Skip to search form
Skip to main content
Skip to account menu
Semantic Scholar
Semantic Scholar's Logo
Search 230,087,198 papers from all fields of science
Search
Sign In
Create Free Account
FGFR2 gene
Known as:
FIBROBLAST GROWTH FACTOR RECEPTOR BEK
, FGFR2
, CEK3
Expand
This gene plays a role in mitogenesis and differentiation and mutations in the gene are associated with craniosynostotic syndromes and bone…
Expand
National Institutes of Health
Create Alert
Alert
Related topics
Related topics
19 relations
Acrocephalosyndactylia
Cell Differentiation process
Cell Proliferation Regulatory Process
Epithelial Cell Proliferation
Expand
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Review
2013
Review
2013
The N 550 K / H Mutations in FGFR 2 Confer Differential Resistance to PD 173074 , Dovitinib , and Ponatinib ATP-Competitive Inhibitors 1
S. Byron
,
Huaibin Chen
,
+7 authors
P. Pollock
2013
Corpus ID: 85450060
We sought to identify fibroblast growth factor receptor 2 (FGFR2) kinase domain mutations that confer resistance to the pan-FGFR…
Expand
2010
2010
Risk of aggressive breast cancer in women of Han nationality carrying TGFB1 rs1982073 C allele and FGFR2 rs1219648 G allele in North China
Xiao-hui Chen
,
Xiao-Qing Li
,
Ying Chen
,
Yu-mei Feng
Breast Cancer Research and Treatment
2010
Corpus ID: 29890121
The high morbidity and aggressive behavior of breast cancer are associated with genetic variations. Single nucleotide…
Expand
2009
2009
Utilization of Lactobacillus fermentum and Saccharomyces cerevisiae as starter cultures in the production of 'dolo'.
R. Glover
,
H. Sawadogo-Lingani
,
B. Diawara
,
L. Jespersen
,
M. Jakobsen
2009
Corpus ID: 83296005
Objective: The present study was carried out to evaluate the potential of representative strains of predominant lactic acid…
Expand
2008
2008
Identification of an Intronic Splicing Enhancer Essential for the Inclusion of FGFR2 Exon IIIc*
P. Seth
,
Heather B. Miller
,
Erika L. Lasda
,
J. Pearson
,
M. Garcia-Blanco
Journal of Biological Chemistry
2008
Corpus ID: 40289595
The ligand specificity of fibroblast growth factor receptor 2 (FGFR2) is determined by the alternative splicing of exons 8 (IIIb…
Expand
2005
2005
A further mutation of the FGFR2 tyrosine kinase domain in mild Crouzon syndrome
T. Ravel
,
I. B. Taylor
,
Alex J T Van Oostveldt
,
J. Fryns
,
A. Wilkie
European Journal of Human Genetics
2005
Corpus ID: 19827091
We report a family heterozygous for a newly identified mutation in the tyrosine kinase I domain of the FGFR2 gene (1576A>G…
Expand
2004
2004
Novel mutation in the tyrosine kinase domain of FGFR2 in a patient with Pfeiffer syndrome
A. Zankl
,
G. Jaeger
,
L. Bonafė
,
E. Boltshauser
,
A. Superti-Furga
American Journal of Medical Genetics. Part A
2004
Corpus ID: 39504414
Mutations in the fibroblast growth factor receptor 2 (FGFR2) cause a variety of craniosynostosis syndromes. The mutational…
Expand
Highly Cited
2004
Highly Cited
2004
MAZ Elements Alter Transcription Elongation and Silencing of the Fibroblast Growth Factor Receptor 2 Exon IIIb*
Nicole D Robson-Dixon
,
M. Garcia-Blanco
Journal of Biological Chemistry
2004
Corpus ID: 20491007
The fibroblast growth factor receptor 2 (FGFR2) gene exons IIIb and IIIc are alternatively spliced in a mutually exclusive and…
Expand
2001
2001
5'- and 3'-terminal nucleotides in the FGFR2 ISAR splicing element core have overlapping roles in exon IIIb activation and exon IIIc repression.
R. Jones
,
R. Carstens
,
Y. Luo
,
W. Mckeehan
Nucleic Acids Research
2001
Corpus ID: 19552815
The cell type-specific, mutually-exclusive alternative splicing of the fibroblast growth factor receptor 2 (FGFR2) pre-mRNA is…
Expand
1998
1998
The feet in Pfeiffer's syndrome.
P. Anderson
,
C. Hall
,
R. Evans
,
B. Jones
,
R. Hayward
The Journal of craniofacial surgery (Print)
1998
Corpus ID: 6143714
Broad toes are the classic clinical finding occurring in the feet in Pfeiffer's syndrome patients, but few cases undergo formal…
Expand
1997
1997
A novel mutation (a886g) in exon 5 of FGFR2 in members of a family with Crouzon phenotype and plagiocephaly.
Daniela Steinberger
,
Hartmut Collmann
,
Bernhard Schmalenberger
,
Ulrich Muller
,
U. Miller
Journal of Medical Genetics
1997
Corpus ID: 20204975
We identified a novel mutation in members of a family with signs of Crouzon syndrome and plagiocephaly. In affected members of…
Expand
By clicking accept or continuing to use the site, you agree to the terms outlined in our
Privacy Policy
(opens in a new tab)
,
Terms of Service
(opens in a new tab)
, and
Dataset License
(opens in a new tab)
ACCEPT & CONTINUE