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Items: 1 to 50 of 51

1.

Age-related retinal degeneration (arrd2) in a novel mouse model due to a nonsense mutation in the Mdm1 gene.

Chang B, Mandal MN, Chavali VR, Hawes NL, Khan NW, Hurd RE, Smith RS, Davisson ML, Kopplin L, Klein BE, Klein R, Iyengar SK, Heckenlively JR, Ayyagari R.

Hum Mol Genet. 2008 Dec 15;17(24):3929-41. doi: 10.1093/hmg/ddn295. Epub 2008 Sep 18.

2.

Iris phenotypes and pigment dispersion caused by genes influencing pigmentation.

Anderson MG, Hawes NL, Trantow CM, Chang B, John SW.

Pigment Cell Melanoma Res. 2008 Oct;21(5):565-78. doi: 10.1111/j.1755-148X.2008.00482.x. Epub 2007 Jun 28.

3.

Allelic variance between GRM6 mutants, Grm6nob3 and Grm6nob4 results in differences in retinal ganglion cell visual responses.

Maddox DM, Vessey KA, Yarbrough GL, Invergo BM, Cantrell DR, Inayat S, Balannik V, Hicks WL, Hawes NL, Byers S, Smith RS, Hurd R, Howell D, Gregg RG, Chang B, Naggert JK, Troy JB, Pinto LH, Nishina PM, McCall MA.

J Physiol. 2008 Sep 15;586(18):4409-24. doi: 10.1113/jphysiol.2008.157289. Epub 2008 Aug 7.

4.

AAV-mediated gene therapy for retinal degeneration in the rd10 mouse containing a recessive PDEbeta mutation.

Pang JJ, Boye SL, Kumar A, Dinculescu A, Deng W, Li J, Li Q, Rani A, Foster TC, Chang B, Hawes NL, Boatright JH, Hauswirth WW.

Invest Ophthalmol Vis Sci. 2008 Oct;49(10):4278-83. doi: 10.1167/iovs.07-1622. Epub 2008 Jun 27.

5.

Dense nuclear cataract caused by the gammaB-crystallin S11R point mutation.

Li L, Chang B, Cheng C, Chang D, Hawes NL, Xia CH, Gong X.

Invest Ophthalmol Vis Sci. 2008 Jan;49(1):304-9. doi: 10.1167/iovs.07-0942.

PMID:
18172107
6.

Genetic background modifies inner ear and eye phenotypes of jag1 heterozygous mice.

Kiernan AE, Li R, Hawes NL, Churchill GA, Gridley T.

Genetics. 2007 Sep;177(1):307-11.

7.

Restoration of cone vision in a mouse model of achromatopsia.

Alexander JJ, Umino Y, Everhart D, Chang B, Min SH, Li Q, Timmers AM, Hawes NL, Pang JJ, Barlow RB, Hauswirth WW.

Nat Med. 2007 Jun;13(6):685-7. Epub 2007 May 21.

8.

Two mouse retinal degenerations caused by missense mutations in the beta-subunit of rod cGMP phosphodiesterase gene.

Chang B, Hawes NL, Pardue MT, German AM, Hurd RE, Davisson MT, Nusinowitz S, Rengarajan K, Boyd AP, Sidney SS, Phillips MJ, Stewart RE, Chaudhury R, Nickerson JM, Heckenlively JR, Boatright JH.

Vision Res. 2007 Mar;47(5):624-33. Epub 2007 Jan 30.

9.

Tool from ancient pharmacopoeia prevents vision loss.

Boatright JH, Moring AG, McElroy C, Phillips MJ, Do VT, Chang B, Hawes NL, Boyd AP, Sidney SS, Stewart RE, Minear SC, Chaudhury R, Ciavatta VT, Rodrigues CM, Steer CJ, Nickerson JM, Pardue MT.

Mol Vis. 2006 Dec 29;12:1706-14.

10.

