(Q62971278)

2

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David K Booth

3

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Thomas Oligino

4

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David Krisky

5

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Peggy Marconi

6

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Joseph C Glorioso

7

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Johnny Huard

8

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J C van Deutekom

1

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S S Floyd

2

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D K Booth

3

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T Oligino

4

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D Krisky

5

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P Marconi

6

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J C Glorioso

7

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J Huard

Systemic delivery of recombinant proteins by genetically modified myoblasts

8

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language of work or name

English

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publication date

May 1998

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published in

Neuromuscular Disorders

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volume

8

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issue

3-4

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page(s)

135-148

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135-48

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cites work

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Expression of human factor IX in mice after injection of genetically modified myoblasts

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Persistent erythropoiesis by myoblast transfer of erythropoietin cDNA.

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Myoblast transfer of human erythropoietin gene in a mouse model of renal failure

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Muscle delivery of human kallikrein gene reduces blood pressure in hypertensive rats

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Intramuscular delivery of rat kallikrein-binding protein gene reverses hypotension in transgenic mice expressing human tissue kallikrein

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

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

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Normal myogenic cells from newborn mice restore normal histology to degenerating muscles of the mdx mouse

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

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Human myoblast transplantation: preliminary results of 4 cases

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Myoblast transfer in Duchenne muscular dystrophy

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Results of a triple blind clinical study of myoblast transplantations without immunosuppressive treatment in young boys with Duchenne muscular dystrophy.

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Gene transfer into skeletal muscles by isogenic myoblasts

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Myoblast Transfer in the Treatment of Duchenne's Muscular Dystrophy

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Rapid death of injected myoblasts in myoblast transfer therapy

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

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Cytotoxicity of a replication-defective mutant of herpes simplex virus type 1

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The potential for gene therapy in Duchenne muscular dystrophy and other genetic muscle diseases

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Adenovirus mediated expression of therapeutic plasma levels of human factor IX in mice

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A differential efficiency of adenovirus-mediated in vivo gene transfer into skeletal muscle cells of different maturity

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Ablation of E2A in recombinant adenoviruses improves transgene persistence and decreases inflammatory response in mouse liver

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Cellular and humoral immune responses to adenoviral vectors containing factor IX gene: tolerization of factor IX and vector antigens allows for long-term expression

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Dystrophin expression in muscles of mdx mice after adenovirus-mediated in vivo gene transfer

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The basal lamina is a physical barrier to herpes simplex virus-mediated gene delivery to mature muscle fibers.

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Impairment of force generation after adenovirus-mediated gene transfer to muscle is alleviated by adenoviral gene inactivation and host CD8+ T cell deficiency

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Viral gene delivery to skeletal muscle: insights on maturation-dependent loss of fiber infectivity for adenovirus and herpes simplex type 1 viral vectors

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Long-term correction of mouse dystrophic degeneration by adenovirus-mediated transfer of a minidystrophin gene

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Retroviral-mediated gene transfer into hepatocytes in vivo

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Culturing satellite cells from living single muscle fiber explants

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Direct retroviral-mediated transfer of a dystrophin minigene into mdx mouse muscle in vivo

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Myosin isoform transitions in regeneration of fast and slow muscles during postnatal development of the rat

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Plasmid DNA is superior to viral vectors for direct gene transfer into adult mouse skeletal muscle

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Cardiotoxin 1 from cobra (Naja naja atra) venom causes necrosis of skeletal muscle in vivo

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Ex vivo gene transfer using adenovirus-mediated full-length dystrophin delivery to dystrophic muscles

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Immunosuppression by FK506 markedly prolongs expression of adenovirus-delivered transgene in skeletal muscles of adult dystrophic [mdx] mice

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FK506 immunosuppression to control the immune reactions triggered by first-generation adenovirus-mediated gene transfer

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7 January 2021

Recombinant IL-12 prevents formation of blocking IgA antibodies to recombinant adenovirus and allows repeated gene therapy to mouse lung.

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7 January 2021

Prevention of immune reactions triggered by first-generation adenoviral vectors by monoclonal antibodies and CTLA4Ig

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Assembly of basement membranes

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Gene transfer in regenerating muscle

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Efficient long-term gene transfer into muscle tissue of immunocompetent mice by adeno-associated virus vector

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Recombinant adeno-associated viral vectors mediate long-term transgene expression in muscle

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Adenovirus targeted to heparan-containing receptors increases its gene delivery efficiency to multiple cell types

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