Variations in Dystrophin Complex in Red and White Caudal Muscles from Torpedo marmorata (Q58103914)

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Gérald Hugon

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François Rivier

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Jean Alain Fehrentz

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Ricardo Paniagua

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Dominique Mornet

Journal of Histochemistry and Cytochemistry

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publication date

July 2001

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published in

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volume

49

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issue

7

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page(s)

857-865

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cites work

The three human syntrophin genes are expressed in diverse tissues, have distinct chromosomal locations, and each bind to dystrophin and its relatives

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Loss of the sarcoglycan complex and sarcospan leads to muscular dystrophy in beta-sarcoglycan-deficient mice

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NO vascular control in Duchenne muscular dystrophy

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Sarcospan, the 25-kDa transmembrane component of the dystrophin-glycoprotein complex

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Characterization and localization of a 77 kDa protein related to the dystrophin gene family

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The developmental morphology ofTorpedo marmorata: Electric organ ? Myogenic phase

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Dystrophin: the protein product of the Duchenne muscular dystrophy locus

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Dystrophin isoforms DP71 and DP427 have distinct roles in myogenic cells.

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Primary structure of dystrophin-associated glycoproteins linking dystrophin to the extracellular matrix

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

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Identification of a novel sarcoglycan gene at 5q33 encoding a sarcolemmal 35 kDa glycoprotein

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Mechanical function of dystrophin in muscle cells

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Gamma1- and gamma2-syntrophins, two novel dystrophin-binding proteins localized in neuronal cells

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Utrophin localization in normal and dystrophin-deficient heart

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Dystrophin and utrophin influence fiber type composition and post-synaptic membrane structure.

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Dystrophin and utrophin complexed with different associated proteins in cardiac Purkinje fibres

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Presence of invertebrate dystrophin-like products in obliquely striated muscle of the leech, Pontobdella muricata (Annelida, Hirudinea).

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Dystrophin is a component of the subsynaptic membrane

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Glycoprotein complex anchoring dystrophin to sarcolemma

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