Smith RS - Search Results

1

Essential iris atrophy, pigment dispersion, and glaucoma in DBA/2J mice.

John SW, Smith RS, Savinova OV, Hawes NL, Chang B, Turnbull D, Davisson M, Roderick TH, Heckenlively JR. John SW, et al. Among authors: smith rs. Invest Ophthalmol Vis Sci. 1998 May;39(6):951-62. Invest Ophthalmol Vis Sci. 1998. PMID: 9579474

2

Mutations in genes encoding melanosomal proteins cause pigmentary glaucoma in DBA/2J mice.

Anderson MG, Smith RS, Hawes NL, Zabaleta A, Chang B, Wiggs JL, John SW. Anderson MG, et al. Among authors: smith rs. Nat Genet. 2002 Jan;30(1):81-5. doi: 10.1038/ng794. Epub 2001 Dec 17. Nat Genet. 2002. PMID: 11743578

3

Inherited glaucoma in DBA/2J mice: pertinent disease features for studying the neurodegeneration.

Libby RT, Anderson MG, Pang IH, Robinson ZH, Savinova OV, Cosma IM, Snow A, Wilson LA, Smith RS, Clark AF, John SW. Libby RT, et al. Among authors: smith rs. Vis Neurosci. 2005 Sep-Oct;22(5):637-48. doi: 10.1017/S0952523805225130. Vis Neurosci. 2005. PMID: 16332275

4

Deficiency of SHP-1 protein-tyrosine phosphatase in "viable motheaten" mice results in retinal degeneration.

Lyons BL, Smith RS, Hurd RE, Hawes NL, Burzenski LM, Nusinowitz S, Hasham MG, Chang B, Shultz LD. Lyons BL, et al. Among authors: smith rs. Invest Ophthalmol Vis Sci. 2006 Mar;47(3):1201-9. doi: 10.1167/iovs.05-1161. Invest Ophthalmol Vis Sci. 2006. PMID: 16505059

5

Inducible nitric oxide synthase, Nos2, does not mediate optic neuropathy and retinopathy in the DBA/2J glaucoma model.

Libby RT, Howell GR, Pang IH, Savinova OV, Mehalow AK, Barter JW, Smith RS, Clark AF, John SW. Libby RT, et al. Among authors: smith rs. BMC Neurosci. 2007 Dec 19;8:108. doi: 10.1186/1471-2202-8-108. BMC Neurosci. 2007. PMID: 18093296 Free PMC article.

6

Strain-Dependent Anterior Segment Dysgenesis and Progression to Glaucoma in Col4a1 Mutant Mice.

Mao M, Smith RS, Alavi MV, Marchant JK, Cosma M, Libby RT, John SW, Gould DB. Mao M, et al. Among authors: smith rs. Invest Ophthalmol Vis Sci. 2015 Oct;56(11):6823-31. doi: 10.1167/iovs.15-17527. Invest Ophthalmol Vis Sci. 2015. PMID: 26567795 Free PMC article.

7

Corn1: a mouse model for corneal surface disease and neovascularization.

Smith RS, Hawes NL, Kuhlmann SD, Heckenlively JR, Chang B, Roderick TH, Sundberg JP. Smith RS, et al. Invest Ophthalmol Vis Sci. 1996 Feb;37(2):397-404. Invest Ophthalmol Vis Sci. 1996. PMID: 8603845

8

Interacting loci cause severe iris atrophy and glaucoma in DBA/2J mice.

Chang B, Smith RS, Hawes NL, Anderson MG, Zabaleta A, Savinova O, Roderick TH, Heckenlively JR, Davisson MT, John SW. Chang B, et al. Among authors: smith rs. Nat Genet. 1999 Apr;21(4):405-9. doi: 10.1038/7741. Nat Genet. 1999. PMID: 10192392

9

Severe ocular abnormalities in C57BL/6 but not in 129/Sv p53-deficient mice.

Ikeda S, Hawes NL, Chang B, Avery CS, Smith RS, Nishina PM. Ikeda S, et al. Among authors: smith rs. Invest Ophthalmol Vis Sci. 1999 Jul;40(8):1874-8. Invest Ophthalmol Vis Sci. 1999. PMID: 10393064

10

Mouse genetics: a tool to help unlock the mechanisms of glaucoma.

John SW, Anderson MG, Smith RS. John SW, et al. Among authors: smith rs. J Glaucoma. 1999 Dec;8(6):400-12. J Glaucoma. 1999. PMID: 10604301 Review.

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