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TBX5 gene
Known as:
T-BOX 5
, T-Box 5 Gene
, TBX5
This gene is involved in transcriptional regulation and mesoderm differentiation.
National Institutes of Health
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Related topics
Related topics
8 relations
Cell Differentiation process
Homo sapiens
Intercellular Communication Process
Limb Development
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Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2016
2016
How fancy pigeons grow feathery feet
Gregory D. Larsen
Lab animal
2016
Corpus ID: 6542826
to overcome several difficulties inherent to catheterization of the cerebral vascular system, including maneuvering the stentrode…
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2016
2016
Author ’ s Accepted Manuscript Gain of function mutations in GATA 6 lead to atrial fibrillation
N. Tucker
,
S. Mahida
,
+10 authors
P. Ellinor
2016
Corpus ID: 207785264
2015
2015
Gata4, Tbx5 and Baf60c induce differentiation of adipose tissue-derived mesenchymal stem cells into beating cardiomyocytes
李琼
2015
Corpus ID: 89671339
2015
2015
HLHS is caused by the up regulation of HIF1α due to hypoxia caused by a polymorphism in eNOS
T. Bruinsma
,
K. Curwick
,
L. Ellman
,
Jared M. Grootwassink
,
T. M. O'Toole
2015
Corpus ID: 55762627
2011
2011
Functional analysis of novel TBX5 T-box mutations associated with Holt-Oram syndrome (vol 88, pg 130, 2010)
C. Boogerd
,
D. Dooijes
,
+8 authors
A. Postma
2011
Corpus ID: 90111188
2011
2011
Detection of NKX2.5, TBX5, GATA4, and MYH6 Gene Mutations in Finding an Association with Sporadic Secundum Atrial Septal Defect
S. Rahayuningsih
2011
Corpus ID: 84090915
Mutations of NKX2.5, TBX5, GATA4, and MYH6 gene had been identified in familial ASD, but until recently reports on GATA4 and MYH6…
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2006
2006
Abstract 3392: A Novel TBX5 Mutation Leads to Enhanced DNA-Binding in a Family with Holt-Oram Syndrome and Paroxysmal Atrial Fibrillation
A. Postma
,
J. V. Meerakker
,
+6 authors
A. Moorman
2006
Corpus ID: 67927709
2005
2005
Identification of new mutations in the TBX5 gene in patients with Holt-Oram syndrome
W. Heinritz
,
A. Moschik
,
+8 authors
U. Froster
Heart
2005
Corpus ID: 11439407
Holt-Oram syndrome (HOS) (MIM 142900), first described by Holt and Oram in 1960, is characterised by malformations of the upper…
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2004
2004
Severe Vertebral anomalies in a patietn with Holt-Oram syndrome and a TBX5 sequence variation
P. Debeer
,
P. Brys
,
C. Huysmans
,
K. Devriendt
,
W. Ven
,
J. Fryns
2004
Corpus ID: 78247474
2002
2002
Elucidating the Molecular and Genetic Interactions Responsible for Congenital Heart Disease
P. Jay
,
S. Izumo
Pediatric Research
2002
Corpus ID: 40593811
Elucidating the Molecular and Genetic Interactions Responsible for Congenital Heart Disease