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FOXC2 gene
Known as:
Forkhead Box C2 Gene
, MFH-1
, FORKHEAD, DROSOPHILA, HOMOLOG-LIKE 14
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This gene plays a role in transcription and adipocyte metabolism.
National Institutes of Health
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Related topics
Related topics
9 relations
FOXB1 gene
Forkhead Box Protein C2
Hereditary lymphedema and yellow nails
Histogenic Process
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FOXC2 wt Allele
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2017
Highly Cited
2017
Antisense lncRNA FOXC2-AS1 promotes doxorubicin resistance in osteosarcoma by increasing the expression of FOXC2.
Chunlin Zhang
,
K. Zhu
,
Xiao-Long Ma
Cancer Letters
2017
Corpus ID: 4857753
Highly Cited
2007
Highly Cited
2007
Mutations in FOXC2 Are Strongly Associated With Primary Valve Failure in Veins of the Lower Limb
R. Mellor
,
G. Brice
,
+6 authors
Peter S. Mortimer
Circulation
2007
Corpus ID: 12371295
Background— Mutations in the FOXC2 gene cause lymphedema distichiasis, an inherited primary lymphedema in which a significant…
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Highly Cited
2006
Highly Cited
2006
The forkhead transcription factors, Foxc1 and Foxc2, are required for arterial specification and lymphatic sprouting during vascular development.
Seungwoon Seo
,
Hideo Fujita
,
A. Nakano
,
Myengmo Kang
,
A. Duarte
,
T. Kume
Developmental Biology
2006
Corpus ID: 19538232
Highly Cited
2003
Highly Cited
2003
FOXC2 haploinsufficient mice are a model for human autosomal dominant lymphedema-distichiasis syndrome.
B. Kriederman
,
T. Myloyde
,
+11 authors
T. Glover
Human Molecular Genetics
2003
Corpus ID: 25652573
Lymphedema-distichiasis (LD) (OMIM 153400) is a rare autosomal-dominant condition characterized by pubertal onset of lower limb…
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Highly Cited
2003
Highly Cited
2003
Reduced expression of FOXC2 and brown adipogenic genes in human subjects with insulin resistance.
Xiaolin Yang
,
S. Enerbäck
,
U. Smith
Obesity Research
2003
Corpus ID: 36260124
OBJECTIVE We investigated subcutaneous adipose tissue expression of FOXC2 and selected genes involved in brown adipogenesis in…
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Highly Cited
2001
Highly Cited
2001
Truncating mutations in FOXC2 cause multiple lymphedema syndromes.
D. Finegold
,
M. Kimak
,
+5 authors
R. Ferrell
Human Molecular Genetics
2001
Corpus ID: 37508891
Hereditary lymphedemas are developmental disorders of the lymphatics resulting in edema of the extremities due to altered…
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Highly Cited
1999
Highly Cited
1999
Roles for the winged helix transcription factors MF1 and MFH1 in cardiovascular development revealed by nonallelic noncomplementation of null alleles.
G. Winnier
,
T. Kume
,
+6 authors
S. Conway
Developmental Biology
1999
Corpus ID: 39535306
The murine Mf1 and Mfh1 genes have overlapping patterns of expression in the embryo and encode forkhead/winged helix…
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Highly Cited
1997
Highly Cited
1997
Essential roles of the winged helix transcription factor MFH-1 in aortic arch patterning and skeletogenesis.
Kiyoshi Iida
,
Haruhiko Koseki
,
+12 authors
N. Miura
Development
1997
Corpus ID: 36915120
Mesenchyme Fork Head-1 (MFH-1) is a forkhead (also called winged helix) transcription factor defined by a common 100-amino acid…
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Highly Cited
1997
Highly Cited
1997
The winged helix transcription factor MFH1 is required for proliferation and patterning of paraxial mesoderm in the mouse embryo.
G. Winnier
,
Linda K. Hargett
,
Brigid L. M. Hogan
Genes & Development
1997
Corpus ID: 25991455
The gene mfh1, encoding a winged helix/forkhead domain transcription factor, is expressed in a dynamic pattern in paraxial and…
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Highly Cited
1996
Highly Cited
1996
Clustered arrangement of winged helix genes fkh-6 and MFH-1: possible implications for mesoderm development.
K. Kaestner
,
S. Bleckmann
,
+4 authors
G. Schütz
Development
1996
Corpus ID: 1003254
The 'winged helix' or 'forkhead' transcription factor gene family is defined by a common 100 amino acid DNA binding domain which…
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