Husnain T - Search Results

1

Ectopia lentis in a consanguineous pakistani family and a novel locus on chromosome 8q.

Kaul H, Riazuddin SA, Qazi ZA, Nasir IA, Zafar AU, Khan SN, Husnain T, Akram J, Hejtmancik JF, Riazuddin S. Kaul H, et al. Among authors: husnain t. Arch Ophthalmol. 2010 Aug;128(8):1046-9. doi: 10.1001/archophthalmol.2010.165. Arch Ophthalmol. 2010. PMID: 20697006 Free PMC article.

2

Mutations of MYO6 are associated with recessive deafness, DFNB37.

Ahmed ZM, Morell RJ, Riazuddin S, Gropman A, Shaukat S, Ahmad MM, Mohiddin SA, Fananapazir L, Caruso RC, Husnain T, Khan SN, Riazuddin S, Griffith AJ, Friedman TB, Wilcox ER. Ahmed ZM, et al. Among authors: husnain t. Am J Hum Genet. 2003 May;72(5):1315-22. doi: 10.1086/375122. Epub 2003 Apr 8. Am J Hum Genet. 2003. PMID: 12687499 Free PMC article.

3

Autosomal recessive retinitis pigmentosa is associated with mutations in RP1 in three consanguineous Pakistani families.

Riazuddin SA, Zulfiqar F, Zhang Q, Sergeev YV, Qazi ZA, Husnain T, Caruso R, Riazuddin S, Sieving PA, Hejtmancik JF. Riazuddin SA, et al. Among authors: husnain t. Invest Ophthalmol Vis Sci. 2005 Jul;46(7):2264-70. doi: 10.1167/iovs.04-1280. Invest Ophthalmol Vis Sci. 2005. PMID: 15980210

4

Somatic embryogenesis in wild relatives of cotton (Gossypium Spp.).

Rao AQ, Hussain SS, Shahzad MS, Bokhari SY, Raza MH, Rakha A, Majeed A, Shahid AA, Saleem Z, Husnain T, Riazuddin S. Rao AQ, et al. Among authors: husnain t. J Zhejiang Univ Sci B. 2006 Apr;7(4):291-8. doi: 10.1631/jzus.2006.B0291. J Zhejiang Univ Sci B. 2006. PMID: 16532531 Free PMC article.

5

Autosomal recessive nonsyndromic deafness locus DFNB63 at chromosome 11q13.2-q13.3.

Khan SY, Riazuddin S, Tariq M, Anwar S, Shabbir MI, Riazuddin SA, Khan SN, Husnain T, Ahmed ZM, Friedman TB, Riazuddin S. Khan SY, et al. Among authors: husnain t. Hum Genet. 2007 Feb;120(6):789-93. doi: 10.1007/s00439-006-0275-1. Epub 2006 Oct 26. Hum Genet. 2007. PMID: 17066295

6

Mutational spectrum of MYO15A: the large N-terminal extension of myosin XVA is required for hearing.

Nal N, Ahmed ZM, Erkal E, Alper OM, Lüleci G, Dinç O, Waryah AM, Ain Q, Tasneem S, Husnain T, Chattaraj P, Riazuddin S, Boger E, Ghosh M, Kabra M, Riazuddin S, Morell RJ, Friedman TB. Nal N, et al. Among authors: husnain t. Hum Mutat. 2007 Oct;28(10):1014-9. doi: 10.1002/humu.20556. Hum Mutat. 2007. PMID: 17546645

7

The autosomal recessive nonsyndromic deafness locus DFNB72 is located on chromosome 19p13.3.

Ain Q, Nazli S, Riazuddin S, Jaleel AU, Riazuddin SA, Zafar AU, Khan SN, Husnain T, Griffith AJ, Ahmed ZM, Friedman TB, Riazuddin S. Ain Q, et al. Among authors: husnain t. Hum Genet. 2007 Dec;122(5):445-50. doi: 10.1007/s00439-007-0418-z. Epub 2007 Aug 10. Hum Genet. 2007. PMID: 17690910

8

Identities, frequencies and origins of TMC1 mutations causing DFNB7/B11 deafness in Pakistan.

Kitajiri SI, McNamara R, Makishima T, Husnain T, Zafar AU, Kittles RA, Ahmed ZM, Friedman TB, Riazuddin S, Griffith AJ. Kitajiri SI, et al. Among authors: husnain t. Clin Genet. 2007 Dec;72(6):546-50. doi: 10.1111/j.1399-0004.2007.00895.x. Epub 2007 Sep 17. Clin Genet. 2007. PMID: 17877751

9

Localization of autosomal recessive congenital cataracts in consanguineous Pakistani families to a new locus on chromosome 1p.

Butt T, Yao W, Kaul H, Xiaodong J, Gradstein L, Zhang Y, Husnain T, Riazuddin S, Hejtmancik JF, Riazuddin SA. Butt T, et al. Among authors: husnain t. Mol Vis. 2007 Sep 10;13:1635-40. Mol Vis. 2007. PMID: 17893665

10

RNA interference: the story of gene silencing in plants and humans.

Mahmood-ur-Rahman, Ali I, Husnain T, Riazuddin S. Mahmood-ur-Rahman, et al. Among authors: husnain t. Biotechnol Adv. 2008 May-Jun;26(3):202-9. doi: 10.1016/j.biotechadv.2007.12.002. Epub 2007 Dec 23. Biotechnol Adv. 2008. PMID: 18221853 Review.

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