Husnain T - Search Results

1

Multiplex Cas9-based excision of CLCuV betasatellite and DNA-A revealed reduction of viral load with asymptomatic cotton plants.

Shakoor S, Rao AQ, Ajmal S, Yasmeen A, Khan MAU, Sadaqat S, Ashraf NM, Wolter F, Pacher M, Husnain T. Shakoor S, et al. Among authors: husnain t. Planta. 2023 Sep 12;258(4):79. doi: 10.1007/s00425-023-04233-w. Planta. 2023. PMID: 37698688

2

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. Among authors: husnain t. 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.

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

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

5

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

6

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.

7

[Isolation and functional analysis of cotton universal stress protein promoter in response to phytohormones and abiotic stresses].

Zahur M, Maqbool A, Ifran M, Barozai MY, Rashid B, Riazuddin S, Husnain T. Zahur M, et al. Among authors: husnain t. Mol Biol (Mosk). 2009 Jul-Aug;43(4):628-35. Mol Biol (Mosk). 2009. PMID: 19807025 Russian.

8

A Common Ancestral Mutation in CRYBB3 Identified in Multiple Consanguineous Families with Congenital Cataracts.

Jiao X, Kabir F, Irum B, Khan AO, Wang Q, Li D, Khan AA, Husnain T, Akram J, Riazuddin S, Hejtmancik JF, Riazuddin SA. Jiao X, et al. Among authors: husnain t. PLoS One. 2016 Jun 21;11(6):e0157005. doi: 10.1371/journal.pone.0157005. eCollection 2016. PLoS One. 2016. PMID: 27326458 Free PMC article.

9

Overexpression of nicotinamidase 3 (NIC3) gene and the exogenous application of nicotinic acid (NA) enhance drought tolerance and increase biomass in Arabidopsis.

Ahmad Z, Bashir K, Matsui A, Tanaka M, Sasaki R, Oikawa A, Hirai MY, Chaomurilege, Zu Y, Kawai-Yamada M, Rashid B, Husnain T, Seki M. Ahmad Z, et al. Among authors: husnain t. Plant Mol Biol. 2021 Sep;107(1-2):63-84. doi: 10.1007/s11103-021-01179-z. Epub 2021 Aug 30. Plant Mol Biol. 2021. PMID: 34460049

10

Splice-site mutations identified in PDE6A responsible for retinitis pigmentosa in consanguineous Pakistani families.

Khan SY, Ali S, Naeem MA, Khan SN, Husnain T, Butt NH, Qazi ZA, Akram J, Riazuddin S, Ayyagari R, Hejtmancik JF, Riazuddin SA. Khan SY, et al. Among authors: husnain t. Mol Vis. 2015 Aug 18;21:871-82. eCollection 2015. Mol Vis. 2015. PMID: 26321862 Free PMC article.

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