This is an amended application for the University of Utah's Research Training in Hematology Program, a program established in 1943 by Dr. M.M. Wintrobe. Eighteen faculty members serve as research preceptors for trainees, and the faculty consists of both physician-scientists and basic scientists from the Departments of Medicine, Biochemistry, Human Genetics, Oncological Sciences, Pathology, and Pediatrics. Research groups participating in the Training Program are the Molecular Regulation of Iron and Heme Metabolism Group and the Hematopoiesis and Stem Cell Group. The special attribute of this multidisciplinary training program is the training faculty that includes both basic and clinical investigators with whom trainees will interact. The unifying element is the objective to train postdoctoral fellows and graduate students who can conduct innovative hematologic research using state of the art technology. Physician-trainees interact with basic science post- doctoral trainees and graduate students in our program, and this interaction promotes an expanded view of hematologic research for all trainees. This amended application expands our program to include newly added faculty with expertise in genetics and genomics. The application requests support for four predoctoral trainees and three postdoctoral fellows.

Public Health Relevance

Hematology has led medical sciences into an era of unprecedented advances in understanding the cellular and molecular basis of many diseases. The leading role of hematology is explained, in part, by the ease of access to blood and bone marrow cells. An expanded core of investigators trained to integrate clinical and basic science investigation is required to exploit new opportunities afforded by advances in technology, and the Hematology Research Training Program at the University of Utah is designed to train these investigators

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Institutional National Research Service Award (T32)
Project #
5T32DK007115-45
Application #
9970276
Study Section
Kidney, Urologic and Hematologic Diseases D Subcommittee (DDK)
Program Officer
Spruance, Victoria Marie
Project Start
1975-07-01
Project End
2021-06-30
Budget Start
2020-07-01
Budget End
2021-06-30
Support Year
45
Fiscal Year
2020
Total Cost
Indirect Cost
Name
University of Utah
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
009095365
City
Salt Lake City
State
UT
Country
United States
Zip Code
84112
Szaniawski, Matthew A; Spivak, Adam M; Cox, James E et al. (2018) SAMHD1 Phosphorylation Coordinates the Anti-HIV-1 Response by Diverse Interferons and Tyrosine Kinase Inhibition. MBio 9:
Wallace, Jared A; O'Connell, Ryan M (2017) MicroRNAs and acute myeloid leukemia: therapeutic implications and emerging concepts. Blood 130:1290-1301
Fidler, Trevor P; Campbell, Robert A; Funari, Trevor et al. (2017) Deletion of GLUT1 and GLUT3 Reveals Multiple Roles for Glucose Metabolism in Platelet and Megakaryocyte Function. Cell Rep 20:881-894
Nielson, Jason R; Fredrickson, Eric K; Waller, T Cameron et al. (2017) Sterol Oxidation Mediates Stress-Responsive Vms1 Translocation to Mitochondria. Mol Cell 68:673-685.e6
Bosque, Alberto; Nilson, Kyle A; Macedo, Amanda B et al. (2017) Benzotriazoles Reactivate Latent HIV-1 through Inactivation of STAT5 SUMOylation. Cell Rep 18:1324-1334
Fidler, Trevor P; Middleton, Elizabeth A; Rowley, Jesse W et al. (2017) Glucose Transporter 3 Potentiates Degranulation and Is Required for Platelet Activation. Arterioscler Thromb Vasc Biol 37:1628-1639
Wallace, Jared A; Kagele, Dominique A; Eiring, Anna M et al. (2017) miR-155 promotes FLT3-ITD-induced myeloproliferative disease through inhibition of the interferon response. Blood 129:3074-3086
Yarrington, Robert M; Goodrum, Jenna M; Stillman, David J (2016) Nucleosomes Are Essential for Proper Regulation of a Multigated Promoter in Saccharomyces cerevisiae. Genetics 202:551-63
Melber, Andrew; Na, Un; Vashisht, Ajay et al. (2016) Role of Nfu1 and Bol3 in iron-sulfur cluster transfer to mitochondrial clients. Elife 5:
Andrade, Daniel; Velinder, Matthew; Singer, Jason et al. (2016) SUMOylation Regulates Growth Factor Independence 1 in Transcriptional Control and Hematopoiesis. Mol Cell Biol 36:1438-50

Showing the most recent 10 out of 143 publications