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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.
2019
2019
MNX1-AS1 is a functional oncogene that induces EMT and activates the AKT/mTOR pathway and MNX1 in breast cancer
Yue Cheng
,
Yi-fei Pan
,
Yiyuan Pan
,
O. Wang
Cancer Management and Research
2019
Corpus ID: 59337820
Purpose lncRNAs have recently been identified as key regulators of basic biological processes as well as the pathogenesis of…
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Review
2017
Review
2017
Currarino syndrome: does the presence of a genetic anomaly correlate with a more severe phenotype? A multicentre study.
S. Costanzo
,
L. Spaccini
,
+12 authors
G. Riccipetitoni
Journal of Pediatric Surgery
2017
Corpus ID: 9985455
2013
2013
Novel MNX1 mutations and clinical analysis of familial and sporadic Currarino cases.
E. Merello
,
P. de Marco
,
M. Ravegnani
,
G. Riccipetitoni
,
A. Cama
,
V. Capra
European Journal of Medical Genetics
2013
Corpus ID: 21049072
2009
2009
MNX1 (HLXB9) mutations in Currarino patients.
M. Garcia-Barcelo
,
V. Lui
,
+9 authors
P. Tam
Journal of Pediatric Surgery
2009
Corpus ID: 66335
2006
2006
Population differences in the polyalanine domain and 6 new mutations in HLXB9 in patients with Currarino syndrome.
M. Garcia-Barcelo
,
M. So
,
+15 authors
P. Tam
Clinical Chemistry
2006
Corpus ID: 205379
BACKGROUND The combination of partial absence of the sacrum, anorectal anomalies, and presacral mass constitutes Currarino…
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2006
2006
Forced expression of the motor neuron determinant HB9 in neural stem cells affects neurogenesis
T. Bréjot
,
S. Blanchard
,
+5 authors
D. Bohl
Experimental Neurology
2006
Corpus ID: 45588653
2006
2006
A previously unreported mutation in a Currarino syndrome kindred
Raymond Y. Wang
,
Julie R. Jones
,
+4 authors
J. Graham
American Journal of Medical Genetics. Part A
2006
Corpus ID: 8552481
Currarino syndrome consists of autosomal dominant hereditary sacral dysgenesis that is caused by mutations of the HOX gene, HLXB9…
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1998
1998
Highly restricted expression at the ectoderm–endoderm boundary of PIHbox 9, a sea urchin homeobox gene related to the human HB9 gene
D. Bellomonte
,
M. D. Bernardo
,
R. Russo
,
G. Caronia
,
G. Spinelli
Mechanisms of Development
1998
Corpus ID: 14886290
1993
1993
High expression of two diverged homeobox genes, HB24 and HB9, in acute leukemias: molecular markers of hematopoietic cell immaturity.
Y. Deguchi
,
Y. Yamanaka
,
C. Theodossiou
,
V. Najfeld
,
J. Kehrl
Leukemia
1993
Corpus ID: 42950335
Homeobox genes encode for sequence-specific DNA-binding proteins which have been implicated in the control of gene expression…
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1991
1991
Monoclonal antibodies VTB‐E3, IB5 and HB9 to the leucocyte/epithelial antigen CD24 resemble BA‐1 in recognizing sialic acid‐dependent epitope(s). Evidence that VIB‐E3 recognizes NeuAcα2‐6GalNAc and…
M. Larkin
,
W. Knapp
,
M. Stoll
,
H. Mehmet
,
T. Feizi
Clinical and Experimental Immunology
1991
Corpus ID: 41422966
The specificities of seven monoclonal antibodies to the human B cell differentiation marker CD24 have been investigated with…
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