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FGF10 gene
Known as:
FGF10
, FIBROBLAST GROWTH FACTOR 10
, Fibroblast Growth Factor 10 Gene
This gene is involved in development and wound healing. It also plays a role in cellular biogenesis, organization and proliferation.
National Institutes of Health
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Related topics
Related topics
13 relations
Angiogenic Process
Cell Differentiation process
Cell Proliferation Regulatory Process
FGF10 protein, human
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Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2019
2019
Polymorphisms in FGF3, FGF10, and FGF13 May Contribute to the Presence of Temporomandibular Disorders in Patients Who Required Orthognathic Surgery.
K. Carpio Horta
,
S. Weiss
,
+7 authors
E. Küchler
The Journal of craniofacial surgery (Print)
2019
Corpus ID: 203640354
BACKGROUND To evaluate whether genetic polymorphisms in FGF3, FGF10, and FGF13 are associated with temporomandibular disorders…
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2019
2019
Intronic Polymorphisms in Gene of Second Heart Field as Risk Factors for Human Congenital Heart Disease in a Chinese Population.
E. Wang
,
Y. Nie
,
Xuesong Fan
,
Zhe Zheng
,
Shengshou Hu
DNA and Cell Biology
2019
Corpus ID: 129942708
Transcriptional factors and signaling factors in the second heart field (SHF) contribute to cardiac development. However, the…
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2018
2018
Increased pregnancy losses following serial somatic cell nuclear transfer in goats.
M. Yang
,
I. Périssé
,
Z. Fan
,
M. Regouski
,
M. Meyer-Ficca
,
I. Polejaeva
Reproduction, Fertility and Development
2018
Corpus ID: 21716302
Serial cloning by somatic cell nuclear transfer (SCNT) is a critical tool for the expansion of precious transgenic lines or…
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2018
2018
Genetic susceptibility to thalidomide embryopathy in humans: Study of candidate development genes.
J. A. Gomes
,
T. W. Kowalski
,
+4 authors
F. Vianna
Birth Defects Research
2018
Corpus ID: 4052882
Thalidomide is a drug used worldwide for several indications, but the molecular mechanisms of its teratogenic property are not…
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2016
2016
Novel FGF10 mutation in autosomal dominant aplasia of lacrimal and salivary glands
F. Seymen
,
M. Koruyucu
,
+7 authors
Jung‐Wook Kim
Clinical Oral Investigations
2016
Corpus ID: 25044498
Aplasia of lacrimal and salivary glands (ALSG) is a rare autosomal dominant inherited disease, characterized by aplasia, atresia…
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2015
2015
Therapeutic efficacy of fibroblast growth factor 10 in a rabbit model of dry eye
Wenjing Zheng
,
Mingming Ma
,
+4 authors
B. Ke
Molecular Medicine Reports
2015
Corpus ID: 15645981
The aim of the present study was to investigate the therapeutic efficacy of fibroblast growth factor 10 (FGF10) in the promotion…
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2013
2013
Association study of fibroblast growth factor 10 (FGF10) polymorphisms with susceptibility to extreme myopia in a Japanese population
Masao Yoshida
,
A. Meguro
,
E. Okada
,
N. Nomura
,
N. Mizuki
Molecular Vision
2013
Corpus ID: 14151891
Purpose The fibroblast growth factor 10 (FGF10) gene polymorphism rs339501 was previously reported to be associated with high…
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2012
2012
Involvement of the WNT and FGF signaling pathways in non-isolated anorectal malformations: sequencing analysis of WNT3A, WNT5A, WNT11, DACT1, FGF10, FGFR2 and the T gene.
Markus Draaken
,
Wiebke Prins
,
+11 authors
M. Ludwig
International Journal of Molecular Medicine
2012
Corpus ID: 29657890
Anorectal malformations (ARMs) comprise a broad spectrum of anomalies, including anal atresia, congenital anal…
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2011
2011
Keratinocyte growth factor 1, fibroblast growth factor 2 and 10 in the healing tympanic membrane following perforation in rats
Peter L. Santa Maria
,
S. Redmond
,
M. Atlas
,
R. Ghassemifar
Journal of Molecular Histology
2011
Corpus ID: 24092077
The aim of this study was to provide a transcriptome profile of Keratinocyte Growth Factor (KGF)-1, Fibroblast Growth Factor (FGF…
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Review
2008
Review
2008
Studies of genes in the FGF signaling pathway and oral clefts with or without dental anomalies
Renato Menezes
,
A. Letra
,
Joe Ruff
,
J. Granjeiro
,
A. Vieira
American Journal of Medical Genetics. Part A
2008
Corpus ID: 36429180
To the Editor: Orofacial clefts comprise a large fraction of all human birth defects, affecting approximately one in every 500…
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