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Showing results (181-190 of 212) with videos related to

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European Journal of Human Genetics : EJHG|January 27, 2011
Type B mandibuloacral dysplasia with congenital myopathy due to homozygous ZMPSTE24 missense mutationRabah Ben Yaou, Claire Navarro, Susana Quijano-Roy, et al.
Soft Matter|March 22, 2014
Spontaneous and field-induced mesomorphism of a silyl-terminated bent-core liquid crystal as determined from second-harmonic generation and resonant X-ray scatteringC L Folcia, J Ortega, J Etxebarria, et al.
Frontiers in Microbiology|October 9, 2023
Hepatitis C virus alters the morphology and function of peroxisomesEsther Martin de Fourchambault, Nathalie Callens, Jean-Michel Saliou, et al.
Biosensors & Bioelectronics|July 28, 2023
Electropolymerization processing of side-chain engineered EDOT for high performance microelectrode arraysMahdi Ghazal, Anna Susloparova, Camille Lefebvre, et al.
Neurology|October 7, 2009
Core-rod myopathy caused by mutations in the nebulin geneN B Romero, V-L Lehtokari, S Quijano-Roy, et al.
Journal of Medical Genetics|June 17, 2003
Possible founder effect of rapsyn N88K mutation and identification of novel rapsyn mutations in congenital myasthenic syndromesP Richard, K Gaudon, F Andreux, et al.
Annals of Neurology|July 12, 2002
Mapping of autosomal recessive chronic distal spinal muscular atrophy to chromosome 11q13Louis Viollet, Annie Barois, Jean G Rebeiz, et al.
Small Science|July 16, 2025
Self-Assembled Silicon@Silica Metasurfaces with High-Quality Resonances in the InfraredMegan A Parker, Raul Barbosa, Cynthia Cibaka-Ndaya, et al.
Science (New York, N.Y.)|September 18, 2025
Transposable elements are vectors of recurrent transgenerational epigenetic inheritancePierre Baduel, Louna De Oliveira, Erwann Caillieux, et al.
Cell Death & Disease|May 14, 2020
Galectin-3 modulates epithelial cell adaptation to stress at the ER-mitochondria interfaceLucie Coppin, Arnaud Jannin, Emilie Ait Yahya, et al.
Pageof 22

Showing results (181-190 of 212) with videos related to

Sort By:
Pageof 22
European Journal of Human Genetics : EJHG|January 27, 2011
Type B mandibuloacral dysplasia with congenital myopathy due to homozygous ZMPSTE24 missense mutationRabah Ben Yaou, Claire Navarro, Susana Quijano-Roy, et al.
Soft Matter|March 22, 2014
Spontaneous and field-induced mesomorphism of a silyl-terminated bent-core liquid crystal as determined from second-harmonic generation and resonant X-ray scatteringC L Folcia, J Ortega, J Etxebarria, et al.
Frontiers in Microbiology|October 9, 2023
Hepatitis C virus alters the morphology and function of peroxisomesEsther Martin de Fourchambault, Nathalie Callens, Jean-Michel Saliou, et al.
Biosensors & Bioelectronics|July 28, 2023
Electropolymerization processing of side-chain engineered EDOT for high performance microelectrode arraysMahdi Ghazal, Anna Susloparova, Camille Lefebvre, et al.
Neurology|October 7, 2009
Core-rod myopathy caused by mutations in the nebulin geneN B Romero, V-L Lehtokari, S Quijano-Roy, et al.
Journal of Medical Genetics|June 17, 2003
Possible founder effect of rapsyn N88K mutation and identification of novel rapsyn mutations in congenital myasthenic syndromesP Richard, K Gaudon, F Andreux, et al.
Annals of Neurology|July 12, 2002
Mapping of autosomal recessive chronic distal spinal muscular atrophy to chromosome 11q13Louis Viollet, Annie Barois, Jean G Rebeiz, et al.
Small Science|July 16, 2025
Self-Assembled Silicon@Silica Metasurfaces with High-Quality Resonances in the InfraredMegan A Parker, Raul Barbosa, Cynthia Cibaka-Ndaya, et al.
Science (New York, N.Y.)|September 18, 2025
Transposable elements are vectors of recurrent transgenerational epigenetic inheritancePierre Baduel, Louna De Oliveira, Erwann Caillieux, et al.
Cell Death & Disease|May 14, 2020
Galectin-3 modulates epithelial cell adaptation to stress at the ER-mitochondria interfaceLucie Coppin, Arnaud Jannin, Emilie Ait Yahya, et al.
Pageof 22