Deficiency of a glycoprotein component of the dystrophin complex in dystrophic muscle (Q59089242)

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25 September 2019

title

Deficiency of a glycoprotein component of the dystrophin complex in dystrophic muscle (English)

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25 September 2019

2

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25 September 2019

Steven Kahl

3

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25 September 2019

Kevin P Campbell

5

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25 September 2019

author name string

Ervasti JM

1

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25 September 2019

Gaver MG

4

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25 September 2019

language of work or name

English

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publication date

1 May 1990

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25 September 2019

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25 September 2019

volume

345

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issue

6273

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25 September 2019

page(s)

315-319

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https://scigraph.springernature.com/pub.10.1038/345315a0

25 September 2019

exact match

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cites work

Dystrophin: the protein product of the Duchenne muscular dystrophy locus

1 reference

7 January 2021

The Duchenne muscular dystrophy gene product is localized in sarcolemma of human skeletal muscle

1 reference

7 January 2021

Immunostaining of skeletal and cardiac muscle surface membrane with antibody against Duchenne muscular dystrophy peptide

1 reference

7 January 2021

Duchenne muscular dystrophy: deficiency of dystrophin at the muscle cell surface

1 reference

7 January 2021

Immunoelectron microscopic localization of dystrophin in myofibres

1 reference

7 January 2021

Characterization of dystrophin in muscle-biopsy specimens from patients with Duchenne's or Becker's muscular dystrophy

1 reference

7 January 2021

The homologue of the Duchenne locus is defective in X-linked muscular dystrophy of dogs

1 reference

7 January 2021

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

1 reference

7 January 2021

alpha-Actinins and the DMD protein contain spectrin-like repeats

1 reference

7 January 2021

Red cell membrane sialoglycoprotein beta in homozygous and heterozygous 4.1(-) hereditary elliptocytosis

1 reference

7 January 2021

Association of dystrophin and an integral membrane glycoprotein.

1 reference

7 January 2021

Duchenne dystrophy: focal alterations in the distribution of concanavalin A binding sites at the muscle cell surface

1 reference

7 January 2021

Altered binding of Ricinus communis I lectin by muscle membranes in Duchenne muscular dystrophy

1 reference

7 January 2021

Lectin blotting of human muscle. Identification of a high molecular weight glycoprotein which is absent or altered in Duchenne muscular dystrophy

1 reference

7 January 2021

Analysis of the red cell membrane in a family with hereditary elliptocytosis--total or partial of protein 4.1.

1 reference

7 January 2021

Deficiency of skeletal membrane protein band 4.1 in homozygous hereditary elliptocytosis. Implications for erythrocyte membrane stability

1 reference

7 January 2021

Increased protein degradation results from elevated free calcium levels found in muscle from mdx mice

1 reference

7 January 2021

Membrane defects in Duchenne dystrophy: protease affecting sarcoplasmic reticulum

1 reference

7 January 2021

Conversion of mdx myofibres from dystrophin-negative to -positive by injection of normal myoblasts

1 reference

7 January 2021

Estimate of the proportion of Duchenne muscular dystrophy with autosomal recessive inheritance

1 reference

7 January 2021

Purification of morphologically intact triad structures from skeletal muscle

1 reference

7 January 2021

Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4

1 reference

7 January 2021

A monoclonal antibody to the Ca2+-ATPase of cardiac sarcoplasmic reticulum cross-reacts with slow type I but not with fast type II canine skeletal muscle fibers: an immunocytochemical and immunochemical study

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7 January 2021

Monoclonal antibodies against the voltage-sensitive sodium channel from rat skeletal muscle: mapping antibody binding sites

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7 January 2021

Identifiers

DOI

10.1038/345315A0

1 reference

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Dimensions Publication ID

25 September 2019

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