Smith RS - Search Results

1

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

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

Col4a1 mutation causes endoplasmic reticulum stress and genetically modifiable ocular dysgenesis.

Gould DB, Marchant JK, Savinova OV, Smith RS, John SW. Gould DB, et al. Among authors: smith rs. Hum Mol Genet. 2007 Apr 1;16(7):798-807. doi: 10.1093/hmg/ddm024. Epub 2007 Feb 22. Hum Mol Genet. 2007. PMID: 17317786

5

Absence of glaucoma in DBA/2J mice homozygous for wild-type versions of Gpnmb and Tyrp1.

Howell GR, Libby RT, Marchant JK, Wilson LA, Cosma IM, Smith RS, Anderson MG, John SW. Howell GR, et al. Among authors: smith rs. BMC Genet. 2007 Jul 3;8:45. doi: 10.1186/1471-2156-8-45. BMC Genet. 2007. PMID: 17608931 Free PMC article.

6

Determining immune components necessary for progression of pigment dispersing disease to glaucoma in DBA/2J mice.

Nair KS, Barbay J, Smith RS, Masli S, John SW. Nair KS, et al. Among authors: smith rs. BMC Genet. 2014 Mar 28;15:42. doi: 10.1186/1471-2156-15-42. BMC Genet. 2014. PMID: 24678736 Free PMC article.

7

Chromosomal localization of a new mouse lens opacity gene (lop18).

Chang B, Hawes NL, Smith RS, Heckenlively JR, Davisson MT, Roderick TH. Chang B, et al. Among authors: smith rs. Genomics. 1996 Aug 15;36(1):171-3. doi: 10.1006/geno.1996.0439. Genomics. 1996. PMID: 8812430

8

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

9

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.

10

Lop12, a mutation in mouse Crygd causing lens opacity similar to human Coppock cataract.

Smith RS, Hawes NL, Chang B, Roderick TH, Akeson EC, Heckenlively JR, Gong X, Wang X, Davisson MT. Smith RS, et al. Genomics. 2000 Feb 1;63(3):314-20. doi: 10.1006/geno.1999.6054. Genomics. 2000. PMID: 10704279

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