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Showing results (801-810 of 844) with videos related to

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The Journal of Physical Chemistry Letters|January 21, 2026
Multi-Orbital Charge Transfer into Nonplanar Cycloarenes Revealed with CO-Functionalized STM TipsAnja Haags, Alexander Reichmann, Zilin Ruan, et al.
Genes|January 11, 2018
Identification of Inherited Retinal Disease-Associated Genetic Variants in 11 Candidate GenesGaluh D N Astuti, L Ingeborgh van den Born, M Imran Khan, et al.
International Journal of Environmental Research and Public Health|February 24, 2024
Consore: A Powerful Federated Data Mining Tool Driving a French Research Network to Accelerate Cancer ResearchJulien Guérin, Amine Nahid, Louis Tassy, et al.
Scientific Reports|September 8, 2016
A new autosomal dominant eye and lung syndrome linked to mutations in TIMP3 geneIsabelle Meunier, Béatrice Bocquet, Gilles Labesse, et al.
The Journal of Clinical Investigation|September 25, 2019
Dominant mutations in mtDNA maintenance gene SSBP1 cause optic atrophy and foveopathyCamille Piro-Mégy, Emmanuelle Sarzi, Aleix Tarrés-Solé, et al.
Frontiers in Oncology|February 13, 2023
Ovarian Real-World International Consortium (ORWIC): A multicentre, real-world analysis of epithelial ovarian cancer treatment and outcomesSue Cheeseman, Bethany Levick, Will Sopwith, et al.
Methods of Information in Medicine|December 16, 2015
Core Standards of the EUBIROD Project. Defining a European Diabetes Data Dictionary for Clinical Audit and Healthcare DeliveryS G Cunningham, F Carinci, M Brillante, et al.
Journal of Medical Genetics|August 21, 2020
Pathogenic variants in <i>IMPG1</i> cause autosomal dominant and autosomal recessive retinitis pigmentosaGuillaume Olivier, Marta Corton, Daniela Intartaglia, et al.
Human Mutation|September 24, 2019
Deep-intronic variants in CNGB3 cause achromatopsia by pseudoexon activationNicole Weisschuh, Marc Sturm, Britta Baumann, et al.
Allergy|January 14, 2026
Unmet Needs in Treatment Escalation for Chronic Spontaneous Urticaria: Findings From the CURE RegistryPavel Kolkhir, Pascale Salameh, Magdalena Zajac, et al.
Pageof 85

Showing results (801-810 of 844) with videos related to

Sort By:
Pageof 85
The Journal of Physical Chemistry Letters|January 21, 2026
Multi-Orbital Charge Transfer into Nonplanar Cycloarenes Revealed with CO-Functionalized STM TipsAnja Haags, Alexander Reichmann, Zilin Ruan, et al.
Genes|January 11, 2018
Identification of Inherited Retinal Disease-Associated Genetic Variants in 11 Candidate GenesGaluh D N Astuti, L Ingeborgh van den Born, M Imran Khan, et al.
International Journal of Environmental Research and Public Health|February 24, 2024
Consore: A Powerful Federated Data Mining Tool Driving a French Research Network to Accelerate Cancer ResearchJulien Guérin, Amine Nahid, Louis Tassy, et al.
Scientific Reports|September 8, 2016
A new autosomal dominant eye and lung syndrome linked to mutations in TIMP3 geneIsabelle Meunier, Béatrice Bocquet, Gilles Labesse, et al.
The Journal of Clinical Investigation|September 25, 2019
Dominant mutations in mtDNA maintenance gene SSBP1 cause optic atrophy and foveopathyCamille Piro-Mégy, Emmanuelle Sarzi, Aleix Tarrés-Solé, et al.
Frontiers in Oncology|February 13, 2023
Ovarian Real-World International Consortium (ORWIC): A multicentre, real-world analysis of epithelial ovarian cancer treatment and outcomesSue Cheeseman, Bethany Levick, Will Sopwith, et al.
Methods of Information in Medicine|December 16, 2015
Core Standards of the EUBIROD Project. Defining a European Diabetes Data Dictionary for Clinical Audit and Healthcare DeliveryS G Cunningham, F Carinci, M Brillante, et al.
Journal of Medical Genetics|August 21, 2020
Pathogenic variants in <i>IMPG1</i> cause autosomal dominant and autosomal recessive retinitis pigmentosaGuillaume Olivier, Marta Corton, Daniela Intartaglia, et al.
Human Mutation|September 24, 2019
Deep-intronic variants in CNGB3 cause achromatopsia by pseudoexon activationNicole Weisschuh, Marc Sturm, Britta Baumann, et al.
Allergy|January 14, 2026
Unmet Needs in Treatment Escalation for Chronic Spontaneous Urticaria: Findings From the CURE RegistryPavel Kolkhir, Pascale Salameh, Magdalena Zajac, et al.
Pageof 85