Haider NB - Search Results

1

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. Mehalow AK, et al. Among authors: haider nb. Hum Mol Genet. 2003 Sep 1;12(17):2179-89. doi: 10.1093/hmg/ddg232. Epub 2003 Jul 15. Hum Mol Genet. 2003. PMID: 12915475

2

Genetic modifiers of vision and hearing.

Haider NB, Ikeda A, Naggert JK, Nishina PM. Haider NB, et al. Hum Mol Genet. 2002 May 15;11(10):1195-206. doi: 10.1093/hmg/11.10.1195. Hum Mol Genet. 2002. PMID: 12015279 Review.

3

Excess cone cell proliferation due to lack of a functional NR2E3 causes retinal dysplasia and degeneration in rd7/rd7 mice.

Haider NB, Naggert JK, Nishina PM. Haider NB, et al. Hum Mol Genet. 2001 Aug 1;10(16):1619-26. doi: 10.1093/hmg/10.16.1619. Hum Mol Genet. 2001. PMID: 11487564

4

The transcription factor Nr2e3 functions in retinal progenitors to suppress cone cell generation.

Haider NB, Demarco P, Nystuen AM, Huang X, Smith RS, McCall MA, Naggert JK, Nishina PM. Haider NB, et al. Vis Neurosci. 2006 Nov-Dec;23(6):917-29. doi: 10.1017/S095252380623027X. Vis Neurosci. 2006. PMID: 17266784

5

Mapping of genetic modifiers of Nr2e3 rd7/rd7 that suppress retinal degeneration and restore blue cone cells to normal quantity.

Haider NB, Zhang W, Hurd R, Ikeda A, Nystuen AM, Naggert JK, Nishina PM. Haider NB, et al. Mamm Genome. 2008 Mar;19(3):145-54. doi: 10.1007/s00335-008-9092-2. Epub 2008 Feb 20. Mamm Genome. 2008. PMID: 18286335

6

Nr2e3-directed transcriptional regulation of genes involved in photoreceptor development and cell-type specific phototransduction.

Haider NB, Mollema N, Gaule M, Yuan Y, Sachs AJ, Nystuen AM, Naggert JK, Nishina PM. Haider NB, et al. Exp Eye Res. 2009 Sep;89(3):365-72. doi: 10.1016/j.exer.2009.04.006. Epub 2009 Apr 18. Exp Eye Res. 2009. PMID: 19379737 Free PMC article. Review.

7

Characterization of a spontaneous retinal neovascular mouse model.

Hasegawa E, Sweigard H, Husain D, Olivares AM, Chang B, Smith KE, Birsner AE, D'Amato RJ, Michaud NA, Han Y, Vavvas DG, Miller JW, Haider NB, Connor KM. Hasegawa E, et al. Among authors: haider nb. PLoS One. 2014 Sep 4;9(9):e106507. doi: 10.1371/journal.pone.0106507. eCollection 2014. PLoS One. 2014. PMID: 25188381 Free PMC article.

8

Positional cloning of a novel gene on chromosome 16q causing Bardet-Biedl syndrome (BBS2).

Nishimura DY, Searby CC, Carmi R, Elbedour K, Van Maldergem L, Fulton AB, Lam BL, Powell BR, Swiderski RE, Bugge KE, Haider NB, Kwitek-Black AE, Ying L, Duhl DM, Gorman SW, Heon E, Iannaccone A, Bonneau D, Biesecker LG, Jacobson SG, Stone EM, Sheffield VC. Nishimura DY, et al. Among authors: haider nb. Hum Mol Genet. 2001 Apr 1;10(8):865-74. doi: 10.1093/hmg/10.8.865. Hum Mol Genet. 2001. PMID: 11285252

9

Rapid communication: the human FEM1B gene maps to chromosome 15q22 and is excluded as the gene for Bardet-Biedl syndrome, type 4.

Ventura-Holman T, Haider NB, Maher JF. Ventura-Holman T, et al. Among authors: haider nb. Am J Med Sci. 2000 Apr;319(4):268-70. doi: 10.1097/00000441-200004000-00014. Am J Med Sci. 2000. PMID: 10768616

10

Mutation of a nuclear receptor gene, NR2E3, causes enhanced S cone syndrome, a disorder of retinal cell fate.

Haider NB, Jacobson SG, Cideciyan AV, Swiderski R, Streb LM, Searby C, Beck G, Hockey R, Hanna DB, Gorman S, Duhl D, Carmi R, Bennett J, Weleber RG, Fishman GA, Wright AF, Stone EM, Sheffield VC. Haider NB, et al. Nat Genet. 2000 Feb;24(2):127-31. doi: 10.1038/72777. Nat Genet. 2000. PMID: 10655056

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