Chang B - Search Results

1

A homologous genetic basis of the murine cpfl1 mutant and human achromatopsia linked to mutations in the PDE6C gene.

Chang B, Grau T, Dangel S, Hurd R, Jurklies B, Sener EC, Andreasson S, Dollfus H, Baumann B, Bolz S, Artemyev N, Kohl S, Heckenlively J, Wissinger B. Chang B, et al. Proc Natl Acad Sci U S A. 2009 Nov 17;106(46):19581-6. doi: 10.1073/pnas.0907720106. Epub 2009 Nov 3. Proc Natl Acad Sci U S A. 2009. PMID: 19887631 Free PMC article.

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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