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Mutations in the human ortholog of Aristaless cause X-linked mental retardation and epilepsy

Nature genetics, 2002-04, Vol.30 (4), p.441-445

2002

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RNA-binding proteins in neurological diseases

Science China. Life sciences, 2014-04, Vol.57 (4), p.432-444

2014

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Mutations in the DLG3 Gene Cause Nonsyndromic X-Linked Mental Retardation

American journal of human genetics, 2004-08, Vol.75 (2), p.318-324

2004

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Infantile spasms, dystonia, and other X-linked phenotypes caused by mutations in Aristaless related homeobox gene, ARX

Brain & development (Tokyo. 1979), 2002-08, Vol.24 (5), p.266

2002

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Human Chromosomal Fragile Site FRA16B Is an Amplified AT-Rich Minisatellite Repeat

Cell, 1997-02, Vol.88 (3), p.367-374

1997

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C9orf72 hexanucleotide repeat expansions in Chinese sporadic amyotrophic lateral sclerosis

Neurobiology of aging, 2015-09, Vol.36 (9), p.2660.e1-2660.e8

2015

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XLMR in MRX families 29, 32, 33 and 38 results from the dup24 mutation in the ARX (Aristaless related homeobox) gene

BMC medical genetics, 2005-04, Vol.6 (1), p.16-16, Article 16

2005

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A non-coding variant in the 5' UTR of DLG3 attenuates protein translation to cause non-syndromic intellectual disability

European journal of human genetics : EJHG, 2016-11, Vol.24 (11), p.1612-1616

2016

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Infantile spasms, dystonia, and other X-linked phenotypes caused by mutations in Aristaless related homeobox gene, ARX

Brain & development (Tokyo. 1979), 2002-08, Vol.24 (5), p.266-268

2002

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Common chromosomal fragile site FRA16D sequence : identification of the FOR gene spanning FRA16D and homozygous deletions and translocation breakpoints in cancer cells

Human molecular genetics, 2000-07, Vol.9 (11), p.1651-1663

2000

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Folate-sensitive fragile site FRA10A is due to an expansion of a CGG repeat in a novel gene, FRA10AC1, encoding a nuclear protein

Genomics (San Diego, Calif.), 2004-07, Vol.84 (1), p.69-81

2004

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FRA10B Structure Reveals Common Elements in Repeat Expansion and Chromosomal Fragile Site Genesis

Molecular cell, 1998-05, Vol.1 (6), p.773-781

1998

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Genetic Heterogeneity in Familial Acute Myelogenous Leukemia: Evidence for a Second Locus at Chromosome 16q21-23.2

American journal of human genetics, 1997-10, Vol.61 (4), p.873-881

1997

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Genomic convergence among ERRα, PROX1, and BMAL1 in the control of metabolic clock outputs

PLoS genetics, 2011-06, Vol.7 (6), p.e1002143-e1002143

2011

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LXRs regulate the balance between fat storage and oxidation

Cell metabolism, 2005-04, Vol.1 (4), p.231-244

2005

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Mutations in the human ortholog of Aristaless cause X-linked mental retardation and epilepsy

RNA-binding proteins in neurological diseases

Mutations in the DLG3 Gene Cause Nonsyndromic X-Linked Mental Retardation

Infantile spasms, dystonia, and other X-linked phenotypes caused by mutations in Aristaless related homeobox gene, ARX

Human Chromosomal Fragile Site FRA16B Is an Amplified AT-Rich Minisatellite Repeat

C9orf72 hexanucleotide repeat expansions in Chinese sporadic amyotrophic lateral sclerosis

XLMR in MRX families 29, 32, 33 and 38 results from the dup24 mutation in the ARX (Aristaless related homeobox) gene

A non-coding variant in the 5' UTR of DLG3 attenuates protein translation to cause non-syndromic intellectual disability

Multiplex families with epilepsy: Success of clinical and molecular genetic characterization

Infantile spasms, dystonia, and other X-linked phenotypes caused by mutations in Aristaless related homeobox gene, ARX

Common chromosomal fragile site FRA16D sequence : identification of the FOR gene spanning FRA16D and homozygous deletions and translocation breakpoints in cancer cells

Construction of a 1-Mb Restriction-Mapped Cosmid Contig Containing the Candidate Region for the Familial Mediterranean Fever Locus (MEFV) on Chromosome 16p13.3

Folate-sensitive fragile site FRA10A is due to an expansion of a CGG repeat in a novel gene, FRA10AC1, encoding a nuclear protein

FRA10B Structure Reveals Common Elements in Repeat Expansion and Chromosomal Fragile Site Genesis

Genetic Heterogeneity in Familial Acute Myelogenous Leukemia: Evidence for a Second Locus at Chromosome 16q21-23.2

A High-Resolution Genetic Map of the Familial Mediterranean Fever Candidate Region Allows Identification of Haplotype-Sharing among Ethnic Groups

Genomic convergence among ERRα, PROX1, and BMAL1 in the control of metabolic clock outputs

LXRs regulate the balance between fat storage and oxidation

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