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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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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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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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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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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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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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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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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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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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Misfolding of fukutin-related protein (FKRP) variants in congenital and limb girdle muscular dystrophies

Frontiers in molecular biosciences, 2023-12, Vol.10, p.1279700

2023

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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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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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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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The neurobiology of Duchenne muscular dystrophy: learning lessons from muscle?

Trends in neurosciences (Regular ed.), 2000-03, Vol.23 (3), p.92-99

2000

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Transcriptional Changes following Cellular Knockdown of the Schizophrenia Risk Gene SETD1A Are Enriched for Common Variant Association with the Disorder

Complex psychiatry, 2019-04, Vol.5 (2), p.109-114

2019

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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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Different Dystrophin-Like Complexes Are Expressed in Neurons and Glia

The Journal of cell biology, 1999-11, Vol.147 (3), p.645-657

1999

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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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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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Myospryn Is a Novel Binding Partner for Dysbindin in Muscle

The Journal of biological chemistry, 2004-03, Vol.279 (11), p.10450-10458

2004

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Abnormal Dysbindin Expression in Cerebellar Mossy Fiber Synapses in the mdx Mouse Model of Duchenne Muscular Dystrophy

The Journal of neuroscience, 2003-07, Vol.23 (16), p.6576-6585

2003

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

The dystrophin–glycoprotein complex in brain development and disease

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

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

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

SGCE mutations cause psychiatric disorders: clinical and genetic characterization

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

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

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

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

Misfolding of fukutin-related protein (FKRP) variants in congenital and limb girdle muscular dystrophies

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

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

The emerging roles of TCF4 in disease and development

The neurobiology of Duchenne muscular dystrophy: learning lessons from muscle?

Transcriptional Changes following Cellular Knockdown of the Schizophrenia Risk Gene SETD1A Are Enriched for Common Variant Association with the Disorder

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

Different Dystrophin-Like Complexes Are Expressed in Neurons and Glia

TRIM32 is an E3 ubiquitin ligase for dysbindin

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

Myospryn Is a Novel Binding Partner for Dysbindin in Muscle

Abnormal Dysbindin Expression in Cerebellar Mossy Fiber Synapses in the mdx Mouse Model of Duchenne Muscular Dystrophy

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

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

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