(Q46980919)

27 December 2017

title

Identification of functional domains in sarcoglycans essential for their interaction and plasma membrane targeting (English)

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27 December 2017

Sarcoglycan, beta (dystrophin-associated glycoprotein)

main subject

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Sarcoglycan, gamma (dystrophin-associated glycoprotein)

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Sarcoglycan, delta (dystrophin-associated glycoprotein)

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Sarcoglycan, alpha (dystrophin-associated glycoprotein)

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Dystrophin, muscular dystrophy

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author name string

Jiwei Chen

1

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27 December 2017

Weixing Shi

2

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27 December 2017

Yuguang Zhang

3

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27 December 2017

Randi Sokol

4

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27 December 2017

Hong Cai

5

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27 December 2017

Mingyue Lun

6

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27 December 2017

Brian F Moore

7

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27 December 2017

Matthew J Farber

8

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27 December 2017

Joel S Stepanchick

9

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27 December 2017

Carsten G Bönnemann

10

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27 December 2017

Yiu-mo Michael Chan

11

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27 December 2017

language of work or name

English

0 references

publication date

9 March 2006

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27 December 2017

Experimental Cell Research

published in

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27 December 2017

volume

312

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27 December 2017

issue

9

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27 December 2017

page(s)

1610-1625

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27 December 2017

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

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1 reference

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

7 January 2021

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

7 January 2021

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

7 January 2021

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

7 January 2021

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

7 January 2021

1 reference

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

7 January 2021

1 reference

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

7 January 2021

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Specific assembly pathway of sarcoglycans is dependent on beta- and delta-sarcoglycan

7 January 2021

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Assembly of the sarcoglycan complex. Insights for muscular dystrophy

7 January 2021

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

7 January 2021

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Mutations in the sarcoglycan genes in patients with myopathy

7 January 2021

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Complete cloning of the duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organization of the DMD gene in normal and affected individuals

7 January 2021

1 reference

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

7 January 2021

1 reference

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Two forms of mouse syntrophin, a 58 kd dystrophin-associated protein, differ in primary structure and tissue distribution

7 January 2021

1 reference

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Cloning and characterization of the human homologue of a dystrophin related phosphoprotein found at the Torpedo electric organ post-synaptic membrane

7 January 2021

1 reference

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

7 January 2021

1 reference

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Membrane organization of the dystrophin-glycoprotein complex

7 January 2021

1 reference

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Identification and characterization of the dystrophin anchoring site on beta-dystroglycan

7 January 2021

1 reference

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Syntrophin binds to an alternatively spliced exon of dystrophin

7 January 2021

1 reference

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Dystrobrevin and dystrophin: an interaction through coiled-coil motifs

7 January 2021

1 reference

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alpha-Dystroglycan is a laminin receptor involved in extracellular matrix assembly on myotubes and muscle cell viability.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2006.01.024

A role for the dystrophin-glycoprotein complex as a transmembrane linker between laminin and actin.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2006.01.024

Muscular dystrophies involving the dystrophin-glycoprotein complex: an overview of current mouse models.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2006.01.024

Muscle degeneration without mechanical injury in sarcoglycan deficiency

7 January 2021

1 reference

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Ecto-ATPase activity of alpha-sarcoglycan (adhalin)

7 January 2021

1 reference

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Genetic compensation for sarcoglycan loss by integrin alpha7beta1 in muscle

7 January 2021

1 reference

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Bidirectional signaling between sarcoglycans and the integrin adhesion system in cultured L6 myocytes

7 January 2021

1 reference

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Loss of sarcolemma nNOS in sarcoglycan-deficient muscle.

7 January 2021

1 reference

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The dystrophin glycoprotein complex: signaling strength and integrity for the sarcolemma

7 January 2021

1 reference

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Molecular organization of sarcoglycan complex in mouse myotubes in culture

7 January 2021

1 reference

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Mutations that disrupt the carboxyl-terminus of gamma-sarcoglycan cause muscular dystrophy

7 January 2021

1 reference

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A first missense mutation in the delta sarcoglycan gene associated with a severe phenotype and frequency of limb-girdle muscular dystrophy type 2F (LGMD2F) in Brazilian sarcoglycanopathies

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2006.01.024

A homozygous nonsense mutation in δ-sarcoglycan exon 3 in a case of LGMD2F

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2006.01.024

Mutations in the delta-sarcoglycan gene are a rare cause of autosomal recessive limb-girdle muscular dystrophy (LGMD2)

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2006.01.024

Mutational analysis of alpha-beta subunit interactions in the delivery of Na,K-ATPase heterodimers to the plasma membrane

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2006.01.024

Characterization and prediction of linker sequences of multi-domain proteins by a neural network.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2006.01.024

A founder mutation in the gamma-sarcoglycan gene of gypsies possibly predating their migration out of India

7 January 2021

1 reference

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Severe gamma-sarcoglycanopathy caused by a novel missense mutation and a large deletion

7 January 2021

1 reference

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A novel gamma-sarcoglycan mutation causing childhood onset, slowly progressive limb girdle muscular dystrophy

7 January 2021

1 reference

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Forced expression of dystrophin deletion constructs reveals structure-function correlations.

7 January 2021

1 reference

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Dp71 can restore the dystrophin-associated glycoprotein complex in muscle but fails to prevent dystrophy.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2006.01.024

Exogenous Dp71 restores the levels of dystrophin associated proteins but does not alleviate muscle damage in mdx mice

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2006.01.024

Intracellular functions of N-linked glycans

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2006.01.024

Plasma membrane localization signals in the light chain of botulinum neurotoxin

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2006.01.024

Fine-tuning the topology of a polytopic membrane protein: role of positively and negatively charged amino acids.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2006.01.024

Filamin 2 (FLN2): A muscle-specific sarcoglycan interacting protein

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2006.01.024

Role for alpha-dystrobrevin in the pathogenesis of dystrophin-dependent muscular dystrophies

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2006.01.024

Sarcospan-deficient mice maintain normal muscle function

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2006.01.024

Defective intracellular transport and processing of CFTR is the molecular basis of most cystic fibrosis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2006.01.024

10.1016/J.YEXCR.2006.01.024

7 January 2021

Identifiers

DOI

1 reference

27 December 2017

release_4lxttnmfkrfjjcgneffoy37ltq

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/4lxttnmfkrfjjcgneffoy37ltq

mapped directly with Wikidata item

24 November 2022

based on heuristic

1 reference

27 December 2017