Butler University

BUTLER UNIVERSITY HIGHER EDUCATION EMERGENCY RELIEF FUND

BUTLER UNIVERSITY HIGHER EDUCATION EMERGENCY RELIEF FUND - INSTITUTIONAL PORTION($2,979,348 HEERF II INSTITUTIONAL ALLOCATION UNDER CRRSAA SECTION 314(A)(1))

INDIANAPOLIS AS A LIVING LABORATORY: SCIENCE LEARNING FOR RESILIENT CITIES

ENGLISH LANGUAGE ACQUISITION: NATIONAL PROFESSIONAL DEVELOPMENT PROGRAM

ELUCIDATING THE MECHANISM AND CONSEQUENCES OF ABERRANT CYCLIN D1 GENE EXPRESSION

THE GROWTH OF THE GERMLINE RING CANALS DURING DROSOPHILA MELANOGASTER OOGENESIS

ENGLISH LANGUAGE ACQUISITION: NATIONAL PROFESSIONAL DEVELOPMENT PROGRAM

INVESTIGATION OF THE G PROTEIN-COUPLED RECEPTOR FSHR-1 IN MULTI-TISSUE NEUROMUSCULAR SIGNALING IN NORMAL AND OXIDATIVE STRESS CONDITIONS - PROJECT SUMMARY/ABSTRACT NEUROLOGICAL AND NEURODEGENERATIVE DISORDERS CHARACTERIZED BY IMBALANCES IN SYNAPTIC TRANSMISSION ARE OFTEN LINKED TO OXIDATIVE DAMAGE. MODIFICATION OF SYNAPTIC SIGNALING IN THE FACE OF DAMAGE IS CRITICAL FOR NERVOUS SYSTEM FUNCTION. INTER-TISSUE SIGNALING IS KEY TO STRESS-INDUCED SYNAPTIC MODULATION, BUT IS NOT FULLY UNDERSTOOD. MY LONG-TERM GOAL IS TO DETERMINE THE MOLECULAR MECHANISMS CONTROLLING SYNAPTIC TRANSMISSION IN THE PRESENCE AND ABSENCE OF OXIDATIVE STRESS. G PROTEIN-COUPLED RECEPTORS (GPCRS) ARE REGULATORS OF SYNAPTIC TRANSMISSION AND MULTI-TISSUE STRESS RESPONSES, YET THE DETAILS OF RELEVANT GPCR PATHWAYS ARE LARGELY UNKNOWN. RECENT WORK FROM MY LAB AND OTHERS IDENTIFIED ROLES FOR THE CONSERVED GPCR FSHR-1 IN REGULATING NEUROMUSCULAR SIGNALING AND OXIDATIVE STRESS RESPONSES. FSHR-1 IS THE SOLE C. ELEGANS HOMOLOG OF A FAMILY OF MAMMALIAN GLYCOPEPTIDE (GP) HORMONE RECEPTORS THAT CONTROL GONAD DEVELOPMENT AND FUNCTION; FSHR DEFICIENCY IS LINKED TO DEPRESSION AND BRAIN OXIDATIVE STRESS IN MICE. IN C. ELEGANS, INTESTINAL FSHR-1 PROMOTES ORGANISM SURVIVAL DURING INFECTION AND OXIDATIVE STRESS; NEURONAL FSHR-1 CAN CELL NON-AUTONOMOUSLY REGULATE INTESTINAL OXIDATIVE STRESS RESPONSES. MY LAB FOUND THAT FSHR-1 NULL ANIMALS HAVE NEUROMUSCULAR DEFECTS EXACERBATED BY OXIDATIVE STRESS, BUT WHERE AND HOW FSHR-1 REGULATES SYNAPTIC SIGNALING UNDER NORMAL OR STRESS CONDITIONS AND THE MECHANISMS BY WHICH FSHR-1 IS ACTIVATED ARE UNKNOWN. THE OBJECTIVE OF THIS PROPOSAL IS TO DETERMINE HOW FSHR-1 CONTROLS SIGNALING AT THE C. ELEGANS NEUROMUSCULAR JUNCTION (NMJ) VIA ACTIVITIES IN MULTIPLE CELL TYPES IN THE PRESENCE AND ABSENCE OF OXIDATIVE STRESS. MY PRELIMINARY DATA INDICATE FSHR-1 CAN ACT IN NEURONS AND THE INTESTINE TO PROMOTE MUSCLE EXCITATION. OUR DATA FURTHER INDICATE THIS EFFECT MAY BE DUE TO FSHR-1’S ABILITY TO ACT CELL NON-AUTONOMOUSLY TO PROMOTE CHOLINERGIC SYNAPTIC VESICLE RELEASE FROM MOTOR NEURONS AND SUGGEST A CANDIDATE GP LIGAND AND DOWNSTREAM SIGNALING PATHWAYS FSHR-1 MAY USE EXERT TO ITS EFFECTS AT THE NMJ. MY CENTRAL HYPOTHESIS IS THAT FSHR-1 ACTS IN A SUBSET OF NON-NMJ CELLS DOWNSTREAM OF THE -GP FLR-2 AND/OR OTHER PEPTIDE LIGANDS TO ACTIVATE PATHWAYS INVOLVING GS AND/OR THE LIPID KINASE SPHK-1 TO INDIRECTLY PROMOTE ACETYLCHOLINE RELEASE AND MUSCLE EXCITATION. AIM 1 WILL USE GENOME EDITING, FLUORESCENCE LOCALIZATION AND CALCIUM IMAGING, CELL-SPECIFIC PROTEIN DEGRADATION, AND BEHAVIOR TO DETERMINE NEURONAL AND NON-NEURONAL SITES OF FSHR-1 ACTION IN CONTROLLING NMJ FUNCTION IN NORMAL AND OXIDATIVE STRESS CONDITIONS. AIM 2 WILL USE GENETICS, IMAGING, AND BEHAVIOR TO DETERMINE IF DOWNSTREAM FSHR-1 EFFECTORS IN OTHER CONTEXTS MEDIATE FSHR-1’S EFFECTS ON NMJ ACTIVITY. AIM 3 WILL USE COMPLEMENTARY GENETIC EPISTASIS AND BIOCHEMICAL APPROACHES TO IDENTIFY FSHR-1 LIGANDS RELEVANT FOR ITS NMJ EFFECTS. THIS RESEARCH IS INNOVATIVE IN ITS USE OF A WHOLE ANIMAL MODEL TO EXPLORE INTER-TISSUE SIGNALING BY A CONSERVED GPCR REGULATING SYNAPTIC TRANSMISSION IN DIVERSE CONDITIONS. IT IS SIGNIFICANT IN DEFINING NOVEL ROLES FOR FSHR-1, WHICH CONTROLS DIVERSE PROCESSES ACROSS PHYLOGENY, AND MAY LAY GROUNDWORK FOR NEW THERAPIES FOR SYNAPTIC DYSFUNCTION AND OXIDATIVE STRESS, HALLMARKS OF AGING AND DISEASE.

