This is a revised application for continued support for a training grant in molecular genetics emphasizing vision research at Baylor College of Medicine. The goal of this proposal is to provide comprehensive training to predoctoral students and postdoctoral fellows in both molecular genetics and visual processes in preparation for careers in vision research. The total number of training faculty is 16, well distributed among full, associate, and assistant professors. All faculty maintain independent, well-funded laboratories conducting research in both genetics and visual processes. Major areas of research include the molecular genetics of human eye disease, studies of fundamental retinal processes using both the mouse and Drosophila as model organisms, phototransduction, cataract formation, lens and corneal development, and glaucoma. In this proposal, we have significantly expanded the number of faculty actively using genetic techniques to pursue vision research, including four new faculty members from the M.D. Anderson Cancer Center located immediately adjacent to Baylor College of Medicine. Indeed, the highly interactive, multi-departmental and institutional nature of our program is a key strength of our proposal. Student training comprises a full year of didactic and interactive coursework, journal clubs, and research rotations. In addition, we have created a new course entitled """"""""Molecular Genetics in Vision Research"""""""" as well as a monthly research seminar series, the """"""""Houston Eye Club,"""""""" in which graduate students and postdoctoral fellows present their work to a group about 30-40 researchers from more than a dozen vision research laboratories in Houston. Following selection of a thesis preceptor, students must pass an oral qualifying exam early in the second year of training and then take an average of four additional years to complete their thesis work. Currently, there are 132 graduate students and 72 postdoctoral fellows eligible for support in the departments associated with this training program. In the last 10 years, 13 graduate students supported by this training grant have received a Ph.D. degree and are now either in residence or postdoctoral training. As an indication of the success of this program, five students who have been supported by this grant and been awarded a Ph.D. have gone on to continue their careers in vision research or medicine

Agency
National Institute of Health (NIH)
Institute
National Eye Institute (NEI)
Type
Institutional National Research Service Award (T32)
Project #
5T32EY007102-14
Application #
6950393
Study Section
Special Emphasis Panel (ZEY1-VSN (08))
Program Officer
Hunter, Chyren
Project Start
1988-09-30
Project End
2007-09-29
Budget Start
2005-09-30
Budget End
2006-09-29
Support Year
14
Fiscal Year
2005
Total Cost
$302,586
Indirect Cost
Name
Baylor College of Medicine
Department
Pathology
Type
Schools of Medicine
DUNS #
051113330
City
Houston
State
TX
Country
United States
Zip Code
77030
Barrasso, Anthony P; Wang, Shang; Tong, Xuefei et al. (2018) Live imaging of developing mouse retinal slices. Neural Dev 13:23
Eblimit, Aiden; Zaneveld, Smriti Agrawal; Liu, Wei et al. (2018) NMNAT1 E257K variant, associated with Leber Congenital Amaurosis (LCA9), causes a mild retinal degeneration phenotype. Exp Eye Res 173:32-43
Barrasso, Anthony P; Tong, Xuefei; Poché, Ross A (2018) The mito::mKate2 mouse: A far-red fluorescent reporter mouse line for tracking mitochondrial dynamics in vivo. Genesis 56:
Agrawal, Smriti A; Burgoyne, Thomas; Eblimit, Aiden et al. (2017) REEP6 deficiency leads to retinal degeneration through disruption of ER homeostasis and protein trafficking. Hum Mol Genet 26:2667-2677
Porto, Fernanda B O; Jones, Evan M; Branch, Justin et al. (2017) Molecular Screening of 43 Brazilian Families Diagnosed with Leber Congenital Amaurosis or Early-Onset Severe Retinal Dystrophy. Genes (Basel) 8:
Galaz-Montoya, Monica; Wright, Sara J; Rodriguez, Gustavo J et al. (2017) ?2-Adrenergic receptor activation mobilizes intracellular calcium via a non-canonical cAMP-independent signaling pathway. J Biol Chem 292:9967-9974
Hull, Sarah; Arno, Gavin; Ku, Cristy A et al. (2016) Molecular and Clinical Findings in Patients With Knobloch Syndrome. JAMA Ophthalmol 134:753-62
Boone, Philip M; Yuan, Bo; Gu, Shen et al. (2016) Hutterite-type cataract maps to chromosome 6p21.32-p21.31, cosegregates with a homozygous mutation in LEMD2, and is associated with sudden cardiac death. Mol Genet Genomic Med 4:77-94
Xu, Mingchu; Gelowani, Violet; Eblimit, Aiden et al. (2015) ATF6 Is Mutated in Early Onset Photoreceptor Degeneration With Macular Involvement. Invest Ophthalmol Vis Sci 56:3889-95
Ge, Zhongqi; Bowles, Kristen; Goetz, Kerry et al. (2015) NGS-based Molecular diagnosis of 105 eyeGENE(®) probands with Retinitis Pigmentosa. Sci Rep 5:18287

Showing the most recent 10 out of 73 publications