Douglas Gould
Affiliations: | University of California, San Francisco, San Francisco, CA |
Area:
extracellular matrixWebsite:
http://vision.ucsf.edu/gould/Gouldlab/Google:
"Douglas Gould"Parents
Sign in to add mentor| Michael Walter | grad student | 2001 | University of Alberta | |
| (Analysis of the genetic basis of Axenfeld Rieger malformations.) | ||||
| Simon WM John | post-doc | 2006 | The Jackson Laboratory (Chemistry Tree) | |
BETA: Related publications
See more...
Publications
|
You can help our author matching system! If you notice any publications incorrectly attributed to this author, please sign in and mark matches as correct or incorrect. |
| Mao M, Ishikawa Y, Labelle-Dumais C, et al. (2025) A multifunction murine Col4a1 allele reveals potential gene therapy parameters for Gould syndrome. The Journal of Cell Biology. 224 |
| Labelle-Dumais C, Mazur C, Kaya S, et al. (2024) Skeletal pathology in mouse models of Gould syndrome is partially alleviated by genetically reducing TGFβ signaling. Matrix Biology : Journal of the International Society For Matrix Biology |
| Cozzitorto C, Peltz Z, Flores LM, et al. (2024) Evaluating neural crest cell migration in a Col4a1 mutant mouse model of ocular anterior segment dysgenesis. Cells & Development. 203926 |
| Mao M, Kuo YM, Yu AK, et al. (2024) TGFβ Signaling Dysregulation May Contribute to COL4A1-Related Glaucomatous Optic Nerve Damage. Investigative Ophthalmology & Visual Science. 65: 15 |
| Yamasaki E, Ali S, Sanchez Solano A, et al. (2023) Faulty TRPM4 channels underlie age-dependent cerebral vascular dysfunction in Gould syndrome. Proceedings of the National Academy of Sciences of the United States of America. 120: e2217327120 |
| Branyan K, Labelle-Dumais C, Wang X, et al. (2022) Elevated TGFβ Signaling Contributes to Cerebral Small Vessel Disease in Mouse Models of Gould Syndrome. Matrix Biology : Journal of the International Society For Matrix Biology |
| Mao M, Labelle-Dumais C, Tufa SF, et al. (2022) Elevated TGFβ signaling contributes to ocular anterior segment dysgenesis in Col4a1 mutant mice. Matrix Biology : Journal of the International Society For Matrix Biology |
| Mao M, Popli T, Jeanne M, et al. (2021) Identification of fibronectin 1 as a candidate genetic modifier in a Col4a1 mutant mouse model of Gould syndrome. Disease Models & Mechanisms. 14 |
| Mao M, Popli T, Jeanne M, et al. (2021) Identification of fibronectin 1 as a candidate genetic modifier in a mutant mouse model of Gould syndrome. Disease Models & Mechanisms |
| Ishikawa Y, Mizuno N, Holden P, et al. (2020) The novel missense mutation Met48Lys in FKBP22 changes its structure and functions. Scientific Reports. 10: 497 |