(Q28185432)

1

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T J R van de Pol

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A I den Hollander

4

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J ten Caat

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V van Limpt

6

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H G Brunner

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H Kremer

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F P M Cremers

Genetics, genomics and gene discovery in the auditory system

9

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language of work or name

English

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publication date

October 2003

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published in

Genomics

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volume

82

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issue

4

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page(s)

480-90

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cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900150-2

7 January 2021

Genetic epidemiology of hearing impairment

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900150-2

7 January 2021

Mutations in a new gene encoding a protein of the hair bundle cause non-syndromic deafness at the DFNB16 locus

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900150-2

7 January 2021

Otoancorin, an inner ear protein restricted to the interface between the apical surface of sensory epithelia and their overlying acellular gels, is defective in autosomal recessive deafness DFNB22.

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900150-2

7 January 2021

Suppression subtractive hybridization: a method for generating differentially regulated or tissue-specific cDNA probes and libraries

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900150-2

7 January 2021

Isolation and mapping of novel candidate genes for retinal disorders using suppression subtractive hybridization

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900150-2

7 January 2021

Mutations in a novel cochlear gene cause DFNA9, a human nonsyndromic deafness with vestibular dysfunction

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900150-2

7 January 2021

Association between X-linked mixed deafness and mutations in the POU domain gene POU3F4

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900150-2

7 January 2021

A novel conserved cochlear gene, OTOR: identification, expression analysis, and chromosomal mapping

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900150-2

7 January 2021

Mutations in the human alpha-tectorin gene cause autosomal dominant non-syndromic hearing impairment

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900150-2

7 January 2021

RHS2, a POU domain-containing gene, and its expression in developing and adult rat

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900150-2

7 January 2021

Fdp, a new fibrocyte-derived protein related to MIA/CD-RAP, has an in vitro effect on the early differentiation of the inner ear mesenchyme

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900150-2

7 January 2021

Consanguineous nuclear families used to identify a new locus for recessive non-syndromic hearing loss on 14q.

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900150-2

7 January 2021

Identification of a locus on chromosome 7q31, DFNB14, responsible for prelingual sensorineural non-syndromic deafness.

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900150-2

7 January 2021

A new locus for autosomal recessive non-syndromal sensorineural hearing impairment (DFNB27) on chromosome 2q23-q31.

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900150-2

7 January 2021

A novel locus for non-syndromic sensorineural deafness (DFN6) maps to chromosome Xp22.

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900150-2

7 January 2021

Cloning genes from an inner ear cDNA library

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900150-2

7 January 2021

Identification of preferentially expressed cochlear genes by systematic sequencing of a rat cochlea cDNA library.

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900150-2

7 January 2021

Expression pattern of mammalian cochlea outer hair cell (OHC) mRNA: screening of a rat OHC cDNA library

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900150-2

7 January 2021

Construction of a cDNA library from microdissected guinea pig organ of Corti

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900150-2

7 January 2021

Otogelin: a glycoprotein specific to the acellular membranes of the inner ear

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900150-2

7 January 2021

Isolation of chicken alpha ENaC splice variants from a cochlear cDNA library

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900150-2

7 January 2021

Molecular markers for cell types of the inner ear and candidate genes for hearing disorders

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900150-2

7 January 2021

Prestin is the motor protein of cochlear outer hair cells

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900150-2

7 January 2021

A subtracted cDNA library from the zebrafish (Danio rerio) embryonic inner ear.

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900150-2

7 January 2021

Isolation of novel and known genes from a human fetal cochlear cDNA library using subtractive hybridization and differential screening

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900150-2

7 January 2021

Molecular cloning of a zinc finger gene eZNF from a human inner ear cDNA library, and in situ expression pattern of its mouse homologue in mouse inner ear

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900150-2

7 January 2021

Human cochlear expressed sequence tags provide insight into cochlear gene expression and identify candidate genes for deafness

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900150-2

7 January 2021

Sequence and tissue distribution of a second protein of hepatic gap junctions, Cx26, as deduced from its cDNA

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900150-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900150-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900150-2

7 January 2021

Abnormal collagen metabolism in cultured cells in osteogenesis imperfecta

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900150-2

7 January 2021

Stop codon in the procollagen II gene (COL2A1) in a family with the Stickler syndrome (arthro-ophthalmopathy)

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900150-2

7 January 2021

A family with Stickler syndrome type 2 has a mutation in the COL11A1 gene resulting in the substitution of glycine 97 by valine in alpha 1 (XI) collagen

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900150-2

7 January 2021

Mutations in COL11A2 cause non-syndromic hearing loss (DFNA13)

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900150-2

7 January 2021

Gapped BLAST and PSI-BLAST: a new generation of protein database search programs

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900150-2

7 January 2021

Isolation of biologically active ribonucleic acid from sources enriched in ribonuclease

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900150-2

7 January 2021

10.1016/S0888-7543(03)00150-2

Identifiers

DOI

1 reference

Consolidated OpenCitations Corpus – April 2017

1312546

1312546

1 reference

Consolidated OpenCitations Corpus – April 2017

Consolidated OpenCitations Corpus – April 2017

1 reference