C V Rojas|E P Hoffman - JoVE Visualize

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Cell|July 31, 1987

Complete cloning of the Duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organization of the DMD gene in normal and affected individualsM Koenig, E P Hoffman, C J Bertelson, et al.

American Journal of Medical Genetics|May 15, 1993

In utero fetal muscle biopsy for the diagnosis of Duchenne muscular dystrophy in a female fetus "suddenly at risk"M I Evans, S A Farrell, A Greb, et al.

Neurology|October 1, 1994

A rippling muscle disease gene is localized to 1q41: evidence for multiple genesD A Stephan, N R Buist, A B Chittenden, et al.

Neurology|August 12, 2005

Early onset of inflammation and later involvement of TGFbeta in Duchenne muscular dystrophyY-W Chen, K Nagaraju, M Bakay, et al.

Acta Neuropathologica|June 23, 1999

Variable histological expression of dystrophinopathy in two femalesC Doriguzzi, L Palmucci, T Mongini, et al.

Human Gene Therapy|September 14, 2002

Delivery of alpha- and beta-sarcoglycan by recombinant adeno-associated virus: efficient rescue of muscle, but differential toxicityD Dressman, K Araishi, M Imamura, et al.

Human Molecular Genetics|October 1, 1992

The genomic structure of the human skeletal muscle sodium channel geneA I McClatchey, C S Lin, J Wang, et al.

American Journal of Medical Genetics|February 2, 1996

X-inactivation patterns in female Leber's hereditary optic neuropathy patients do not support a strong X-linked determinantE Pegoraro, V Carelli, M Zeviani, et al.

Neuromuscular Disorders : NMD|May 23, 2001

Massive muscle cell degeneration in the early stage of merosin-deficient congenital muscular dystrophyY K Hayashi, Z Tezak, T Momoi, et al.

Annals of Neurology|December 16, 1998

A dystrophin missense mutation showing persistence of dystrophin and dystrophin-associated proteins yet a severe phenotypeL R Goldberg, I Hausmanowa-Petrusewicz, A Fidzianska, et al.

Pageof 19

Showing results (111-120 of 181) with videos related to

Sort By:

Pageof 19

Cell|July 31, 1987

Complete cloning of the Duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organization of the DMD gene in normal and affected individualsM Koenig, E P Hoffman, C J Bertelson, et al.

American Journal of Medical Genetics|May 15, 1993

In utero fetal muscle biopsy for the diagnosis of Duchenne muscular dystrophy in a female fetus "suddenly at risk"M I Evans, S A Farrell, A Greb, et al.

Neurology|October 1, 1994

A rippling muscle disease gene is localized to 1q41: evidence for multiple genesD A Stephan, N R Buist, A B Chittenden, et al.

Neurology|August 12, 2005

Early onset of inflammation and later involvement of TGFbeta in Duchenne muscular dystrophyY-W Chen, K Nagaraju, M Bakay, et al.

Acta Neuropathologica|June 23, 1999

Variable histological expression of dystrophinopathy in two femalesC Doriguzzi, L Palmucci, T Mongini, et al.

Human Gene Therapy|September 14, 2002

Delivery of alpha- and beta-sarcoglycan by recombinant adeno-associated virus: efficient rescue of muscle, but differential toxicityD Dressman, K Araishi, M Imamura, et al.

Human Molecular Genetics|October 1, 1992

The genomic structure of the human skeletal muscle sodium channel geneA I McClatchey, C S Lin, J Wang, et al.

American Journal of Medical Genetics|February 2, 1996

X-inactivation patterns in female Leber's hereditary optic neuropathy patients do not support a strong X-linked determinantE Pegoraro, V Carelli, M Zeviani, et al.

Neuromuscular Disorders : NMD|May 23, 2001

Massive muscle cell degeneration in the early stage of merosin-deficient congenital muscular dystrophyY K Hayashi, Z Tezak, T Momoi, et al.

Annals of Neurology|December 16, 1998

A dystrophin missense mutation showing persistence of dystrophin and dystrophin-associated proteins yet a severe phenotypeL R Goldberg, I Hausmanowa-Petrusewicz, A Fidzianska, et al.

Pageof 19