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Cellular and molecular mechanisms underlying muscular dystrophy

The Journal of cell biology, 2013-05, Vol.201 (4), p.499-510

2013

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CD82 Is a Marker for Prospective Isolation of Human Muscle Satellite Cells and Is Linked to Muscular Dystrophies

Cell stem cell, 2016-12, Vol.19 (6), p.800-807

2016

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Regulation of IRS1/Akt insulin signaling by microRNA-128a during myogenesis

Journal of cell science, 2013-06, Vol.126 (Pt 12), p.2678-2691

2013

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MicroRNA-199a is induced in dystrophic muscle and affects WNT signaling, cell proliferation, and myogenic differentiation

Cell death and differentiation, 2013-09, Vol.20 (9), p.1194-1208

2013

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Emerging preclinical animal models for FSHD

Trends in molecular medicine, 2015-05, Vol.21 (5), p.295-306

2015

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Effects of RAS on the genesis of embryonal rhabdomyosarcoma

Genes & development, 2007-06, Vol.21 (11), p.1382-1395

2007

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To dystrophin and beyond: an interview with Louis Kunkel

Disease models & mechanisms, 2020-02, Vol.13 (2)

2020

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miRNAS in normal and diseased skeletal muscle

Journal of cellular and molecular medicine, 2009-01, Vol.13 (1), p.2-11

2009

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Loss of FilaminC (FLNc) Results in Severe Defects in Myogenesis and Myotube Structure

Molecular and Cellular Biology, 2006-09, Vol.26 (17), p.6522-6534

2006

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Muscle dysfunction in a zebrafish model of Duchenne muscular dystrophy

Physiological genomics, 2016-11, Vol.48 (11), p.850-860

2016

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Muscular dystrophies: genes to pathogenesis

Current opinion in genetics & development, 2003-06, Vol.13 (3), p.231-238

2003

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Regulation of DMD pathology by an ankyrin-encoded miRNA

Skeletal muscle, 2011-08, Vol.1 (1), p.27-27, Article 27

2011

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Expression profiling and identification of novel genes involved in myogenic differentiation

The FASEB journal, 2004-02, Vol.18 (2), p.1-23

2004

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Filamin 2 (FLN2): A Muscle-Specific Sarcoglycan Interacting Protein

The Journal of cell biology, 2000-01, Vol.148 (1), p.115-126

2000

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The fate of individual myoblasts after transplantation into muscles of DMD patients

Nature medicine, 1997-09, Vol.3 (9), p.970-977

1997

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Jagged 1 Rescues the Duchenne Muscular Dystrophy Phenotype

Cell, 2015-11, Vol.163 (5), p.1204-1213

2015

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Demystifying SP cell purification: viability, yield, and phenotype are defined by isolation parameters

Experimental cell research, 2004-08, Vol.298 (1), p.144-154

2004

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Characterization of zebrafish dysferlin by morpholino knockdown

Biochemical and biophysical research communications, 2011-09, Vol.413 (2), p.358-363

2011

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Syntrophin Binds to an Alternatively Spliced Exon of Dystrophin

The Journal of cell biology, 1995-02, Vol.128 (3), p.363-371

1995

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Dystrophin: The protein product of the duchenne muscular dystrophy locus

Cell, 1987-12, Vol.51 (6), p.919-928

1987

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Human ϵ-sarcoglycan is highly related to α-sarcoglycan (adhalin), the limb girdle muscular dystrophy 2D gene

FEBS letters, 1998-01, Vol.422 (1), p.27-32

1998

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Molecular Organization of Sarcoglycan Complex in Mouse Myotubes in Culture

The Journal of cell biology, 1998-12, Vol.143 (7), p.2033-2044

1998

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The complete sequence of dystrophin predicts a rod-shaped cytoskeletal protein

Cell, 1988-04, Vol.53 (2), p.219-228

1988

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Fam65b is important for formation of the HDAC6‐dysferlin protein complex during myogenic cell differentiation

The FASEB journal, 2014-07, Vol.28 (7), p.2955-2969

2014

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α‐Actinin‐2 deficiency results in sarcomeric defects in zebrafish that cannot be rescued by α‐actinin‐3 revealing functional differences between sarcomeric isoforms

The FASEB journal, 2012-05, Vol.26 (5), p.1892-1908

2012

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Cellular and molecular mechanisms underlying muscular dystrophy

CD82 Is a Marker for Prospective Isolation of Human Muscle Satellite Cells and Is Linked to Muscular Dystrophies

Regulation of IRS1/Akt insulin signaling by microRNA-128a during myogenesis

MicroRNA-199a is induced in dystrophic muscle and affects WNT signaling, cell proliferation, and myogenic differentiation

Emerging preclinical animal models for FSHD

Effects of RAS on the genesis of embryonal rhabdomyosarcoma

To dystrophin and beyond: an interview with Louis Kunkel

miRNAS in normal and diseased skeletal muscle

Loss of FilaminC (FLNc) Results in Severe Defects in Myogenesis and Myotube Structure

Muscle dysfunction in a zebrafish model of Duchenne muscular dystrophy

Muscular dystrophies: genes to pathogenesis

Regulation of DMD pathology by an ankyrin-encoded miRNA

Expression profiling and identification of novel genes involved in myogenic differentiation

Filamin 2 (FLN2): A Muscle-Specific Sarcoglycan Interacting Protein

The fate of individual myoblasts after transplantation into muscles of DMD patients

Jagged 1 Rescues the Duchenne Muscular Dystrophy Phenotype

Demystifying SP cell purification: viability, yield, and phenotype are defined by isolation parameters

Characterization of zebrafish dysferlin by morpholino knockdown

Syntrophin Binds to an Alternatively Spliced Exon of Dystrophin

Dystrophin: The protein product of the duchenne muscular dystrophy locus

Human ϵ-sarcoglycan is highly related to α-sarcoglycan (adhalin), the limb girdle muscular dystrophy 2D gene

Molecular Organization of Sarcoglycan Complex in Mouse Myotubes in Culture

The complete sequence of dystrophin predicts a rod-shaped cytoskeletal protein

Fam65b is important for formation of the HDAC6‐dysferlin protein complex during myogenic cell differentiation

α‐Actinin‐2 deficiency results in sarcomeric defects in zebrafish that cannot be rescued by α‐actinin‐3 revealing functional differences between sarcomeric isoforms

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