Expression of human full-length and minidystrophin in transgenic mdx mice: implications for gene therapy of Duchenne muscular dystrophy. / Wells, D J; Wells, K E; Asante, E A; Turner, G; Sunada, Y; Campbell, K P; Walsh, F S; Dickson, G.

In: Human Molecular Genetics, Vol. 4, No. 8, 1995, p. 1245-50.

Research output: Contribution to journalArticlepeer-review

Published

Standard

Expression of human full-length and minidystrophin in transgenic mdx mice: implications for gene therapy of Duchenne muscular dystrophy. / Wells, D J; Wells, K E; Asante, E A; Turner, G; Sunada, Y; Campbell, K P; Walsh, F S; Dickson, G.

In: Human Molecular Genetics, Vol. 4, No. 8, 1995, p. 1245-50.

Research output: Contribution to journalArticlepeer-review

Harvard

Wells, DJ, Wells, KE, Asante, EA, Turner, G, Sunada, Y, Campbell, KP, Walsh, FS & Dickson, G 1995, 'Expression of human full-length and minidystrophin in transgenic mdx mice: implications for gene therapy of Duchenne muscular dystrophy', Human Molecular Genetics, vol. 4, no. 8, pp. 1245-50.

APA

Wells, D. J., Wells, K. E., Asante, E. A., Turner, G., Sunada, Y., Campbell, K. P., Walsh, F. S., & Dickson, G. (1995). Expression of human full-length and minidystrophin in transgenic mdx mice: implications for gene therapy of Duchenne muscular dystrophy. Human Molecular Genetics, 4(8), 1245-50.

Vancouver

Wells DJ, Wells KE, Asante EA, Turner G, Sunada Y, Campbell KP et al. Expression of human full-length and minidystrophin in transgenic mdx mice: implications for gene therapy of Duchenne muscular dystrophy. Human Molecular Genetics. 1995;4(8):1245-50.

Author

Wells, D J ; Wells, K E ; Asante, E A ; Turner, G ; Sunada, Y ; Campbell, K P ; Walsh, F S ; Dickson, G. / Expression of human full-length and minidystrophin in transgenic mdx mice: implications for gene therapy of Duchenne muscular dystrophy. In: Human Molecular Genetics. 1995 ; Vol. 4, No. 8. pp. 1245-50.

BibTeX

@article{3c9f0b3712d54167b7d06908aa3dbcc4,
title = "Expression of human full-length and minidystrophin in transgenic mdx mice: implications for gene therapy of Duchenne muscular dystrophy",
keywords = "Animals, Base Sequence, DNA Primers, DNA, Complementary, Dystrophin, Female, Gene Expression, Gene Therapy, Humans, Male, Mice, Mice, Inbred C57BL, Mice, Inbred CBA, Mice, Mutant Strains, Mice, Transgenic, Molecular Sequence Data, Muscular Dystrophies, Muscular Dystrophy, Animal, Phenotype, Sequence Deletion",
author = "Wells, {D J} and Wells, {K E} and Asante, {E A} and G Turner and Y Sunada and Campbell, {K P} and Walsh, {F S} and G Dickson",
year = "1995",
language = "English",
volume = "4",
pages = "1245--50",
journal = "Human Molecular Genetics",
issn = "0964-6906",
publisher = "Oxford University Press",
number = "8",

}

RIS

TY - JOUR

T1 - Expression of human full-length and minidystrophin in transgenic mdx mice: implications for gene therapy of Duchenne muscular dystrophy

AU - Wells, D J

AU - Wells, K E

AU - Asante, E A

AU - Turner, G

AU - Sunada, Y

AU - Campbell, K P

AU - Walsh, F S

AU - Dickson, G

PY - 1995

Y1 - 1995

KW - Animals

KW - Base Sequence

KW - DNA Primers

KW - DNA, Complementary

KW - Dystrophin

KW - Female

KW - Gene Expression

KW - Gene Therapy

KW - Humans

KW - Male

KW - Mice

KW - Mice, Inbred C57BL

KW - Mice, Inbred CBA

KW - Mice, Mutant Strains

KW - Mice, Transgenic

KW - Molecular Sequence Data

KW - Muscular Dystrophies

KW - Muscular Dystrophy, Animal

KW - Phenotype

KW - Sequence Deletion

M3 - Article

C2 - 7581360

VL - 4

SP - 1245

EP - 1250

JO - Human Molecular Genetics

JF - Human Molecular Genetics

SN - 0964-6906

IS - 8

ER -