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Knockdown of human TCF4 affects multiple signaling pathways involved in cell survival, epithelial to mesenchymal transition and neuronal differentiation

PloS one, 2013-08, Vol.8 (8), p.e73169-e73169

2013

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Meta-Analysis of Cell Therapy Studies in Heart Failure and Acute Myocardial Infarction

Circulation research, 2018-07, Vol.123 (2), p.301-308

2018

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The dystrophin–glycoprotein complex in brain development and disease

Trends in neurosciences (Regular ed.), 2012-08, Vol.35 (8), p.487-496

2012

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Reduced C9orf72 protein levels in frontal cortex of amyotrophic lateral sclerosis and frontotemporal degeneration brain with the C9ORF72 hexanucleotide repeat expansion

Neurobiology of aging, 2014-07, Vol.35 (7), p.1779.e5-1779.e13

2014

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The Psychiatric Risk Gene Transcription Factor 4 (TCF4) Regulates Neurodevelopmental Pathways Associated With Schizophrenia, Autism, and Intellectual Disability

Schizophrenia bulletin, 2018-08, Vol.44 (5), p.1100-1110

2018

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The emerging roles of TCF4 in disease and development

Trends in molecular medicine, 2014-06, Vol.20 (6), p.322-331

2014

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C9orf72 ablation in mice does not cause motor neuron degeneration or motor deficits

Annals of neurology, 2015-09, Vol.78 (3), p.426-438

2015

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Proteomic investigation of the Alzheimer's risk gene MEF2C in microglial like cells

Alzheimer's & dementia, 2021-12, Vol.17 (S3), p.e050631-n/a

2021

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Synaptic dysbindin-1 reductions in schizophrenia occur in an isoform-specific manner indicating their subsynaptic location

PloS one, 2011-03, Vol.6 (3), p.e16886-e16886

2011

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Transcriptional programs regulating neuronal differentiation are disrupted in DLG2 knockout human embryonic stem cells and enriched for schizophrenia and related disorders risk variants

Nature communications, 2022-01, Vol.13 (1), p.27-27, Article 27

2022

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TRIM32 is an E3 ubiquitin ligase for dysbindin

Human molecular genetics, 2009-07, Vol.18 (13), p.2344-2358

2009

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Function and Genetics of Dystrophin and Dystrophin-Related Proteins in Muscle

Physiological reviews, 2002-04, Vol.82 (2), p.291-329

2002

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Adeno-associated Virus 9 Mediated FKRP Gene Therapy Restores Functional Glycosylation of α-dystroglycan and Improves Muscle Functions

Molecular therapy, 2013-10, Vol.21 (10), p.1832-1840

2013

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CMYA5 is a novel interaction partner of FHL2 in cardiac myocytes

The FEBS journal, 2022-08, Vol.289 (15), p.4622-4645

2022

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Role of major and brain-specific Sgce isoforms in the pathogenesis of myoclonus-dystonia syndrome

Neurobiology of disease, 2017-02, Vol.98, p.52-65

2017

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An isolated sacral promyelocytic sarcoma in a child: A rare case report with emphasis on cytomorphology

Diagnostic cytopathology, 2024-06, Vol.52 (6), p.E145-E149

2024

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SGCE mutations cause psychiatric disorders: clinical and genetic characterization

Brain (London, England : 1878), 2013, Vol.136 (Pt 1), p.294-303

2013

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Myoclonus dystonia and muscular dystrophy: ɛ-sarcoglycan is part of the dystrophin-associated protein complex in brain

Movement disorders, 2016-11, Vol.31 (11), p.1694-1703

2016

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Fukutin-related protein is essential for mouse muscle, brain and eye development and mutation recapitulates the wide clinical spectrums of dystroglycanopathies

Human molecular genetics, 2010-10, Vol.19 (20), p.3995-4006

2010

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Convergent Evidence That ZNF804A Is a Regulator of Pre-messenger RNA Processing and Gene Expression

Schizophrenia bulletin, 2019-10, Vol.45 (6), p.1267-1278

2019

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Dysbindin-1 is reduced in intrinsic, glutamatergic terminals of the hippocampal formation in schizophrenia

The Journal of clinical investigation, 2004-05, Vol.113 (9), p.1353-1363

2004

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Effect of Trinucleotide Repeat Expansion on the Expression of TCF4 mRNA in Fuchs' Endothelial Corneal Dystrophy

Investigative ophthalmology & visual science, 2019-02, Vol.60 (2), p.779-786

2019

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The neurobiology of the dystrophin-associated glycoprotein complex

Annals of medicine (Helsinki), 2009, Vol.41 (5), p.344-359

2009

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Ryanodine receptors are part of the myospryn complex in cardiac muscle

Scientific reports, 2017-07, Vol.7 (1), p.6312-12, Article 6312

2017

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Functional analysis of TCF4 missense mutations that cause Pitt-Hopkins syndrome

Human mutation, 2012-12, Vol.33 (12), p.1676-1686

2012

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Knockdown of human TCF4 affects multiple signaling pathways involved in cell survival, epithelial to mesenchymal transition and neuronal differentiation

Meta-Analysis of Cell Therapy Studies in Heart Failure and Acute Myocardial Infarction

The dystrophin–glycoprotein complex in brain development and disease

Reduced C9orf72 protein levels in frontal cortex of amyotrophic lateral sclerosis and frontotemporal degeneration brain with the C9ORF72 hexanucleotide repeat expansion

The Psychiatric Risk Gene Transcription Factor 4 (TCF4) Regulates Neurodevelopmental Pathways Associated With Schizophrenia, Autism, and Intellectual Disability

The emerging roles of TCF4 in disease and development

C9orf72 ablation in mice does not cause motor neuron degeneration or motor deficits

Proteomic investigation of the Alzheimer's risk gene MEF2C in microglial like cells

Synaptic dysbindin-1 reductions in schizophrenia occur in an isoform-specific manner indicating their subsynaptic location

Transcriptional programs regulating neuronal differentiation are disrupted in DLG2 knockout human embryonic stem cells and enriched for schizophrenia and related disorders risk variants

TRIM32 is an E3 ubiquitin ligase for dysbindin

Function and Genetics of Dystrophin and Dystrophin-Related Proteins in Muscle

Adeno-associated Virus 9 Mediated FKRP Gene Therapy Restores Functional Glycosylation of α-dystroglycan and Improves Muscle Functions

CMYA5 is a novel interaction partner of FHL2 in cardiac myocytes

Role of major and brain-specific Sgce isoforms in the pathogenesis of myoclonus-dystonia syndrome

An isolated sacral promyelocytic sarcoma in a child: A rare case report with emphasis on cytomorphology

SGCE mutations cause psychiatric disorders: clinical and genetic characterization

Myoclonus dystonia and muscular dystrophy: ɛ-sarcoglycan is part of the dystrophin-associated protein complex in brain

Fukutin-related protein is essential for mouse muscle, brain and eye development and mutation recapitulates the wide clinical spectrums of dystroglycanopathies

Convergent Evidence That ZNF804A Is a Regulator of Pre-messenger RNA Processing and Gene Expression

Dysbindin-1 is reduced in intrinsic, glutamatergic terminals of the hippocampal formation in schizophrenia

Effect of Trinucleotide Repeat Expansion on the Expression of TCF4 mRNA in Fuchs' Endothelial Corneal Dystrophy

The neurobiology of the dystrophin-associated glycoprotein complex

Ryanodine receptors are part of the myospryn complex in cardiac muscle

Functional analysis of TCF4 missense mutations that cause Pitt-Hopkins syndrome

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