epsilon-Sarcoglycan, a broadly expressed homologue of the gene mutated in limb-girdle muscular dystrophy 2D (Q24314855)

limb-girdle muscular dystrophy

GOA release 2020-03-11

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A J Ettinger

1

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G Feng

series ordinal

2

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J R Sanes

series ordinal

3

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language of work or name

English

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publication date

19 December 1997

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published in

Journal of Biological Chemistry

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volume

272

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issue

51

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page(s)

32534-8

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cites work

Dystroglycan mRNA expression during normal and mdx mouse embryogenesis: a comparison with utrophin and the apo-dystrophins.

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7 January 2021

Dystroglycan expression in the wild type and mdx mouse neural retina: synaptic colocalization with dystrophin, dystrophin-related protein but not laminin

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7 January 2021

Expression of a dystrophin-sarcoglycan complex in serum-deprived BC3H1 cells and involvement of alpha-sarcoglycan in substrate attachment

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7 January 2021

Mouse adhalin: primary structure and expression during late stages of muscle differentiation in vitro

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7 January 2021

Transient expression of Dp140, a product of the Duchenne muscular dystrophy locus, during kidney tubulogenesis.

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7 January 2021

Expression of the dystrophin-related protein 2 (Drp2) transcript in the mouse

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Single-Step Method of RNA Isolation by Acid Guanidinium Thiocyanate–Phenol–Chloroform Extraction

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7 January 2021

Absence of gamma-sarcoglycan (35 DAG) in autosomal recessive muscular dystrophy linked to chromosome 13q12

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7 January 2021

Point mutations define a sequence flanking the AUG initiator codon that modulates translation by eukaryotic ribosomes

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Membrane organization of the dystrophin-glycoprotein complex

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Missense mutations in the adhalin gene linked to autosomal recessive muscular dystrophy

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Developmental expression of dystrophin, dystrophin-associated glycoproteins and other membrane cytoskeletal proteins in human skeletal and heart muscle.

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Expression of dystrophin-associated glycoproteins during human fetal muscle development: a preliminary immunocytochemical study.

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Utrophin-dystrophin-deficient mice as a model for Duchenne muscular dystrophy

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Skeletal and cardiac myopathies in mice lacking utrophin and dystrophin: a model for Duchenne muscular dystrophy

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Dystroglycan: an extracellular matrix receptor linked to the cytoskeleton.

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Autosomal recessive muscular dystrophy and mutations of the sarcoglycan complex

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7 January 2021

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

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7 January 2021

Amelioration of the dystrophic phenotype of mdx mice using a truncated utrophin transgene

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The structural and functional diversity of dystrophin

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Autosomal recessive limb-girdle muscular dystrophy, LGMD2F, is caused by a mutation in the delta-sarcoglycan gene

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7 January 2021

β–sarcoglycan: characterization and role in limb–girdle muscular dystrophy linked to 4q12

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7 January 2021

Beta-sarcoglycan (A3b) mutations cause autosomal recessive muscular dystrophy with loss of the sarcoglycan complex

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7 January 2021

Isoform diversity of dystrobrevin, the murine 87-kDa postsynaptic protein

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7 January 2021

Characterization of delta-sarcoglycan, a novel component of the oligomeric sarcoglycan complex involved in limb-girdle muscular dystrophy

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7 January 2021

A role of dystroglycan in schwannoma cell adhesion to laminin

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7 January 2021

Non-muscle alpha-dystroglycan is involved in epithelial development

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7 January 2021

A new model for the interaction of dystrophin with F-actin

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7 January 2021

The sarcoglycan complex in the six autosomal recessive limb-girdle muscular dystrophies

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7 January 2021

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

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7 January 2021

Dystroglycan is essential for early embryonic development: disruption of Reichert's membrane in Dag1-null mice

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7 January 2021

A new method for predicting signal sequence cleavage sites

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7 January 2021

Dissociation of the complex of dystrophin and its associated proteins into several unique groups by n-octyl beta-D-glucoside

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7 January 2021

Utrophin: a structural and functional comparison to dystrophin

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7 January 2021

Mutations in the dystrophin-associated protein gamma-sarcoglycan in chromosome 13 muscular dystrophy

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7 January 2021

Mutational diversity and hot spots in the alpha-sarcoglycan gene in autosomal recessive muscular dystrophy (LGMD2D)

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7 January 2021

Abnormal expression of laminin suggests disturbance of sarcolemma-extracellular matrix interaction in Japanese patients with autosomal recessive muscular dystrophy deficient in adhalin.

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7 January 2021