Positions
- Associate Professor
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Integrative Physiology
91国产视频
Houston, TX, US
- Member
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Dan L Duncan Comprehensive Cancer Center
91国产视频
Houston, Texas, United States
Addresses
- BCM-Ben Taub Research Center (Lab)
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Room: T440 (Lab) T424 (Office)
Houston, TX, 77030
United States
Education
- BS from The University of New Orleans
- 07/2001 - New Orleans, Louisiana, United States
- PhD from 91国产视频
- 07/2007 - Houston, Texas, United States
- Postdoctoral Fellowship at 91国产视频
- 07/2012 - Houston, Texas, United States
Professional Interests
- Regenerative Medicine
- Vision Sciences
- Mouse Molecular Genetics
- Developmental Biology
Professional Statement
One of my lab's long-term goals is to elucidate the transcriptional and epigenetic mechanisms regulating retinal progenitor cell proliferation and differentiation, leading to new therapeutic interventions to restore sight and treat cancers such as retinoblastoma. Toward that end, projects aimed at characterizing mouse mutants suffering from defects in retinogenesis are ongoing. One specific aspect of our research is to determine precisely how mitochondrial activity and other bioenergetic pathways interface with cell cycle progression during development. Additionally, we aim to identify new strategies to promote retinal regeneration in response to photoreceptor damage. Here, we are interested in determining whether the mouse retina retains latent regenerative potential akin to other vertebrates such as the zebrafish and whether we can genetically "re-awaken" that potential to restore sight.
Our second focus is on the generation and characterization of novel mouse models recapitulating human craniofacial and neurodevelopmental birth defects. Recently, we have uncovered a previously unknown transcription factor network that is responsible for development of the neural crest-derived craniofacial skeleton.
In the lab, we employ a multi-disciplinary approach utilizing genetic loss- and gain-of-function experiments, molecular biology and live retinal confocal microscopy.
Our second focus is on the generation and characterization of novel mouse models recapitulating human craniofacial and neurodevelopmental birth defects. Recently, we have uncovered a previously unknown transcription factor network that is responsible for development of the neural crest-derived craniofacial skeleton.
In the lab, we employ a multi-disciplinary approach utilizing genetic loss- and gain-of-function experiments, molecular biology and live retinal confocal microscopy.
Selected Publications
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Martin JF, Poch茅 RA.. " " Development. 2019 Dec 2; 146 (23)
Pubmed PMID: . -
Rueda EM, Hall BM, Hill MC, Swinton PG, Tong X, Martin JF, Poch茅 RA. " " Cell Reports. 2019 May 7; 27 (6) : 1637-1649.
Pubmed PMID: . -
Barrasso AP, Wang S, Tong X, Christiansen AE, Larina IV, Poch茅 RA. " " Neural Dev.. 2018 Sep 15; 13
Pubmed PMID: . -
Barrasso AP, Tong X, Poch茅 RA.. " " Genesis. 2018 Dec 15;
Pubmed PMID: .
Funding
-
鈥淩onin (Thap11) in Neural Crest Cell Development鈥
#R01 DE028298 - (07/15/2019 - 04/30/2024)
- NIH/NIDCR
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鈥淗ippo Pathway Regulation of M眉ller Glial Cell-mediated Retinal Regeneration鈥
- (09/01/2019 - 06/30/2023)
- NIH/NEI
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鈥淭ranscriptional Regulation of Retinal Mitochondrial Function and Cell Cycle鈥
- (12/01/2014 - 11/30/2020)
- NIH/NEI
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鈥淩eawakening the Regenerative Potential of Mammalian M眉ller Glial Cells鈥
- (07/01/2018 - 06/30/2021)
- Bright Focus Foundation
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