Literature DB >> 16158433

A new locus for nonsyndromic deafness DFNB51 maps to chromosome 11p13-p12.

Rehan Sadiq Shaikh, Khushnooda Ramzan, Sabiha Nazli, Sameera Sattar, Shaheen N Khan, Saima Riazuddin, Zubair M Ahmed, Thomas B Friedman, Sheikh Riazuddin.   

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Year:  2005        PMID： 16158433      PMCID： PMC2572776          DOI： 10.1002/ajmg.a.30949

Source DB:  PubMed          Journal:  Am J Med Genet A        ISSN： 1552-4825            Impact factor:   2.802


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  27 in total

1.  The HUGO Gene Nomenclature Committee (HGNC).

Authors:  S Povey; R Lovering; E Bruford; M Wright; M Lush; H Wain
Journal:  Hum Genet       Date:  2001-10-24       Impact factor: 4.132

Review 2.  The molecular architecture of the inner ear.

Authors:  Andrew Forge; Tony Wright
Journal:  Br Med Bull       Date:  2002       Impact factor: 4.291

3.  Myosin XVa and whirlin, two deafness gene products required for hair bundle growth, are located at the stereocilia tips and interact directly.

Authors:  Benjamin Delprat; Vincent Michel; Richard Goodyear; Yasuhiro Yamasaki; Nicolas Michalski; Aziz El-Amraoui; Isabelle Perfettini; Pierre Legrain; Guy Richardson; Jean-Pierre Hardelin; Christine Petit
Journal:  Hum Mol Genet       Date:  2004-12-08       Impact factor: 6.150

4.  Origins and frequencies of SLC26A4 (PDS) mutations in east and south Asians: global implications for the epidemiology of deafness.

Authors:  H-J Park; S Shaukat; X-Z Liu; S H Hahn; S Naz; M Ghosh; H-N Kim; S-K Moon; S Abe; K Tukamoto; S Riazuddin; M Kabra; R Erdenetungalag; J Radnaabazar; S Khan; A Pandya; S-I Usami; W E Nance; E R Wilcox; S Riazuddin; A J Griffith
Journal:  J Med Genet       Date:  2003-04       Impact factor: 6.318

5.  Association of unconventional myosin MYO15 mutations with human nonsyndromic deafness DFNB3.

Authors:  A Wang; Y Liang; R A Fridell; F J Probst; E R Wilcox; J W Touchman; C C Morton; R J Morell; K Noben-Trauth; S A Camper; T B Friedman
Journal:  Science       Date:  1998-05-29       Impact factor: 47.728

6.  Myosin-XVa is required for tip localization of whirlin and differential elongation of hair-cell stereocilia.

Authors:  Inna A Belyantseva; Erich T Boger; Sadaf Naz; Gregory I Frolenkov; James R Sellers; Zubair M Ahmed; Andrew J Griffith; Thomas B Friedman
Journal:  Nat Cell Biol       Date:  2005-01-16       Impact factor: 28.824

7.  Novel mutations of MYO15A associated with profound deafness in consanguineous families and moderately severe hearing loss in a patient with Smith-Magenis syndrome.

Authors:  N Liburd; M Ghosh; S Riazuddin; S Naz; S Khan; Z Ahmed; S Riazuddin; Y Liang; P S Menon; T Smith; A C Smith; K S Chen; J R Lupski; E R Wilcox; L Potocki; T B Friedman
Journal:  Hum Genet       Date:  2001-10-03       Impact factor: 4.132

8.  Insertion of beta-satellite repeats identifies a transmembrane protease causing both congenital and childhood onset autosomal recessive deafness.

Authors:  H S Scott; J Kudoh; M Wattenhofer; K Shibuya; A Berry; R Chrast; M Guipponi; J Wang; K Kawasaki; S Asakawa; S Minoshima; F Younus; S Q Mehdi; U Radhakrishna; M P Papasavvas; C Gehrig; C Rossier; M Korostishevsky; A Gal; N Shimizu; B Bonne-Tamir; S E Antonarakis
Journal:  Nat Genet       Date:  2001-01       Impact factor: 38.330

9.  Novel mutations of TMPRSS3 in four DFNB8/B10 families segregating congenital autosomal recessive deafness.

Authors:  T Ben-Yosef; M Wattenhofer; S Riazuddin; Z M Ahmed; H S Scott; J Kudoh; K Shibuya; S E Antonarakis; B Bonne-Tamir; U Radhakrishna; S Naz; Z Ahmed; S Riazuddin; A Pandya; W E Nance; E R Wilcox; T B Friedman; R J Morell
Journal:  J Med Genet       Date:  2001-06       Impact factor: 6.318

Review 10.  Regulation of cortical structure by the ezrin-radixin-moesin protein family.

Authors:  A Bretscher
Journal:  Curr Opin Cell Biol       Date:  1999-02       Impact factor: 8.382
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  6 in total

1.  CD44 is a marker for the outer pillar cells in the early postnatal mouse inner ear.

Authors:  Ronna Hertzano; Chandrakala Puligilla; Siaw-Lin Chan; Caroline Timothy; Didier A Depireux; Zubair Ahmed; Jeffrey Wolf; David J Eisenman; Thomas B Friedman; Sheikh Riazuddin; Matthew W Kelley; Scott E Strome
Journal:  J Assoc Res Otolaryngol       Date:  2010-04-13

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

Authors:  Shahid Y Khan; Saima Riazuddin; Muhammad Tariq; Saima Anwar; Muhammad I Shabbir; S Amer Riazuddin; Shaheen N Khan; Tayyab Husnain; Zubair M Ahmed; Thomas B Friedman; Sheikh Riazuddin
Journal:  Hum Genet       Date:  2006-10-26       Impact factor: 4.132

3.  A study on the prevalence of a tick-transmitted pathogen, Theileria annulata, and hematological profile of cattle from Southern Punjab (Pakistan).

Authors:  S Shahnawaz; M Ali; M A Aslam; R Fatima; Z I Chaudhry; M U Hassan; M Ali; Furhan Iqbal
Journal:  Parasitol Res       Date:  2011-03-31       Impact factor: 2.289

4.  A novel locus DFNA59 for autosomal dominant nonsyndromic hearing loss maps at chromosome 11p14.2-q12.3.

Authors:  Arunima Chatterjee; Rajeev Jalvi; Nishtha Pandey; R Rangasayee; Anuranjan Anand
Journal:  Hum Genet       Date:  2008-11-22       Impact factor: 4.132

5.  Detection of Babesia bovis in blood samples and its effect on the hematological and serum biochemical profile in large ruminants from Southern Punjab.

Authors:  Samreen Zulfiqar; Sadia Shahnawaz; Muhammad Ali; Arif Mahmood Bhutta; Shahid Iqbal; Sikandar Hayat; Shazia Qadir; Muhammad Latif; Nazia Kiran; Ali Saeed; Muhammad Ali; Furhan Iqbal
Journal:  Asian Pac J Trop Biomed       Date:  2012-02

6.  A study on the determination of risk factors associated with babesiosis and prevalence of Babesia sp., by PCR amplification, in small ruminants from Southern Punjab (Pakistan).

Authors:  F Iqbal; M Fatima; S Shahnawaz; M Naeem; Rs Shaikh; M Ali; As Shaikh; M Aktas; M Ali
Journal:  Parasite       Date:  2011-08       Impact factor: 3.000
  6 in total

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