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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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2016
2016
MNX1 Is Oncogenically Upregulated in African-American Prostate Cancer.
Incidence and mortality rates for prostate cancer are higher in African-American (AA) men than in European-American (EA) men, but… Expand
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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
Understanding transcriptional regulation of pancreatic development is required to advance current efforts in developing beta cell… Expand
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2013
2013
Novel MNX1 mutations and clinical analysis of familial and sporadic Currarino cases.
Currarino Syndrome (CS) is a rare congenital malformation characterized by three major clinical aspects: sacral anomalies… Expand
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2012
2012
RNA profiling and chromatin immunoprecipitation-sequencing reveal that PTF1a stabilizes pancreas progenitor identity via the control of MNX1/HLXB9 and a network of other transcription factors.
Pancreas development is initiated by the specification and expansion of a small group of endodermal cells. Several transcription… Expand
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2011
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… Expand
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2009
2009
MNX1 (HLXB9) mutations in Currarino patients.
PURPOSE The combination of partial absence of the sacrum, anorectal anomalies, and presacral mass constitutes Currarino syndrome… Expand
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2006
2006
Population differences in the polyalanine domain and 6 new mutations in HLXB9 in patients with Currarino syndrome.
BACKGROUND The combination of partial absence of the sacrum, anorectal anomalies, and presacral mass constitutes Currarino… Expand
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2005
2005
Omphalocoele-Exstrophy-Imperforate Anus-Spinal Defects Complex in Dizygotic Twins
OEIS complex refers to a combination of defects consisting of omphalocoele, exstrophy of the cloaca, imperforate anus, and spinal… Expand
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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… Expand
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1994
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… Expand
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