Premature truncation of a novel protein, RD3, exhibiting subnuclear localization is associated with retinal degeneration.

Friedman JS, Chang B, Kannabiran C, Chakarova C, Singh HP, Jalali S, Hawes NL, Branham K, Othman M, Filippova E, Thompson DA, Webster AR, Andréasson S, Jacobson SG, Bhattacharya SS, Heckenlively JR, Swaroop A.

Am J Hum Genet. 2006 Dec;79(6):1059-70. Epub 2006 Oct 23. Erratum in: Am J Hum Genet. 2007 Feb;80(2):388.

11.

Cone photoreceptor function loss-3, a novel mouse model of achromatopsia due to a mutation in Gnat2.

Chang B, Dacey MS, Hawes NL, Hitchcock PF, Milam AH, Atmaca-Sonmez P, Nusinowitz S, Heckenlively JR.

Invest Ophthalmol Vis Sci. 2006 Nov;47(11):5017-21.

PMID:
17065522
12.

The nob2 mouse, a null mutation in Cacna1f: anatomical and functional abnormalities in the outer retina and their consequences on ganglion cell visual responses.

Chang B, Heckenlively JR, Bayley PR, Brecha NC, Davisson MT, Hawes NL, Hirano AA, Hurd RE, Ikeda A, Johnson BA, McCall MA, Morgans CW, Nusinowitz S, Peachey NS, Rice DS, Vessey KA, Gregg RG.

Vis Neurosci. 2006 Jan-Feb;23(1):11-24.

13.

Early transposable element insertion in intron 9 of the Hsf4 gene results in autosomal recessive cataracts in lop11 and ldis1 mice.

Talamas E, Jackson L, Koeberl M, Jackson T, McElwee JL, Hawes NL, Chang B, Jablonski MM, Sidjanin DJ.

Genomics. 2006 Jul;88(1):44-51. Epub 2006 Apr 3.

14.

Deficiency of SHP-1 protein-tyrosine phosphatase in "viable motheaten" mice results in retinal degeneration.

Lyons BL, Smith RS, Hurd RE, Hawes NL, Burzenski LM, Nusinowitz S, Hasham MG, Chang B, Shultz LD.

Invest Ophthalmol Vis Sci. 2006 Mar;47(3):1201-9.

PMID:
16505059
15.

Mouse models of ocular diseases.

Chang B, Hawes NL, Hurd RE, Wang J, Howell D, Davisson MT, Roderick TH, Nusinowitz S, Heckenlively JR.

Vis Neurosci. 2005 Sep-Oct;22(5):587-93.

PMID:
16332269
16.

Retinal degeneration 12 (rd12): a new, spontaneously arising mouse model for human Leber congenital amaurosis (LCA).

Pang JJ, Chang B, Hawes NL, Hurd RE, Davisson MT, Li J, Noorwez SM, Malhotra R, McDowell JH, Kaushal S, Hauswirth WW, Nusinowitz S, Thompson DA, Heckenlively JR.

Mol Vis. 2005 Feb 28;11:152-62.

17.

Mouse models of USH1C and DFNB18: phenotypic and molecular analyses of two new spontaneous mutations of the Ush1c gene.

Johnson KR, Gagnon LH, Webb LS, Peters LL, Hawes NL, Chang B, Zheng QY.

Hum Mol Genet. 2003 Dec 1;12(23):3075-86. Epub 2003 Sep 30.

18.

Mouse model of subretinal neovascularization with choroidal anastomosis.

Heckenlively JR, Hawes NL, Friedlander M, Nusinowitz S, Hurd R, Davisson M, Chang B.

Retina. 2003 Aug;23(4):518-22.

PMID:
12972764
19.

A missense mutation in the mouse Col2a1 gene causes spondyloepiphyseal dysplasia congenita, hearing loss, and retinoschisis.

Donahue LR, Chang B, Mohan S, Miyakoshi N, Wergedal JE, Baylink DJ, Hawes NL, Rosen CJ, Ward-Bailey P, Zheng QY, Bronson RT, Johnson KR, Davisson MT.

