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sarcoglycan

Overview page. Subjects: Chemistry — Medicine and Health.

A family of transmembrane proteins involved in the dystrophin-associated protein complex and that, together with dystrophin, dystroglycans, and syntrophins, link the contractile system of...

See overview in Oxford Index

sarcoglycan

Overview page. Subjects: Chemistry — Medicine and Health.

A family of transmembrane proteins involved in the dystrophin-associated protein complex and that, together with dystrophin, dystroglycans, and syntrophins, link the contractile system of...

See overview in Oxford Index

sarcoglycans

John Lackie.

in A Dictionary of Biomedicine

January 2010; p ublished online January 2010 .

Reference Entry. Subjects: Clinical Medicine. 61 words.

A family of transmembrane proteins involved in the *dystrophin-associated protein complex and that, together with dystrophin, *dystroglycans,

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sarcoglycan

Edited by Richard Cammack, Teresa Atwood, Peter Campbell, Howard Parish, Anthony Smith, Frank Vella and John Stirling.

in Oxford Dictionary of Biochemistry and Molecular Biology

January 2006; p ublished online January 2008 .

Reference Entry. Subjects: Biochemistry. 74 words.

a complex of proteins found in skeletal and cardiac muscle, associated with the dystrophin glycoprotein complex but of unknown function.

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ζ-Sarcoglycan, a novel component of the sarcoglycan complex, is reduced in muscular dystrophy

Matthew T. Wheeler, Sara Zarnegar and Elizabeth M. McNally.

in Human Molecular Genetics

September 2002; p ublished online September 2002 .

Journal Article. Subjects: Genetics and Genomics. 4703 words.

The dystrophin glycoprotein complex (DGC) is found at the plasma membrane of muscle cells, where it provides a link between the cytoskeleton and the extracellular matrix. A subcomplex within...

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Loss of the Sarcoglycan Complex and Sarcospan Leads to Muscular Dystrophy in β-Sarcoglycan-Deficient Mice

Kenji Araishi, Toshikuni Sasaoka, Michihiro Imamura, Satoru Noguchi, Hiroshi Hama, Eriko Wakabayashi, Mikiharu Yoshida, Tetsuro Hori and Eijiro Ozawa.

in Human Molecular Genetics

September 1999; p ublished online September 1999 .

Journal Article. Subjects: Genetics and Genomics. 7416 words.

β-Sarcoglycan, one of the subunits of the sarcoglycan complex, is a transmembranous glycoprotein which associates with dystrophin and is the molecule responsible for β-sarcoglycanopathy, a...

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ε-Sarcoglycan compensates for lack of α-sarcoglycan in a mouse model of limb-girdle muscular dystrophy

Michihiro Imamura, Yasushi Mochizuki, Eva Engvall and Shin'ichi Takeda.

in Human Molecular Genetics

March 2005; p ublished online February 2005 .

Journal Article. Subjects: Genetics and Genomics. 5608 words.

Dystrophin and the dystrophin-associated protein (DAP) complex protect the sarcolemma against contraction-induced injury and serve as a mechanical link between the extracellular matrix and...

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Reduced life span with heart and muscle dysfunction in <i>Drosophila</i> sarcoglycan mutants

Michael J. Allikian, Gira Bhabha, Patrick Dospoy, Ahlke Heydemann, Pearl Ryder, Judy U. Earley, Matthew J. Wolf, Howard A. Rockman and Elizabeth M. McNally.

in Human Molecular Genetics

December 2007; p ublished online September 2007 .

Journal Article. Subjects: Genetics and Genomics. 6539 words.

In humans, genetically diverse forms of muscular dystrophy are associated with a disrupted sarcoglycan complex. The sarcoglycan complex resides at the muscle plasma membrane where it...

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Molecular and genetic characterization of sarcospan: insights into sarcoglycan–sarcospan interactions

Rachelle H. Crosbie, Leland E. Lim, Steven A. Moore, Michio Hirano, Arthur P. Hays, Simon W. Maybaum, Huguette Collin, Sherri A. Dovico, Catherine A. Stolle, Michel Fardeau, Fernando M.S. Tomé and Kevin P. Campbell.

in Human Molecular Genetics

August 2000; p ublished online August 2000 .

Journal Article. Subjects: Genetics and Genomics. 6883 words.

Autosomal recessive limb girdle muscular dystrophies 2C–2F represent a family of diseases caused by primary mutations in the sarcoglycan genes. We show that sarcospan, a novel tetraspan-like...

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Mutations That Disrupt the Carboxyl-Terminus of γ-Sarcoglycan Cause Muscular Dystrophy

Elizabeth M. McNally, David Duggan, J. Rafael Gorospe, Carsten G. Bönnemann, Marina Fanin, Elena Pegoraro, Hart G. W. Lidov, Satoru Noguchi, Eijiro Ozawa, Richard S. Finkel, Robert P. Cruse, Corrado Angelini, Louis M. Kunkel and Eric P. Hoffman.

in Human Molecular Genetics

November 1996 .

Journal Article. Subjects: Genetics and Genomics. 4927 words.

Recently, mutations in the genes encoding several of the dystrophin-associated proteins have been identified that produce phenotypes ranging from severe Duchenne-like autosomal recessive...

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Sub-physiological sarcoglycan expression contributes to compensatory muscle protection in mdx mice

Dejia Li, Chun Long, Yongping Yue and Dongsheng Duan.

in Human Molecular Genetics

April 2009; p ublished online January 2009 .

Journal Article. Subjects: Genetics and Genomics. 6630 words.

Sarcoglycans are a group of single-pass transmembrane glycoproteins. In striated muscle, sarcoglycans interact with dystrophin and other dystrophin-associated proteins (DAPs) to form the...

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