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TBX3 wt Allele

Known as: T-Box 3 wt Allele, TBX3-ISO, UMS 
Human TBX3 wild-type allele is located in the vicinity of 12q24.1 and is approximately 14 kb in length. This allele, which encodes T-box… 
National Institutes of Health

Related topics

Related topics

10 relations
12q24.1Homo sapiensLimb DevelopmentMorphogenesis

Broader (1)

TBX3 gene

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2016
Highly Cited
2016
Effect of Ozone Treatment on Deoxynivalenol and Wheat Quality
Deoxynivalenol (DON) is a secondary metabolite produced by Fusarium fungi, which is found in a wide range of agricultural… 
Highly Cited
2013
Highly Cited
2013
Consumption of coffee associated with reduced risk of liver cancer: a meta-analysis
BackgroundEpidemiologic studies have reported inconsistent results regarding coffee consumption and the risk of liver cancer. We… 
Review
2013
Review
2013
The T-box Transcription Factors TBX2 and TBX3 in Mammary Gland Development and Breast Cancer
TBX2 and TBX3, closely related members of the T-box family of transcription factor genes, are expressed in mammary tissue in both… 
Highly Cited
2013
Highly Cited
2013
MicroRNA-17-92, a Direct Ap-2α Transcriptional Target, Modulates T-Box Factor Activity in Orofacial Clefting
Among the most common human congenital anomalies, cleft lip and palate (CL/P) affects up to 1 in 700 live births. MicroRNA (miR)s… 
Highly Cited
2009
Highly Cited
2009
Ulnar mammary syndrome and TBX3: Expanding the phenotype
We present a patient with features of Ulnar Mammary syndrome (UMS) consisting of bilateral ulnar defects, inverted nipples, short… 
Review
2006
Review
2006
Novel TBX3 mutation data in families with ulnar-mammary syndrome indicate a genotype-phenotype relationship: mutations that do not disrupt the T-domain are associated with less severe limb defects.
Review
2004
Review
2004
The Role of Tbx2 and Tbx3 in Mammary Development and Tumorigenesis
TBX2 and TBX3 are members of a family of genes encoding developmental transcription factors, characterized by a 200 amino acid… 
Highly Cited
2001
Highly Cited
2001
A dominant repression domain in Tbx3 mediates transcriptional repression and cell immortalization: relevance to mutations in Tbx3 that cause ulnar-mammary syndrome.
Mutations in Tbx3 are responsible for ulnar-mammary syndrome (UMS), an autosomal dominant disorder affecting limb, tooth, hair… 
Highly Cited
2000
Highly Cited
2000
Geochemical and Sm-Nd isotopic study of amphibolites in the Cathaysia Block, southeastern China: evidence for an extremely depleted mantle in the Paleoproterozoic
Highly Cited
1999
Highly Cited
1999
Limb mammary syndrome: a new genetic disorder with mammary hypoplasia, ectrodactyly, and other Hand/Foot anomalies maps to human chromosome 3q27.
We report on a large Dutch family with a syndrome characterized by severe hand and/or foot anomalies, and hypoplasia/aplasia of… 
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