(Q40132147)

17 September 2017

title

Human immortalized chondrocytes carrying heterozygous FGFR3 mutations: an in vitro model to study chondrodysplasias (English)

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17 September 2017

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5

Arnold Munnich

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17 September 2017

author name string

Catherine Benoist-Lasselin

1

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17 September 2017

Linda Gibbs

2

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Solange Heuertz

3

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Thierry Odent

4

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Laurence Legeai-Mallet

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language of work or name

English

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publication date

8 May 2007

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17 September 2017

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volume

581

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issue

14

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page(s)

2593-2598

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Mutations in the gene encoding fibroblast growth factor receptor-3 in achondroplasia

17 September 2017

cites work

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https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2007.04.079

Mutations in the transmembrane domain of FGFR3 cause the most common genetic form of dwarfism, achondroplasia

21 January 2018

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https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2007.04.079

A recurrent mutation in the tyrosine kinase domain of fibroblast growth factor receptor 3 causes hypochondroplasia

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2007.04.079

Stop codon FGFR3 mutations in thanatophoric dwarfism type 1.

21 January 2018

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https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2007.04.079

Missense FGFR3 mutations create cysteine residues in thanatophoric dwarfism type I (TD1)

21 January 2018

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https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2007.04.079

A novel skeletal dysplasia with developmental delay and acanthosis nigricans is caused by a Lys650Met mutation in the fibroblast growth factor receptor 3 gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2007.04.079

Graded activation of fibroblast growth factor receptor 3 by mutations causing achondroplasia and thanatophoric dysplasia

21 January 2018

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https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2007.04.079

Overexpression of FGFR3, Stat1, Stat5 and p21Cip1 correlates with phenotypic severity and defective chondrocyte differentiation in FGFR3-related chondrodysplasias

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2007.04.079

Sustained ERK1/2 but not STAT1 or 3 activation is required for thanatophoric dysplasia phenotypes in PC12 cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2007.04.079

FGF signaling inhibits chondrocyte proliferation and regulates bone development through the STAT-1 pathway

21 January 2018

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https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2007.04.079

Constitutive activation of MEK1 in chondrocytes causes Stat1-independent achondroplasia-like dwarfism and rescues the Fgfr3-deficient mouse phenotype

21 January 2018

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https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2007.04.079

Activation of Stat1 by mutant fibroblast growth-factor receptor in thanatophoric dysplasia type II dwarfism

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2007.04.079

Novel FGFR3 mutations creating cysteine residues in the extracellular domain of the receptor cause achondroplasia or severe forms of hypochondroplasia

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2007.04.079

Immortalized human adult articular chondrocytes maintain cartilage-specific phenotype and responses to interleukin-1beta

21 January 2018

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https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2007.04.079

Tissue engineering strategies for cartilage generation--micromass and three dimensional cultures using human chondrocytes and a continuous cell line.

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2007.04.079

Sox9 is required for cartilage formation

21 January 2018

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https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2007.04.079

Toward understanding SOX9 function in chondrocyte differentiation

21 January 2018

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https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2007.04.079

A Lys644Glu substitution in fibroblast growth factor receptor 3 (FGFR3) causes dwarfism in mice by activation of STATs and ink4 cell cycle inhibitors

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2007.04.079

Effect of transmembrane and kinase domain mutations on fibroblast growth factor receptor 3 chimera signaling in PC12 cells. A model for the control of receptor tyrosine kinase activation

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2007.04.079

The thanatophoric dysplasia type II mutation hampers complete maturation of fibroblast growth factor receptor 3 (FGFR3), which activates signal transducer and activator of transcription 1 (STAT1) from the endoplasmic reticulum

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2007.04.079

The kinase activity of fibroblast growth factor receptor 3 with activation loop mutations affects receptor trafficking and signaling

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2007.04.079

A network of transcriptional and signaling events is activated by FGF to induce chondrocyte growth arrest and differentiation

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2007.04.079

Expression of simian virus 40 large T (tumor) oncogene in mouse chondrocytes induces cell proliferation without loss of the differentiated phenotype

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2007.04.079

An established rat cell line expressing chondrocyte properties.

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2007.04.079

SV40-immortalization of rabbit articular chondrocytes: alteration of differentiated functions

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2007.04.079

Molecular phenotyping of human chondrocyte cell lines T/C-28a2, T/C-28a4, and C-28/I2.

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2007.04.079

Phenotypic characterization of human chondrocyte cell line C-20/A4: a comparison between monolayer and alginate suspension culture.

21 January 2018

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https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2007.04.079

10.1016/J.FEBSLET.2007.04.079

21 January 2018

Identifiers

DOI

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17 September 2017

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