Jonathan M. Skarie, Ph.D. - Publications
Affiliations: | 2008 | Medical College of Wisconsin, Milwaukee, WI, United States |
Area:
retinal developmentYear | Citation | Score | |||
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2014 | French CR, Seshadri S, Destefano AL, Fornage M, Arnold CR, Gage PJ, Skarie JM, Dobyns WB, Millen KJ, Liu T, Dietz W, Kume T, Hofker M, Emery DJ, Childs SJ, et al. Mutation of FOXC1 and PITX2 induces cerebral small-vessel disease. The Journal of Clinical Investigation. 124: 4877-81. PMID 25250569 DOI: 10.1172/Jci75109 | 0.4 | |||
2009 | Skarie JM, Link BA. FoxC1 is essential for vascular basement membrane integrity and hyaloid vessel morphogenesis. Investigative Ophthalmology & Visual Science. 50: 5026-34. PMID 19458328 DOI: 10.1167/Iovs.09-3447 | 0.522 | |||
2008 | Skarie JM, Link BA. The primary open-angle glaucoma gene WDR36 functions in ribosomal RNA processing and interacts with the p53 stress-response pathway. Human Molecular Genetics. 17: 2474-85. PMID 18469340 DOI: 10.1093/Hmg/Ddn147 | 0.516 | |||
2008 | Berry FB, Skarie JM, Mirzayans F, Fortin Y, Hudson TJ, Raymond V, Link BA, Walter MA. FOXC1 is required for cell viability and resistance to oxidative stress in the eye through the transcriptional regulation of FOXO1A. Human Molecular Genetics. 17: 490-505. PMID 17993506 DOI: 10.1093/Hmg/Ddm326 | 0.549 | |||
2006 | Tamimi Y, Skarie JM, Footz T, Berry FB, Link BA, Walter MA. FGF19 is a target for FOXC1 regulation in ciliary body-derived cells. Human Molecular Genetics. 15: 3229-40. PMID 17000708 DOI: 10.1093/Hmg/Ddl400 | 0.525 | |||
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