J Bone Miner Res. 2003 Sep;18(9):1612-21. Erratum in: J Bone Miner Res. 2007 Dec;22(12):2011.

20.

CRB1 is essential for external limiting membrane integrity and photoreceptor morphogenesis in the mammalian retina.

Mehalow AK, Kameya S, Smith RS, Hawes NL, Denegre JM, Young JA, Bechtold L, Haider NB, Tepass U, Heckenlively JR, Chang B, Naggert JK, Nishina PM.

Hum Mol Genet. 2003 Sep 1;12(17):2179-89. Epub 2003 Jul 15.

PMID:
12915475
21.

Mfrp, a gene encoding a frizzled related protein, is mutated in the mouse retinal degeneration 6.

Kameya S, Hawes NL, Chang B, Heckenlively JR, Naggert JK, Nishina PM.

Hum Mol Genet. 2002 Aug 1;11(16):1879-86.

PMID:
12140190
22.

Fierce: a new mouse deletion of Nr2e1; violent behaviour and ocular abnormalities are background-dependent.

Young KA, Berry ML, Mahaffey CL, Saionz JR, Hawes NL, Chang B, Zheng QY, Smith RS, Bronson RT, Nelson RJ, Simpson EM.

Behav Brain Res. 2002 May 14;132(2):145-58.

23.

A Gja8 (Cx50) point mutation causes an alteration of alpha 3 connexin (Cx46) in semi-dominant cataracts of Lop10 mice.

Chang B, Wang X, Hawes NL, Ojakian R, Davisson MT, Lo WK, Gong X.

Hum Mol Genet. 2002 Mar 1;11(5):507-13.

PMID:
11875045
24.

Retinal degeneration mutants in the mouse.

Chang B, Hawes NL, Hurd RE, Davisson MT, Nusinowitz S, Heckenlively JR.

Vision Res. 2002 Feb;42(4):517-25. Review.

25.

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.

Nat Genet. 2002 Jan;30(1):81-5. Epub 2001 Dec 17.

PMID:
11743578
26.

Haploinsufficient Bmp4 ocular phenotypes include anterior segment dysgenesis with elevated intraocular pressure.

Chang B, Smith RS, Peters M, Savinova OV, Hawes NL, Zabaleta A, Nusinowitz S, Martin JE, Davisson ML, Cepko CL, Hogan BL, John SW.

BMC Genet. 2001;2:18. Epub 2001 Nov 6.

27.

Mouse paracentric inversion In(3)55Rk mutates the urate oxidase gene.

Cook SA, Akeson EC, Calvano C, Johnson KR, Mandell J, Hawes NL, Bronson RT, Roderick TH, Davisson MT.

Cytogenet Cell Genet. 2001;93(1-2):77-82.

PMID:
11474184
28.

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.

BMC Genet. 2001;2:1. Epub 2001 Jan 15.

29.

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.

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

PMID:
10967077
30.

A deletion in a photoreceptor-specific nuclear receptor mRNA causes retinal degeneration in the rd7 mouse.

Akhmedov NB, Piriev NI, Chang B, Rapoport AL, Hawes NL, Nishina PM, Nusinowitz S, Heckenlively JR, Roderick TH, Kozak CA, Danciger M, Davisson MT, Farber DB.

Proc Natl Acad Sci U S A. 2000 May 9;97(10):5551-6.

31.

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.

Genomics. 2000 Feb 1;63(3):314-20.

PMID:
10704279
32.

The bst locus on mouse chromosome 16 is associated with age-related subretinal neovascularization.

Smith RS, John SW, Zabeleta A, Davisson MT, Hawes NL, Chang B.

Proc Natl Acad Sci U S A. 2000 Feb 29;97(5):2191-5.

33.

Mouse fundus photography and angiography: a catalogue of normal and mutant phenotypes.

