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Nuclear and nuclear envelope localization of dystrophin Dp71 and dystrophin-associated proteins (DAPs) in the C2C12 muscle cells: DAPs nuclear localization is modulated during myogenesis

Journal of cellular biochemistry, 2008-10, Vol.105 (3), p.735-745

2008

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TRIM24 protein promotes and TRIM32 protein inhibits cardiomyocyte hypertrophy via regulation of dysbindin protein levels

The Journal of biological chemistry, 2017-06, Vol.292 (24), p.10180-10196

2017

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Role of dystrophin and utrophin for assembly and function of the dystrophin glycoprotein complex in non-muscle tissue

Cellular and molecular life sciences : CMLS, 2006-07, Vol.63 (14), p.1614-1631

2006

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Dysbindin as a novel biomarker for pancreatic ductal adenocarcinoma identified by proteomic profiling

International journal of cancer, 2016-10, Vol.139 (8), p.1821-1829

2016

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LXR Agonism Upregulates the Macrophage ABCA1/Syntrophin Protein Complex That Can Bind ApoA‑I and Stabilized ABCA1 Protein, but Complex Loss Does Not Inhibit Lipid Efflux

Biochemistry (Easton), 2015-11, Vol.54 (46), p.6931-6941

2015

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The Dystrophin Complex: Structure, Function, and Implications for Therapy

Comprehensive Physiology, 2015-07, Vol.5 (3), p.1223-1239

2015

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Molecular scaffolds underpinning macroglial polarization: An analysis of retinal Müller cells and brain astrocytes in mouse

Glia, 2012-12, Vol.60 (12), p.2018-2026

2012

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Circulating miRNAs are generic and versatile therapeutic monitoring biomarkers in muscular dystrophies

Scientific reports, 2016-06, Vol.6 (1), p.28097, Article 28097

2016

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Phosphorylation within the cysteine-rich region of dystrophin enhances its association with β-dystroglycan and identifies a potential novel therapeutic target for skeletal muscle wasting

Human molecular genetics, 2014-12, Vol.23 (25), p.6697-6711

2014

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Costamere proteins and their involvement in myopathic processes

Expert reviews in molecular medicine, 2015-01, Vol.17, p.e12-e12, Article e12

2015

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Equilibrium Unfolding of the PDZ Domain of β2-Syntrophin

Biophysical journal, 2012-06, Vol.102 (12), p.2835-2844

2012

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Dystrophin R16/17-syntrophin PDZ fusion protein restores sarcolemmal nNOSμ

Skeletal muscle, 2018-11, Vol.8 (1), p.36-36, Article 36

2018

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Identification of two novel mutations in FAM136A and DTNA genes in autosomal-dominant familial Meniere's disease

Human molecular genetics, 2015-02, Vol.24 (4), p.1119-1126

2015

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β2-Syntrophin is a Cdk5 substrate that restrains the motility of insulin secretory granules

PloS one, 2010-09, Vol.5 (9), p.e12929-e12929

2010

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Expression of multiple AQP4 pools in the plasma membrane and their association with the dystrophin complex

Journal of neurochemistry, 2008-06, Vol.105 (6), p.2156-2165

2008

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Distinct roles of the dystrophin-glycoprotein complex: α-dystrobrevin and α-syntrophin in the maintenance of the postsynaptic apparatus of the neuromuscular synapse

Human molecular genetics, 2022-07, Vol.31 (14), p.2370-2385

2022

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Pharmacological advances for treatment in Duchenne muscular dystrophy

Current opinion in pharmacology, 2017-06, Vol.34, p.36-48

2017

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BLOC-1 is required for selective membrane protein trafficking from endosomes to primary cilia

The Journal of cell biology, 2017-07, Vol.216 (7), p.2131-2150

2017

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Cerebellar synaptic defects and abnormal motor behavior in mice lacking alpha- and beta-dystrobrevin

The Journal of neuroscience, 2006-03, Vol.26 (11), p.2841-2851

2006

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Haemostatic role of intermediate filaments in adhered platelets: Importance of the membranous system stability

