(Q24324566)

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Identification of CRYM as a candidate responsible for nonsyndromic deafness, through cDNA microarray analysis of human cochlear and vestibular tissues.

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Europe PubMed Central

PubMed publication ID

23 June 2017

Identification of CRYM as a candidate responsible for nonsyndromic deafness, through cDNA microarray analysis of human cochlear and vestibular tissues. (English)

1 reference

Europe PubMed Central

PubMed publication ID

23 June 2017

1 reference

GOA release 2020-03-11

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GOA release 2020-03-11

author name string

Satoko Abe

1

1 reference

Europe PubMed Central

PubMed publication ID

23 June 2017

Toyomasa Katagiri

2

1 reference

Europe PubMed Central

PubMed publication ID

23 June 2017

Akihiko Saito-Hisaminato

3

1 reference

Europe PubMed Central

PubMed publication ID

23 June 2017

Shin-ichi Usami

4

1 reference

Europe PubMed Central

PubMed publication ID

23 June 2017

Yasuhiro Inoue

5

1 reference

Europe PubMed Central

PubMed publication ID

23 June 2017

Tatsuhiko Tsunoda

6

1 reference

Europe PubMed Central

PubMed publication ID

23 June 2017

Yusuke Nakamura

7

1 reference

Europe PubMed Central

PubMed publication ID

23 June 2017

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publication date

6 December 2002

1 reference

Europe PubMed Central

PubMed publication ID

23 June 2017

American Journal of Human Genetics

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Europe PubMed Central

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23 June 2017

72

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Europe PubMed Central

PubMed publication ID

23 June 2017

1

1 reference

Europe PubMed Central

PubMed publication ID

23 June 2017

73-82

1 reference

Europe PubMed Central

PubMed publication ID

23 June 2017

A defect in harmonin, a PDZ domain-containing protein expressed in the inner ear sensory hair cells, underlies Usher syndrome type 1C

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=420014

19 March 2017

Identification of the gene responsible for gelatinous drop-like corneal dystrophy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=420014

19 March 2017

A mutation in OTOF, encoding otoferlin, a FER-1-like protein, causes DFNB9, a nonsyndromic form of deafness

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=420014

19 March 2017

Purification, molecular cloning, and functional expression of the human nicodinamide-adenine dinucleotide phosphate-regulated thyroid hormone-binding protein

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=420014

19 March 2017

mu-crystallin is a mammalian homologue of Agrobacterium ornithine cyclodeaminase and is expressed in human retina

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=420014

19 March 2017

Two roles for mu-crystallin: a lens structural protein in diurnal marsupials and a possible enzyme in mammalian retinas

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=420014

19 March 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=420014

19 March 2017

Targeted disruption of otog results in deafness and severe imbalance

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=420014

19 March 2017

Identification of the stef gene that encodes a novel guanine nucleotide exchange factor specific for Rac1

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=420014

19 March 2017

Heteroligomerization of an Aquaporin-2 mutant with wild-type Aquaporin-2 and their misrouting to late endosomes/lysosomes explains dominant nephrogenic diabetes insipidus

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=420014

27 September 2017

A genetic approach to understanding auditory function

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=420014

27 September 2017

Prevalent connexin 26 gene (GJB2) mutations in Japanese

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=420014

27 September 2017

Prevalence of mitochondrial gene mutations among hearing impaired patients

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=420014

27 September 2017

Gene expression profiles of laser-captured adjacent neuronal subtypes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=420014

27 September 2017

Juvenile form of mucopolysaccharidosis VI (Maroteaux-Lamy syndrome). A C-terminal extension causes instability but increases catalytic efficiency of arylsulfatase B.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=420014

27 September 2017

The fine structure of spiral ligament cells relates to ion return to the stria and varies with place-frequency

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=420014

30 May 2018

Periods of sensitivity to thyroid hormone during the development of the organ of Corti.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=420014

30 May 2018

Genome-wide profiling of gene expression in 29 normal human tissues with a cDNA microarray

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=420014

29 November 2018

Identification by cDNA microarray of genes involved in ovarian carcinogenesis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=420014

29 November 2018

Genetic epidemiological studies of early-onset deafness in the U.S. school-age population

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=420014

29 November 2018

Responsiveness of α1, and β1Cochlear Na, K-ATPase Isoforms to Thyroid Hormone

1 reference

https://pubmed.ncbi.nlm.nih.gov/12471561

12 December 2020

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1 reference

Europe PubMed Central

PubMed publication ID

23 June 2017

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1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

PMC publication ID

1 reference

Consolidated OpenCitations Corpus – April 2017

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PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

23 June 2017

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