Skip to search formSkip to main contentSkip to account menu

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

Semantic Scholar uses AI to extract papers important to this topic.
2017
2017
Is there a role for epithelial-mesenchymal transition in adrenocortical tumors?
PurposeEpithelial-mesenchymal transition (EMT) is a biological dynamic process by which epithelial cells lose their epithelial… 
Review
2015
Review
2015
Intrinsic regulations in neural fate commitment
Neural fate commitment is an early embryonic event that a group of cells in ectoderm, which do not ingress through primitive… 
2015
2015
SIP 1 predicts progression and poor prognosis in pharyngeal squamous cell carcinoma
transition (EMT) is a crucial process in tumorigenesis that enables tumor cells to invade and metastasize. The transcription… 
2010
2010
Mowat-Wilson syndrome: the first two Malaysian cases.
Mowat-Wilson syndrome (MWS) is a recently delineated mental retardation; a multiple congenital anomaly syndrome characterised by… 
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… 
2007
2007
Nonsense mutations of the ZFHX1B gene in two Japanese girls with Mowat-Wilson syndrome.
Mowat-Wilson syndrome (MWS) is a multiple congenital anomaly-mental retardation complex caused by mutations in the Zinc Finger… 
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… 
2002
2002
Purification and characterization of Snf1 kinase complexes containing a defined Beta subunit composition.
The Snf1 kinase complex of Saccharomyces cerevisiae contains one of three possible beta subunits encoded by either SIP1, SIP2, or… 
2002
2002
Increased expression level of the splicing variant of SIP1 in motor neuron diseases.
2000
2000
An essential SMN interacting protein (SIP1) is not involved in the phenotypic variability of spinal muscular atrophy (SMA)
The survival motor neuron (SMN) protein and the SMN interacting protein 1 (SIP1) are part of a 300 kD protein complex with a… 
By clicking accept or continuing to use the site, you agree to the terms outlined in our Privacy Policy (opens in a new tab), Terms of Service (opens in a new tab), and Dataset License (opens in a new tab)