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MNX1 gene

Known as: MNX1, HOMEOBOX GENE HB9, Motor Neuron and Pancreas Homeobox 1 Gene 
This gene plays a role in both the regulation of transcription and DNA binding.
National Institutes of Health

Related topics

Related topics

9 relations
Cell Differentiation processCurrarino triadHomo sapiensHumoral Immunity
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MNX1 wt Allele

Papers overview

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Highly Cited
2014
Highly Cited
2014
Analysis of Transcription Factors Key for Mouse Pancreatic Development Establishes NKX2-2 and MNX1 Mutations as Causes of Neonatal Diabetes in Man
2013
2013
Pancreatic differentiation of human dental pulp CD117⁺ stem cells.
AIM Adult stem cells cannot proliferate to produce enough cells for human transplantation with keeping stem cell characteristics… 
2012
2012
Characterization and regulation of the hb9/mnx1 beta-cell progenitor specific enhancer in zebrafish
Highly Cited
2011
Highly Cited
2011
Zebrafish mnx1 controls cell fate choice in the developing endocrine pancreas
The vertebrate endocrine pancreas has the crucial function of maintaining blood sugar homeostasis. This role is dependent upon… 
Review
2008
Review
2008
Spectrum of HLXB9 gene mutations in Currarino syndrome and genotype–phenotype correlation
Currarino syndrome (CS) is a rare congenital malformation described in 1981 as the association of three main features: typical… 
Highly Cited
2004
Highly Cited
2004
Analysis of embryonic motoneuron gene regulation: derepression of general activators function in concert with enhancer factors
The underlying transcriptional mechanisms that establish the proper spatial and temporal pattern of gene expression required for… 
Highly Cited
2004
Highly Cited
2004
Zebrafish mnx genes in endocrine and exocrine pancreas formation.
Highly Cited
2001
Highly Cited
2001
Spectrum of mutations and genotype–phenotype analysis in Currarino syndrome
The triad of a presacral tumour, sacral agenesis and anorectal malformation constitutes the Currarino syndrome which is caused by… 
Highly Cited
1999
Highly Cited
1999
A physical and transcriptional map of the preaxial polydactyly locus on chromosome 7q36.
Preaxial polydactyly is a congenital hand malformation that includes duplicated thumbs, various forms of triphalangeal thumbs… 
Highly Cited
1994
Highly Cited
1994
A novel human homeobox gene distantly related to proboscipedia is expressed in lymphoid and pancreatic tissues.
A novel human homeobox gene, HB9, was isolated from a cDNA library prepared from in vitro stimulated human tonsil B lymphocytes… 
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