(Q48409882)

11 February 2018

title

Auditory function associated with Col11a1 haploinsufficiency in chondrodysplasia (cho) mice. (English)

1 reference

11 February 2018

main subject

haploinsufficiency

0 references

author name string

Yvonne M Szymko-Bennett

1

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11 February 2018

Kiyoto Kurima

2

1 reference

11 February 2018

Bjorn Olsen

3

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11 February 2018

Robert Seegmiller

4

1 reference

11 February 2018

Andrew J Griffith

5

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11 February 2018

publication date

1 January 2003

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11 February 2018

published in

Hearing Research

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11 February 2018

volume

175

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11 February 2018

issue

1-2

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11 February 2018

page(s)

178-182

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11 February 2018

Hearing loss in the nonocular Stickler syndrome caused by a COL11A2 mutation.

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900736-0

7 January 2021

Splicing mutations of 54-bp exons in the COL11A1 gene cause Marshall syndrome, but other mutations cause overlapping Marshall/Stickler phenotypes

1 reference

https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900736-0

7 January 2021

Structural macromolecules and supramolecular organisation of the vitreous gel.

1 reference

https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900736-0

7 January 2021

Marshall syndrome associated with a splicing defect at the COL11A1 locus

1 reference

https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900736-0

7 January 2021

Audiovestibular phenotype associated with a COL11A1 mutation in Marshall syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900736-0

7 January 2021

A major gene affecting age-related hearing loss in C57BL/6J mice

1 reference

https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900736-0

7 January 2021

A major gene affecting age-related hearing loss is common to at least ten inbred strains of mice.

1 reference

https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900736-0

7 January 2021

A fibrillar collagen gene, Col11a1, is essential for skeletal morphogenesis

1 reference

https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900736-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900736-0

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%2FS0378-5955%2802%2900736-0

7 January 2021

A new chondrodystrophic mutant in mice. Electron microscopy of normal and abnormal chondrogenesis

1 reference

https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900736-0

7 January 2021

Studies on cartilage. VI. A genetically determined defect in tracheal cartilage

1 reference

https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900736-0

7 January 2021

Stickler syndrome without eye involvement is caused by mutations in COL11A2, the gene encoding the alpha2(XI) chain of type XI collagen

1 reference

https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900736-0

7 January 2021

Type II and type IX collagen form heterotypic fibers in the tectorial membrane of the inner ear

1 reference

https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900736-0

7 January 2021

Auditory dysfunction in Stickler syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900736-0

7 January 2021

Collagen of accessory structures of organ of Corti

1 reference

https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900736-0

7 January 2021

Autosomal dominant and recessive osteochondrodysplasias associated with the COL11A2 locus

1 reference

https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900736-0

7 January 2021

Assessment of hearing in 80 inbred strains of mice by ABR threshold analyses

1 reference

https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900736-0

7 January 2021

10.1016/S0378-5955(02)00736-0

Identifiers

DOI

1 reference

11 February 2018

PubMed ID

12527136

1 reference

11 February 2018