Dwarfism and age-associated spinal degeneration of heterozygote cmd mice defective in aggrecan (Q36243774)

13 August 2017

Dwarfism and age-associated spinal degeneration of heterozygote cmd mice defective in aggrecan (English)

1 reference

13 August 2017

Watanabe H

1

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13 August 2017

Nakata K

2

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13 August 2017

Kimata K

3

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13 August 2017

Nakanishi I

4

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13 August 2017

Yamada Y

5

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13 August 2017

language of work or name

English

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publication date

1 June 1997

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Proceedings of the National Academy of Sciences of the United States of America

13 August 2017

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13 August 2017

94

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13 August 2017

13

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13 August 2017

6943-6947

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The chondrocyte, architect of cartilage. Biomechanics, structure, function and molecular biology of cartilage matrix macromolecules

13 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=21264

Mutations in collagen genes resulting in metaphyseal and epiphyseal dysplasias

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=21264

Aggrecan degradation in osteoarthritis and rheumatoid arthritis.

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=21264

A type X collagen mutation causes Schmid metaphyseal chondrodysplasia

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=21264

Mutations in type 1 procollagen that cause osteogenesis imperfecta: effects of the mutations on the assembly of collagen into fibrils, the basis of phenotypic variations, and potential antisense therapies

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=21264

Molecular basis of osteogenesis imperfecta and related disorders of bone.

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=21264

Complete coding sequence, deduced primary structure, chromosomal localization, and structural analysis of murine aggrecan

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=21264

Heritable diseases of cartilage caused by mutations in collagen genes.

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=21264

Changes in cartilage metabolism in arthritis are reflected by altered serum and synovial fluid levels of the cartilage proteoglycan aggrecan. Implications for pathogenesis

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=21264

Absence of proteoglycan core protein in cartilage from the cmd/cmd (cartilage matrix deficiency) mouse

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=21264

Identification of the molecular defect in a family with spondyloepiphyseal dysplasia

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=21264

Proteoglycans: many forms and many functions

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=21264

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

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=21264

Mouse aggrecan, a large cartilage proteoglycan: protein sequence, gene structure and promoter sequence

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=21264

Abnormal collagen fibrillogenesis in epiphyseal cartilage of CMD (cartilage matrix deficiency) mouse.

29 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=21264

Glycine to serine substitution in the triple helical domain of pro-alpha 1 (II) collagen results in a lethal perinatal form of short-limbed dwarfism

29 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=21264

Kniest and Stickler dysplasia phenotypes caused by collagen type II gene (COL2A1) defect

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=21264

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

22 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=21264

Effects of proteoglycan extraction on the tensile behavior of articular cartilage

22 September 2018

1 reference

12 December 2020

The turnover of adult rabbit articular cartilage

1 reference

12 December 2020

Cartilage matrix deficiency (cmd): a new autosomal recessive lethal mutation in the mouse

1 reference

12 December 2020

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

1 reference

12 December 2020

Proteoglycans: isolation and characterization

1 reference

12 December 2020

Stickler syndrome. A mutation in the nonhelical 3' end of type II procollagen gene

1 reference

12 December 2020

Differential levels of synovial fluid aggrecan aggregate components in experimental osteoarthritis and joint disuse

1 reference

12 December 2020

Self-assembly of collagen I from a proband homozygous for a mutation that substituted serine for glycine at position 661 in the alpha 2(I) chain. Possible relationship between the effects of mutations on critical concentration and the severity of th

1 reference

12 December 2020

Identifiers

DOI

10.1073/PNAS.94.13.6943

1 reference

13 August 2017

0 references

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13 August 2017

PubMed publication ID

9192671

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