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ZFIN ID:
ZDB-PERS-090121-5
Skarie, Jonathan M.
Email:
jskarie@mcw.edu
URL:
Affiliation:
Link Lab
Address:
Department of Cell Biology, Neurobiology, and Anatomy Medical College of Wisconsin 8701 Watertown Plank Road Milwaukee, WI 53226-0509 USA
Country:
United States
Phone:
414-456-8509
Fax:
ORCID ID:
BIOGRAPHY AND RESEARCH INTERESTS
PUBLICATIONS
French, C.R., Seshadri, S., Destefano, A.L., Fornage, M., Arnold, C.R., Gage, P.J., Skarie, J.M., Dobyns, W.B., Millen, K.J., Liu, T., Dietz, W., Kume, T., Hofker, M., Emery, D.J., Childs, S.J., Waskiewicz, A.J., Lehmann, O.J. (2014) Mutation of FOXC1 and PITX2 induces cerebral small-vessel disease. J. Clin. Invest.. 124(11):4877-81
Skarie, J.M., and Link, B.A. (2009) FoxC1 is essential for vascular basement membrane integrity and hyaloid vessel morphogenesis. Investigative ophthalmology & visual science. 50(11):5026-5034
Skarie, J.M., and Link, B.A. (2008) The Primary open-angle glaucoma gene WDR36 functions in ribosomal RNA processing and interacts with the p53 stress–response pathway. Human molecular genetics. 17(16):2474-2485
Berry, F.B., Skarie, J.M., Mirzayans, F., Fortin, Y., Hudson, T.J., Raymond, V., Link, B.A., and Walter, M.A. (2008) FOXC1 is required for cell viability and resistance to oxidative stress in the eye through the transcriptional regulation of FOXO1A. Human molecular genetics. 17(4):490-505
Skarie, J.M. (2008) Utilization of the zebrafish to examine the function of genes associated with glaucoma. Ph.D. Thesis. :273p
Tamimi, Y., Skarie, J.M., Footz, T., Berry, F.B., Link, B.A., and Walter, M.A. (2006) FGF19 is a target for FOXC1 regulation in ciliary body derived cells. Human molecular genetics. 15(21):3229-3240
NON-ZEBRAFISH PUBLICATIONS
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