Journal of cellular biochemistry, 2013-09, Vol.114 (9), p.2050-2060

2013

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Characterization of the expression of dystrophins and dystrophin-associated proteins during embryonic neural stem/progenitor cell differentiation

Neuroscience letters, 2020-09, Vol.736, p.135247-135247, Article 135247

2020

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Finding the Sweet Spot: Assembly and Glycosylation of the Dystrophin‐Associated Glycoprotein Complex

Anatomical record (Hoboken, N.J. : 2007), 2014-09, Vol.297 (9), p.1694-1705

Townsend, Dewayne

2014

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Ordered disorder of the astrocytic dystrophin-associated protein complex in the norm and pathology

PloS one, 2013-08, Vol.8 (8), p.e73476-e73476

2013

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Mice lacking α-, β1- and β2-syntrophins exhibit diminished function and reduced dystrophin expression in both cardiac and skeletal muscle

Human molecular genetics, 2019-02, Vol.28 (3), p.386-395

2019

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Dystrobrevins in muscle and non-muscle tissues

Neuromuscular disorders : NMD, 2007-02, Vol.17 (2), p.123-134

2007

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Nuclear and nuclear envelope localization of dystrophin Dp71 and dystrophin-associated proteins (DAPs) in the C2C12 muscle cells: DAPs nuclear localization is modulated during myogenesis

TRIM24 protein promotes and TRIM32 protein inhibits cardiomyocyte hypertrophy via regulation of dysbindin protein levels

Role of dystrophin and utrophin for assembly and function of the dystrophin glycoprotein complex in non-muscle tissue

Dysbindin as a novel biomarker for pancreatic ductal adenocarcinoma identified by proteomic profiling

LXR Agonism Upregulates the Macrophage ABCA1/Syntrophin Protein Complex That Can Bind ApoA‑I and Stabilized ABCA1 Protein, but Complex Loss Does Not Inhibit Lipid Efflux

The Dystrophin Complex: Structure, Function, and Implications for Therapy

Molecular scaffolds underpinning macroglial polarization: An analysis of retinal Müller cells and brain astrocytes in mouse

Circulating miRNAs are generic and versatile therapeutic monitoring biomarkers in muscular dystrophies

Phosphorylation within the cysteine-rich region of dystrophin enhances its association with β-dystroglycan and identifies a potential novel therapeutic target for skeletal muscle wasting

Costamere proteins and their involvement in myopathic processes

Equilibrium Unfolding of the PDZ Domain of β2-Syntrophin

Dystrophin R16/17-syntrophin PDZ fusion protein restores sarcolemmal nNOSμ

Identification of two novel mutations in FAM136A and DTNA genes in autosomal-dominant familial Meniere's disease

β2-Syntrophin is a Cdk5 substrate that restrains the motility of insulin secretory granules

Expression of multiple AQP4 pools in the plasma membrane and their association with the dystrophin complex

Distinct roles of the dystrophin-glycoprotein complex: α-dystrobrevin and α-syntrophin in the maintenance of the postsynaptic apparatus of the neuromuscular synapse

Pharmacological advances for treatment in Duchenne muscular dystrophy

BLOC-1 is required for selective membrane protein trafficking from endosomes to primary cilia

Cerebellar synaptic defects and abnormal motor behavior in mice lacking alpha- and beta-dystrobrevin

Haemostatic role of intermediate filaments in adhered platelets: Importance of the membranous system stability

Characterization of the expression of dystrophins and dystrophin-associated proteins during embryonic neural stem/progenitor cell differentiation

Finding the Sweet Spot: Assembly and Glycosylation of the Dystrophin‐Associated Glycoprotein Complex

Ordered disorder of the astrocytic dystrophin-associated protein complex in the norm and pathology

Mice lacking α-, β1- and β2-syntrophins exhibit diminished function and reduced dystrophin expression in both cardiac and skeletal muscle

Dystrobrevins in muscle and non-muscle tissues

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