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Contribution of VANGL2 mutations to isolated neural tube defects

Clinical genetics, 2011-07, Vol.80 (1), p.76-82

2011

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Disruption of the non-canonical Wnt gene PRICKLE2 leads to autism-like behaviors with evidence for hippocampal synaptic dysfunction

Molecular psychiatry, 2013-10, Vol.18 (10), p.1077-1089

2013

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SCARB2 mutations in progressive myoclonus epilepsy (PME) without renal failure

Annals of neurology, 2009-10, Vol.66 (4), p.532-536

2009

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In cis autosomal dominant mutation of Senataxin associated with tremor/ataxia syndrome

Neurogenetics, 2007, Vol.8 (1), p.45-49

2007

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Whole genomewide linkage screen for neural tube defects reveals regions of interest on chromosomes 7 and 10

Journal of medical genetics, 2005-12, Vol.42 (12), p.940-946

2005

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Alexander disease with serial MRS and a new mutation in the glial fibrillary acidic protein gene

Neurology, 2003-10, Vol.61 (7), p.1014

2003

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Activation of the granulocyte-macrophage colony-stimulating factor promoter in T cells requires cooperative binding of Elf-1 and AP-1 transcription factors

Molecular and Cellular Biology, 1994-02, Vol.14 (2), p.1153-1159

1994

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A child with spinal cord AVM presenting with raised intracranial pressure

Neurology, 2003-05, Vol.60 (10), p.1724

2003

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The non-canonical Wnt ligand Wnt5a rescues morphological deficits in Prickle2-deficient hippocampal neurons

Molecular psychiatry, 2013-10, Vol.18 (10), p.1049-1049

2013

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Disruption of the non-canonical Wnt gene PRICKLE2 leads to autism-like behaviors with evidence for hippocampal synaptic dysfunction

Molecular psychiatry, 2014-06, Vol.19 (6), p.742

2014

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A direct physical association between ETS and AP-1 transcription factors in normal human T cells

Immunity (Cambridge, Mass.), 1995-08, Vol.3 (2), p.223-237

1995

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Expression pattern of the Ets-related transcription factor Elf-1

Molecular medicine (Cambridge, Mass.), 1998-06, Vol.4 (6), p.392-401

1998

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Physical interactions between Ets and NF- Kappa B/NFAT proteins play an important role in their cooperative activation of the human immunodeficiency virus enhancer in T cells

Journal of virology, 1997-05, Vol.71 (5), p.3563-3573

1997

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Functional validation of a human CAPN5 exome variant by lentiviral transduction into mouse retina

Human molecular genetics, 2014-05, Vol.23 (10), p.2665-2677

2014

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The Role of Ets Transcription Factors in the Development and Function of the Mammalian Immune System

Advances in Immunology, 1997, Vol.64, p.65-104

1997

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SNPs in the neural cell adhesion molecule 1 gene (NCAM1) may be associated with human neural tube defects

Human genetics, 2005-07, Vol.117 (2-3), p.133-142

2005

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Neural Tube Defects and Folate Pathway Genes: Family-Based Association Tests of Gene-Gene and Gene-Environment Interactions

Environmental health perspectives, 2006-10, Vol.114 (10), p.1547-1552

2006

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Copy number variation analysis implicates the cell polarity gene glypican 5 as a human spina bifida candidate gene

Human molecular genetics, 2013-03, Vol.22 (6), p.1097-1111

2013

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Presence of Epilepsy-Associated Variants in Large Exome Databases

Journal of neurogenetics, 2013-06, Vol.27 (1-2), p.1-4

2013

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Drug repositioning in epilepsy reveals novel antiseizure candidates

Annals of clinical and translational neurology, 2019-02, Vol.6 (2), p.295-309

2019

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Erratum: Disruption of the non-canonical Wnt gene PRICKLE2 leads to autism-like behaviors with evidence for hippocampal synaptic dysfunction

Molecular psychiatry, 2014-06, Vol.19 (6), p.742-742

2014

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TERC is not a major gene in human neural tube defects

Birth defects research. A Clinical and molecular teratology, 2004-08, Vol.70 (8), p.531-533

2004

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Physical interactions between Ets and NF-kappaB/NFAT proteins play an important role in their cooperative activation of the human immunodeficiency virus enhancer in T cells

Journal of Virology, 1997-05, Vol.71 (5), p.3563-3573

1997

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Monozygotic twins with CAPN5 autosomal dominant neovascular inflammatory vitreoretinopathy

Clinical ophthalmology (Auckland, N.Z.), 2012-01, Vol.6 (default), p.2037-2044

2012

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Contribution of VANGL2 mutations to isolated neural tube defects

Disruption of the non-canonical Wnt gene PRICKLE2 leads to autism-like behaviors with evidence for hippocampal synaptic dysfunction

SCARB2 mutations in progressive myoclonus epilepsy (PME) without renal failure

In cis autosomal dominant mutation of Senataxin associated with tremor/ataxia syndrome

Whole genomewide linkage screen for neural tube defects reveals regions of interest on chromosomes 7 and 10

Alexander disease with serial MRS and a new mutation in the glial fibrillary acidic protein gene

Activation of the granulocyte-macrophage colony-stimulating factor promoter in T cells requires cooperative binding of Elf-1 and AP-1 transcription factors

A child with spinal cord AVM presenting with raised intracranial pressure

The non-canonical Wnt ligand Wnt5a rescues morphological deficits in Prickle2-deficient hippocampal neurons

Disruption of the non-canonical Wnt gene PRICKLE2 leads to autism-like behaviors with evidence for hippocampal synaptic dysfunction

A direct physical association between ETS and AP-1 transcription factors in normal human T cells

Expression pattern of the Ets-related transcription factor Elf-1

A Homozygous Mutation in Human PRICKLE1 Causes an Autosomal-Recessive Progressive Myoclonus Epilepsy-Ataxia Syndrome

Physical interactions between Ets and NF- Kappa B/NFAT proteins play an important role in their cooperative activation of the human immunodeficiency virus enhancer in T cells

Functional validation of a human CAPN5 exome variant by lentiviral transduction into mouse retina

The Role of Ets Transcription Factors in the Development and Function of the Mammalian Immune System

SNPs in the neural cell adhesion molecule 1 gene (NCAM1) may be associated with human neural tube defects

Neural Tube Defects and Folate Pathway Genes: Family-Based Association Tests of Gene-Gene and Gene-Environment Interactions

Copy number variation analysis implicates the cell polarity gene glypican 5 as a human spina bifida candidate gene

Presence of Epilepsy-Associated Variants in Large Exome Databases

Drug repositioning in epilepsy reveals novel antiseizure candidates

Erratum: Disruption of the non-canonical Wnt gene PRICKLE2 leads to autism-like behaviors with evidence for hippocampal synaptic dysfunction

TERC is not a major gene in human neural tube defects

Physical interactions between Ets and NF-kappaB/NFAT proteins play an important role in their cooperative activation of the human immunodeficiency virus enhancer in T cells

Monozygotic twins with CAPN5 autosomal dominant neovascular inflammatory vitreoretinopathy

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