This is a revised application for a renewal of the Baylor College of Medicine (BCM) Hematology Training Grant that has been successfully running for 5 years and has trained, or is training, 23 young investigators, 5 of whom are from under-represented minorities. These trainees have published a total of 65 papers directly related to their hematology training. All of our trainees have advanced substantially in their biomedical research careers, and one has become a tenured Associate Professor at BCM, and four others have junior faculty positions. The overall goal of the BCM Hematology Training Program (HTP) supported through this Grant is to foster and strengthen the research base for trainees in basic and clinical research disciplines of Hematology. Training is provided to researchers in both adult and pediatric hematology who include MD, MD/PhD and PhD trainees. The BCM HTP provides its trainees with the mentorship, research skills and experience to ultimately become productive and successful investigators in the field. The program is structured to ensure close mentorship from accomplished senior researchers at Baylor College of Medicine, and to support junior faculty to develop their own mentorship skills. The 31 faculty mentors participating in the HTP have vast teaching and training experience and share a sincere commitment to train young physician scientists in hematology research. Their expertise covers a wide range of hematology research areas including stem cell biology, hemoglobin function, iron metabolism, thrombosis, neutrophil function, myeloid cell differentiation, stem cell transplantation and cell and gene therapy. Important components of the BCM HTP are a structured training scheme involving mentored research, a didactic program, and preparation for grant writing. The PI and Co-Directors, Margaret Goodell, David Poplack, and Martha Mims have a history of close productive interaction with each other and a strong record of past trainees, assuring a close interaction and integration of basic research with clinical adult and pediatric hematology programs. Renewal of the Hematology Training Program will ensure continued training of outstanding physician-scientists in hematology at BCM.
The goal of this program is to train young scientists and clinicians to conduct research in the area of hematology (the study of blood). There are many disorders that affect the blood, and because blood is critical to life, it is essential to keep improving our understanding of blood cells, and what goes awry with disease. Funding from this grant will help train the next generation of researchers to continue to move this crucial field forward in both basic research, and in applying our new findings to the treatment of patients.
|Yang, Liubin; Rodriguez, Benjamin; Mayle, Allison et al. (2016) DNMT3A Loss Drives Enhancer Hypomethylation in FLT3-ITD-Associated Leukemias. Cancer Cell 29:922-34|
|Matatall, Katie A; Jeong, Mira; Chen, Siyi et al. (2016) Chronic Infection Depletes Hematopoietic Stem Cells through Stress-Induced Terminal Differentiation. Cell Rep 17:2584-2595|
|Rajagopal, Abbhirami; Homan, Erica P; Joeng, Kyu Sang et al. (2016) Restoration of the serum level of SERPINF1 does not correct the bone phenotype in Serpinf1 null mice. Mol Genet Metab 117:378-82|
|Eckstein, Olive S; Wang, Linghua; Punia, Jyotinder N et al. (2016) Mixed-phenotype acute leukemia (MPAL) exhibits frequent mutations in DNMT3A and activated signaling genes. Exp Hematol 44:740-4|
|Ho, Shiuh-Rong; Lee, Yu-Ju; Lin, Weei-Chin (2015) Regulation of RNF144A E3 Ubiquitin Ligase Activity by Self-association through Its Transmembrane Domain. J Biol Chem 290:23026-38|
|Cullen, Sean M; Goodell, Margaret A (2015) Dynamic DNA methylation discovered during HSC differentiation. Cell Cycle 14:693-4|
|Arasaratnam, Reuben J; Leen, Ann M (2015) Adoptive T cell therapy for the treatment of viral infections. Ann Transl Med 3:278|
|Hudson, David M; Joeng, Kyu Sang; Werther, Rachel et al. (2015) Post-translationally abnormal collagens of prolyl 3-hydroxylase-2 null mice offer a pathobiological mechanism for the high myopia linked to human LEPREL1 mutations. J Biol Chem 290:8613-22|
|Arber, Caroline; Feng, Xiang; Abhyankar, Harshal et al. (2015) Survivin-specific T cell receptor targets tumor but not T cells. J Clin Invest 125:157-68|
|Chen, Shan; Grover, Monica; Sibai, Tarek et al. (2015) Losartan increases bone mass and accelerates chondrocyte hypertrophy in developing skeleton. Mol Genet Metab 115:53-60|
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