Sundin O - Search Results

1

A spontaneous mutation affects programmed cell death during development of the rat eye.

Sinha D, Hose S, Zhang C, Neal R, Ghosh M, O'Brien TP, Sundin O, Goldberg MF, Robison WG Jr, Russell P, Lo WK, Samuel Zigler J Jr. Sinha D, et al. Among authors: o brien tp, sundin o. Exp Eye Res. 2005 Mar;80(3):323-35. doi: 10.1016/j.exer.2004.09.014. Exp Eye Res. 2005. PMID: 15721615

2

betaA3/A1-crystallin in astroglial cells regulates retinal vascular remodeling during development.

Sinha D, Klise A, Sergeev Y, Hose S, Bhutto IA, Hackler L Jr, Malpic-Llanos T, Samtani S, Grebe R, Goldberg MF, Hejtmancik JF, Nath A, Zack DJ, Fariss RN, McLeod DS, Sundin O, Broman KW, Lutty GA, Zigler JS Jr. Sinha D, et al. Among authors: sundin o. Mol Cell Neurosci. 2008 Jan;37(1):85-95. doi: 10.1016/j.mcn.2007.08.016. Epub 2007 Aug 31. Mol Cell Neurosci. 2008. PMID: 17931883 Free PMC article.

3

A Spontaneous Missense Mutation in Branched Chain Keto Acid Dehydrogenase Kinase in the Rat Affects Both the Central and Peripheral Nervous Systems.

Zigler JS Jr, Hodgkinson CA, Wright M, Klise A, Sundin O, Broman KW, Hejtmancik F, Huang H, Patek B, Sergeev Y, Hose S, Brayton C, Xaiodong J, Vasquez D, Maragakis N, Mori S, Goldman D, Hoke A, Sinha D. Zigler JS Jr, et al. Among authors: sundin o. PLoS One. 2016 Jul 29;11(7):e0160447. doi: 10.1371/journal.pone.0160447. eCollection 2016. PLoS One. 2016. PMID: 27472223 Free PMC article.

4

Fuchs corneal dystrophy: aberrant collagen distribution in an L450W mutant of the COL8A2 gene.

Gottsch JD, Zhang C, Sundin OH, Bell WR, Stark WJ, Green WR. Gottsch JD, et al. Invest Ophthalmol Vis Sci. 2005 Dec;46(12):4504-11. doi: 10.1167/iovs.05-0497. Invest Ophthalmol Vis Sci. 2005. PMID: 16303941

5

Immunohistochemistry and electron microscopy of early-onset fuchs corneal dystrophy in three cases with the same L450W COL8A2 mutation.

Zhang C, Bell WR, Sundin OH, De La Cruz Z, Stark WJ, Green WR, Gottsch JD. Zhang C, et al. Trans Am Ophthalmol Soc. 2006;104:85-97. Trans Am Ophthalmol Soc. 2006. PMID: 17471329 Free PMC article.

6

Redefining papillorenal syndrome: an underdiagnosed cause of ocular and renal morbidity.

Parsa CF, Silva ED, Sundin OH, Goldberg MF, De Jong MR, Sunness JS, Zeimer R, Hunter DG. Parsa CF, et al. Among authors: sundin oh. Ophthalmology. 2001 Apr;108(4):738-49. doi: 10.1016/s0161-6420(00)00661-8. Ophthalmology. 2001. PMID: 11297491

7

A CRX null mutation is associated with both Leber congenital amaurosis and a normal ocular phenotype.

Silva E, Yang JM, Li Y, Dharmaraj S, Sundin OH, Maumenee IH. Silva E, et al. Among authors: sundin oh. Invest Ophthalmol Vis Sci. 2000 Jul;41(8):2076-9. Invest Ophthalmol Vis Sci. 2000. PMID: 10892846

8

Sequence and location of SIX3, a homeobox gene expressed in the human eye.

Leppert GS, Yang JM, Sundin OH. Leppert GS, et al. Among authors: sundin oh. Ophthalmic Genet. 1999 Mar;20(1):7-21. doi: 10.1076/opge.20.1.7.2298. Ophthalmic Genet. 1999. PMID: 10415461

9

Developmental basis of nanophthalmos: MFRP Is required for both prenatal ocular growth and postnatal emmetropization.

Sundin OH, Dharmaraj S, Bhutto IA, Hasegawa T, McLeod DS, Merges CA, Silval ED, Maumenee IH, Lutty GA. Sundin OH, et al. Ophthalmic Genet. 2008 Mar;29(1):1-9. doi: 10.1080/13816810701651241. Ophthalmic Genet. 2008. PMID: 18363166 Free PMC article.

10

Extreme hyperopia is the result of null mutations in MFRP, which encodes a Frizzled-related protein.

Sundin OH, Leppert GS, Silva ED, Yang JM, Dharmaraj S, Maumenee IH, Santos LC, Parsa CF, Traboulsi EI, Broman KW, Dibernardo C, Sunness JS, Toy J, Weinberg EM. Sundin OH, et al. Proc Natl Acad Sci U S A. 2005 Jul 5;102(27):9553-8. doi: 10.1073/pnas.0501451102. Epub 2005 Jun 23. Proc Natl Acad Sci U S A. 2005. PMID: 15976030 Free PMC article.

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