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Generation of Fgfr3 conditional knockout mice
scientific article
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instance of
scholarly article
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title
Generation of Fgfr3 conditional knockout mice
(English)
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main subject
knockout mouse
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fibroblast growth factor receptor 3
1 reference
stated in
GOA release 2020-03-11
bone maturation
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stated in
GOA release 2020-03-11
Fibroblast growth factor receptor 3
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stated in
GOA release 2020-03-11
author name string
Nan Su
series ordinal
1
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Xiaoling Xu
series ordinal
2
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Cuiling Li
series ordinal
3
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Qifen He
series ordinal
4
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Ling Zhao
series ordinal
5
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Can Li
series ordinal
6
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Siyu Chen
series ordinal
7
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Fengtao Luo
series ordinal
8
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Lingxian Yi
series ordinal
9
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Xiaolan Du
series ordinal
10
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Haiyang Huang
series ordinal
11
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Chuxia Deng
series ordinal
12
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Lin Chen
series ordinal
13
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language of work or name
English
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publication date
2010
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published in
International Journal of Biological Sciences
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volume
6
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issue
4
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page(s)
327-32
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cites work
A novel mutation in FGFR3 causes camptodactyly, tall stature, and hearing loss (CATSHL) syndrome
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2892296
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19 March 2017
Cell responses to FGFR3 signalling: growth, differentiation and apoptosis
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2892296
retrieved
19 March 2017
Fibroblast growth factor receptor 3 is a negative regulator of bone growth
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2892296
retrieved
19 March 2017
Disruption of fibroblast growth factor receptor 3 signaling results in defects in cellular differentiation, neuronal patterning, and hearing impairment
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2892296
retrieved
19 March 2017
Efficient in vivo manipulation of mouse genomic sequences at the zygote stage
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2892296
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7 April 2017
FGF signaling: its role in bone development and human skeleton diseases
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PubMed Central
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27 September 2017
Skeletal overgrowth is mediated by deficiency in a specific isoform of fibroblast growth factor receptor 3.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2892296
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27 September 2017
Fibroblast growth factor receptor-3 is expressed in undifferentiated intestinal epithelial cells during murine crypt morphogenesis
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2892296
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27 September 2017
FGF signaling pathways in endochondral and intramembranous bone development and human genetic disease
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2892296
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27 September 2017
Gly369Cys mutation in mouse FGFR3 causes achondroplasia by affecting both chondrogenesis and osteogenesis
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2892296
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27 September 2017
A Lys644Glu substitution in fibroblast growth factor receptor 3 (FGFR3) causes dwarfism in mice by activation of STATs and ink4 cell cycle inhibitors
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2892296
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27 September 2017
Human fibroblast growth factor receptor 3 gene (FGFR3): genomic sequence and primer set information for gene analysis
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stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2892296
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27 September 2017
Common mutations in the fibroblast growth factor receptor 3 (FGFR 3) gene account for achondroplasia, hypochondroplasia, and thanatophoric dwarfism
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2892296
retrieved
27 September 2017
Mutations in the transmembrane domain of FGFR3 cause the most common genetic form of dwarfism, achondroplasia
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2892296
retrieved
27 September 2017
Fibroblast growth factor receptor (FGFR) 3. Alternative splicing in immunoglobulin-like domain III creates a receptor highly specific for acidic FGF/FGF-1.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2892296
retrieved
27 September 2017
Skeletal overgrowth and deafness in mice lacking fibroblast growth factor receptor 3.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2892296
retrieved
30 May 2018
Different members of the fibroblast growth factor receptor family are specific to distinct cell types in the developing chicken embryo
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2892296
retrieved
30 May 2018
Gly374Arg mutation in Fgfr3 causes achondroplasia in mice
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2892296
retrieved
29 November 2018
Defective bone mineralization and osteopenia in young adult FGFR3-/- mice
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2892296
retrieved
29 November 2018
Fgfr3 expression by astrocytes and their precursors: evidence that astrocytes and oligodendrocytes originate in distinct neuroepithelial domains
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2892296
retrieved
29 November 2018
FGF signaling in skeletal development.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2892296
retrieved
29 November 2018
Mutations in the gene encoding fibroblast growth factor receptor-3 in achondroplasia
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2892296
retrieved
29 November 2018
Thanatophoric dysplasia (types I and II) caused by distinct mutations in fibroblast growth factor receptor 3.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2892296
retrieved
29 November 2018
Generation of Fgfr1 conditional knockout mice
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/20582225
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Direct removal in the mouse of a floxed neo gene from a three-loxP conditional knockout allele by two novel approaches
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/20582225
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Defects in articular cartilage metabolism and early arthritis in fibroblast growth factor receptor 3 deficient mice
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/20582225
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.7150/IJBS.6.327
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
2503613
OpenCitations bibliographic resource ID
2503613
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
2503613
PMC publication ID
2892296
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
2503613
PubMed publication ID
20582225
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
2503613
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