SITES. BY DOING SO, THE PROJECT ENDEAVORS TO USHER IN A TRANSFORMATIVE ERA OF REMOTE ACCESS TO HEALTHCARE AND MENTAL HEALTH SERVICES FOR THE UNDERSERVED POPULATIONS IN SUBSTANCE USE RECOVERY WHO RESIDE IN THESE COUNTIES. WITH A ONE-YEAR PLANNING GRANT, SERVE WILL AIM TO ACCOMPLISH THREE MAIN FOCUS AREAS THAT ALIGN WITH THE AIMS OF THIS FUNDING OPPORTUNITY: 1. EVALUATE HEALTHCARE ACCESS IN THE TARGET COMMUNITIES BY CONDUCTING A COMPREHENSIVE COUNTY-BY-COUNTY NEEDS ASSESSMENT. IDENTIFY CRITICAL HEALTHCARE ACCESS NEEDS, EXPAND COLLABORATION WITH COMMUNITY MEMBERS AND HEALTHCARE ENTITIES, AND FORMULATE A STRATEGIC PLAN TO ADDRESS ACCESS CHALLENGES WITHIN THE SERVE HEALTHCARE NETWORK, ULTIMATELY FOSTERING A MORE RESPONSIVE AND EFFECTIVE HEALTHCARE INFRASTRUCTURE (ALIGNS WITH AIM #1: ACHIEVE EFFICIENCIES) 2. DEVELOP AN IMPLEMENTATION PLAN TO EXPAND ACCESS TO, COORDINATE, AND IMPROVE THE QUALITY OF BASIC HEALTH CARE AND MENTAL HEALTH SERVICES IN FANNIN, GILMER, GORDON, AND POLK COUNTIES. (ALIGNS WITH AIM #2: EXPAND ACCESS TO, COORDINATE, AND I MPROVE THE QUALITY OF BASIC HEALTH CARE SERVICES) 3. CREATE A PLAN TO ENHANCE THE RESILIENCE AND EFFECTIVENESS OF THE RURAL HEALTH CARE SYSTEM IN POLK, GORDON, FANNIN, AND GILMER COUNTIES THROUGH STRATEGIES, INCLUDING THE PLANNING OF A TELEHEALTH NETWORK, INNOVATIVE COMMUNITY HEALTH WORKER TRAINING PROGRAMS, AND COMMUNITY-ENGAGED INITIATIVES. (ALIGNS WITH AIM #3: STRENGTHEN THE RURAL HEALTH CARE SYSTEM) THE PROJECT'S CORE MISSION IS TO SIGNIFICANTLY IMPROVE ACCESS TO HEALTHCARE AND MENTAL HEALTH SERVICES THROUGH A SUSTAINABLE NETWORK DESIGNED TO MEET THE COMMUNITY'S SPECIFIC NEEDS. THIS NETWORK IS EXPECTED TO PROVIDE NOT ONLY ENHANCED CARE QUALITY BUT ALSO EMPLOYMENT OPPORTUNITIES, THEREBY STRENGTHENING THE OVERALL HEALTH INFRASTRUCTURE. BY EVALUATING TECHNICAL, LOGISTICAL, AND ENGAGEMENT STRATEGIES DURING THE PLANNING PHASE, SERVE WILL ENSURE THAT THE NETWORK IS WELL-SUITED TO MOVE INTO AN IMPLEMENTATION PHASE AND CREATE A PROGRAM THAT SERVES THE COMMUNITIES IN A MEANINGFUL AND VALUABLE CAPACITY. THE ULTIMATE GOAL IS TO REDUCE HEALTHCARE INEQUITIES BY EMPLOYING TELEHEALTH AND WORKFORCE DEVELOPMENT INNOVATIONS, CREATING A MORE ACCESSIBLE AND RESILIENT HEALTHCARE ENVIRONMENT