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I Richard

Showing results (151-160 of 157) with videos related to

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European Journal of Neurology|October 14, 2020
Clinical correlations and long-term follow-up in 100 patients with sarcoglycanopathiesR Guimarães-Costa, G Fernández-Eulate, K Wahbi, et al.
Neuromuscular Disorders : NMD|December 1, 1996
Identification of muscle-specific calpain and beta-sarcoglycan genes in progressive autosomal recessive muscular dystrophiesJ S Beckmann, I Richard, O Broux, et al.
American Journal of Human Genetics|May 20, 1999
Calpainopathy-a survey of mutations and polymorphismsI Richard, C Roudaut, A Saenz, et al.
Neurology|July 27, 2001
Genomic organization of the dysferlin gene and novel mutations in Miyoshi myopathyM Aoki, J Liu, I Richard, et al.
Neurobiology of Disease|March 4, 2025
2024 VCP International Conference: Exploring multi-disciplinary approaches from basic science of valosin containing protein, an AAA+ ATPase protein, to the therapeutic advancement for VCP-associated multisystem proteinopathyA Peck, A Dadi, Z Yavarow, et al.
Nature|March 31, 2012
Systematic identification of genomic markers of drug sensitivity in cancer cellsMathew J Garnett, Elena J Edelman, Sonja J Heidorn, et al.
Nature Communications|May 13, 2025
Clinical response to azacitidine in MDS is associated with distinct DNA methylation changes in HSPCsJulie A I Thoms, Feng Yan, Henry R Hampton, et al.
Pageof 16

Showing results (151-160 of 157) with videos related to

Sort By:
Pageof 16
You have reached the last page of results.This site can display upto 157 results.
European Journal of Neurology|October 14, 2020
Clinical correlations and long-term follow-up in 100 patients with sarcoglycanopathiesR Guimarães-Costa, G Fernández-Eulate, K Wahbi, et al.
Neuromuscular Disorders : NMD|December 1, 1996
Identification of muscle-specific calpain and beta-sarcoglycan genes in progressive autosomal recessive muscular dystrophiesJ S Beckmann, I Richard, O Broux, et al.
American Journal of Human Genetics|May 20, 1999
Calpainopathy-a survey of mutations and polymorphismsI Richard, C Roudaut, A Saenz, et al.
Neurology|July 27, 2001
Genomic organization of the dysferlin gene and novel mutations in Miyoshi myopathyM Aoki, J Liu, I Richard, et al.
Neurobiology of Disease|March 4, 2025
2024 VCP International Conference: Exploring multi-disciplinary approaches from basic science of valosin containing protein, an AAA+ ATPase protein, to the therapeutic advancement for VCP-associated multisystem proteinopathyA Peck, A Dadi, Z Yavarow, et al.
Nature|March 31, 2012
Systematic identification of genomic markers of drug sensitivity in cancer cellsMathew J Garnett, Elena J Edelman, Sonja J Heidorn, et al.
Nature Communications|May 13, 2025
Clinical response to azacitidine in MDS is associated with distinct DNA methylation changes in HSPCsJulie A I Thoms, Feng Yan, Henry R Hampton, et al.
Pageof 16