Format
Sort by
Items per page

Send to

Choose Destination

Search results

Items: 1 to 50 of 52

1.

Candidate genes for chromosomes 6 and 10 quantitative trait loci for age-related retinal degeneration in mice.

Ogando DG, Dahlquist KD, Alizadeh M, Kunchithapautham K, Li J, Yu N, LaVail MM, Rohrer B, Vollrath D, Danciger M.

Mol Vis. 2010 Jun 5;16:1004-18.

2.

Loss of the metalloprotease ADAM9 leads to cone-rod dystrophy in humans and retinal degeneration in mice.

Parry DA, Toomes C, Bida L, Danciger M, Towns KV, McKibbin M, Jacobson SG, Logan CV, Ali M, Bond J, Chance R, Swendeman S, Daniele LL, Springell K, Adams M, Johnson CA, Booth AP, Jafri H, Rashid Y, Banin E, Strom TM, Farber DB, Sharon D, Blobel CP, Pugh EN Jr, Pierce EA, Inglehearn CF.

Am J Hum Genet. 2009 May;84(5):683-91. doi: 10.1016/j.ajhg.2009.04.005. Epub 2009 Apr 30.

3.

A missense mutation in the nuclear localization signal sequence of CERKL (p.R106S) causes autosomal recessive retinal degeneration.

Ali M, Ramprasad VL, Soumittra N, Mohamed MD, Jafri H, Rashid Y, Danciger M, McKibbin M, Kumaramanickavel G, Inglehearn CF.

Mol Vis. 2008;14:1960-4. Epub 2008 Oct 30.

4.

Influence of a quantitative trait locus on mouse chromosome 19 to the light-adapted electroretinogram.

Reynolds AL, Danciger M, Farrar GJ, Humphries P, Kenna PF.

Invest Ophthalmol Vis Sci. 2008 Sep;49(9):4058-63. doi: 10.1167/iovs.07-1620. Epub 2008 Mar 14.

PMID:
18344449
5.

Genetic modifiers of retinal degeneration in the rd3 mouse.

Danciger M, Ogando D, Yang H, Matthes MT, Yu N, Ahern K, Yasumura D, Williams RW, Lavail MM.

Invest Ophthalmol Vis Sci. 2008 Jul;49(7):2863-9. doi: 10.1167/iovs.08-1715. Epub 2008 Mar 14.

6.

Evidence for retinal remodelling in retinitis pigmentosa caused by PDE6B mutation.

Jacobson SG, Sumaroka A, Aleman TS, Cideciyan AV, Danciger M, Farber DB.

Br J Ophthalmol. 2007 May;91(5):699-701. No abstract available.

7.
8.

Quantitative genetics of age-related retinal degeneration: a second F1 intercross between the A/J and C57BL/6 strains.

Danciger M, Yang H, Ralston R, Liu Y, Matthes MT, Peirce J, Lavail MM.

Mol Vis. 2007 Jan 25;13:79-85.

9.

Disruption of the gene encoding the beta1-subunit of transducin in the Rd4/+ mouse.

Kitamura E, Danciger M, Yamashita C, Rao NP, Nusinowitz S, Chang B, Farber DB.

Invest Ophthalmol Vis Sci. 2006 Apr;47(4):1293-301.

PMID:
16565360
10.

Constant light-induced retinal damage and the RPE65-MET450 variant: assessment of the NZW/LacJ mouse.

Danciger M, Yang H, Handschumacher L, LaVail MM.

Mol Vis. 2005 May 27;11:374-9.

11.

A substitution of G to C in the cone cGMP-phosphodiesterase gamma subunit gene found in a distinctive form of cone dystrophy.

Piri N, Gao YQ, Danciger M, Mendoza E, Fishman GA, Farber DB.

Ophthalmology. 2005 Jan;112(1):159-66.

PMID:
15629837
12.

New retinal light damage QTL in mice with the light-sensitive RPE65 LEU variant.

Danciger M, Lyon J, Worrill D, Hoffman S, Lem J, Reme CE, Wenzel A, Grimm C.

Mamm Genome. 2004 Apr;15(4):277-83.

PMID:
15112105
13.

Electroretinographic evidence for altered phototransduction gain and slowed recovery from photobleaches in albino mice with a MET450 variant in RPE65.

Nusinowitz S, Nguyen L, Radu R, Kashani Z, Farber D, Danciger M.

Exp Eye Res. 2003 Nov;77(5):627-38.

PMID:
14550405
14.

A strong and highly significant QTL on chromosome 6 that protects the mouse from age-related retinal degeneration.

Danciger M, Lyon J, Worrill D, LaVail MM, Yang H.

Invest Ophthalmol Vis Sci. 2003 Jun;44(6):2442-9.

PMID:
12766041
15.

CORD9 a new locus for arCRD: mapping to 8p11, estimation of frequency, evaluation of a candidate gene.