COLLABORATIVE RESEARCH: ROL: REVEALING A NEW MECHANISM OF ACTION FOR EUKARYOTIC TRANSCRIPTIONAL ACTIVATION DOMAINS

CULTIVATING SCIENTIFIC LITERACY AND ACTION THROUGH PLACE-BASED EXPERIENTIAL LEARNING: EXPANDING THE USE OF A CAMPUS FARM AS AN INTERDISCIPLINARY LEARNING HUB

SCHOLARSHIPS FOR ECONOMICALLY DISADVANTAGED STUDENTS FROM INDIANAPOLIS

BEHAVIORAL HEALTH WORKFORCE EDUCATION AND TRAINING PROGRAM- AMERICAN RESCUE PLAN

MRI: ACQUISITION OF SPINNING DISK CONFOCAL FOR MULTI-DISCIPLINARY RESEARCH AND UNDERGRADUATE TEACHING AND TRAINING

INVESTIGATION OF CHROMATIN REMODELING MECHANISMS AT THE PROMOTERS OF HEAT SHOCK GENES

INVESTIGATION OF ANAPHASE PROMOTING COMPLEX FUNCTION IN SYNAPTIC TRANSMISSION

INVESTIGATION OF MYCOBACTERIAL HYDROLASES AND THEIR ROLE IN LIPOLYSIS.

