(Q41572953)

4 October 2017

Efficient adenovirus-mediated transfer of a human minidystrophin gene to skeletal muscle of mdx mice (English)

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Michel Jean Robert Perricaudet

4 October 2017

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10

object named as

Perricaudet M

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4 October 2017

Ragot T

1

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4 October 2017

Vincent N

2

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4 October 2017

Chafey P

3

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4 October 2017

Vigne E

4

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4 October 2017

Gilgenkrantz H

5

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4 October 2017

Couton D

6

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4 October 2017

Cartaud J

7

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4 October 2017

Briand P

8

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4 October 2017

Kaplan JC

9

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4 October 2017

language of work or name

English

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publication date

1 February 1993

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4 October 2017

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4 October 2017

361

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4 October 2017

647-650

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4 October 2017

6413

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https://scigraph.springernature.com/pub.10.1038/361647a0

4 October 2017

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cites work

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

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7 January 2021

Association of dystrophin and an integral membrane glycoprotein.

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7 January 2021

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

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7 January 2021

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

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7 January 2021

Human myoblast transplantation: preliminary results of 4 cases

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7 January 2021

Normal dystrophin transcripts detected in Duchenne muscular dystrophy patients after myoblast transplantation

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7 January 2021

Human dystrophin expression in mdx mice after intramuscular injection of DNA constructs

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7 January 2021

Evaluation of the transfer and expression in mice of an enzyme-encoding gene using a human adenovirus vector

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7 January 2021

Adenovirus-mediated transfer of a recombinant alpha 1-antitrypsin gene to the lung epithelium in vivo

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7 January 2021

In vivo transfer of the human cystic fibrosis transmembrane conductance regulator gene to the airway epithelium

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7 January 2021

Adenovirus as an expression vector in muscle cells in vivo

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7 January 2021

Widespread long-term gene transfer to mouse skeletal muscles and heart

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7 January 2021

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

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7 January 2021

X chromosome-linked muscular dystrophy (mdx) in the mouse

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7 January 2021

The molecular basis of muscular dystrophy in the mdx mouse: a point mutation

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7 January 2021

Dystrophin abnormalities in Duchenne/Becker muscular dystrophy

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7 January 2021

Characteristics of a human cell line transformed by DNA from human adenovirus type 5

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7 January 2021

Defective and nondefective adenovirus vectors for expressing foreign genes in vitro and in vivo

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7 January 2021

Localization of dystrophin and dystrophin-related protein at the electromotor synapse and neuromuscular junction in Torpedo marmorata

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7 January 2021

Somatic reversion/suppression of the mouse mdx phenotype in vivo.

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7 January 2021

Construction of dystrophin fusion proteins to raise targeted antibodies to different epitopes

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7 January 2021

The mdx mouse diaphragm reproduces the degenerative changes of Duchenne muscular dystrophy

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7 January 2021

Direct gene transfer into nonhuman primate myofibers in vivo

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7 January 2021

Distal transcript of the dystrophin gene initiated from an alternative first exon and encoding a 75-kDa protein widely distributed in nonmuscle tissues

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7 January 2021

Identifiers

DOI

10.1038/361647A0

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Dimensions Publication ID

4 October 2017

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