Hawes NL - Search Results

1

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. Among authors: hawes nl. Genomics. 1997 Jun 15;42(3):393-6. doi: 10.1006/geno.1997.4717. Genomics. 1997. PMID: 9205110

2

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: hawes nl. Invest Ophthalmol Vis Sci. 1994 Mar;35(3):1071-6. Invest Ophthalmol Vis Sci. 1994. PMID: 8125718

3

New mouse primary retinal degeneration (rd-3).

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

4

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

5

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: hawes nl. Invest Ophthalmol Vis Sci. 1998 May;39(6):951-62. Invest Ophthalmol Vis Sci. 1998. PMID: 9579474

6

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

7

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: hawes nl. Genomics. 2000 Feb 1;63(3):314-20. doi: 10.1006/geno.1999.6054. Genomics. 2000. PMID: 10704279

8

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. Invest Ophthalmol Vis Sci. 2000 Sep;41(10):3149-57. Invest Ophthalmol Vis Sci. 2000. PMID: 10967077

9

Genetic modification of glaucoma associated phenotypes between AKXD-28/Ty and DBA/2J mice.

Anderson MG, Smith RS, Savinova OV, Hawes NL, Chang B, Zabaleta A, Wilpan R, Heckenlively JR, Davisson M, John SW. Anderson MG, et al. Among authors: hawes nl. BMC Genet. 2001;2:1. doi: 10.1186/1471-2156-2-1. Epub 2001 Jan 15. BMC Genet. 2001. PMID: 11178107 Free PMC article.

10

Retinal degeneration mutants in the mouse.

Chang B, Hawes NL, Hurd RE, Davisson MT, Nusinowitz S, Heckenlively JR. Chang B, et al. Among authors: hawes nl. Vision Res. 2002 Feb;42(4):517-25. doi: 10.1016/s0042-6989(01)00146-8. Vision Res. 2002. PMID: 11853768 Free article. Review.

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