CULTIVATING SCIENTIFIC LITERACY AND ACTION THROUGH PLACE: USING A CAMPUS FARM AS AN INTERDISCIPLINARY LEARNING HUB

FLOW: AN INNOVATIVE EDUCATIONAL TOOLKIT FOR RIVER AWARENESS

RUI: DUAL REGULATED CONTROL OVER THE CATALYTIC AND MEMBRANE BINDING ACTIVITY OF ACYL PROTEIN THIOESTERASES

RUI: CHIRAL DEEP EUTECTIC SOLVENTS: DEVELOPING CIRCULARLY POLARIZED LIGHT EMITTING MATERIALS -IN THIS PROJECT, FUNDED BY THE CHEMICAL STRUCTURE, DYNAMICS, AND MECHANISMS B PROGRAM OF THE CHEMISTRY DIVISION, PROFESSOR HOPKINS OF BUTLER UNIVERSITY IS STUDYING CIRCULARLY POLARIZED LIGHT EMITTING MATERIALS BASED ON DEEP EUTECTIC SOLVENTS AND LUMINESCENT LANTHANIDES. CIRCULARLY POLARIZED LIGHT EMITTING MATERIALS ARE POTENTIALLY USEFUL IN A NUMBER OF APPLICATIONS, INCLUDING QUANTUM COMPUTING, AS SECURITY LABELS, AND AS A WAY TO INCREASE THE BRIGHTNESS OF A DISPLAY. DEEP EUTECTIC SOLVENTS ARE FORMED BY MIXING TWO OR MORE COMPONENTS TO YIELD A UNIQUE SOLVENT WITH CONTROLLABLE PROPERTIES. THIS PROJECT EXPLORES THE DESIGN OF NEW DEEP EUTECTIC SOLVENTS WITH PROPERTIES THAT IMPROVE THE EFFICIENCY OF CIRCULARLY POLARIZED LIGHT EMISSION BY DISSOLVED LUMINESCENT LANTHANIDES. THE RESULTING DEEP EUTECTIC SOLVENT-LANTHANIDE COMBINATIONS ARE EXPLORED AS EMITTING LAYERS IN CIRCULARLY POLARIZED ORGANIC LIGHT EMITTING DIODES. THE RESULTS OF THIS PROJECT WILL CONTRIBUTE TO A PUBLICLY AVAILABLE DATABASE OF DEEP EUTECTIC SOLVENTS MAINTAINED BY DR. HOPKINS? RESEARCH GROUP. THIS PROJECT WILL RESULT IN TRAINING AND RESEARCH EXPERIENCES FOR UNDERGRADUATE STUDENTS. THE PROJECT WILL ENGAGE UNDERGRADUATE STUDENTS IN RESEARCH AT THE INTERFACE OF PHYSICAL, INORGANIC, AND MATERIALS CHEMISTRY. THE STUDENTS ENROLLED IN A PHYSICAL CHEMISTRY LABORATORY COURSE WILL COLLABORATE ON THE RESEARCH PROJECT, AND TOPICS RELATED TO DEEP EUTECTIC SOLVENTS AND LIGHT EMITTING MATERIALS WILL BE INCORPORATED INTO THE PHYSICAL CHEMISTRY LECTURE CURRICULUM. THE GOAL OF THIS PROJECT IS TO DEVELOP CIRCULARLY POLARIZED LIGHT EMITTING MATERIALS BASED ON CHIRAL DEEP EUTECTIC SOLVENTS (DES)/EUTECTIC MIXTURES THAT SERVE AS SOLVENTS TO LUMINESCENT LANTHANIDE COMPLEXES. IN ORDER TO ACHIEVE THE OBJECTIVE, THE PROJECT WILL 1) DEVELOP AND CHARACTERIZE BINARY AND TERNARY DES/EUTECTIC MIXTURES WITH CHIRAL COMPONENTS; AND 2) CHARACTERIZE THE PHOTO- AND ELECTROLUMINESCENT CIRCULARLY POLARIZED LUMINESCENCE (CPL) PROPERTIES OF LUMINESCENT LANTHANIDE COMPLEXES DISSOLVED IN THE DEVELOPED CHIRAL DES/EUTECTIC MIXTURES. DEEP EUTECTIC SOLVENTS/EUTECTIC MIXTURES ARE MIXTURES THAT HAVE A LOWER MELTING POINT THAN THE COMPONENTS (TWO OR MORE), AND THEIR PROPERTIES, SUCH AS CHIRAL RECOGNITION, CAN BE CONTROLLED BY CHOICE OF COMPONENTS. THIS PROJECT WILL EXPLORE THE ROLE OF BOTH CHIRAL AND ACHIRAL COMPONENTS OF BINARY AND TERNARY DES/MIXTURES IN THEIR ABILITY TO INDUCE CPL FROM DISSOLVED LUMINESCENT LANTHANIDE COMPLEXES. THE SUCCESSFUL COMBINATIONS OF CHIRAL DES + LANTHANIDE COMPLEX WILL BE INCORPORATED INTO CIRCULARLY POLARIZED ORGANIC LIGHT EMITTING DIODES (CP-OLEDS) TO DETERMINE THEIR SUITABILITY AS CIRCULARLY POLARIZED LIGHT EMITTING MATERIALS. WHEN COMPLETED, THE PROJECT WOULD PROVIDE NEW STRATEGIES TO OPTIMIZE MATERIALS THAT DISPLAY CIRCULARLY POLARIZED LUMINESCENCE. 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.

