(Q28290790)

9

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Eric Hoffman

10

object named as

E P Hoffman

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author name string

C G Bönnemann

1

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R Modi

2

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S Noguchi

3

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Y Mizuno

4

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M Yoshida

5

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E M McNally

7

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D J Duggan

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

8

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language of work or name

English

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publication date

November 1995

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published in

Nature Genetics

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volume

11

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issue

3

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page(s)

266-73

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cites work

1 reference

https://api.crossref.org/works/10.1038%2FNG1195-266

7 January 2021

Dystrophin: the protein product of the Duchenne muscular dystrophy locus

1 reference

https://api.crossref.org/works/10.1038%2FNG1195-266

7 January 2021

Association of dystrophin and an integral membrane glycoprotein.

1 reference

https://api.crossref.org/works/10.1038%2FNG1195-266

7 January 2021

Glycoprotein complex anchoring dystrophin to sarcolemma

1 reference

https://api.crossref.org/works/10.1038%2FNG1195-266

7 January 2021

Heterogeneity of dystrophin-associated proteins

1 reference

https://api.crossref.org/works/10.1038%2FNG1195-266

7 January 2021

Membrane organization of the dystrophin-glycoprotein complex

1 reference

https://api.crossref.org/works/10.1038%2FNG1195-266

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG1195-266

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/10.1038%2FNG1195-266

7 January 2021

Human dystroglycan: skeletal muscle cDNA, genomic structure, origin of tissue specific isoforms and chromosomal localization

1 reference

https://api.crossref.org/works/10.1038%2FNG1195-266

7 January 2021

Molecular organization at the glycoprotein-complex-binding site of dystrophin. Three dystrophin-associated proteins bind directly to the carboxy-terminal portion of dystrophin

1 reference

https://api.crossref.org/works/10.1038%2FNG1195-266

7 January 2021

A dystrophin-associated glycoprotein, A3a (one of 43DAG doublets), is retained in Duchenne muscular dystrophy muscle

1 reference

https://api.crossref.org/works/10.1038%2FNG1195-266

7 January 2021

Severe childhood muscular dystrophy affecting both sexes and frequent in Tunisia

1 reference

https://api.crossref.org/works/10.1038%2FNG1195-266

7 January 2021

Linkage of Tunisian autosomal recessive Duchenne-like muscular dystrophy to the pericentromeric region of chromosome 13q.

1 reference

https://api.crossref.org/works/10.1038%2FNG1195-266

7 January 2021

Linkage analysis of families with severe childhood autosomal recessive muscular dystrophy in Morocco indicates genetic homogeneity of the disease in north Africa

1 reference

https://api.crossref.org/works/10.1038%2FNG1195-266

7 January 2021

Genetic heterogeneity for Duchenne-like muscular dystrophy (DLMD) based on linkage and 50 DAG analysis.

1 reference

https://api.crossref.org/works/10.1038%2FNG1195-266

7 January 2021

Assessment of the 50-kDa dystrophin-associated glycoprotein in Brazilian patients with severe childhood autosomal recessive muscular dystrophy.

1 reference

https://api.crossref.org/works/10.1038%2FNG1195-266

7 January 2021

A common missense mutation in the adhalin gene in three unrelated Brazilian families with a relatively mild form of autosomal recessive limb-girdle muscular dystrophy

1 reference

https://api.crossref.org/works/10.1038%2FNG1195-266

7 January 2021

Deficiency of the 50K dystrophin-associated glycoprotein in severe childhood autosomal recessive muscular dystrophy

1 reference

https://api.crossref.org/works/10.1038%2FNG1195-266

7 January 2021

The frequency of patients with 50-kd dystrophin-associated glycoprotein (50DAG or adhalin) deficiency in a muscular dystrophy patient population in Japan: immunocytochemical analysis of 50DAG, 43DAG, dystrophin, and utrophin

