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MNX1 gene
Known as:
MNX1
, HOMEOBOX GENE HB9
, Motor Neuron and Pancreas Homeobox 1 Gene
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This gene plays a role in both the regulation of transcription and DNA binding.
National Institutes of Health
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Related topics
Related topics
9 relations
Cell Differentiation process
Currarino triad
Homo sapiens
Humoral Immunity
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MNX1 wt Allele
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
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
S. Flanagan
,
E. De Franco
,
+14 authors
A. Hattersley
Cell metabolism
2014
Corpus ID: 8877794
2013
2013
Pancreatic differentiation of human dental pulp CD117⁺ stem cells.
N. Ishkitiev
,
K. Yaegaki
,
+5 authors
T. Imai
Regenerative medicine
2013
Corpus ID: 24434145
AIM Adult stem cells cannot proliferate to produce enough cells for human transplantation with keeping stem cell characteristics…
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2012
2012
Characterization and regulation of the hb9/mnx1 beta-cell progenitor specific enhancer in zebrafish
V. Arkhipova
,
B. Wendik
,
N. Devos
,
O. Ek
,
B. Peers
,
D. Meyer
Developmental biology
2012
Corpus ID: 31731735
Highly Cited
2011
Highly Cited
2011
Zebrafish mnx1 controls cell fate choice in the developing endocrine pancreas
G. Dalgin
,
A. B. Ward
,
L. Hao
,
C. Beattie
,
A. Nechiporuk
,
V. Prince
Development
2011
Corpus ID: 28958
The vertebrate endocrine pancreas has the crucial function of maintaining blood sugar homeostasis. This role is dependent upon…
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Review
2008
Review
2008
Spectrum of HLXB9 gene mutations in Currarino syndrome and genotype–phenotype correlation
C. Cretolle
,
A. Pelet
,
+8 authors
S. Lyonnet
Human mutation
2008
Corpus ID: 27068280
Currarino syndrome (CS) is a rare congenital malformation described in 1981 as the association of three main features: typical…
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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
Soo-Kyung Lee
,
L. Jurata
,
J. Funahashi
,
Esmeralda C Ruiz
,
S. Pfaff
Development
2004
Corpus ID: 1078561
The underlying transcriptional mechanisms that establish the proper spatial and temporal pattern of gene expression required for…
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Highly Cited
2004
Highly Cited
2004
Zebrafish mnx genes in endocrine and exocrine pancreas formation.
B. Wendik
,
Esther C. Maier
,
D. Meyer
Developmental biology
2004
Corpus ID: 5839479
Highly Cited
2001
Highly Cited
2001
Spectrum of mutations and genotype–phenotype analysis in Currarino syndrome
J. Köchling
,
Mohsen Karbasiyan
,
A. Reis
European Journal of Human Genetics
2001
Corpus ID: 8900576
The triad of a presacral tumour, sacral agenesis and anorectal malformation constitutes the Currarino syndrome which is caused by…
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Highly Cited
1999
Highly Cited
1999
A physical and transcriptional map of the preaxial polydactyly locus on chromosome 7q36.
H. Heus
,
A. Hing
,
+11 authors
P. Heutink
Genomics
1999
Corpus ID: 638712
Preaxial polydactyly is a congenital hand malformation that includes duplicated thumbs, various forms of triphalangeal thumbs…
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Highly Cited
1994
Highly Cited
1994
A novel human homeobox gene distantly related to proboscipedia is expressed in lymphoid and pancreatic tissues.
K. Harrison
,
K. Druey
,
Y. Deguchi
,
J. Tuscano
,
J. Kehrl
The Journal of biological chemistry
1994
Corpus ID: 683063
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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