A novel conserved cochlear gene, OTOR: identification, expression analysis, and chromosomal mapping (Q22254343)

GOA release 2020-03-11

hearing

1 reference

GOA release 2020-03-11

N G Robertson

1

N G

Robertson

1 reference

8 February 2023

S Heller

2

S

Heller

1 reference

8 February 2023

J S Lin

3

J S

Lin

1 reference

8 February 2023

B L Resendes

4

B L

Resendes

1 reference

8 February 2023

S Weremowicz

5

S

Weremowicz

1 reference

8 February 2023

C S Denis

6

C S

Denis

1 reference

8 February 2023

A M Bell

7

A M

Bell

1 reference

8 February 2023

A J Hudspeth

8

A J

Hudspeth

1 reference

8 February 2023

C C Morton

9

C C

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

Morton

1 reference

8 February 2023

language of work or name

English

0 references

publication date

15 June 2000

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published in

Genomics

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volume

66

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issue

3

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page(s)

242-8

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cites work

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Effects of retinoic acid on cartilage differentiation in a chondrogenic cell line

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Responsiveness to retinoic acid changes during chondrocyte maturation.

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

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Cloning of the genes encoding two murine and human cochlear unconventional type I myosins

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Mapping and characterization of a novel cochlear gene in human and in mouse: a positional candidate gene for a deafness disorder, DFNA9

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A single protocol to detect transcripts of various types and expression levels in neural tissue and cultured cells: in situ hybridization using digoxigenin-labelled cRNA probes

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Noncollagenous, nonproteoglycan macromolecules of cartilage

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"A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity". Addendum

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A simple method for displaying the hydropathic character of a protein

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Expression and localization of COL2A1 mRNA and type II collagen in human fetal cochlea.

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Isolation of biologically active ribonucleic acid from sources enriched in ribonuclease

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Beginning of a molecular era in hearing and deafness

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Local application of retinoic acid to the limb bond mimics the action of the polarizing region

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7 January 2021

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

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7 January 2021

Mutations in the human Jagged1 gene are responsible for Alagille syndrome

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7 January 2021

Alagille syndrome is caused by mutations in human Jagged1, which encodes a ligand for Notch1

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7 January 2021

Hybridization of denatured RNA and small DNA fragments transferred to nitrocellulose

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7 January 2021

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

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7 January 2021

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

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7 January 2021

Cloning of a retinoic acid-sensitive mRNA expressed in cartilage and during chondrogenesis

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7 January 2021

Localization of a gene for otosclerosis to chromosome 15q25-q26.

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7 January 2021

A Pro51Ser mutation in the COCH gene is associated with late onset autosomal dominant progressive sensorineural hearing loss with vestibular defects

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7 January 2021

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

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7 January 2021

High prevalence of symptoms of Menière's disease in three families with a mutation in the COCH gene

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7 January 2021

A comprehensive set of sequence analysis programs for the VAX

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A new method for predicting signal sequence cleavage sites

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7 January 2021

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

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7 January 2021

Clinical and molecular genetics of Alagille syndrome

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7 January 2021

Genetic epidemiology of hearing impairment

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7 January 2021

mRNA encoding a novel growth regulatory factor is coexpressed with type II procollagen during chondrogenesis.

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7 January 2021

Purification of the human NF-E2 complex: cDNA cloning of the hematopoietic cell-specific subunit and evidence for an associated partner

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Alagille syndrome and deletion of 20p.

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Rat calvarial cell lines immortalized with SV-40 large T antigen: constitutive and retinoic acid-inducible expression of osteoblastic features

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7 January 2021