Literature DB >> 10354578

Deafness genes: expressions of surprise.

K P Steel1, T J Bussoli.   

Abstract

Recent rapid progress in identifying genes involved in deafness has suggested that a wide range of different types of gene products can result in hearing impairment, which, given the complexity of the auditory system, is not surprising. However, what has given some surprises are the unexpected expression patterns within the ear of some of these genes, which suggests that cochlear physiologists need to look again at some of the cell types involved.

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Year:  1999        PMID： 10354578     DOI： 10.1016/s0168-9525(99)01753-9

Source DB:  PubMed          Journal:  Trends Genet        ISSN： 0168-9525            Impact factor:   11.639


  15 in total

Review 1.  Science, medicine, and the future: New interventions in hearing impairment.

Authors:  K P Steel
Journal:  BMJ       Date:  2000-03-04

2.  Heritability and segregation analysis of deafness in U.S. Dalmatians.

Authors:  E J Cargill; T R Famula; G M Strain; K E Murphy
Journal:  Genetics       Date:  2004-03       Impact factor: 4.562

3.  Translation initiation in Saccharomyces cerevisiae mitochondria: functional interactions among mitochondrial ribosomal protein Rsm28p, initiation factor 2, methionyl-tRNA-formyltransferase and novel protein Rmd9p.

Authors:  Elizabeth H Williams; Christine A Butler; Nathalie Bonnefoy; Thomas D Fox
Journal:  Genetics       Date:  2006-12-28       Impact factor: 4.562

4.  Mapping of a novel autosomal recessive nonsyndromic deafness locus (DFNB46) to chromosome 18p11.32-p11.31.

Authors:  Asif Mir; Muhammad Ansar; Maria H Chahrour; Thanh L Pham; Muhammad Wajid; Sayedul Haque; Kai Yan; Wasim Ahmad; Suzanne M Leal
Journal:  Am J Med Genet A       Date:  2005-02-15       Impact factor: 2.802

5.  Characterisation and genetic mapping of a new X linked deafness syndrome.

Authors:  D M Martin; F J Probst; S A Camper; E M Petty
Journal:  J Med Genet       Date:  2000-11       Impact factor: 6.318

6.  DFNB44, a novel autosomal recessive non-syndromic hearing impairment locus, maps to chromosome 7p14.1-q11.22.

Authors:  Muhammad Ansar; Maria H Chahrour; Mohammad Amin Ud Din; Muhammad Arshad; Sayedul Haque; Thanh L Pham; Kai Yan; Wasim Ahmad; Suzanne M Leal
Journal:  Hum Hered       Date:  2004       Impact factor: 0.444

7.  A novel autosomal recessive non-syndromic hearing impairment locus (DFNB47) maps to chromosome 2p25.1-p24.3.

Authors:  Muhammad Jawad Hassan; Regie Lyn P Santos; Muhammad Arshad Rafiq; Maria H Chahrour; Thanh L Pham; Muhammad Wajid; Nadine Hijab; Michael Wambangco; Kwanghyuk Lee; Muhammad Ansar; Kai Yan; Wasim Ahmad; Suzanne M Leal
Journal:  Hum Genet       Date:  2005-10-29       Impact factor: 4.132

8.  Pendred syndrome among patients with congenital hypothyroidism detected by neonatal screening: identification of two novel PDS/SLC26A4 mutations.

Authors:  Karolina Banghova; Eva Al Taji; Ondrej Cinek; Dana Novotna; Radka Pourova; Jirina Zapletalova; Olga Hnikova; Jan Lebl
Journal:  Eur J Pediatr       Date:  2007-09-18       Impact factor: 3.183

9.  Probing the Xenopus laevis inner ear transcriptome for biological function.

Authors:  TuShun R Powers; Selene M Virk; Casilda Trujillo-Provencio; Elba E Serrano
Journal:  BMC Genomics       Date:  2012-06-08       Impact factor: 3.969

10.  Headbobber: a combined morphogenetic and cochleosaccular mouse model to study 10qter deletions in human deafness.

Authors:  Annalisa Buniello; Rachel E Hardisty-Hughes; Johanna C Pass; Eva Bober; Richard J Smith; Karen P Steel
Journal:  PLoS One       Date:  2013-02-14       Impact factor: 3.240
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