This program will provide integrated pre-doctoral training in the pharmacological sciences and funding for 11 students in the Division of Basic Sciences (DBS), the interdisciplinary graduate curriculum of the University of Texas Southwestern Medical Center. Graduates of the program will be well-prepared to pursue postdoctoral training or other career paths that lead to independent research programs focused on theoretical, molecular, cellular, and organismal approaches to understanding the mechanism of action of drugs, hormones, and other regulatory molecules. Recognizing the interdisciplinary nature of modern pharmacology, students will also receive instruction in biochemistry, quantitative biology, molecular and cell biology, and physiology. Training in quantitative methods, grant writing skills, journal clubs, student research seminars, and dissertation research projects will complete the training experience. Students will also receive opportunities to present their work orally or in posters at national and international meetings. All students wil be encouraged to finish their training within 5 years of matriculating. Trainees: Students with strong undergraduate training in physical and biological science who have completed the integrated first year curriculum of the DBS or the first two years of our M.D./Ph.D. program will be eligible for appointment as a trainee. Most students will be within the first two years of matriculation, but exceptions for uniquely qualified advanced students will be considered. Selection by the Steering Committee will be based on a student's academic performance, the mentor's research program, and the commitment of the student to pursue training consistent with goals of the program. Particular emphasis will be placed on candidates that are diamonds-in-the-rough and show potential beyond their didactic training credentials. Faculty: The 69 members of the training faculty come from 19 different departments, 5 different Centers, and represent 9 of the 10 interdisciplinary graduate programs of the DBS. Many students and mentors participate in the Cell Regulation graduate program of the DBS. These individuals bring a wealth of experience (including Nobel laureates and National Academy members) and provide substantial diversity in their approaches to problems of pharmacological interest. Senior, mid-level, and junior faculty are represented, and the UT Southwestern Endowed Scholars program continues to provide a yearly influx of talented new junior faculty to the program.

Public Health Relevance

The decline in early stage drug discovery research in the U.S. has resulted in a paucity of new approaches to develop therapeutic agents to treat human diseases. Nevertheless, recent technological breakthroughs and the ability to map intra- and intercellular regulatory networks in great detail have created unique opportunities to discover and characterize novel therapeutics. This program seeks to train the next generation of scientists who will make these discoveries and insure that scientific research on human health remains vibrant and at the cutting edge.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Institutional National Research Service Award (T32)
Project #
5T32GM007062-46
Application #
9948661
Study Section
NIGMS Initial Review Group (TWD)
Program Officer
Koduri, Sailaja
Project Start
1975-07-01
Project End
2021-06-30
Budget Start
2020-07-01
Budget End
2021-06-30
Support Year
46
Fiscal Year
2020
Total Cost
Indirect Cost
Name
University of Texas Sw Medical Center Dallas
Department
Pharmacology
Type
Schools of Medicine
DUNS #
800771545
City
Dallas
State
TX
Country
United States
Zip Code
75390
Cozza, Giorgio; Moro, Enrico; Black, Miles et al. (2018) The Golgi 'casein kinase' Fam20C is a genuine 'phosvitin kinase' and phosphorylates polyserine stretches devoid of the canonical consensus. FEBS J 285:4674-4683
Pendleton, Kathryn E; Park, Sung-Kyun; Hunter, Olga V et al. (2018) Balance between MAT2A intron detention and splicing is determined cotranscriptionally. RNA 24:778-786
Meng, Delong; Frank, Anderson R; Jewell, Jenna L (2018) mTOR signaling in stem and progenitor cells. Development 145:
Doxtader, Katelyn A; Wang, Ping; Scarborough, Anna M et al. (2018) Structural Basis for Regulation of METTL16, an S-Adenosylmethionine Homeostasis Factor. Mol Cell 71:1001-1011.e4
Doyle, Wayne I; Meeks, Julian P (2018) Excreted Steroids in Vertebrate Social Communication. J Neurosci 38:3377-3387
Fan, Chen; Yarravarapu, Nageswari; Chen, Hua et al. (2018) Regulation of tankyrase activity by a catalytic domain dimer interface. Biochem Biophys Res Commun 503:1780-1785
Gibbs, Zane A; Whitehurst, Angelique W (2018) Emerging Contributions of Cancer/Testis Antigens to Neoplastic Behaviors. Trends Cancer 4:701-712
Pendleton, Kathryn E; Chen, Beibei; Liu, Kuanqing et al. (2017) The U6 snRNA m6A Methyltransferase METTL16 Regulates SAM Synthetase Intron Retention. Cell 169:824-835.e14
Nguyen, Thu P; Frank, Anderson R; Jewell, Jenna L (2017) Amino acid and small GTPase regulation of mTORC1. Cell Logist 7:e1378794
Elkin, Sarah R; Lakoduk, Ashley M; Schmid, Sandra L (2016) Endocytic pathways and endosomal trafficking: a primer. Wien Med Wochenschr 166:196-204

Showing the most recent 10 out of 178 publications