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) | |
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Publications
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| 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 |
| Labelle-Dumais C, Schuitema V, Hayashi G, et al. (2019) COL4A1 Mutations Cause Neuromuscular Disease with Tissue-Specific Mechanistic Heterogeneity. American Journal of Human Genetics. 104: 847-860 |
| Hayashi G, Labelle-Dumais C, Gould DB. (2018) Use of 4-phenylbutyrate to define therapeutic parameters for reducing intracerebral hemorrhage and myopathy in mutant mice. Disease Models & Mechanisms |
| Protas ME, Weh E, Footz T, et al. (2017) Mutations of conserved non-coding elements of PITX2 in patients with ocular dysgenesis and developmental glaucoma. Human Molecular Genetics. 26: 3630-3638 |
| Mao M, Kiss M, Ou Y, et al. (2017) Genetic dissection of anterior segment dysgenesis caused by a Col4a1 mutation. Disease Models & Mechanisms |