Danciger M, Hendrickson J, Lyon J, Toomes C, McHale JC, Fishman GA, Inglehearn CF, Jacobson SG, Farber DB.

Invest Ophthalmol Vis Sci. 2001 Oct;42(11):2458-65.

PMID:
11581183
16.

Mutation analysis of ocular genes.

Danciger M.

Methods Mol Med. 2001;47:237-50. doi: 10.1385/1-59259-085-3:237.

PMID:
21394588
17.

A homozygous deletion in RPE65 in a small Sardinian family with autosomal recessive retinal dystrophy.

Poehner WJ, Fossarello M, Rapoport AL, Aleman TS, Cideciyan AV, Jacobson SG, Wright AF, Danciger M, Farber DB.

Mol Vis. 2000 Oct 30;6:192-8.

18.

Disease expression of RP1 mutations causing autosomal dominant retinitis pigmentosa.

Jacobson SG, Cideciyan AV, Iannaccone A, Weleber RG, Fishman GA, Maguire AM, Affatigato LM, Bennett J, Pierce EA, Danciger M, Farber DB, Stone EM.

Invest Ophthalmol Vis Sci. 2000 Jun;41(7):1898-908.

PMID:
10845615
19.

A QTL on distal chromosome 3 that influences the severity of light-induced damage to mouse photoreceptors.

Danciger M, Matthes MT, Yasamura D, Akhmedov NB, Rickabaugh T, Gentleman S, Redmond TM, La Vail MM, Farber DB.

Mamm Genome. 2000 Jun;11(6):422-7.

PMID:
10818205
20.

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.

21.

A nonsense mutation in a novel gene is associated with retinitis pigmentosa in a family linked to the RP1 locus.

Guillonneau X, Piriev NI, Danciger M, Kozak CA, Cideciyan AV, Jacobson SG, Farber DB.

Hum Mol Genet. 1999 Aug;8(8):1541-6.

PMID:
10401003
22.

Screening of the gene encoding the alpha'-subunit of cone cGMP-PDE in patients with retinal degenerations.

Gao YQ, Danciger M, Longmuir R, Piriev NI, Zhao DY, Heckenlively JR, Fishman GA, Weleber RG, Jacobson SG, Stone EM, Farber DB.

Invest Ophthalmol Vis Sci. 1999 Jul;40(8):1818-22.

PMID:
10393054
23.

Genetic and physical maps of the mouse rd3 locus; exclusion of the ortholog of USH2A.

Danciger JS, Danciger M, Nusinowitz S, Rickabaugh T, Farber DB.

Mamm Genome. 1999 Jul;10(7):657-61.

PMID:
10384036
24.

The mouse X-linked juvenile retinoschisis cDNA: expression in photoreceptors.

Reid SN, Akhmedov NB, Piriev NI, Kozak CA, Danciger M, Farber DB.

Gene. 1999 Feb 18;227(2):257-66.

PMID:
10023077
25.

Exon screening of the genes encoding the beta- and gamma-subunits of cone transducin in patients with inherited retinal disease.

Gao YQ, Danciger M, Akhmedov NB, Zhao DY, Heckenlively JR, Fishman GA, Weleber RG, Jacobson SG, Farber DB.

Mol Vis. 1998 Sep 17;4:16.

26.

Identification of genes causing photoreceptor degenerations leading to blindness.

Farber DB, Danciger M.

Curr Opin Neurobiol. 1997 Oct;7(5):666-73. Review.

PMID:
9384551
27.

A homozygous PDE6B mutation in a family with autosomal recessive retinitis pigmentosa.

Danciger M, Heilbron V, Gao YQ, Zhao DY, Jacobson SG, Farber DB.

Mol Vis. 1996 Sep 17;2:10. No abstract available.

28.

Chromosomal localization of murine and human oligodendrocyte-specific protein genes.

Bronstein JM, Kozak CA, Chen XN, Wu S, Danciger M, Korenberg JR, Farber DB.

Genomics. 1996 Jun 1;34(2):255-7.

PMID:
8661061
29.

Screening of the PDE6B gene in patients with autosomal dominant retinitis pigmentosa.

Gao YQ, Danciger M, Zhao DY, Blaney J, Piriev NI, Shih J, Jacobson SG, Heckenlively JH, Farber DB.

Exp Eye Res. 1996 Feb;62(2):149-54.

PMID:
8698075
30.

Mutations in the PDE6B gene in autosomal recessive retinitis pigmentosa.

Danciger M, Blaney J, Gao YQ, Zhao DY, Heckenlively JR, Jacobson SG, Farber DB.

Genomics. 1995 Nov 1;30(1):1-7.

PMID:
8595886
31.

Chromosomal localization of the genes for five zinc finger proteins expressed in mouse lens.

Danciger M, Brady J, Adamson MC, Farber DB, Piatigorsky J, Kozak CA.

Genomics. 1995 Jul 1;28(1):39-43.

PMID:
7590745
32.

Localization of three genes expressed in retina on mouse chromosome 11.

