Haider NB - Search Results

1

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.

2

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

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

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

5

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.

6

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

7

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

8

Pitfalls in homozygosity mapping.

Miano MG, Jacobson SG, Carothers A, Hanson I, Teague P, Lovell J, Cideciyan AV, Haider N, Stone EM, Sheffield VC, Wright AF. Miano MG, et al. Am J Hum Genet. 2000 Nov;67(5):1348-51. doi: 10.1016/S0002-9297(07)62966-8. Epub 2000 Sep 27. Am J Hum Genet. 2000. PMID: 11007652 Free PMC article.

9

Complement factor H gene mutation associated with autosomal recessive atypical hemolytic uremic syndrome.

Ying L, Katz Y, Schlesinger M, Carmi R, Shalev H, Haider N, Beck G, Sheffield VC, Landau D. Ying L, et al. Am J Hum Genet. 1999 Dec;65(6):1538-46. doi: 10.1086/302673. Am J Hum Genet. 1999. PMID: 10577907 Free PMC article.

10

Orally active multi-functional antioxidants are neuroprotective in a rat model of light-induced retinal damage.

Randazzo J, Zhang Z, Hoff M, Kawada H, Sachs A, Yuan Y, Haider N, Kador P. Randazzo J, et al. PLoS One. 2011;6(7):e21926. doi: 10.1371/journal.pone.0021926. Epub 2011 Jul 14. PLoS One. 2011. PMID: 21779355 Free PMC article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

47 results

Search Page