(Q47573323)

4 February 2018

editorial

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title

Therapeutic possibilities in muscular dystrophy: the hope versus the hype (English)

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4 February 2018

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Victor Dubowitz

1

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4 February 2018

publication date

1 February 2002

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4 February 2018

published in

Neuromuscular Disorders

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4 February 2018

volume

12

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4 February 2018

issue

2

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4 February 2018

page(s)

113-116

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4 February 2018

Muscle transplantation and regeneration in the dystrophic hamster. Part 1. Histological studies

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Use of mononuclear precursor cells to insert allogeneic genes into growing mouse muscles

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Partial correction of an inherited biochemical defect of skeletal muscle by grafts of normal muscle precursor cells

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

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Myoblast transfer in Duchenne muscular dystrophy

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

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Dystrophin expression in the mdx mouse restored by stem cell transplantation

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7 January 2021

Successful myoblast transplantation in primates depends on appropriate cell delivery and induction of regeneration in the host muscle

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7 January 2021

Myoblast transplantation in whole muscle of nonhuman primates

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

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Gene therapy: present situation and future prospects

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Human dystrophin expression corrects the myopathic phenotype in transgenic mdx mice

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

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

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Aminoglycoside antibiotics restore dystrophin function to skeletal muscles of mdx mice

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Duchenne muscular dystrophy improved by gentamicin

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An agrin minigene rescues dystrophic symptoms in a mouse model for congenital muscular dystrophy.

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7 January 2021

10.1016/S0960-8966(01)00319-4

Identifiers

DOI

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4 February 2018

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4 February 2018