RUI: DEEP EUTECTIC SOLVENTS FOR CHIROPTICAL MATERIALS

COLLABORATIVE RESEARCH: PURSUIT: SPECIES DIVERSITY AND EVOLUTION OF PARASITIC MICROFUNGI

AN INTEGRATED SERIES OF STUDENT-DRIVEN, RESEARCH-BASED UNDERGRADUATE LABORATORY COURSES LINKING CHEMICAL BIOLOGY, BIOCHEMISTRY, AND NEUROBIOLOGY

PARTNERS IN REACHING POTENTIAL (PREP): PREPARING AN INTERDISCIPLINARY WORKFORCE FOR FAMILY ENGAGEMENT IN DEAF EDUCATION

CRII: OAC: DEVELOPMENT OF A MODULAR FRAMEWORK FOR THE MODELING OF PEPTIDE AND PROTEIN BINDING TO MEMBRANES -MEMBRANE PROTEINS BIND MEMBRANES TO SERVE THEIR BIOLOGICAL FUNCTIONS, SUCH AS RECEPTORS AND TRANSPORTERS, WHOSE FUNCTIONS ARE CRITICAL FOR HUMAN HEALTH. THEY CONSTITUTE THE TARGETS OF NEARLY HALF OF ALL APPROVED DRUGS AND THUS ARE IMPORTANT TARGETS FOR TREATING MYRIAD DISEASES. RESEARCH EFFORTS TO UNDERSTAND THESE DISEASE MECHANISMS BENEFIT FROM PREDICTING THE ACCURATE PLACEMENT OF PROTEINS IN MEMBRANES. HOWEVER, THE EXISTING COMPUTATIONAL PREDICTION METHODS TYPICALLY PERFORM AS STANDALONE APPLICATIONS, AND THEIR USE IN CONJUNCTION WITH OTHER PROTEIN MODELING TOOLS CANNOT BE AUTOMATED. TO ADDRESS THESE GAPS, THIS WORK DEVELOPS AN EFFICIENT FRAMEWORK FOR THE ACCURATE PLACEMENT OF MEMBRANE PROTEINS IN CELL MEMBRANES WHILE ENABLING INTEGRATION WITH OTHER COMPUTATIONAL TOOLS FREQUENTLY USED TO DESIGN OR ASSESS MEMBRANE PROTEIN STRUCTURE IN A MODULAR MANNER. THIS APPROACH FACILITATES THE MODELING OF PROTEINS AND PEPTIDES WITH POTENTIAL THERAPEUTIC USE, INCLUDING DEVELOPING ANTIMICROBIAL PEPTIDES AND PROTEINS SPECIFICALLY DESIGNED TO ASSUME FUNCTIONS AND THE INVESTIGATION OF PROTEIN VARIANTS THAT CAUSE VARIOUS DISEASES. THIS WORK AIMS TO DEVELOP COMPUTATIONAL TOOLS FOR MODELING PROTEIN BINDING TO MEMBRANES THAT CAN BE USED IN MULTIPLE WAYS, USING THE ROSETTA SUITE AS A PLATFORM. THE DESIGNED TOOLS CAN BE USED WITHIN OR OUTSIDE THE ROSETTA FRAMEWORK. THE INTELLECTUAL MERIT OF THIS PROJECT IS ITS APPROACH THAT OPTIMIZES THE PERFORMANCE, ROBUSTNESS, AND ACCURACY OF MEMBRANE COORDINATE PREDICTION METHODS IN A MODULAR AND FLEXIBLE MANNER. THE TOOLS DESIGNED AS PART OF THIS PROJECT WILL ENCOMPASS THE DEVELOPMENT OF A) A ROSETTA MOVER IMPLEMENTED TO THE ROSETTA C++ SOURCE CODE TO PREDICT MEMBRANE PLACEMENT OF ANY GIVEN PROTEIN OR PEPTIDE, B) AN APPLICATION OF THIS MOVER COMPATIBLE WITH THE ROSETTASCRIPTS FRAMEWORK, C) STANDALONE AND CONTAINERIZED PYTHON SCRIPTS THAT CAN BE PIPELINED WITH EXTERNAL MODELING SOFTWARE, AND D) A WEB SERVER FOR THE PREDICTION OF PROTEIN BINDING TO MEMBRANES. 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.