IN THESE TRADITIONALLY UNDERSERVED AREAS. LEGISLATIVE AIMS: AIM #1: ACHIEVE EFFICIENCIES AIM #2: EXPAND ACCESS TO, COORDINATE, AND IMPROVE THE QUALITY OF BASIC HEALTH CARE SERVICES) AIM #3: STRENGTHEN THE RURAL HEALTH CARE SYSTEM FOCUS AREA: MERCER UNIVERSITY SCHOOL OF MEDICINE’S FOCUS AREA IS TO IMPROVE ACCESS TO HEALTH CARE FOR RURAL AND MEDICALLY UNDERSERVED PEOPLE RESIDING IN FANNIN, GILMER, GORDON, AND POLK COUNTIES. PROPOSED SERVICE REGIONS: FANNIN COUNTY, GA (FIPS 13-111) GILMER COUNTY, GA (FIPS 13-123) GORDON COUNTY, GA (FIPS 13-129) POLK COUNTY, GA (FIPS 13-233) ALL HRSA-DESIGNATED AS RURAL (ENTIRE COUNTY) FUNDING PREFERENCE: MEDICALLY UNDERSERVED AREAS HEALTHCARE PROFESSIONAL SHORTAGE AREAS
Department of Health and Human Services
$94.6K
NURSE FACULTY LOAN PROGRAM
Environmental Protection Agency
$91.9K
THIS ACTION APPROVES AN AWARD IN THE AMOUNT OF $91,886 TO THE CORPORATION OF MERCER UNIVERSITY TO INCREASE THE BLOOD LEAD TESTING RATES IN HIGH RISK
National Science Foundation
$79.5K
MRI: ACQUISITION OF A WIDE RANGE PARTICLE SPECTROMETER
Environmental Protection Agency
$75K
DESCRIPTION:THE GOAL OF THIS PROJECT IS TO EVALUATE THE ENVIRONMENTAL PERFORMANCE OF SECOND-GENERATION BIOFUELS PRODUCED VIA HYDROTHERMAL LIQUEFACTION (HTL) CONVERSION OF FOOD WASTE USING A RANGE OF EXPERIMENTAL METHODS AND LIFE-CYCLE AND COST ASSESSMENT TECHNIQUES. ACTIVITIES:THE OBJECTIVES OF THE PROJECT ARE TO: (1) CHARACTERIZE AND OPTIMIZE FOOD WASTE FEEDSTOCKS AND THEIR CORRESPONDING POST-HTL PRODUCTS (I.E., BIOCRUDE, BIOCHAR, AND AQUEOUS CO-PRODUCT (ACP)) AND (2) PERFORM LIFE-CYCLE ASSESSMENT (LCA) AND LIFE-CYCLE COST (LCC) ASSESSMENT OF HYPOTHETICAL REGIONAL COLLECTION AND CONVERSION SYSTEMS FOR BIOCRUDE AND POST-HTL PRODUCTS RECOVERED FROM FOOD WASTE STREAMS. SUBRECIPIENT:NO SUBAWARDS ARE INCLUDED IN THIS ASSISTANCE AGREEMENT.OUTCOMES:DELIVERABLES INCLUDE ANNUAL AND FINAL REPORTS. THE EXPECTED OUTCOME OF THIS PROJECT IS TO ASSESS FEASIBILITY AND SUSTAINABILITY OF WASTE-TO-ENERGY SYSTEMS VIA HTL CONVERSION AND DISSEMINATE FINDINGS FROM A FULL-SCALE LCA AND LCC ASSESSMENT MODEL. DIRECT BENEFICIARIES OF THIS PROJECT INCLUDE FOOD WASTE STREAMS, THE RENEWABLE ENERGY SECTOR, THE ENVIRONMENT, HUMAN HEALTH, AND THE GENERAL PUBLIC.
