Thomas M. Glaser
Affiliations: | University of Michigan, Ann Arbor, Ann Arbor, MI | ||
| University of California, Davis, Davis, CA |
Area:
Genetics, Neuroscience Biology, OphthalmologyGoogle:
"Thomas Glaser"Mean distance: 21373.2
Children
Sign in to add trainee| Kristen L. Coulter | grad student | 2004 | University of Michigan |
| Joseph A. Brzezinski | grad student | 2005 | University of Michigan |
| Edward R. Oliver | grad student | 2005 | University of Michigan |
| Sara M. Saul | grad student | 2007 | University of Michigan |
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Publications
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| Shao A, Lopez AJ, Chen J, et al. (2022) Arap1 loss causes retinal pigment epithelium phagocytic dysfunction and subsequent photoreceptor death. Disease Models & Mechanisms |
| Davis ES, Voss G, Miesfeld JB, et al. (2020) The rax homeobox gene is mutated in the eyeless axolotl, Ambystoma mexicanum Developmental Dynamics |
| Miesfeld JB, Ghiasvand NM, Marsh-Armstrong B, et al. (2020) The remote enhancer provides transcriptional robustness during retinal ganglion cell development. Proceedings of the National Academy of Sciences of the United States of America |
| Kwon YS, Tham A, Lopez AJ, et al. (2019) Cytoglobin deficiency potentiates Crb1-mediated retinal degeneration in rd8 mice. Developmental Biology |
| Lam PT, Padula SL, Hoang TV, et al. (2019) Considerations for the use of Cre recombinase for conditional gene deletion in the mouse lens. Human Genomics. 13: 10 |
| Kaukonen M, Woods S, Ahonen S, et al. (2018) Maternal Inheritance of a Recessive RBP4 Defect in Canine Congenital Eye Disease. Cell Reports. 23: 2643-2652 |
| Miesfeld JB, Glaser T, Brown NL. (2017) The dynamics of native Atoh7 protein expression during mouse retinal histogenesis, revealed with a new antibody. Gene Expression Patterns : Gep. 27: 114-121 |
| O'Sullivan ML, Puñal VM, Kerstein PC, et al. (2017) Astrocytes follow ganglion cell axons to establish an angiogenic template during retinal development. Glia |
| Moshiri A, Humpal D, Leonard BC, et al. (2017) Arap1 Deficiency Causes Photoreceptor Degeneration in Mice. Investigative Ophthalmology & Visual Science. 58: 1709-1718 |
| Chou CM, Nelson C, Tarlé SA, et al. (2015) Biochemical Basis for Dominant Inheritance, Variable Penetrance, and Maternal Effects in RBP4 Congenital Eye Disease. Cell. 161: 634-46 |