Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Institutional National Research Service Award (T32)
Project #
5T32GM008307-15
Application #
6756427
Study Section
National Institute of General Medical Sciences Initial Review Group (BRT)
Program Officer
Rhoades, Marcus M
Project Start
1990-07-01
Project End
2006-06-30
Budget Start
2004-07-01
Budget End
2006-06-30
Support Year
15
Fiscal Year
2004
Total Cost
$186,623
Indirect Cost
Name
Baylor College of Medicine
Department
Genetics
Type
Schools of Medicine
DUNS #
051113330
City
Houston
State
TX
Country
United States
Zip Code
77030
Davis, Shaun M; Thomas, Amanda L; Liu, Lingzhi et al. (2018) Isolation of Aggressive Behavior Mutants in Drosophila Using a Screen for Wing Damage. Genetics 208:273-282
Chapple, Richard H; Tseng, Yu-Jung; Hu, Tianyuan et al. (2018) Lineage tracing of murine adult hematopoietic stem cells reveals active contribution to steady-state hematopoiesis. Blood Adv 2:1220-1228
White, Janson J; Mazzeu, Juliana F; Coban-Akdemir, Zeynep et al. (2018) WNT Signaling Perturbations Underlie the Genetic Heterogeneity of Robinow Syndrome. Am J Hum Genet 102:27-43
Wei, Christina; Stock, Lauren; Valanejad, Leila et al. (2018) Correction of GSK3? at young age prevents muscle pathology in mice with myotonic dystrophy type 1. FASEB J 32:2073-2085
Coban-Akdemir, Zeynep; White, Janson J; Song, Xiaofei et al. (2018) Identifying Genes Whose Mutant Transcripts Cause Dominant Disease Traits by Potential Gain-of-Function Alleles. Am J Hum Genet 103:171-187
Emerson, Charlene H; Lopez, Christopher R; Ribes-Zamora, Albert et al. (2018) Ku DNA End-Binding Activity Promotes Repair Fidelity and Influences End-Processing During Nonhomologous End-Joining in Saccharomyces cerevisiae. Genetics 209:115-128
Jordan, Valerie K; Beck, Tyler F; Hernandez-Garcia, Andres et al. (2018) The role of FREM2 and FRAS1 in the development of congenital diaphragmatic hernia. Hum Mol Genet 27:2064-2075
Li, Huajin; Jones, Evan M; Li, Hui et al. (2018) Clinical and genetic features of eight Chinese autosomal-dominant optic atrophy pedigrees with six novel OPA1 pathogenic variants. Ophthalmic Genet 39:569-576
Gillentine, Madelyn A; Lozoya, Ricardo; Yin, Jiani et al. (2018) CHRNA7 copy number gains are enriched in adolescents with major depressive and anxiety disorders. J Affect Disord 239:247-252
Choi, Byung-Kwon; Dayaram, Tajhal; Parikh, Neha et al. (2018) Literature-based automated discovery of tumor suppressor p53 phosphorylation and inhibition by NEK2. Proc Natl Acad Sci U S A 115:10666-10671

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