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H Lochmuller

Showing results (1-10 of 12) with videos related to

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Journal of Virology|April 5, 2001
Muscle-specific overexpression of the adenovirus primary receptor CAR overcomes low efficiency of gene transfer to mature skeletal muscleJ Nalbantoglu, N Larochelle, E Wolf, et al.
Neuromuscular Disorders : NMD|July 1, 1997
Use of the dog model for Duchenne muscular dystrophy in gene therapy trialsJ M Howell, S Fletcher, B A Kakulas, et al.
Journal of Virology|May 30, 1998
Combinatorial blockade of calcineurin and CD28 signaling facilitates primary and secondary therapeutic gene transfer by adenovirus vectors in dystrophic (mdx) mouse musclesG H Guibinga, H Lochmuller, B Massie, et al.
Cell Death and Differentiation|August 4, 2007
Characterization of hereditary inclusion body myopathy myoblasts: possible primary impairment of apoptotic eventsS Amsili, Z Shlomai, R Levitzki, et al.
Gene Therapy|June 6, 1998
Adenovirus-mediated dystrophin minigene transfer improves muscle strength in adult dystrophic (MDX) miceL Yang, H Lochmuller, J Luo, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|August 16, 2016
Why are some patients with Duchenne muscular dystrophy dying young: An analysis of causes of death in North East EnglandH J A Van Ruiten, C Marini Bettolo, T Cheetham, et al.
Journal of Medical Genetics|October 5, 2001
Frequency of mitochondrial transfer RNA mutations and deletions in 225 patients presenting with respiratory chain deficienciesM Jaksch, S Kleinle, C Scharfe, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|April 1, 1999
Intracerebral adenovirus-mediated p53 tumor suppressor gene therapy for experimental human gliomaH Li, M Alonso-Vanegas, M A Colicos, et al.
Brain & Development|May 12, 2020
Successful treatment of intractable epilepsy with ketogenic diet therapy in twins with ALG3-CDGC Paketci, P Edem, S Hiz, et al.
Neurology|October 24, 2001
Homozygosity (E140K) in SCO2 causes delayed infantile onset of cardiomyopathy and neuropathyM Jaksch, R Horvath, N Horn, et al.
Pageof 2

Showing results (1-10 of 12) with videos related to

Sort By:
Pageof 2
Journal of Virology|April 5, 2001
Muscle-specific overexpression of the adenovirus primary receptor CAR overcomes low efficiency of gene transfer to mature skeletal muscleJ Nalbantoglu, N Larochelle, E Wolf, et al.
Neuromuscular Disorders : NMD|July 1, 1997
Use of the dog model for Duchenne muscular dystrophy in gene therapy trialsJ M Howell, S Fletcher, B A Kakulas, et al.
Journal of Virology|May 30, 1998
Combinatorial blockade of calcineurin and CD28 signaling facilitates primary and secondary therapeutic gene transfer by adenovirus vectors in dystrophic (mdx) mouse musclesG H Guibinga, H Lochmuller, B Massie, et al.
Cell Death and Differentiation|August 4, 2007
Characterization of hereditary inclusion body myopathy myoblasts: possible primary impairment of apoptotic eventsS Amsili, Z Shlomai, R Levitzki, et al.
Gene Therapy|June 6, 1998
Adenovirus-mediated dystrophin minigene transfer improves muscle strength in adult dystrophic (MDX) miceL Yang, H Lochmuller, J Luo, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|August 16, 2016
Why are some patients with Duchenne muscular dystrophy dying young: An analysis of causes of death in North East EnglandH J A Van Ruiten, C Marini Bettolo, T Cheetham, et al.
Journal of Medical Genetics|October 5, 2001
Frequency of mitochondrial transfer RNA mutations and deletions in 225 patients presenting with respiratory chain deficienciesM Jaksch, S Kleinle, C Scharfe, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|April 1, 1999
Intracerebral adenovirus-mediated p53 tumor suppressor gene therapy for experimental human gliomaH Li, M Alonso-Vanegas, M A Colicos, et al.
Brain & Development|May 12, 2020
Successful treatment of intractable epilepsy with ketogenic diet therapy in twins with ALG3-CDGC Paketci, P Edem, S Hiz, et al.
Neurology|October 24, 2001
Homozygosity (E140K) in SCO2 causes delayed infantile onset of cardiomyopathy and neuropathyM Jaksch, R Horvath, N Horn, et al.
Pageof 2