Department of Health and Human Services
$67.8K
ARRA - SCHOLARSHIPS FOR DISADVANTAGED STUDENTS
Department of Health and Human Services
$38.9K
SCHOLARSHIPS FOR DISADVANTAGED STUDENTS
Department of Health and Human Services
$35K
ALCOHOL RESEARCH CONFERENCE DAYS, 12TH ANNUAL CONFERENCE OF THE INTERNATIONAL NETWORK ON BRIEF INTERVENTION FOR ALCOHOL AND DRUGS (INEBRIA)
Department of Health and Human Services
$25.5K
ARRA - SCHOLARSHIPS FOR DISADVANTAGED STUDENTS
Department of Health and Human Services
$20.6K
DRUG RESEARCH DAY, 12TH ANNUAL CONFERENCE OF THE INTERNATIONAL NETWORK ON BRIEF INTERVENTION FOR ALCOHOL AND DRUGS (INEBRIA)
Department of Health and Human Services
$20.3K
NURSE ANESTHETIST TRAINEESHIPS
Department of Health and Human Services
$17.8K
ADVANCED EDUCATION NURSING TRAINEESHIP
Environmental Protection Agency
$15K
THIS TEAM IS DESIGNING A SYSTEM THAT USES BIOFILTRATION TECHNOLOGY AND AN IN GROUND DETENTION TANK TO TREAT GRAY WATER PRODUCED IN HOUSEHOLD'S TO BE USED FOR OUTDOOR APPLICATION, NAMELY IRRIGATION. DESIGNING A SYSTEM THAT USES THE GRAY WATER ALREADY PRODUCED IN DAILY HOUSEHOLD ACTIVITIES FOR THE USE OF IRRIGATION HAS THE CAPABILITY OF DECREASING THE DEMAND FOR TREATED WATER. THE SYSTEM'S BENEFITS COULD INCLUDE A REDUCTION OF DOMESTIC WATER CONSUMPTION, CONSERVING WATER AND ENERGY RESOURCES, AND DECREASING DEMAND OF WATER FROM NATURAL RESERVOIRS.
National Science Foundation
$13.1K
TWENTY-NINTH SOUTHEASTERN-ATLANTIC CONFERENCE ON DIFFERENTIAL EQUATIONS; MACON, GA
National Science Foundation
$12.1K
COALITION OF HISPANIC, AFRICAN AND NATIVE AMERICANS FOR THE NEXT GENERATION OF ENGINEERS AND SCIENTISTS (CHANGES) ORGANIZATIONAL WORKSHOP
National Endowment for the Arts
$8,730.7
TO SUPPORT THE DEVELOPMENT OF A NEW DOCUMENTARY THEATER PIECE ABOUT THOSE LIVING WITH METASTATIC BREAST CANCER AND THE ONLINE DISTRIBUTION OF AN ACCOMPANYING VIDEO DOCUMENTARY.
Department of Health and Human Services
$0
PCL - ALLOPATHIC MEDICINE - LOAN GRANT WITH FUNDS FOR NEW BUDGET PERIOD
National Science Foundation
$0
CONFERENCE: FUNCTIONAL LOGIC OF NEURAL CIRCUITS: DIAMONDS IN THE ROUGH (FLNDR) -NATURAL BEHAVIOR IS THE RESULT OF COMPLEX INTERACTIONS BETWEEN NEURONS, BETWEEN NEURONS AND THE BODY, AND BETWEEN THE BODY AND THE ENVIRONMENT. UNDERSTANDING THE NEURAL CIRCUITS UNDERPINNING ANIMAL BEHAVIOR, THEREFORE, INVOLVES UNRAVELLING THIS WEB OF INTERACTIONS AND HAS CAPTURED THE IMAGINATION AND EFFORTS OF BIOLOGISTS, PHYSICISTS, MATHEMATICIANS, ENGINEERS, AND ARTIFICIAL INTELLIGENCE RESEARCHERS ALIKE. THIS AWARD PROVIDES FUNDING FOR RESEARCHERS IN THESE VARIOUS DISCIPLINES TO COME TOGETHER AND FIND COMMON DIRECTION, EXCHANGE IDEAS AND INSIGHTS, AND CREATE NEW COLLABORATIONS. THE ORGANIZERS WILL PRODUCE AND LEAD A WORKSHOP ON THE FUNCTIONAL LOGIC OF NEURAL CIRCUITS. THE WORKSHOP WILL TAKE PLACE IN PUERTO RICO IN FEBRUARY 2023. THE GOAL OF THE WORKSHOP IS TO CREATE A HIGHLY INTERACTIVE ENVIRONMENT THAT FOSTERS MAXIMUM INFORMATION EXCHANGE AMONGST A DIVERSE SET OF RESEARCHERS FROM EXPERIMENTAL, COMPUTATIONAL, AND THEORETICAL NEUROSCIENCE, STRUCTURAL AND FUNCTIONAL CONNECTOMICS, GENOMICS, AND ARTIFICIAL INTELLIGENCE. TO ACCOMPLISH THIS GOAL, THE WORKSHOP INCLUDES SEVERAL PLANNED ACTIVITIES INCLUDING CHALK TALKS, PANEL DISCUSSIONS, AND RANDOM GROUP BREAKOUTS. THE WORKSHOP WILL RESULT IN A COMPREHENSIVE SUMMARY THAT WILL BE WIDELY DISSEMINATED FOR THE PURPOSE OF FOSTERING NEW COMMUNITY EFFORTS AROUND THIS CHALLENGING SCIENTIFIC PROBLEM. THIS AWARD REFLECTS NSF'S STATUTORY MISSION AND HAS BEEN DEEMED WORTHY OF SUPPORT THROUGH EVALUATION USING THE FOUNDATION'S INTELLECTUAL MERIT AND BROADER IMPACTS REVIEW CRITERIA.
