Chang B - Search Results

1

Mouse models of age-related macular degeneration.

Elizabeth Rakoczy P, Yu MJ, Nusinowitz S, Chang B, Heckenlively JR. Elizabeth Rakoczy P, et al. Among authors: chang b. Exp Eye Res. 2006 May;82(5):741-52. doi: 10.1016/j.exer.2005.10.012. Epub 2005 Dec 1. Exp Eye Res. 2006. PMID: 16325179 Review.

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

4

New mouse primary retinal degeneration (rd-3).

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

5

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: chang b. Invest Ophthalmol Vis Sci. 1996 Feb;37(2):397-404. Invest Ophthalmol Vis Sci. 1996. PMID: 8603845

6

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

7

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: chang b. Genomics. 1997 Jun 15;42(3):393-6. doi: 10.1006/geno.1997.4717. Genomics. 1997. PMID: 9205110

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

9

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

10

Identification of a missense mutation in the alphaA-crystallin gene of the lop18 mouse.

Chang B, Hawes NL, Roderick TH, Smith RS, Heckenlively JR, Horwitz J, Davisson MT. Chang B, et al. Mol Vis. 1999 Sep 10;5:21. Mol Vis. 1999. PMID: 10493778 Free article.

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