Kozak CA, Danciger M, Bowes C, Adamson MC, Palczewski K, Polans AS, Farber DB.

Mamm Genome. 1995 Feb;6(2):142-4. No abstract available.

PMID:
7767000
33.

Transcription factor IID probes localize a single gene to the proximal region of mouse chromosome 17.

Danciger M, Kozak CA, Suzuki S, Chang MR, Shinohara T, Farber DB.

Gene. 1993 Aug 25;130(2):283-6.

PMID:
8359696
34.

Genetic mapping of three GABAA receptor-subunit genes in the mouse.

Danciger M, Farber DB, Kozak CA.

Genomics. 1993 May;16(2):361-5.

PMID:
8390964
35.

Localization of a retroviral element within the rd gene coding for the beta subunit of cGMP phosphodiesterase.

Bowes C, Li T, Frankel WN, Danciger M, Coffin JM, Applebury ML, Farber DB.

Proc Natl Acad Sci U S A. 1993 Apr 1;90(7):2955-9.

36.

Localization of the gene for a third G protein beta-subunit to mouse chromosome 6 near Raf-1.

Danciger M, Chakraborti A, Farber DB, Kozak CA.

Genomics. 1992 Apr;12(4):688-92.

PMID:
1572642
37.

Chromosomal localization of the murine genes for the alpha- and beta-subunits of calcium/calmodulin-dependent protein kinase II.

Danciger M, Kozak CA, Adamson MC, Farber DB.

Mamm Genome. 1992;3(2):122-5. No abstract available.

PMID:
1319776
38.

Studies leading to the isolation of a cDNA for the gene causing retinal degeneration in the rd mouse.

Farber DB, Bowes C, Danciger M.

Prog Clin Biol Res. 1991;362:67-86. Review. No abstract available.

PMID:
1848365
39.

The gene for retinal rod 33-kDa protein is on mouse chromosome 1, near Lamb2.

Danciger M, Kozak CA, Abe T, Shinohara T, Farber DB.

Cytogenet Cell Genet. 1991;56(3-4):202-5.

PMID:
1675982
40.

Localization of the gene for interphotoreceptor retinoid-binding protein to mouse chromosome 14 near Np-1.

Danciger M, Kozak CA, Nickerson J, Redmond TM, Farber DB.

Genomics. 1990 Dec;8(4):727-31.

PMID:
2276745
41.

Retinal degeneration in the rd mouse is caused by a defect in the beta subunit of rod cGMP-phosphodiesterase.

Bowes C, Li T, Danciger M, Baxter LC, Applebury ML, Farber DB.

Nature. 1990 Oct 18;347(6294):677-80.

PMID:
1977087
42.

Genetic mapping demonstrates that the alpha-subunit of retinal cGMP-phosphodiesterase is not the site of the rd mutation.

Danciger M, Kozak CA, Li T, Applebury ML, Farber DB.

Exp Eye Res. 1990 Aug;51(2):185-9.

PMID:
2167232
43.

Fine mapping of a putative rd cDNA and its co-segregation with rd expression.

Danciger M, Bowes C, Kozak CA, LaVail MM, Farber DB.

Invest Ophthalmol Vis Sci. 1990 Aug;31(8):1427-32.

PMID:
1974892
44.

Isolation and characterization of cDNA encoding the gamma-subunit of cGMP phosphodiesterase in human retina.

Tuteja N, Danciger M, Klisak I, Tuteja R, Inana G, Mohandas T, Sparkes RS, Farber DB.

Gene. 1990 Apr 16;88(2):227-32.

PMID:
2161380
46.

Isolation of a candidate cDNA for the gene causing retinal degeneration in the rd mouse.

Bowes C, Danciger M, Kozak CA, Farber DB.

Proc Natl Acad Sci U S A. 1989 Dec;86(24):9722-6. Erratum in: Proc Natl Acad Sci U S A 1990 Feb;87(4):1625.

47.

The gene for retinal S-antigen (48-kDa protein) maps to the centromeric portion of mouse chromosome 1 near Idh-1.

Danciger M, Kozak CA, Tsuda M, Shinohara T, Farber DB.

Genomics. 1989 Aug;5(2):378-81.

PMID:
2571583
48.

The gene for the alpha-subunit of retinal rod transducin is on mouse chromosome 9.

Danciger M, Kozak CA, Farber DB.

Genomics. 1989 Feb;4(2):215-7.

PMID:
2737680
49.

The gene for the gamma-subunit of retinal cGMP-phosphodiesterase is on mouse chromosome 11.

Danciger M, Tuteja N, Kozak CA, Farber DB.

Exp Eye Res. 1989 Feb;48(2):303-8.

PMID:
2538340
50.

Assignment to mouse chromosomes of candidate genes for the rd mutation.

Farber DB, Kozak CA, Danciger M.

Prog Clin Biol Res. 1989;314:143-53. No abstract available.

PMID:
2558380

Supplemental Content

Loading ...
Support Center