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Showing results (791-800 of 844) with videos related to

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British Journal of Cancer|May 5, 2011
Immunohistochemical and molecular analyses of HER2 status in breast cancers are highly concordant and complementary approachesJ Lehmann-Che, F Amira-Bouhidel, E Turpin, et al.
Human Mutation|May 7, 2019
Mutation spectrum and clinical investigation of achromatopsia patients with mutations in the GNAT2 geneJulia Felden, Britta Baumann, Manir Ali, et al.
JAMA Network Open|April 3, 2024
Tucatinib Combination Treatment After Trastuzumab-Deruxtecan in Patients With ERBB2-Positive Metastatic Breast CancerJean-Sebastien Frenel, Jean Zeghondy, Catherine Guérin-Charbonnel, et al.
International Journal of Molecular Sciences|July 2, 2021
Novel <i>TTLL5</i> Variants Associated with Cone-Rod Dystrophy and Early-Onset Severe Retinal DystrophyVasily Smirnov, Olivier Grunewald, Jean Muller, et al.
Human Molecular Genetics|October 4, 2017
A novel duplication of PRMD13 causes North Carolina macular dystrophy: overexpression of PRDM13 orthologue in drosophila eye reproduces the human phenotypeGaël Manes, Willy Joly, Thomas Guignard, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 22, 2025
Identification of IDH3G, encoding the gamma subunit of mitochondrial isocitrate dehydrogenase, as a novel candidate gene for X-linked retinitis pigmentosaLorenzo Bianco, Julien Navarro, Christelle Michiels, et al.
Journal for Immunotherapy of Cancer|October 17, 2020
Natural killer cells in the human lung tumor microenvironment display immune inhibitory functionsJules Russick, Pierre-Emmanuel Joubert, Mélanie Gillard-Bocquet, et al.
ACS Nano|November 13, 2020
Kekulene: On-Surface Synthesis, Orbital Structure, and Aromatic StabilizationAnja Haags, Alexander Reichmann, Qitang Fan, et al.
The Journal of Allergy and Clinical Immunology|July 5, 2022
RNF213-associated urticarial lesions with hypercytokinemiaCamille Louvrier, Fawaz Awad, Anne Cosnes, et al.
Human Molecular Genetics|January 9, 2016
A dominant mutation in MAPKAPK3, an actor of p38 signaling pathway, causes a new retinal dystrophy involving Bruch's membrane and retinal pigment epitheliumIsabelle Meunier, Guy Lenaers, Béatrice Bocquet, et al.
Pageof 85

Showing results (791-800 of 844) with videos related to

Sort By:
Pageof 85
British Journal of Cancer|May 5, 2011
Immunohistochemical and molecular analyses of HER2 status in breast cancers are highly concordant and complementary approachesJ Lehmann-Che, F Amira-Bouhidel, E Turpin, et al.
Human Mutation|May 7, 2019
Mutation spectrum and clinical investigation of achromatopsia patients with mutations in the GNAT2 geneJulia Felden, Britta Baumann, Manir Ali, et al.
JAMA Network Open|April 3, 2024
Tucatinib Combination Treatment After Trastuzumab-Deruxtecan in Patients With ERBB2-Positive Metastatic Breast CancerJean-Sebastien Frenel, Jean Zeghondy, Catherine Guérin-Charbonnel, et al.
International Journal of Molecular Sciences|July 2, 2021
Novel <i>TTLL5</i> Variants Associated with Cone-Rod Dystrophy and Early-Onset Severe Retinal DystrophyVasily Smirnov, Olivier Grunewald, Jean Muller, et al.
Human Molecular Genetics|October 4, 2017
A novel duplication of PRMD13 causes North Carolina macular dystrophy: overexpression of PRDM13 orthologue in drosophila eye reproduces the human phenotypeGaël Manes, Willy Joly, Thomas Guignard, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 22, 2025
Identification of IDH3G, encoding the gamma subunit of mitochondrial isocitrate dehydrogenase, as a novel candidate gene for X-linked retinitis pigmentosaLorenzo Bianco, Julien Navarro, Christelle Michiels, et al.
Journal for Immunotherapy of Cancer|October 17, 2020
Natural killer cells in the human lung tumor microenvironment display immune inhibitory functionsJules Russick, Pierre-Emmanuel Joubert, Mélanie Gillard-Bocquet, et al.
ACS Nano|November 13, 2020
Kekulene: On-Surface Synthesis, Orbital Structure, and Aromatic StabilizationAnja Haags, Alexander Reichmann, Qitang Fan, et al.
The Journal of Allergy and Clinical Immunology|July 5, 2022
RNF213-associated urticarial lesions with hypercytokinemiaCamille Louvrier, Fawaz Awad, Anne Cosnes, et al.
Human Molecular Genetics|January 9, 2016
A dominant mutation in MAPKAPK3, an actor of p38 signaling pathway, causes a new retinal dystrophy involving Bruch's membrane and retinal pigment epitheliumIsabelle Meunier, Guy Lenaers, Béatrice Bocquet, et al.
Pageof 85