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Membrane Targeting and Stabilization of Sarcospan Is Mediated by the Sarcoglycan Subcomplex

The Journal of cell biology, 1999-04, Vol.145 (1), p.153-165

1999

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Progressive Muscular Dystrophy in α-Sarcoglycan-Deficient Mice

The Journal of cell biology, 1998-09, Vol.142 (6), p.1461-1471

1998

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Biosynthesis of dystroglycan: processing of a precursor propeptide

FEBS letters, 2000-02, Vol.468 (1), p.79-83

2000

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Sarcospan, the 25-kDa Transmembrane Component of the Dystrophin-Glycoprotein Complex

The Journal of biological chemistry, 1997-12, Vol.272 (50), p.31221-31224

1997

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Functional Rescue of the Sarcoglycan Complex in the BIO 14.6 Hamster Using δ-Sarcoglycan Gene Transfer

Molecular cell, 1998-05, Vol.1 (6), p.841-848

1998

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Caveolin-3 is not an integral component of the dystrophin glycoprotein complex

FEBS letters, 1998-05, Vol.427 (2), p.279-282

1998

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Sarcospan-Deficient Mice Maintain Normal Muscle Function

Molecular and Cellular Biology, 2000-03, Vol.20 (5), p.1669-1677

2000

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ε-Sarcoglycan Replaces α-Sarcoglycan in Smooth Muscle to Form a Unique Dystrophin-Glycoprotein Complex

The Journal of biological chemistry, 1999-09, Vol.274 (39), p.27989-27996

1999

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Molecular Pathogenesis of Muscle Degeneration in the δ-Sarcoglycan-Deficient Hamster

The American journal of pathology, 1998-11, Vol.153 (5), p.1623-1630

1998

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β Subunit Heterogeneity in N-type Ca2+ Channels (∗)

The Journal of biological chemistry, 1996-02, Vol.271 (6), p.3207-3212

1996

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Characterization of δ-Sarcoglycan, a Novel Component of the Oligomeric Sarcoglycan Complex Involved in Limb-Girdle Muscular Dystrophy

The Journal of biological chemistry, 1996-12, Vol.271 (50), p.32321-32329

1996

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glycans of soybean peroxidase

Glycobiology (Oxford), 1996-01, Vol.6 (1), p.23-32

1996

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Molecular pathogenesis of muscle degeneration in the (delta-sarcoglycan-deficient hamster)

The American journal of pathology, 1998-11, Vol.153 (5), p.1623

1998

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Îµ-Sarcoglycan Replaces Î±-Sarcoglycan in Smooth Muscle to Form a Unique Dystrophin-Glycoprotein Complex

The Journal of biological chemistry, 1999-09, Vol.274 (39), p.27989

1999

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Subunit Heterogeneity in N-type Ca Channels

The Journal of biological chemistry, 1996-02, Vol.271 (6), p.3207

1996

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Characterization of Î´-Sarcoglycan, a Novel Component of the Oligomeric Sarcoglycan Complex Involved in Limb-Girdle Muscular Dystrophy

The Journal of biological chemistry, 1996-12, Vol.271 (50), p.32321

1996

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Molecular Pathogenesis of Muscle Degeneration in the {delta}-Sarcoglycan-Deficient Hamster

The American journal of pathology, 1998-11, Vol.153 (5), p.1623

1998

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Structural basis of laminin binding to the LARGE glycans on dystroglycan

Nature chemical biology, 2016-10, Vol.12 (10), p.810-814

2016

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LARGE glycans on dystroglycan function as a tunable matrix scaffold to prevent dystrophy

Nature (London), 2013-11, Vol.503 (7474), p.136-140

2013

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ISPD loss-of-function mutations disrupt dystroglycan O-mannosylation and cause Walker-Warburg syndrome

Nature genetics, 2012-05, Vol.44 (5), p.575-580

2012

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SGK196 is a glycosylation-specific O-mannose kinase required for dystroglycan function

Science (American Association for the Advancement of Science), 2013-08, Vol.341 (6148), p.896-899

2013

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N-terminal domain on dystroglycan enables LARGE1 to extend matriglycan on α-dystroglycan and prevents muscular dystrophy

eLife, 2023-02, Vol.12

2023

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The glucuronyltransferase B4GAT1 is required for initiation of LARGE-mediated α-dystroglycan functional glycosylation

eLife, 2014-10, Vol.3

2014

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POMK regulates dystroglycan function via LARGE1-mediated elongation of matriglycan

eLife, 2020-09, Vol.9

2020

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Structure of protein O-mannose kinase reveals a unique active site architecture

eLife, 2016-11, Vol.5

2016

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Glycosylation
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Membrane Targeting and Stabilization of Sarcospan Is Mediated by the Sarcoglycan Subcomplex

Progressive Muscular Dystrophy in α-Sarcoglycan-Deficient Mice

Biosynthesis of dystroglycan: processing of a precursor propeptide

Sarcospan, the 25-kDa Transmembrane Component of the Dystrophin-Glycoprotein Complex

Functional Rescue of the Sarcoglycan Complex in the BIO 14.6 Hamster Using δ-Sarcoglycan Gene Transfer

Caveolin-3 is not an integral component of the dystrophin glycoprotein complex

Sarcospan-Deficient Mice Maintain Normal Muscle Function

ε-Sarcoglycan Replaces α-Sarcoglycan in Smooth Muscle to Form a Unique Dystrophin-Glycoprotein Complex

Molecular Pathogenesis of Muscle Degeneration in the δ-Sarcoglycan-Deficient Hamster

β Subunit Heterogeneity in N-type Ca2+ Channels (∗)

Characterization of δ-Sarcoglycan, a Novel Component of the Oligomeric Sarcoglycan Complex Involved in Limb-Girdle Muscular Dystrophy

glycans of soybean peroxidase

Molecular pathogenesis of muscle degeneration in the (delta-sarcoglycan-deficient hamster)

Îµ-Sarcoglycan Replaces Î±-Sarcoglycan in Smooth Muscle to Form a Unique Dystrophin-Glycoprotein Complex

Subunit Heterogeneity in N-type Ca Channels

Characterization of Î´-Sarcoglycan, a Novel Component of the Oligomeric Sarcoglycan Complex Involved in Limb-Girdle Muscular Dystrophy

Molecular Pathogenesis of Muscle Degeneration in the {delta}-Sarcoglycan-Deficient Hamster

Structural basis of laminin binding to the LARGE glycans on dystroglycan

LARGE glycans on dystroglycan function as a tunable matrix scaffold to prevent dystrophy

ISPD loss-of-function mutations disrupt dystroglycan O-mannosylation and cause Walker-Warburg syndrome

SGK196 is a glycosylation-specific O-mannose kinase required for dystroglycan function

N-terminal domain on dystroglycan enables LARGE1 to extend matriglycan on α-dystroglycan and prevents muscular dystrophy

The glucuronyltransferase B4GAT1 is required for initiation of LARGE-mediated α-dystroglycan functional glycosylation

POMK regulates dystroglycan function via LARGE1-mediated elongation of matriglycan

Structure of protein O-mannose kinase reveals a unique active site architecture

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