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I Richard

Showing results (141-150 of 157) with videos related to

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The Review of Scientific Instruments|October 2, 2017
Reactor for nano-focused x-ray diffraction and imaging under catalytic in situ conditionsM-I Richard, S Fernández, J P Hofmann, et al.
Brain : a Journal of Neurology|October 8, 1998
Limb-girdle muscular dystrophy in Guipúzcoa (Basque Country, Spain)M Urtasun, A Sáenz, C Roudaut, et al.
Muscle & Nerve|October 15, 1998
Clinical, pathological, and genetic features of limb-girdle muscular dystrophy type 2A with new calpain 3 gene mutations in seven patients from three Japanese familiesH Kawai, M Akaike, M Kunishige, et al.
Nature Medicine|May 6, 1999
Calpain 3 deficiency is associated with myonuclear apoptosis and profound perturbation of the IkappaB alpha/NF-kappaB pathway in limb-girdle muscular dystrophy type 2AS Baghdiguian, M Martin, I Richard, et al.
Nature Genetics|September 10, 1998
A gene related to Caenorhabditis elegans spermatogenesis factor fer-1 is mutated in limb-girdle muscular dystrophy type 2BR Bashir, S Britton, T Strachan, et al.
Nucleic Acids Research|November 28, 2012
Genomics of Drug Sensitivity in Cancer (GDSC): a resource for therapeutic biomarker discovery in cancer cellsWanjuan Yang, Jorge Soares, Patricia Greninger, et al.
Annals of Neurology|August 1, 1997
A biochemical, genetic, and clinical survey of autosomal recessive limb girdle muscular dystrophies in TurkeyP Dinçer, F Leturcq, I Richard, et al.
European Journal of Neurology|February 14, 2018
Novel mutations in DNAJB6 cause LGMD1D and distal myopathy in French familiesP H Jonson, J Palmio, M Johari, et al.
American Journal of Human Genetics|May 1, 1997
Multiple independent molecular etiology for limb-girdle muscular dystrophy type 2A patients from various geographical originsI Richard, L Brenguier, P Dinçer, et al.
Human Molecular Genetics|December 14, 2001
Mutations in the fukutin-related protein gene (FKRP) identify limb girdle muscular dystrophy 2I as a milder allelic variant of congenital muscular dystrophy MDC1CM Brockington, Y Yuva, P Prandini, et al.
Pageof 16

Showing results (141-150 of 157) with videos related to

Sort By:
Pageof 16
The Review of Scientific Instruments|October 2, 2017
Reactor for nano-focused x-ray diffraction and imaging under catalytic in situ conditionsM-I Richard, S Fernández, J P Hofmann, et al.
Brain : a Journal of Neurology|October 8, 1998
Limb-girdle muscular dystrophy in Guipúzcoa (Basque Country, Spain)M Urtasun, A Sáenz, C Roudaut, et al.
Muscle & Nerve|October 15, 1998
Clinical, pathological, and genetic features of limb-girdle muscular dystrophy type 2A with new calpain 3 gene mutations in seven patients from three Japanese familiesH Kawai, M Akaike, M Kunishige, et al.
Nature Medicine|May 6, 1999
Calpain 3 deficiency is associated with myonuclear apoptosis and profound perturbation of the IkappaB alpha/NF-kappaB pathway in limb-girdle muscular dystrophy type 2AS Baghdiguian, M Martin, I Richard, et al.
Nature Genetics|September 10, 1998
A gene related to Caenorhabditis elegans spermatogenesis factor fer-1 is mutated in limb-girdle muscular dystrophy type 2BR Bashir, S Britton, T Strachan, et al.
Nucleic Acids Research|November 28, 2012
Genomics of Drug Sensitivity in Cancer (GDSC): a resource for therapeutic biomarker discovery in cancer cellsWanjuan Yang, Jorge Soares, Patricia Greninger, et al.
Annals of Neurology|August 1, 1997
A biochemical, genetic, and clinical survey of autosomal recessive limb girdle muscular dystrophies in TurkeyP Dinçer, F Leturcq, I Richard, et al.
European Journal of Neurology|February 14, 2018
Novel mutations in DNAJB6 cause LGMD1D and distal myopathy in French familiesP H Jonson, J Palmio, M Johari, et al.
American Journal of Human Genetics|May 1, 1997
Multiple independent molecular etiology for limb-girdle muscular dystrophy type 2A patients from various geographical originsI Richard, L Brenguier, P Dinçer, et al.
Human Molecular Genetics|December 14, 2001
Mutations in the fukutin-related protein gene (FKRP) identify limb girdle muscular dystrophy 2I as a milder allelic variant of congenital muscular dystrophy MDC1CM Brockington, Y Yuva, P Prandini, et al.
Pageof 16