(Q46050411)

19 December 2017

title

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

1 reference

19 December 2017

Duchenne muscular dystrophy

main subject

myoblast

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patient

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1

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19 December 2017

Helen Blau

7

object named as

Blau HM

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19 December 2017

Grace K. Pavlath

2

object named as

Pavlath GK

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author name string

Lanctot AM

3

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19 December 2017

Sharma KR

4

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19 December 2017

Miller RG

5

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19 December 2017

Steinman L

6

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19 December 2017

language of work or name

English

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publication date

1 April 1992

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19 December 2017

published in

Nature

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19 December 2017

volume

356

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19 December 2017

issue

6368

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19 December 2017

page(s)

435-438

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19 December 2017

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

cites work

1 reference

7 January 2021

Accelerated age-related decline in replicative life-span of Duchenne muscular dystrophy myoblasts: implications for cell and gene therapy

1 reference

7 January 2021

Preferential deletion of exons in Duchenne and Becker muscular dystrophies

1 reference

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

1 reference

7 January 2021

A cDNA clone from the Duchenne/Becker muscular dystrophy gene.

1 reference

7 January 2021

Deletion screening of the Duchenne muscular dystrophy locus via multiplex DNA amplification

1 reference

7 January 2021

Detection of 98% of DMD/BMD gene deletions by polymerase chain reaction

1 reference

7 January 2021

Dystrophin: the protein product of the Duchenne muscular dystrophy locus

1 reference

7 January 2021

Characterization of dystrophin in muscle-biopsy specimens from patients with Duchenne's or Becker's muscular dystrophy

1 reference

7 January 2021

Dystrophin abnormalities in Duchenne/Becker muscular dystrophy

1 reference

7 January 2021

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

1 reference

7 January 2021

Migration of myoblasts across basal lamina during skeletal muscle development

1 reference

7 January 2021

Muscle fiber pattern is independent of cell lineage in postnatal rodent development

1 reference

7 January 2021

Systemic delivery of human growth hormone by injection of genetically engineered myoblasts.

1 reference

7 January 2021

Systemic delivery of recombinant proteins by genetically modified myoblasts

1 reference

7 January 2021

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

1 reference

7 January 2021

Isolation and characterization of human muscle cells

1 reference

7 January 2021

Isolation of human myoblasts with the fluorescence-activated cell sorter

1 reference

7 January 2021

Transcription of the dystrophin gene in human muscle and non-muscle tissue

1 reference

7 January 2021

Direct diagnosis of carriers of Duchenne and Becker muscular dystrophy by amplification of lymphocyte RNA

1 reference

7 January 2021

Invited review: myoblast transfer: a possible therapy for inherited myopathies?

1 reference

7 January 2021

Dystrophin production induced by myoblast transfer therapy in Duchenne muscular dystrophy

1 reference

7 January 2021

Mosaic expression of dystrophin in symptomatic carriers of Duchenne's muscular dystrophy

1 reference

7 January 2021

Dystrophin distribution in heterozygote MDX mice

1 reference

7 January 2021

Monoclonal antibodies against defined regions of the muscular dystrophy protein, dystrophin

1 reference

7 January 2021

Identifiers

DOI

10.1038/356435A0

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19 December 2017

Dimensions Publication ID

1025801133

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1 reference

19 December 2017