DEVELOPMENT OF THEMATIC MODULAR LABORATORY EXPERIENCES FOR INCORPORATING PROBLEM-BASED LEARNING INTO THE UNDERGRADUATE ANALYTICAL CHEMISTRY CURRICULU

IMPLEMENTATION OF MODERN PEDAGOGY, REACTIONS, TECHNOLOGY, AND TECHNIQUES INTO THE SYNTHETIC CURRICULUM

RUI-SYNTHESIS AND APPLICATIONS OF CYCLIC BORONIC HALF ACIDS

THE MANDAEAN BOOK OF JOHN: CRITICAL EDITION TRANSLATION AND COMMENTARY

BUSINESS AND INTERNATIONAL EDUCATION

COLLABORATIVE RESEARCH: MULTI-CONFIGURATIONAL METHODS FOR CHARGE TRANSPORT IN NANOSCALE ELECTRONICS -PROFESSORS ERIK HOY OF ROWAN UNIVERSITY AND ANDREW SAND OF BUTLER UNIVERSITY ARE SUPPORTED BY AN AWARD FROM THE CHEMICAL THEORY, MODELS AND COMPUTATIONAL METHODS (CTMC) PROGRAM IN THE DIVISION OF CHEMISTRY TO CHARACTERIZE NOVEL CHARGE TRANSPORT PROCESSES AT THE QUANTUM LEVEL. UNDERSTANDING CHARGE TRANSPORT IS VITAL TO PURSUING NEW DEVELOPMENTS IN AREAS CONSIDERED CRITICALLY IMPORTANT TO LONG-TERM NATIONAL ECONOMIC SUCCESS INCLUDING ELECTRONICS, SOLAR ENERGY, AND MATERIALS DEVELOPMENT. NANOSCALE ORGANIC ELECTRONIC DEVICES DISPLAY UNIQUE CHARGE TRANSPORT PROPERTIES THAT CAN BE USED TO DESIGN IMPROVED ELECTRONIC DEVICES (EX. TRANSISTORS, RESISTORS), BUT IT IS CHALLENGING TO DESCRIBE CHARGE TRANSPORT IN MANY OF THESE DEVICES USING EXISTING COMPUTATIONAL METHODS. THE JOINT ROWAN AND BUTLER TEAM WILL DEVELOP NEW COMPUTATIONAL TOOLS FOR GENERATING THE CHARGE TRANSPORT DATA NEEDED TO DESIGN THE NEXT GENERATION OF ELECTRONIC DEVICES BASED ON NON-CLASSICAL CHARGE TRANSPORT EFFECTS. THE DEVELOPED COMPUTATIONAL TOOLS WILL BE INCORPORATED INTO THE OPENMOLCAS SOFTWARE PACKAGE, WHICH IS WIDELY USED IN BOTH EDUCATIONAL AND RESEARCH EFFORTS. BOTH BUTLER UNIVERSITY AND ROWAN UNIVERSITY HAVE STRONG COMMITMENTS TO UNDERGRADUATE EDUCATION, AND A CORE EDUCATIONAL OUTCOME OF THIS PROJECT IS THE DEVELOPMENT OF COMPUTATIONALLY-ENGAGED UNDERGRADUATE STUDENTS FIT FOR EITHER ACADEMIC OR INDUSTRY POSITIONS. THROUGH STUDENT RECRUITMENT PARTNERSHIPS WITH MENTORSHIP PROGRAMS AND LOCAL COMMUNITY COLLEGES, THIS PROJECT PROVIDES A PATHWAY INTO RESEARCH FOR STUDENTS FROM NON-TRADITIONAL BACKGROUNDS AND UNDERREPRESENTED GROUPS IN THE COMPUTATIONAL SCIENCES. NANOSCALE ORGANIC ELECTRONIC DEVICES THAT OPERATE AT THE SINGLE-MOLECULE LEVEL ARE A KEY EXPERIMENTAL PLATFORM FOR ENHANCING THE SCIENTIFIC COMMUNITY?S UNDERSTANDING OF CHARGE TRANSPORT AT THE QUANTUM LEVEL. CREATED BY COMBINING SINGLE ORGANIC MOLECULES WITH METAL OR CARBON-BASED ELECTRODES, SINGLE-MOLECULE DEVICES HOLD THE POTENTIAL TO BE THE FOUNDATION FOR THE NEXT GENERATION OF TRANSISTORS, RESISTORS, AND SWITCHES FOR NANOSCALE ELECTRONICS. LARGE GAPS REMAIN IN OUR THEORETICAL UNDERSTANDING OF NON-CLASSICAL CHARGE TRANSPORT EFFECTS IN NANOSCALE ELECTRONICS SUCH AS THE REVERSAL OF THE EXPECTED ELECTRICAL CONDUCTANCE DECAY WITH INCREASING MOLECULAR LENGTH. A KEY REASON FOR THIS IS THE LIMITED TREATMENT OF ELECTRON-ELECTRON INTERACTIONS (ELECTRON CORRELATION) BY EXISTING TRANSPORT METHODS PARTICULARLY STRONG/MULTIREFERENCE CORRELATION. TO RESOLVE THIS, THE HOY/SAND RESEARCH TEAM WILL DEVELOP A FULLY-QUANTUM FAMILY OF MULTICONFIGURATIONAL CHARGE TRANSPORT METHODS BASED ON MULTICONFIGURATION PAIR DENSITY FUNCTIONAL THEORY (MC-PDFT) COMBINED WITH THE NON-EQUILIBRIUM GREEN?S FUNCTION FORMALISM (NEGF). KEY OBJECTIVES INCLUDE THE DEVELOPMENT OF NEW MC-PDFT-BASED EFFECTIVE HAMILTONIANS AND SELF-CONSISTENT OPTIMIZATION SCHEMES FOR MULTICONFIGURATIONAL GREEN?S FUNCTION TRANSPORT THEORIES. THE INTEGRATION OF THESE DEVELOPMENTS WITHIN AN OPEN-SOURCE MODULAR PYTHON FRAMEWORK ALLOWS FOR THE CHARACTERIZATION OF MULTIREFERENCE CORRELATION EFFECTS IN QUANTUM TRANSPORT PHENOMENA. USING THESE NEGF-MCPDFT METHODOLOGIES, THE TEAM WILL INVESTIGATE INCLUDING REVERSED CONDUCTANCE DECAY, COULOMB BLOCKADES, AND KONDO RESONANCES TO ENHANCE THE SCIENTIFIC COMMUNITY?S UNDERSTANDING OF QUANTUM CHARGE TRANSPORT PHENOMENA. 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.

