(Q28183558)

7

object named as

Knight AE

1 reference

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29 September 2022

author name string

J M Tinsley

1

0 references

D J Blake

2

0 references

B C Byth

6

0 references

A E Knight

7

0 references

J Kendrick-Jones

8

0 references

G K Suthers

9

0 references

Tinsley JM

1

1 reference

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29 September 2022

Blake DJ

2

1 reference

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29 September 2022

Roche A

3

1 reference

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29 September 2022

Fairbrother U

4

1 reference

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29 September 2022

Riss J

5

1 reference

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29 September 2022

Byth BC

6

1 reference

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29 September 2022

Kendrick-Jones J

8

1 reference

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29 September 2022

Suthers GK

9

1 reference

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29 September 2022

Love DR

10

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1461283

Characterization of a 4.8kb transcript from the Duchenne muscular dystrophy locus expressed in Schwannoma cells

29 September 2022

language of work or name

English

0 references

publication date

10 December 1992

0 references

published in

Nature

0 references

volume

360

0 references

page(s)

591-3

0 references

issue

6404

0 references

cites work

1 reference

7 January 2021

Tissue distribution of the dystrophin-related gene product and expression in the mdx and dy mouse

1 reference

7 January 2021

Immunolocalization and developmental expression of dystrophin related protein in skeletal muscle.

1 reference

7 January 2021

A homologue of dystrophin is expressed at the neuromuscular junctions of normal individuals and DMD patients, and of normal andmdxmice Immunological evidence

1 reference

7 January 2021

1 reference

7 January 2021

Expression of a dystrophin-related protein associated with the skeletal muscle cell membrane

1 reference

7 January 2021

Localization of the DMDL gene-encoded dystrophin-related protein using a panel of nineteen monoclonal antibodies: presence at neuromuscular junctions, in the sarcolemma of dystrophic skeletal muscle, in vascular and other smooth muscles, and in prol

1 reference

7 January 2021

1 reference

7 January 2021

An autosomal transcript in skeletal muscle with homology to dystrophin

1 reference

7 January 2021

A homologue of dystrophin is expressed at the blood vessel membrane of DMD and BMD patients: immunological evidence

1 reference

7 January 2021

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

1 reference

7 January 2021

Analysis of the actin-binding domain of alpha-actinin by mutagenesis and demonstration that dystrophin contains a functionally homologous domain

1 reference

7 January 2021

Expression of the N-terminal domain of dystrophin in E. coli and demonstration of binding to F-actin.

1 reference

7 January 2021

The interaction of actin with dystrophin

1 reference

7 January 2021

The identification and characterisation of an actin-binding site in alpha-actinin by mutagenesis

1 reference

7 January 2021

Very mild muscular dystrophy associated with the deletion of 46% of dystrophin

1 reference

7 January 2021

Membrane organization of the dystrophin-glycoprotein complex

1 reference

7 January 2021

Glycoprotein-binding site of dystrophin is confined to the cysteine-rich domain and the first half of the carboxy-terminal domain

1 reference

7 January 2021

Preservation of the C-terminus of dystrophin molecule in the skeletal muscle from Becker muscular dystrophy

1 reference

7 January 2021

A comprehensive set of sequence analysis programs for the VAX

1 reference

7 January 2021

Nucleotide sequence of chicken dystrophin cDNA.

1 reference

7 January 2021