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UnknownIdentification and validation of the phosphorylation sites on Aristaless-related homeobox protein.
Not available
S-EPMC7364481 | biostudies-literature
UnknownDysgenesis of enteroendocrine cells in Aristaless-Related Homeobox polyalanine expansion mutations.
Not available
S-EPMC4308495 | biostudies-literature
ProteomicsComparative brain proteomics in Arx transgenic mice for lissencephaly and epileptic encephalopathy
Aristaless-related homeobox (ARX) is an X-linked gene encoding a bi-functional morphogenetic transcription factor with a key role in neuronal migration and brain development. Mutations in ARX have been identified in patients with X-linked Lissencephaly with Abnormal Genitalia (XLAG) and Early-infant...
ORGANISM(S): Mus musculus (Mouse) 
2024-06-14 | PXD021358 | Pride
Aristaless-related homeobox Neuroproteomics Lc-ms/ms 
UnknownAristaless Related Homeobox (ARX) Interacts with β-Catenin, BCL9, and P300 to Regulate Canonical Wnt Signaling.
Not available
S-EPMC5245867 | biostudies-literature
TranscriptomicsIdentification by ChIP-on-Chip of ARX target genes, a transcription factor implicated in mental retardation and epilepsy
Genetic investigations of X-linked intellectual disabilities have implicated the ARX (Aristaless-related homeobox) gene in a wide spectrum of disorders extending from phenotypes characterised by severe neuronal migration defects such as lissencephaly, to mild or moderate forms of mental retardation ...
ORGANISM(S): Mus musculus 
2011-12-22 | E-GEOD-29985 | biostudies-arrayexpress
TranscriptomicsComparison of gene expression between Arx-transfected N2a cells and cells transfected by the corresponding empty vector
Genetic investigations of X-linked intellectual disabilities have implicated the ARX (Aristaless-related homeobox) gene in a wide spectrum of disorders extending from phenotypes characterised by severe neuronal migration defects such as lissencephaly, to mild or moderate forms of mental retardation ...
ORGANISM(S): Mus musculus 
2011-12-22 | E-GEOD-30190 | biostudies-arrayexpress
UnknownThe roles of multiple importins for nuclear import of murine aristaless-related homeobox protein.
Not available
S-EPMC2740467 | biostudies-literature
UnknownAristaless-Like Homeobox protein 1 (ALX1) variant associated with craniofacial structure and frontonasal dysplasia in Burmese cats.
Not available
S-EPMC4724490 | biostudies-literature
UnknownHomeobox gene Prx3 expression in rodent brain and extraneural tissues.
Not available
S-EPMC24251 | biostudies-literature
UnknownFrontorhiny, a distinctive presentation of frontonasal dysplasia caused by recessive mutations in the ALX3 homeobox gene.
Not available
S-EPMC2681074 | biostudies-literature
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