Literature DB >> 23273769

Clue to a new deafness gene: a large Chinese nonsyndromic hearing loss family linked to DFNA4.

Liang Zong, Chunye Lu, Yali Zhao, Qian Li, Dongyi Han, Weiyan Yang, Yan Shen, Qingyin Zheng, Qiuju Wang.   

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Year:  2012        PMID： 23273769      PMCID： PMC3685490          DOI： 10.1016/j.jgg.2012.11.002

Source DB:  PubMed          Journal:  J Genet Genomics        ISSN： 1673-8527            Impact factor:   4.275


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  22 in total

1.  Deafness linked to DFNA2: one locus but how many genes?

Authors:  P Van Hauwe; P J Coucke; F Declau; H Kunst; R J Ensink; H A Marres; C W Cremers; B Djelantik; S D Smith; P Kelley; P H Van de Heyning; G Van Camp
Journal:  Nat Genet       Date:  1999-03       Impact factor: 38.330

2.  Orphan glutamate receptor delta1 subunit required for high-frequency hearing.

Authors:  Jiangang Gao; Stéphane F Maison; Xudong Wu; Keiko Hirose; Sherri M Jones; Ildar Bayazitov; Yong Tian; Guy Mittleman; Douglas B Matthews; Stanislav S Zakharenko; M Charles Liberman; Jian Zuo
Journal:  Mol Cell Biol       Date:  2007-04-16       Impact factor: 4.272

3.  A chloride conductance in VGLUT1 underlies maximal glutamate loading into synaptic vesicles.

Authors:  Stephan Schenck; Sonja M Wojcik; Nils Brose; Shigeo Takamori
Journal:  Nat Neurosci       Date:  2009-01-25       Impact factor: 24.884

4.  Mutations in the KCNQ4 gene are responsible for autosomal dominant deafness in four DFNA2 families.

Authors:  P J Coucke; P Van Hauwe; P M Kelley; H Kunst; I Schatteman; D Van Velzen; J Meyers; R J Ensink; M Verstreken; F Declau; H Marres; K Kastury; S Bhasin; W T McGuirt; R J Smith; C W Cremers; P Van de Heyning; P J Willems; S D Smith; G Van Camp
Journal:  Hum Mol Genet       Date:  1999-07       Impact factor: 6.150

5.  Carcinoembryonic antigen-related cell adhesion molecule 16 interacts with alpha-tectorin and is mutated in autosomal dominant hearing loss (DFNA4).

Authors:  Jing Zheng; Katharine K Miller; Tao Yang; Michael S Hildebrand; A Eliot Shearer; Adam P DeLuca; Todd E Scheetz; Jennifer Drummond; Steve E Scherer; P Kevin Legan; Richard J Goodyear; Guy P Richardson; Mary Ann Cheatham; Richard J Smith; Peter Dallos
Journal:  Proc Natl Acad Sci U S A       Date:  2011-02-22       Impact factor: 11.205

6.  Nonsyndromic hereditary hearing loss.

Authors:  Raye L Alford
Journal:  Adv Otorhinolaryngol       Date:  2011-02-24

Review 7.  An overview of hereditary hearing loss.

Authors:  Yildirim A Bayazit; Metin Yilmaz
Journal:  ORL J Otorhinolaryngol Relat Spec       Date:  2006-01-20       Impact factor: 1.538

8.  Genetic heterogeneity of deafness phenotypes linked to DFNA4.

Authors:  Tao Yang; Markus Pfister; Nikolaus Blin; Hans P Zenner; Carsten M Pusch; Richard J H Smith
Journal:  Am J Med Genet A       Date:  2005-11-15       Impact factor: 2.802

Review 9.  The impact of next-generation sequencing on genomics.

Authors:  Jun Zhang; Rod Chiodini; Ahmed Badr; Genfa Zhang
Journal:  J Genet Genomics       Date:  2011-03-15       Impact factor: 4.275

10.  Impairment of SLC17A8 encoding vesicular glutamate transporter-3, VGLUT3, underlies nonsyndromic deafness DFNA25 and inner hair cell dysfunction in null mice.

Authors:  Jérôme Ruel; Sarah Emery; Régis Nouvian; Tiphaine Bersot; Bénédicte Amilhon; Jana M Van Rybroek; Guy Rebillard; Marc Lenoir; Michel Eybalin; Benjamin Delprat; Theru A Sivakumaran; Bruno Giros; Salah El Mestikawy; Tobias Moser; Richard J H Smith; Marci M Lesperance; Jean-Luc Puel
Journal:  Am J Hum Genet       Date:  2008-08       Impact factor: 11.025
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  4 in total

1.  Comparative proteomic analysis of human lung telocytes with fibroblasts.

Authors:  Yonghua Zheng; Dragos Cretoiu; Guoquan Yan; Sanda Maria Cretoiu; Laurentiu M Popescu; Xiangdong Wang
Journal:  J Cell Mol Med       Date:  2014-03-28       Impact factor: 5.310

2.  Exome sequencing identifies a novel CEACAM16 mutation associated with autosomal dominant nonsyndromic hearing loss DFNA4B in a Chinese family.

Authors:  Honghan Wang; Xinwei Wang; Chufeng He; Haibo Li; Jie Qing; Mhamed Grati; Zhengmao Hu; Jiada Li; Yiqiao Hu; Kun Xia; Lingyun Mei; Xingwei Wang; Jianjun Yu; Hongsheng Chen; Lu Jiang; Yalan Liu; Meichao Men; Hailin Zhang; Liping Guan; Jingjing Xiao; Jianguo Zhang; Xuezhong Liu; Yong Feng
Journal:  J Hum Genet       Date:  2015-01-15       Impact factor: 3.172

3.  Isolated human uterine telocytes: immunocytochemistry and electrophysiology of T-type calcium channels.

Authors:  Sanda Maria Cretoiu; Beatrice Mihaela Radu; Adela Banciu; Daniel Dumitru Banciu; Dragos Cretoiu; Laura Cristina Ceafalan; Laurentiu Mircea Popescu
Journal:  Histochem Cell Biol       Date:  2014-09-12       Impact factor: 4.304

4.  TLR4 drives the pathogenesis of acquired cholesteatoma by promoting local inflammation and bone destruction.

Authors:  Yu Si; Yu Bin Chen; Sui Jun Chen; Yi Qing Zheng; Xiang Liu; Yi Liu; Huai Li Jiang; Guo Xu; Zhuo Hao Li; Qiu Hong Huang; Hao Xiong; Zhi Gang Zhang
Journal:  Sci Rep       Date:  2015-12-07       Impact factor: 4.379
  4 in total

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