22-NUSTAR22-0028 ROBING RAPID VARIABILITY IN BLACK HOLE X-RAY BINARY JETS

COLLABORATIVE RESEARCH/RUI: FACTORS THAT AFFECT THE LIKELIHOOD OF PREJUDICE CONFRONTATION

PROBING RAPID VARIABILITY IN BLACK HOLE X RAY BINARY JETS

RUI, SBP, COLLABORATIVE RESEARCH: EXPLORING THE UNIQUE EFFECTS OF SHARED PAST ADVERSITY FOR ENHANCING SOCIAL CONNECTION AND IDENTITY-SAFETY IN STEM

SELECTIVE INHIBITORS OF HUMAN HSF2

NEH ENDURING QUESTIONS COURSE ON FREEDOM

BLACK HOLE JET LAUNCHING PHYSICS TRIGGERING JWST WITH SWIFT BUTLER UNIVERSITY

NEH ENDURING QUESTIONS COURSE ON COMEDY AND THE HUMAN EXPERIENCE

PURPOSE: TO SUPPORT EDUCATIONAL PROGRAMMING AND PERFORMANCES FEATURING THE UNITED STATES NAVY BAND BRASS QUINTET IN RECOGNITION OF FREEDOM 250. 

CANADIAN NUMBER THEORY ASSOCIATION MEETING 2016

ANALYTIC METHODS OF DIOPHANTINE

CONFERENCE: EIGHTH ALGORITHMIC NUMBER THEORY SYMPOSIUM