(Q24558691)

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WISP3, the gene responsible for the human skeletal disease progressive pseudorheumatoid dysplasia, is not essential for skeletal function in mice

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WISP3, the gene responsible for the human skeletal disease progressive pseudorheumatoid dysplasia, is not essential for skeletal function in mice (English)

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author name string

Wendy E Kutz

1

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Yaoqin Gong

2

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Matthew L Warman

3

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language of work or name

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publication date

January 2005

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Molecular and Cellular Biology

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25

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414-21

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1

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Connective tissue growth factor coordinates chondrogenesis and angiogenesis during skeletal development

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=538768

24 March 2017

CYR61 (CCN1) is essential for placental development and vascular integrity

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=538768

24 March 2017

Cartilage oligomeric matrix protein-deficient mice have normal skeletal development

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=538768

24 March 2017

NOV (nephroblastoma overexpressed) and the CCN family of genes: structural and functional issues

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=538768

24 March 2017

Overexpression of connective tissue growth factor/hypertrophic chondrocyte-specific gene product 24 decreases bone density in adult mice and induces dwarfism

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=538768

24 March 2017

WISP3-dependent regulation of type II collagen and aggrecan production in chondrocytes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=538768

27 September 2017

Matrilin-3 is dispensable for mouse skeletal growth and development

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=538768

27 September 2017

Lifelong voluntary joint loading increases osteoarthritis in mice housing a deletion mutation in type II procollagen gene, and slightly also in non-transgenic mice

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=538768

27 September 2017

WISP3 is a novel tumor suppressor gene of inflammatory breast cancer

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=538768

27 September 2017

In vivo morphometry and functional analysis of human articular cartilage with quantitative magnetic resonance imaging--from image to data, from data to theory

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=538768

27 September 2017

Mutations in the CCN gene family member WISP3 cause progressive pseudorheumatoid dysplasia.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=538768

27 September 2017

The connective tissue growth factor/cysteine-rich 61/nephroblastoma overexpressed (CCN) family

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=538768

27 September 2017

Progressive pseudorheumatoid dysplasia: report of a family and review

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=538768

27 September 2017

Identification of a phenotype-specific enhancer in the first intron of the rat collagen II gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=538768

27 September 2017

Vascular events associated with the appearance of the secondary center of ossification in the murine distal femoral epiphysis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=538768

27 September 2017

Radiographic features of progressive pseudorheumatoid arthritis.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=538768

30 May 2018

The CCN family of genes: a brief history

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=538768

28 November 2018

Identification of a minimum enhancer sequence for the type II collagen gene reveals several core sequence motifs in common with the link protein gene.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=538768

28 November 2018

Progressive pseudorheumatoid arthropathy of childhood (PPAC): a hereditary disorder simulating juvenile rheumatoid arthritis.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=538768

28 November 2018

Transgenic mice expressing bovine GH develop arthritic disorder and self-antibodies

1 reference

https://pubmed.ncbi.nlm.nih.gov/15601861

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mega os trigonum in progressive pseudorheumatoid dysplasia

1 reference

https://pubmed.ncbi.nlm.nih.gov/15601861

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

WNT-inducible signaling pathway protein 3, WISP-3, is mutated in microsatellite unstable gastrointestinal carcinomas but not in endometrial carcinomas

1 reference

https://pubmed.ncbi.nlm.nih.gov/15601861

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Osteoarthritis-like changes and decreased mechanical function of articular cartilage in the joints of mice with the chondrodysplasia gene (cho)

1 reference

https://pubmed.ncbi.nlm.nih.gov/15601861

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clinical, radiographic, and genetic diagnosis of progressive pseudorheumatoid dysplasia in a patient with severe polyarthropathy

1 reference

https://pubmed.ncbi.nlm.nih.gov/15601861

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Spondylo-epiphysial dysplasia tarda with progressive arthropathy. A "new" disorder of autosomal recessive inheritance

1 reference

https://pubmed.ncbi.nlm.nih.gov/15601861

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Progressive pseudorheumatoid chondrodysplasia: a report of nine cases in three families

1 reference

https://pubmed.ncbi.nlm.nih.gov/15601861

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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