Hawes NL, Smith RS, Chang B, Davisson M, Heckenlively JR, John SW.

Mol Vis. 1999 Sep 15;5:22.

34.

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.

Mol Vis. 1999 Sep 10;5:21.

35.

Severe ocular abnormalities in C57BL/6 but not in 129/Sv p53-deficient mice.

Ikeda S, Hawes NL, Chang B, Avery CS, Smith RS, Nishina PM.

Invest Ophthalmol Vis Sci. 1999 Jul;40(8):1874-8.

PMID:
10393064
36.

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.

Nat Genet. 1999 Apr;21(4):405-9.

PMID:
10192392
37.

Lens epithelial proliferation cataract in segmental trisomy involving mouse Chromosomes 4 and 17.

Smith RS, Johnson KR, Hawes NL, Harris BS, Sundberg JP, Davisson MT.

Mamm Genome. 1999 Feb;10(2):102-6.

PMID:
9922387
38.

Characterization of the mouse Prox1 gene.

Tomarev SI, Zinovieva RD, Chang B, Hawes NL.

Biochem Biophys Res Commun. 1998 Jul 30;248(3):684-9.

PMID:
9703987
39.

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.

Invest Ophthalmol Vis Sci. 1998 May;39(6):951-62. Erratum in: Invest Ophthalmol Vis Sci 1998 Aug;39(9):1641.

PMID:
9579474
40.

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

Roderick TH, Chang B, Hawes NL, Heckenlively JR.

Genomics. 1997 Jun 15;42(3):393-6.

PMID:
9205110
41.

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

Chang B, Hawes NL, Smith RS, Heckenlively JR, Davisson MT, Roderick TH.

Genomics. 1996 Aug 15;36(1):171-3. Erratum in: Genomics 1997 Jan 15;39(2):237.

PMID:
8812430
42.

Ocular retardation mouse caused by Chx10 homeobox null allele: impaired retinal progenitor proliferation and bipolar cell differentiation.

Burmeister M, Novak J, Liang MY, Basu S, Ploder L, Hawes NL, Vidgen D, Hoover F, Goldman D, Kalnins VI, Roderick TH, Taylor BA, Hankin MH, McInnes RR.

Nat Genet. 1996 Apr;12(4):376-84.

PMID:
8630490
43.

Corn1: a mouse model for corneal surface disease and neovascularization.

Smith RS, Hawes NL, Kuhlmann SD, Heckenlively JR, Chang B, Roderick TH, Sundberg JP.

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

PMID:
8603845
44.

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.

Proc Natl Acad Sci U S A. 1995 Nov 21;92(24):11100-4.

45.

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.

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

PMID:
8125718
46.

New mouse primary retinal degeneration (rd-3).

Chang B, Heckenlively JR, Hawes NL, Roderick TH.

Genomics. 1993 Apr;16(1):45-9.

PMID:
8486383
47.

Autosomal dominant mouse cataract (Lop-10). Consistent differences of expression in heterozygotes.

Runge PE, Hawes NL, Heckenlively JR, Langley SH, Roderick TH.

Invest Ophthalmol Vis Sci. 1992 Oct;33(11):3202-8. Review.

PMID:
1399425
48.

The hairy ears (Eh) mutation is closely associated with a chromosomal rearrangement in mouse chromosome 15.

Davisson MT, Roderick TH, Akeson EC, Hawes NL, Sweet HO.

Genet Res. 1990 Oct-Dec;56(2-3):167-78.

PMID:
2272507
49.

Mitochondrial malate dehydrogenase (Mor-1) in the mouse: linkage to chromosome 5 markers.

Womack JE, Hawes NL, Soares ER, Roderick TH.

Biochem Genet. 1975 Oct;13(9-10):519-25.

PMID:
1203052
50.

Nineteen paracentric chromosomal inversions in mice.

Roderick TH, Hawes NL.

Genetics. 1974 Jan;76(1):109-17.

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