(Q48082300)

8 February 2018

title

Mouse cartilage matrix deficiency (cmd) caused by a 7 bp deletion in the aggrecan gene. (English)

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8 February 2018

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Watanabe H

1

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8 February 2018

Kimata K

2

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8 February 2018

Line S

3

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8 February 2018

Strong D

4

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8 February 2018

Gao LY

5

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8 February 2018

Kozak CA

6

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8 February 2018

Yamada Y

7

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8 February 2018

language of work or name

English

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publication date

1 June 1994

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8 February 2018

published in

Nature Genetics

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8 February 2018

volume

7

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8 February 2018

page(s)

154-157

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8 February 2018

issue

2

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8 February 2018

https://scigraph.springernature.com/pub.10.1038/ng0694-154

exact match

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cites work

Presence of link protein in cartilage from cmd/cmd (cartilage matrix deficiency) mice

1 reference

https://api.crossref.org/works/10.1038%2FNG0694-154

7 January 2021

Molecular genetic markers spanning mouse chromosome 10

1 reference

https://api.crossref.org/works/10.1038%2FNG0694-154

7 January 2021

The mouse homolog of the Gibbon ape leukemia virus receptor: genetic mapping and a possible receptor function in rodents

1 reference

https://api.crossref.org/works/10.1038%2FNG0694-154

7 January 2021

Characterization and chromosomal mapping of a cDNA encoding tryptophan hydroxylase from a mouse mastocytoma cell line

1 reference

https://api.crossref.org/works/10.1038%2FNG0694-154

7 January 2021

Genetic mapping of three GABAA receptor-subunit genes in the mouse.

1 reference

https://api.crossref.org/works/10.1038%2FNG0694-154

7 January 2021

Absence of proteoglycan core protein in the cartilage mutant nanomelia

1 reference

https://api.crossref.org/works/10.1038%2FNG0694-154

7 January 2021

Chondrocytes from the cartilage proteoglycan-deficient mutant, nanomelia, synthesize greatly reduced levels of the proteoglycan core protein transcript

1 reference

https://api.crossref.org/works/10.1038%2FNG0694-154

7 January 2021

Molecular basis of heritable connective tissue disease

1 reference

https://api.crossref.org/works/10.1038%2FNG0694-154

7 January 2021

The Stickler syndrome: evidence for close linkage to the structural gene for type II collagen

1 reference

https://api.crossref.org/works/10.1038%2FNG0694-154

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/10.1038%2FNG0694-154

7 January 2021

Identification of the molecular defect in a family with spondyloepiphyseal dysplasia

1 reference

https://api.crossref.org/works/10.1038%2FNG0694-154

7 January 2021

Correction of abnormal matrix formed by cmd/cmd chondrocytes in culture by exogenously added cartilage proteoglycan

1 reference

https://api.crossref.org/works/10.1038%2FNG0694-154

7 January 2021

Identifiers

DOI

10.1038/NG0694-154

1 reference

8 February 2018

PubMed ID

7920633

1 reference

8 February 2018