(Q24314855)

limb-girdle muscular dystrophy

GOA release 2020-03-11

1 reference

A J Ettinger

1

0 references

G Feng

series ordinal

2

0 references

J R Sanes

series ordinal

3

0 references

language of work or name

English

0 references

publication date

19 December 1997

0 references

published in

Journal of Biological Chemistry

0 references

volume

272

0 references

page(s)

32534-8

0 references

issue

51

0 references

cites work

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.51.32534

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.51.32534

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.51.32534

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.51.32534

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.51.32534

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.51.32534

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.51.32534

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.51.32534

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.51.32534

7 January 2021

Membrane organization of the dystrophin-glycoprotein complex

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.51.32534

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.51.32534

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.51.32534

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.51.32534

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.51.32534

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.51.32534

7 January 2021

Dystroglycan: an extracellular matrix receptor linked to the cytoskeleton.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.51.32534

7 January 2021

Autosomal recessive muscular dystrophy and mutations of the sarcoglycan complex

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.51.32534

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.51.32534

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.51.32534

7 January 2021

The structural and functional diversity of dystrophin

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.51.32534

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.51.32534

7 January 2021

Beta-sarcoglycan: characterization and role in limb-girdle muscular dystrophy linked to 4q12

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.51.32534

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.51.32534

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.51.32534

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.51.32534

7 January 2021

A role of dystroglycan in schwannoma cell adhesion to laminin

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.51.32534

7 January 2021

Non-muscle alpha-dystroglycan is involved in epithelial development

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.51.32534

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.51.32534

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.51.32534

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.51.32534

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.51.32534

7 January 2021

A new method for predicting signal sequence cleavage sites

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.51.32534

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.51.32534

7 January 2021

Utrophin: a structural and functional comparison to dystrophin

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.51.32534

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.51.32534

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.51.32534

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.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.51.32534

7 January 2021