1 reference

https://api.crossref.org/works/10.1038%2FNG1195-266

7 January 2021

Selective defect of sarcoglycan complex in severe childhood autosomal recessive muscular dystrophy muscle

1 reference

https://api.crossref.org/works/10.1038%2FNG1195-266

7 January 2021

Human adhalin is alternatively spliced and the gene is located on chromosome 17q21

1 reference

https://api.crossref.org/works/10.1038%2FNG1195-266

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG1195-266

7 January 2021

Primary adhalinopathy: a common cause of autosomal recessive muscular dystrophy of variable severity

1 reference

https://api.crossref.org/works/10.1038%2FNG1195-266

7 January 2021

Compilation and analysis of sequences upstream from the translational start site in eukaryotic mRNAs

1 reference

https://api.crossref.org/works/10.1038%2FNG1195-266

7 January 2021

Cloning of human basic A1, a distinct 59-kDa dystrophin-associated protein encoded on chromosome 8q23-24

1 reference

https://api.crossref.org/works/10.1038%2FNG1195-266

7 January 2021

Protein targeting signals

1 reference

https://api.crossref.org/works/10.1038%2FNG1195-266

7 January 2021

Mapping the whole human genome by fingerprinting yeast artificial chromosomes

1 reference

https://api.crossref.org/works/10.1038%2FNG1195-266

7 January 2021

The 1993-94 Généthon human genetic linkage map

1 reference

https://api.crossref.org/works/10.1038%2FNG1195-266

7 January 2021

The limb-girdle muscular dystrophies--proposal for a new nomenclature.

1 reference

https://api.crossref.org/works/10.1038%2FNG1195-266

7 January 2021

Expression of dystrophin-associated protein 35DAG (A4) and 50DAG (A2) is confined to striated muscles

1 reference

https://api.crossref.org/works/10.1038%2FNG1195-266

7 January 2021

The structural and functional diversity of dystrophin

1 reference

https://api.crossref.org/works/10.1038%2FNG1195-266

7 January 2021

Increasing complexity of the dystrophin-associated protein complex

1 reference

https://api.crossref.org/works/10.1038%2FNG1195-266

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG1195-266

7 January 2021

Duchenne muscular dystrophy: deficiency of dystrophin-associated proteins in the sarcolemma

1 reference

https://api.crossref.org/works/10.1038%2FNG1195-266

7 January 2021

Expression of utrophin (dystrophin-related protein) and dystrophin-associated glycoproteins in muscles from patients with Duchenne muscular dystrophy

1 reference

https://api.crossref.org/works/10.1038%2FNG1195-266

7 January 2021

Proteinase-sensitive sites on isolated rabbit dystrophin

1 reference

https://api.crossref.org/works/10.1038%2FNG1195-266

7 January 2021

Production and separation of peptides from proteins stained with Coomassie brilliant blue R-250 after separation by sodium dodecyl sulfate-polyacrylamide gel electrophoresis

1 reference

https://api.crossref.org/works/10.1038%2FNG1195-266

7 January 2021

Basic local alignment search tool

1 reference

https://api.crossref.org/works/10.1038%2FNG1195-266

7 January 2021

Characterization of NIGMS human/rodent somatic cell hybrid mapping panel 2 by PCR

1 reference

https://api.crossref.org/works/10.1038%2FNG1195-266

7 January 2021

High-resolution mapping of human chromosome 11 by in situ hybridization with cosmid clones

1 reference

https://api.crossref.org/works/10.1038%2FNG1195-266

7 January 2021

Deglycosylation of asparagine-linked glycans by peptide:N-glycosidase F.

1 reference

https://api.crossref.org/works/10.1038%2FNG1195-266

7 January 2021

Dystrophinopathy in isolated cases of myopathy in females

1 reference

https://api.crossref.org/works/10.1038%2FNG1195-266

7 January 2021

A simple salting out procedure for extracting DNA from human nucleated cells

1 reference

https://api.crossref.org/works/10.1038%2FNG1195-266

7 January 2021