Riazuddin S - Search Results

1

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: riazuddin s. 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.

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: riazuddin s. 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: riazuddin s. Invest Ophthalmol Vis Sci. 2005 Jul;46(7):2264-70. doi: 10.1167/iovs.04-1280. Invest Ophthalmol Vis Sci. 2005. PMID: 15980210

4

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: riazuddin sa, riazuddin s. Hum Genet. 2007 Feb;120(6):789-93. doi: 10.1007/s00439-006-0275-1. Epub 2006 Oct 26. Hum Genet. 2007. PMID: 17066295

5

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: riazuddin s. Hum Mutat. 2007 Oct;28(10):1014-9. doi: 10.1002/humu.20556. Hum Mutat. 2007. PMID: 17546645

6

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: riazuddin sa, riazuddin s. Hum Genet. 2007 Dec;122(5):445-50. doi: 10.1007/s00439-007-0418-z. Epub 2007 Aug 10. Hum Genet. 2007. PMID: 17690910

7

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: riazuddin sa, riazuddin s. Mol Vis. 2007 Sep 10;13:1635-40. Mol Vis. 2007. PMID: 17893665

8

Identification of micro-RNAs in cotton.

Khan Barozai MY, Irfan M, Yousaf R, Ali I, Qaisar U, Maqbool A, Zahoor M, Rashid B, Hussnain T, Riazuddin S. Khan Barozai MY, et al. Among authors: riazuddin s. Plant Physiol Biochem. 2008 Aug-Sep;46(8-9):739-51. doi: 10.1016/j.plaphy.2008.05.009. Epub 2008 May 28. Plant Physiol Biochem. 2008. PMID: 18603441

9

Ascochyta blight of chickpea: production of phytotoxins and disease management.

Shahid AA, Husnain T, Riazuddin S. Shahid AA, et al. Among authors: riazuddin s. Biotechnol Adv. 2008 Nov-Dec;26(6):511-5. doi: 10.1016/j.biotechadv.2008.06.001. Epub 2008 Jun 22. Biotechnol Adv. 2008. PMID: 18616995 Review.

10

Molecular basis of DFNB73: mutations of BSND can cause nonsyndromic deafness or Bartter syndrome.

Riazuddin S, Anwar S, Fischer M, Ahmed ZM, Khan SY, Janssen AG, Zafar AU, Scholl U, Husnain T, Belyantseva IA, Friedman PL, Riazuddin S, Friedman TB, Fahlke C. Riazuddin S, et al. Am J Hum Genet. 2009 Aug;85(2):273-80. doi: 10.1016/j.ajhg.2009.07.003. Epub 2009 Jul 30. Am J Hum Genet. 2009. PMID: 19646679 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

390 results

Search Page