Literature DB >> 15121790

Modifier controls severity of a novel dominant low-frequency MyosinVIIA (MYO7A) auditory mutation.

V A Street, J C Kallman, K L Kiemele.   

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Year:  2004        PMID： 15121790      PMCID： PMC1735774          DOI： 10.1136/jmg.2003.013557

Source DB:  PubMed          Journal:  J Med Genet        ISSN： 0022-2593            Impact factor:   6.318


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  11 in total

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3.  A DNA variant within the MYO7A promoter regulates YY1 transcription factor binding and gene expression serving as a potential dominant DFNA11 auditory genetic modifier.

Authors:  Valerie A Street; Jin Li; Carol A Robbins; Jeremy C Kallman
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4.  Variable hearing impairment in a DFNB2 family with a novel MYO7A missense mutation.

Authors:  M S Hildebrand; N P Thorne; C J Bromhead; K Kahrizi; J A Webster; Z Fattahi; M Bataejad; W J Kimberling; D Stephan; H Najmabadi; M Bahlo; R J H Smith
Journal:  Clin Genet       Date:  2010-02-04       Impact factor: 4.438

5.  In search of the DFNA11 myosin VIIA low- and mid-frequency auditory genetic modifier.

Authors:  Jeremy C Kallman; James O Phillips; Naomi F Bramhall; John P Kelly; Valerie A Street
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6.  A Myo7a mutation cosegregates with stereocilia defects and low-frequency hearing impairment.

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Review 7.  Function and expression pattern of nonsyndromic deafness genes.

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Journal:  Curr Mol Med       Date:  2009-06       Impact factor: 2.222

Review 8.  Development and Patterning of the Cochlea: From Convergent Extension to Planar Polarity.

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Journal:  Cold Spring Harb Perspect Med       Date:  2020-01-02       Impact factor: 6.915

9.  Identification and functional study of a new missense mutation in the motor head domain of myosin VIIA in a family with autosomal dominant hearing impairment (DFNA11).

Authors:  Qing Sang; Xukun Yan; Huan Wang; Ruizhi Feng; Xiang Fei; Duan Ma; Qinghe Xing; Qiaoli Li; Xinzhi Zhao; Li Jin; Lin He; Huawei Li; Lei Wang
Journal:  PLoS One       Date:  2013-01-29       Impact factor: 3.240

10.  A novel WFS1 mutation in a family with dominant low frequency sensorineural hearing loss with normal VEMP and EcochG findings.

Authors:  Naomi F Bramhall; Jeremy C Kallman; Aimee M Verrall; Valerie A Street
Journal:  BMC Med Genet       Date:  2008-06-02       Impact factor: 2.103
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