Roderick TH - Search Results

1

New mouse primary retinal degeneration (rd-3).

Chang B, Heckenlively JR, Hawes NL, Roderick TH. Chang B, et al. Among authors: roderick th. Genomics. 1993 Apr;16(1):45-9. doi: 10.1006/geno.1993.1138. Genomics. 1993. PMID: 8486383

2

Mouse model for Usher syndrome: linkage mapping suggests homology to Usher type I reported at human chromosome 11p15.

Heckenlively JR, Chang B, Erway LC, Peng C, Hawes NL, Hageman GS, Roderick TH. Heckenlively JR, et al. Among authors: roderick th. Proc Natl Acad Sci U S A. 1995 Nov 21;92(24):11100-4. doi: 10.1073/pnas.92.24.11100. Proc Natl Acad Sci U S A. 1995. PMID: 7479945 Free PMC article.

3

Retinal degeneration in motor neuron degeneration: a mouse model of ceroid lipofuscinosis.

Chang B, Bronson RT, Hawes NL, Roderick TH, Peng C, Hageman GS, Heckenlively JR. Chang B, et al. Among authors: roderick th. Invest Ophthalmol Vis Sci. 1994 Mar;35(3):1071-6. Invest Ophthalmol Vis Sci. 1994. PMID: 8125718

4

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. Among authors: roderick th. Invest Ophthalmol Vis Sci. 1996 Feb;37(2):397-404. Invest Ophthalmol Vis Sci. 1996. PMID: 8603845

5

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: roderick th. Genomics. 1996 Aug 15;36(1):171-3. doi: 10.1006/geno.1996.0439. Genomics. 1996. PMID: 8812430

6

A new dominant retinal degeneration (Rd4) associated with a chromosomal inversion in the mouse.

Roderick TH, Chang B, Hawes NL, Heckenlively JR. Roderick TH, et al. Genomics. 1997 Jun 15;42(3):393-6. doi: 10.1006/geno.1997.4717. Genomics. 1997. PMID: 9205110

7

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: roderick th. Nat Genet. 1999 Apr;21(4):405-9. doi: 10.1038/7741. Nat Genet. 1999. PMID: 10192392

8

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. Among authors: roderick th. Genomics. 2000 Feb 1;63(3):314-20. doi: 10.1006/geno.1999.6054. Genomics. 2000. PMID: 10704279

9

Retinal degeneration 6 (rd6): a new mouse model for human retinitis punctata albescens.

Hawes NL, Chang B, Hageman GS, Nusinowitz S, Nishina PM, Schneider BS, Smith RS, Roderick TH, Davisson MT, Heckenlively JR. Hawes NL, et al. Among authors: roderick th. Invest Ophthalmol Vis Sci. 2000 Sep;41(10):3149-57. Invest Ophthalmol Vis Sci. 2000. PMID: 10967077

10

Mouse models of ocular diseases.

Chang B, Hawes NL, Hurd RE, Wang J, Howell D, Davisson MT, Roderick TH, Nusinowitz S, Heckenlively JR. Chang B, et al. Among authors: roderick th. Vis Neurosci. 2005 Sep-Oct;22(5):587-93. doi: 10.1017/S0952523805225075. Vis Neurosci. 2005. PMID: 16332269

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