National Science Foundation
$0
CAREER: EQUITY FOCUSED ELEMENTARY MATHEMATICS: CREATING VIRTUAL MATHEMATICS COMMUNITIES IN RURAL GEORGIA -ACCESS TO HIGH QUALITY STEM EDUCATION IS HIGHLY VARIABLE DEPENDING ON WHERE ONE LIVES. IN ADDITION, EARLY CAREER TEACHERS NEED SUPPORT DURING THEIR FIRST YEARS OF TEACHING TO BE SUCCESSFUL AND HELP THEM STAY IN THE PROFESSION. THIS PROJECT AIMS TO PROVIDE IN-SERVICE AND BEGINNING ELEMENTARY SCHOOL TEACHERS INCREASED OPPORTUNITIES TO REFINE THEIR MATHEMATICS TEACHING TO SUPPORT MINORITIZED YOUTH IN RACIALLY DIVERSE RURAL COMMUNITIES IN GEORGIA THAT HAVE LESS ACCESS TO ELEMENTARY MATHEMATICS SPECIALISTS. THIS PROJECT FOLLOWS AND SUPPORTS BOTH BEGINNING TEACHERS (BTS) AND ELEMENTARY MATHEMATICS COACHES (EMCS) OVER 5 YEARS TO DEVELOP AND REFINE THEIR MATHEMATICS TEACHING AND COACHING, RESPECTIVELY, USING EQUITY-BASED TOOLS TO GUIDE REFLECTION AND CONVERSATIONS ABOUT BOTH THE BTS? INSTRUCTIONAL PRACTICES AND THE EMCS? COACHING PRACTICES. THE TOOLS PROVIDE DATA TO UNCOVER BIASES AND ASPIRATIONAL PEDAGOGICAL TARGETS FOR EQUITABLE DISCOURSE AND TASK DESIGN. THE GOALS OF THE PROJECT INCLUDE: A) ESTABLISHING A VIRTUAL DISTANCE LEARNING COMMUNITY TO SUPPORT EQUITY FOCUSED ELEMENTARY MATHEMATICS COACHES ACROSS RURAL COUNTIES IN GEORGIA, B) DEVELOPING AND REFINING A FULLY ONLINE ELEMENTARY MATHEMATICS AND COACHING GRADUATE COURSEWORK SEQUENCE TO PREPARE EMCS, AND C) IMPLEMENTING AN INNOVATIVE MODEL OF UNIVERSITY SUPERVISION AND INDUCTION FOR BTS. OVER THE 5-YEAR PERIOD, TEN EMCS WILL ENGAGE IN COURSEWORK, AND BE SUPPORTED THROUGH A VIRTUAL COMMUNITY TO DEVELOP ELEMENTARY MATHEMATICS TEACHING AND LEARNING IN THEIR SCHOOLS AND DISTRICTS. THE COACHES WILL SUPPORT AT LEAST TEN BEGINNING TEACHERS TO DEVELOP EQUITABLE MATHEMATICS LEARNING COMMUNITIES AS THEY ENTER THE FIELD DURING THEIR FIRST YEARS OF TEACHING. THIS APPROACH IS IMPORTANT BECAUSE FORMALIZED INDUCTION SUPPORT IS RARE IN MOST DISTRICTS IN GEORGIA, AND TEACHERS ARE LEAVING THE FIELD IN RECORD NUMBERS BECAUSE THEY FEEL UNPREPARED. DATA SOURCES WILL INCLUDE VIDEOS OF TEACHING EPISODES, TEACHER REFLECTIONS, NARRATIVE INTERVIEWS, AND DOCUMENT ANALYSIS. THE STUDY WILL EMPLOY CASE STUDY AND NARRATIVE METHODOLOGIES IN ANALYZING THE VARIED AND RICH DATA COLLECTED WITH BTS AND EMCS. THE PROJECT?S GOAL OF PREPARING AND SUPPORTING EMCS HAS POTENTIAL TO DRAMATICALLY SHIFT THE PROFESSIONAL DEVELOPMENT OF BTS, AND TO RE-PROFESSIONALIZE TEACHER EDUCATION AND PROVIDE MORE EQUITABLE MATHEMATICS EDUCATION FOR ALL STUDENTS. THIS PROPOSED STUDY COULD SERVE