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ZEB2 wt Allele

Known as: KIAA0569, ZFX1B, ZFHX1B 
Human ZEB2 wild-type allele is located in the vicinity of 2q22 and is approximately 132 kb in length. This allele, which encodes zinc finger E-box… 
National Institutes of Health

Related topics

Related topics

9 relations
2q22Homo sapiensTranscriptional RegulationTranscriptional Repression

Broader (1)

ZEB2 gene

Papers overview

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Highly Cited
2011
Highly Cited
2011
The F-box protein Ppa is a common regulator of core EMT factors Twist, Snail, Slug, and Sip1
The core EMT regulatory factors Twist, Snail, Slug, and Sip1, while structurally diverse, are coordinately regulated by a common… 
Highly Cited
2010
Highly Cited
2010
Multifactorial Regulation of E-Cadherin Expression: An Integrative Study
E-cadherin (E-cad) is an adhesion molecule associated with tumor invasion and metastasis. Its down-regulation is associated with… 
Highly Cited
2008
Highly Cited
2008
A Novel ARID DNA-Binding Protein Interacts with SymRK and Is Expressed during Early Nodule Development in Lotus japonicus1[C][W][OA]
During the establishment of symbiosis in legume roots, the rhizobial Nod factor signal is perceived by the host cells via… 
2008
2008
Zebrafish sip1a and sip1b are essential for normal axial and neural patterning
Smad‐interacting protein‐1 (SIP1) has been implicated in the development of Mowat‐Wilson syndrome whose patients exhibit… 
Highly Cited
2006
Highly Cited
2006
Involvement of Ets-1 transcription factor in inducing matrix metalloproteinase-2 expression by epithelial-mesenchymal transition in human squamous carcinoma cells.
Epithelial-mesenchymal transition (EMT) is a crucial event in cancer progression. We previously reported that EMT up-regulates… 
Highly Cited
2005
Highly Cited
2005
Mutations of the RET gene in isolated and syndromic Hirschsprung’s disease in human disclose major and modifier alleles at a single locus
Background: In Hirschsprung’s disease (HSCR), a hypomorphic allele of a major gene, RET, accounts for most isolated (non… 
2005
2005
Recurrence of Mowat–Wilson syndrome in siblings with the same proven mutation
Mowat–Wilson syndrome (MWS) is a mental retardation syndrome associated with distinctive facial features, microcephaly, epilepsy… 
Review
2003
Review
2003
Hirschsprung disease, mental retardation, characteristic facial features, and mutation in the gene ZFHX1B (SIP1): Confirmation of the Mowat‐Wilson syndrome
We read with interest the article ‘‘Hirschsprung disease, microcephaly, mental retardation, and characteristic facial features… 
2002
2002
Clinical features of a form of Hirschsprung's disease caused by a novel genetic abnormality.
BACKGROUND/PURPOSE The aim of this report is to describe the pattern of similarities among the patients, exemplifying a newly… 
2002
2002
Late infantile Hirschsprung disease–mental retardation syndrome with a 3-bp deletion in ZFHX1B
A 48-year-old woman with late infantile onset mental retardation developed megacolon. Although the patient had no typical… 
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