ThemissionoftheCBItrainingprogramattheUniversityofMaryland,Baltimore County(UMBC)istoprovidetraineeswithcuttingedgeresearchopportunitiesandhandson,cross-disciplinary trainingacrossnotonlydiscipline,butdepartmentallines.UMBCisaleaderinpromotingdiversitywithinscience, technology,engineering,andmathematics(STEM)fieldsatboththeundergraduateandgraduatelevelsandthe CBIprogramhashadsignificantsuccessinproducingstrongandsuccessfulPhDstudentsthathavegoneonto excellentpositionsinacademia,biotechandpharmaceuticalcompanies,governmentagenciesandpatentlaw. UMBC?s CBI program has four participating programs: UMBC?s Department of Chemistry & Biochemistry, the Biological Sciences and Molecular and Cellular Biology programs, and UMB?s Pharmaceutical Sciences, The CBIprogramwasinitiallyfundedin2004with15studentsandhasgrownsignificantlysincethattime.Currently thereare48studentsparticipatingintheprogram-32secondyearandbeyondfullmembers,and16firstyear students.Ofthese,43areTGEandtwelvearefromunderrepresented(UR)groups.Fivestudents(4arefrom UR groups) are currently supported by the NIH training grant, however all of the full members (2nd year and beyond) participate in the same programmatic requirements as those supported on the grant. The students selectedtobesupportedontheNIHgrantaretypicallyintheir3rdyearandbeyondtoaideinhavingmoretime to make progress on their cross training. There are also currently 43 participating faculty from the three Departments. The CBI program requirements include doing (i) hands on cross disciplinary research in a collaborator?s laboratory that gives added value to the students? dissertation research, (ii) taking an upper level course in anotherdiscipline,and(iii)presentingatnationalandinternationalmeetingsinadditionto(iv)participatinginthe weekly course, CHEM 715 ?Issues at the Chemistry Biology Interface?. Because the students who are not supportedontheCBIgrantstillhavetodothesamerequirementsastheNIH-supportedFellows,thePDhas leveragedthesignificantprogrammaticsupportprovidedbythethreedepartments,theDeanofUMBC?sCollege ofScienceandMathematics,UMBC?sVicePresidentforResearchandUMBC?sProvost,totaling$100K.This providestravelandsuppliesmoneyforthestudentstopresenttheirresearchatconferences,aswellastouse thefundsfortheircrosstraining.Insummary,theCBIprogramplanstocontinuetoprovideameaningfultraining experienceforalargecohortofstrongstudentstoincreasethedepth,breadthanddiversityofthebiomedical workforce.

Public Health Relevance

ThemissionoftheCBItrainingprogramatUMBCandUMBistoprovidePhDseekingtrainees withcuttingedgeresearchopportunitiesandhandson,cross-disciplinarytrainingacrossnot onlydiscipline,butdepartmentallines,inanumberofhealth-anddisease-relatedareas.The48 participatingstudentsand43facultycomefromtheChemistry&Biochemistry,Biology, MolecularandCellularBiologyandPharmaceuticalSciencesprogramsandareinvolvedin manydifferentareasofresearch.Someofthekeytrainingcomponentsinvolvehands-on,cross disciplinaryresearch,takingacourseinanotherdisciplineandpresentingtheirresearchat nationalandinternationalconferences,allactivitiesthathelpleadtostronger,morecompetitive scientistsforthebiomedicalworkforce.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Institutional National Research Service Award (T32)
Project #
2T32GM066706-16
Application #
9572658
Study Section
NIGMS Initial Review Group (TWD)
Program Officer
Fabian, Miles
Project Start
2004-07-01
Project End
2024-06-30
Budget Start
2019-07-01
Budget End
2020-06-30
Support Year
16
Fiscal Year
2019
Total Cost
Indirect Cost
Name
University of Maryland Balt CO Campus
Department
Chemistry
Type
Schools of Arts and Sciences
DUNS #
061364808
City
Baltimore
State
MD
Country
United States
Zip Code
21250
Cawrse, Brian M; Lapidus, Rena S; Cooper, Brandon et al. (2018) Anticancer Properties of Halogenated Pyrrolo[3,2-d]pyrimidines with Decreased Toxicity via N5 Substitution. ChemMedChem 13:178-185
Heinzl, Geoffrey A; Huang, Weiliang; Robinson, Elizabeth et al. (2018) The Asp99-Arg188 salt bridge of the Pseudomonas aeruginosa HemO is critical in allowing conformational flexibility during catalysis. J Biol Inorg Chem 23:1057-1070
Childers, Kenneth C; Garcin, Elsa D (2018) Structure/function of the soluble guanylyl cyclase catalytic domain. Nitric Oxide 77:53-64
Melendez, Johan H; Hardick, Justin; Barnes, Mathilda et al. (2018) Molecular Characterization of Markers Associated With Antimicrobial Resistance in Neisseria gonorrhoeae Identified From Residual Clinical Samples. Sex Transm Dis 45:312-315
Shimberg, Geoffrey D; Pritts, Jordan D; Michel, Sarah L J (2018) Iron-Sulfur Clusters in Zinc Finger Proteins. Methods Enzymol 599:101-137
Yates, Mary K; Seley-Radtke, Katherine L (2018) The evolution of antiviral nucleoside analogues: A review for chemists and non-chemists. Part II: Complex modifications to the nucleoside scaffold. Antiviral Res 162:5-21
Knoblauch, Rachael; Bui, Brian; Raza, Ammar et al. (2018) Heavy carbon nanodots: a new phosphorescent carbon nanostructure. Phys Chem Chem Phys 20:15518-15527
Sestok, Alexandrea E; Linkous, Richard O; Smith, Aaron T (2018) Toward a mechanistic understanding of Feo-mediated ferrous iron uptake. Metallomics 10:887-898
Valdez-Lopez, Juan C; Donohue, Mary W; Bok, Michael J et al. (2018) Sequence, Structure, and Expression of Opsins in the Monochromatic Stomatopod Squilla empusa. Integr Comp Biol 58:386-397
Hedrich, William D; Fandy, Tamer E; Ashour, Hossam M et al. (2018) Antibody-Drug Conjugates: Pharmacokinetic/Pharmacodynamic Modeling, Preclinical Characterization, Clinical Studies, and Lessons Learned. Clin Pharmacokinet 57:687-703

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