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Yann Fichou

Showing results (31-40 of 96) with videos related to

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Transfusion|February 28, 2019
Functional analysis of novel RHD variants: splicing disruption is likely to be a common mechanism of variant D phenotypeLoann Raud, Chandran Ka, Isabelle Gourlaouen, et al.
Transfusion|May 5, 2017
First report of Rh<sub>null</sub> individuals in the Indian population and characterization of the underlying molecular mechanismsSwati S Kulkarni, Kasiviswanathan Vasantha, Harita Gogri, et al.
JACS Au|May 29, 2026
Local Organization of Biological Membranes Modulates Tau-Lipid Interactions and Fibril formationClara Piersson, Victoria Lublin, Mathieu Duttine, et al.
The Journal of Physical Chemistry. B|June 29, 2022
Total Internal Reflection Tip-Enhanced Raman Spectroscopy of Tau FibrilsDavid Talaga, Gary S Cooney, Vicky Ury-Thiery, et al.
Biochimica Et Biophysica Acta|September 18, 2007
Annexin V is directly involved in cystic fibrosis transmembrane conductance regulator's chloride channel functionPascal Trouvé, Marie-Anne Le Drévo, Mathieu Kerbiriou, et al.
Neurogenetics|November 27, 2008
The first missense mutation causing Rett syndrome specifically affecting the MeCP2_e1 isoformYann Fichou, Juliette Nectoux, Nadia Bahi-Buisson, et al.
Transfusion|April 5, 2013
A convenient qualitative and quantitative method to investigate RHD-RHCE hybrid genesYann Fichou, Cédric Le Maréchal, Laurence Bryckaert, et al.
Journal of Visualized Experiments : Jove|May 16, 2022
High-resolution Neutron Spectroscopy to Study Picosecond-nanosecond Dynamics of Proteins and Hydration WaterKevin Pounot, Markus Appel, Christian Beck, et al.
Angewandte Chemie (International Ed. in English)|October 31, 2023
Chemical Imaging of RNA-Tau Amyloid Fibrils at the Nanoscale Using Tip-Enhanced Raman SpectroscopyGary Sean Cooney, David Talaga, Vicky Ury-Thiery, et al.
Journal of Molecular Medicine (Berlin, Germany)|November 26, 2010
Cell cloning-based transcriptome analysis in cyclin-dependent kinase-like 5 mutation patients with severe epileptic encephalopathyJuliette Nectoux, Yann Fichou, Nicolas Cagnard, et al.
Pageof 10

Showing results (31-40 of 96) with videos related to

Sort By:
Pageof 10
Transfusion|February 28, 2019
Functional analysis of novel RHD variants: splicing disruption is likely to be a common mechanism of variant D phenotypeLoann Raud, Chandran Ka, Isabelle Gourlaouen, et al.
Transfusion|May 5, 2017
First report of Rh<sub>null</sub> individuals in the Indian population and characterization of the underlying molecular mechanismsSwati S Kulkarni, Kasiviswanathan Vasantha, Harita Gogri, et al.
JACS Au|May 29, 2026
Local Organization of Biological Membranes Modulates Tau-Lipid Interactions and Fibril formationClara Piersson, Victoria Lublin, Mathieu Duttine, et al.
The Journal of Physical Chemistry. B|June 29, 2022
Total Internal Reflection Tip-Enhanced Raman Spectroscopy of Tau FibrilsDavid Talaga, Gary S Cooney, Vicky Ury-Thiery, et al.
Biochimica Et Biophysica Acta|September 18, 2007
Annexin V is directly involved in cystic fibrosis transmembrane conductance regulator's chloride channel functionPascal Trouvé, Marie-Anne Le Drévo, Mathieu Kerbiriou, et al.
Neurogenetics|November 27, 2008
The first missense mutation causing Rett syndrome specifically affecting the MeCP2_e1 isoformYann Fichou, Juliette Nectoux, Nadia Bahi-Buisson, et al.
Transfusion|April 5, 2013
A convenient qualitative and quantitative method to investigate RHD-RHCE hybrid genesYann Fichou, Cédric Le Maréchal, Laurence Bryckaert, et al.
Journal of Visualized Experiments : Jove|May 16, 2022
High-resolution Neutron Spectroscopy to Study Picosecond-nanosecond Dynamics of Proteins and Hydration WaterKevin Pounot, Markus Appel, Christian Beck, et al.
Angewandte Chemie (International Ed. in English)|October 31, 2023
Chemical Imaging of RNA-Tau Amyloid Fibrils at the Nanoscale Using Tip-Enhanced Raman SpectroscopyGary Sean Cooney, David Talaga, Vicky Ury-Thiery, et al.
Journal of Molecular Medicine (Berlin, Germany)|November 26, 2010
Cell cloning-based transcriptome analysis in cyclin-dependent kinase-like 5 mutation patients with severe epileptic encephalopathyJuliette Nectoux, Yann Fichou, Nicolas Cagnard, et al.
Pageof 10