AS A MODEL TO BUILD ADDITIONAL NETWORKS OF STEM COACHES ACROSS RURAL AREAS. THE AWARD IS FUNDED BY THE DISCOVERY RESEARCH PREK-12 PROGRAM (DRK-12) WHICH SEEKS TO SIGNIFICANTLY ENHANCE THE LEARNING AND TEACHING OF SCIENCE, TECHNOLOGY, ENGINEERING AND MATHEMATICS (STEM) BY PREK-12 STUDENTS AND TEACHERS, THROUGH RESEARCH AND DEVELOPMENT OF INNOVATIVE RESOURCES, MODELS AND TOOLS. PROJECTS IN THE DRK-12 PROGRAM BUILD ON FUNDAMENTAL RESEARCH IN STEM EDUCATION AND PRIOR RESEARCH AND DEVELOPMENT EFFORTS THAT PROVIDE THEORETICAL AND EMPIRICAL JUSTIFICATION FOR PROPOSED PROJECTS. THIS AWARD REFLECTS NSF'S STATUTORY MISSION AND HAS BEEN DEEMED WORTHY OF SUPPORT THROUGH EVALUATION USING THE FOUNDATION'S INTELLECTUAL MERIT AND BROADER IMPACTS REVIEW CRITERIA.
Department of Homeland Security
-$86.1K
RESEARCH ON PERSONAL AREA NETWORK (PAN) INTERFERENCE & COMPATABILITY ISSUES FOR PUBLIC SAFETY PERSONAL PROTECTIVE EQUIPMENT
Source: Federal Audit Clearinghouse (fac.gov)
Total Audits
10
Clean Audits
10
Material Weakness
No
Noncompliance Issues
No
| Year | Status | Financial Report | Federal Expenditure | Low Risk | Accepted |
|---|---|---|---|---|---|
| 2025 | Clean | Unmodified (Clean) | $196.8M | Yes | 2026-03-31 |
| 2024 | Clean | Unmodified (Clean) | $186.5M | Yes | 2025-02-28 |
| 2023 | Clean | Unmodified (Clean) | $186.6M | Yes | 2024-03-29 |
| 2022 | Clean | Unmodified (Clean) | $191.8M | Yes | 2023-01-12 |
| 2021 | Clean | Unmodified (Clean) | $196.6M | Yes | 2021-12-15 |
| 2020 | Clean | Unmodified (Clean) | $188M | Yes | 2021-03-04 |
| 2019 | Clean | Unmodified (Clean) | $176.6M | Yes | 2020-03-30 |
| 2018 | Clean | Unmodified (Clean) | $164.3M | Yes | 2019-01-06 |
| 2017 | Clean | Unmodified (Clean) | $166M | Yes | 2018-03-19 |
| 2016 | Clean | Unmodified (Clean) | $169.2M | Yes | 2017-03-22 |
Financial Report
Unmodified (Clean)
Federal Expenditure
$196.8M
Financial Report
Unmodified (Clean)
Federal Expenditure
$186.5M
Financial Report
Unmodified (Clean)
Federal Expenditure
$186.6M
Financial Report
Unmodified (Clean)
Federal Expenditure
$191.8M
Financial Report
Unmodified (Clean)
Federal Expenditure
$196.6M
Financial Report
Unmodified (Clean)
Federal Expenditure
$188M
Financial Report
Unmodified (Clean)
Federal Expenditure
$176.6M
Financial Report
Unmodified (Clean)
Federal Expenditure
$164.3M
Financial Report
Unmodified (Clean)
Federal Expenditure
$166M
Financial Report
Unmodified (Clean)
Federal Expenditure
$169.2M
Source: IRS e-Filed Form 990
No officer or director compensation data available for this organization.
