Inner ear and kidney anomalies caused by IAP insertion in an intron of the Eya1 gene in a mouse model of BOR syndrome (Q28593604)

31 January 2017

title

Inner ear and kidney anomalies caused by IAP insertion in an intron of the Eya1 gene in a mouse model of BOR syndrome (English)

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EYA transcriptional coactivator and phosphatase 1

31 January 2017

main subject

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GOA release 2020-03-11

K. R. Johnson

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31 January 2017

S. A. Cook

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31 January 2017

L. C. Erway

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31 January 2017

A. N. Matthews

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31 January 2017

L. P. Sanford

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31 January 2017

N. E. Paradies

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31 January 2017

R. A. Friedman

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31 January 2017

language of work or name

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1 April 1999

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31 January 2017

published in

Human Molecular Genetics

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31 January 2017

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31 January 2017

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31 January 2017

page(s)

645–653

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Genetic epidemiology of hearing impairment

31 January 2017

cites work

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The fundamental and medical impacts of recent progress in research on hereditary hearing loss

21 January 2018

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Genetic deafness--progress with mouse models

21 January 2018

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Inherited hearing defects in mice

21 January 2018

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A type VII myosin encoded by the mouse deafness gene shaker-1

21 January 2018

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HIV-1: gambling on the evolution of drug resistance?

21 January 2018

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Mutations in the myosin VIIA gene cause non-syndromic recessive deafness

21 January 2018

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Defective myosin VIIA gene responsible for Usher syndrome type 1B

21 January 2018

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Correction of deafness in shaker-2 mice by an unconventional myosin in a BAC transgene.

21 January 2018

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

21 January 2018

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A human homologue of the Drosophila eyes absent gene underlies branchio-oto-renal (BOR) syndrome and identifies a novel gene family

21 January 2018

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Clustering of mutations responsible for branchio-oto-renal (BOR) syndrome in the eyes absent homologous region (eyaHR) of EYA1

21 January 2018

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Neomorphic agouti mutations in obese yellow mice

21 January 2018

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The mouse pale ear ( ep ) mutation is the homologue of human Hermansky–Pudlak syndrome

21 January 2018

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IAP insertion in the murine LamB3 gene results in junctional epidermolysis bullosa

21 January 2018

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Reln(rl-Alb2), an allele of reeler isolated from a chlorambucil screen, is due to an IAP insertion with exon skipping

21 January 2018

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Inherited somatic mosaicism caused by an intracisternal A particle insertion in the mouse tyrosinase gene

21 January 2018

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Intracisternal A-particle element transposition into the murine beta-glucuronidase gene correlates with loss of enzyme activity: a new model for beta-glucuronidase deficiency in the C3H mouse

21 January 2018

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A Macintosh program for storage and analysis of experimental genetic mapping data

21 January 2018

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Genetics of age-related hearing loss in mice: I. Inbred and F1 hybrid strains

21 January 2018

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21 January 2018

Identifiers

DOI

10.1093/HMG/8.4.645

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