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Homeobox Protein ARX
Known as:
Aristaless-Like 4
, Aristaless-Related Homeobox
, Homeobox Protein Aristaless-Like 4
Homeobox protein aristaless-like 4 (411 aa, ~44 kDa) is encoded by the human ALX4 gene. This protein is involved in the regulation of transcription…
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National Institutes of Health
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Related topics
Related topics
11 relations
ALX4 gene
ARX gene
DNA-Binding Proteins
Genes, Regulator
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Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2014
2014
O-010 Comparative Neuropathology Of Lissencephaly With Arx Mutation: Consideration Of Neocortical Interneuron Distribution
M. Itoh
Archives of Disease in Childhood
2014
Corpus ID: 58034574
Background X-linked lissencephaly with abnormal genitalia (XLAG) is established as one disease entity. XLAG, showing severe…
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2013
2013
Aristaless-Related Homeobox Plays a Key Role in Hyperplasia of the Pancreas Islet α–Like Cells in Mice Deficient in Proglucagon-Derived Peptides
Sai-Ya Xu
,
Y. Hayashi
,
Y. Takagishi
,
M. Itoh
,
Y. Murata
PLoS ONE
2013
Corpus ID: 17845704
Defects in glucagon action can cause hyperplasia of islet α-cells, however, the underlying mechanisms remain largely to be…
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2013
2013
Nuclear import of aristaless-related homeobox protein via its NLS1 regulates its transcriptional function
Wenduo Ye
,
Wenbo Lin
,
A. Tartakoff
,
Qilin Ma
,
T. Tao
Molecular and Cellular Biochemistry
2013
Corpus ID: 254799471
Nucleocytoplasmic transport of transcription factors is essential in eukaryotes. We previously reported the presence of two…
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2012
2012
Mutational screening of ARX gene in Iranian families with X-linked intellectual disability.
S. S. Abedini
,
K. Kahrizi
,
F. Behjati
,
Sussan Banihashemi
,
Saghar Ghasemi Firoozabadi
,
H. Najmabadi
Archives of Iranian medicine
2012
Corpus ID: 36512477
BACKGROUND Mutations in the human aristaless-related homeobox (ARX) gene are amongst the major causes of developmental and…
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2010
2010
Westward Ho! Pioneering Mouse Models for X-Linked Infantile Spasms Syndrome
J. Naegele
Epilepsy Currents
2010
Corpus ID: 44911827
Targeted Loss of Arx Results in a Developmental Epilepsy Mouse Model and Recapitulates the Human Phenotype in Heterozygous…
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2009
2009
The Roles of Multiple Importins for Nuclear Import of Murine Aristaless-related Homeobox Protein*
Wenbo Lin
,
Wenduo Ye
,
+8 authors
T. Tao
Journal of Biological Chemistry
2009
Corpus ID: 12317051
Nuclear import of proteins with nuclear localization signals (NLSs) is mediated by shuttling carriers, the importins. Some…
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2009
2009
An 11‐month‐old boy with intractable epilepsy from birth
M. Itoh
Neuropathology (Kyoto. )
2009
Corpus ID: 28807895
The patient, a male infant, was born following an uneventful pregnancy, and was delivered at 38-weeks gestation from non…
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2008
2008
Signaling pathways regulating the expression of Prx1 and Prx2 in the chick mandibular mesenchyme
Aikaterini‐El Doufexi
,
M. Mina
Developmental Dynamics
2008
Corpus ID: 3497172
Prx1 and Prx2 are members of the aristaless‐related homeobox genes shown to play redundant but essential roles in morphogenesis…
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2004
2004
X-Linked Lissencephaly with Abnormal Genitalia Associated with Renal Phosphate Wasting
A. Hahn
,
C. Gross
,
+4 authors
B. Neubauer
Neuropediatrics
2004
Corpus ID: 37554663
(ARX)
2002
2002
The Xenopus arx gene is expressed in the developing rostral forebrain
H. El-Hodiri
,
Xiuyan Qi
,
D. Seufert
Development, Genes and Evolution
2002
Corpus ID: 9422287
Abstract. The human aristaless-related homeobox (ARX) gene is mutated in several patients with X-linked mental retardation and/or…
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