This data is sourced from IRS Form 990, Part VII. It may not be available if the organization files Form 990-N (e-Postcard) or has not yet been enriched.
Source: IRS Publication 78, Auto-Revocation List & e-Postcard Data
Tax-deductible contributions: Yes
Deductibility code: PC
990-N (e-Postcard) Filing History
This organization files simplified Form 990-N (annual gross receipts ≤ $50,000).
Sources: IRS e-Filed Form 990 (XML) & ProPublica Nonprofit Explorer
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| Year | Revenue | Contributions | Expenses | Assets | Net Assets |
|---|---|---|---|---|---|
| 2023 | $434.7M | $62.4M | $415M | $1B | $661.9M |
| 2022 | $443M | $74.3M | $417M | $969.8M | $608.4M |
| 2021 | $444M | $83.2M | $389.3M | $975.5M | $629.1M |
| 2020 | $406.5M | $105.2M | $378.4M | $834M |
Sources: ProPublica Nonprofit Explorer & IRS e-File Index
| Tax Year | Form Type | Source | Documents |
|---|---|---|---|
| 2024 | 990 | IRS e-File | PDF not yet published by IRSView Filing → |
| 2023 | 990 | DataIRS e-File | PDF not yet published by IRSView Filing → |
| 2022 | 990 | DataIRS e-File |
Financial data: IRS Form 990 via ProPublica Nonprofit Explorer (Tax Year 2023)
Federal grants: USAspending.gov (live)
Organization info: IRS Business Master File · ProPublica Nonprofit Explorer
Tax-deductibility: IRS Publication 78
| $479.5M |
| 2019 | $396M | $95.9M | $370.5M | $808.7M | $456.8M |
| 2018 | $376.1M | $88.3M | $352.9M | $743.9M | $422.6M |
| 2017 | $360.6M | $86.3M | $343.4M | $733M | $383.3M |
| 2016 | $341.1M | $76.8M | $335.6M | $697.7M | $335.7M |
| 2015 | $341M | $79.6M | $325.2M | $605.8M | $342M |
| 2014 | $317.3M | $66.2M | $308.1M | $574.3M | $333.3M |
| 2013 | $297.7M | $65.8M | $289.3M | $547.2M | $295.6M |
| 2012 | $281.4M | $65.7M | $274.7M | $514.7M | $270.8M |
| 2021 | 990 | Data | PDF not yet published by IRS |
| 2020 | 990 | Data |
| 2019 | 990 | Data |
| 2018 | 990 | Data |
| 2017 | 990 | Data |
| 2016 | 990 | Data |
| 2015 | 990 | Data |
| 2014 | 990 | Data |
| 2013 | 990 | Data |
| 2012 | 990 | Data |
| 2011 | 990 | — |
| 2010 | 990 | — |
| 2009 | 990 | — |
| 2008 | 990 | — |
| 2007 | 990 | — |
| 2006 | 990 | — |
| 2005 | 990 | — |
| 2004 | 990 | — |
| 2003 | 990 | — |
| 2002 | 990 | — |
| 2001 | 990 | — |