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Yann Fichou

Showing results (61-70 of 96) with videos related to

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Transfusion|March 17, 2012
Weak D caused by a founder deletion in the RHD geneYann Fichou, Jian-Min Chen, Cédric Le Maréchal, et al.
Transfusion|June 10, 2021
Missense RHD single nucleotide variants induce weakened D antigen expression by altering splicing and/or protein expressionLoann Raud, Marlène Le Tertre, Léonie Vigneron, et al.
Journal of Lipid Research|April 8, 2026
The impact of charge on chlorpromazine interaction with lipid membranesAna Gorse, Nicolò Paracini, Marion Mathelié-Guinlet, et al.
Transfusion|December 12, 2012
Establishment of a medium-throughput approach for the genotyping of RHD variants and report of nine novel rare allelesYann Fichou, Cédric Le Maréchal, Déborah Jamet, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 13, 2018
Cofactors are essential constituents of stable and seeding-active tau fibrilsYann Fichou, Yanxian Lin, Jennifer N Rauch, et al.
Blood Transfusion = Trasfusione Del Sangue|November 13, 2018
Comprehensive phenotypic and molecular investigation of RhD and RhCE variants in Moroccan blood donorsHouria El Housse, Mariam El Wafi, Zainab Ouabdelmoumene, et al.
Blood Transfusion = Trasfusione Del Sangue|February 5, 2024
First investigation of RH gene polymorphism in patients with sickle cell disease and associated blood donors in Cameroon, Central AfricaJeanne Manga Messina Mbeti, Caroline Bénech, Françoise Ngo Sack, et al.
Frontiers in Genetics|August 23, 2021
Splicing Outcomes of 5' Splice Site GT>GC Variants That Generate Wild-Type Transcripts Differ Significantly Between Full-Length and Minigene Splicing AssaysJin-Huan Lin, Hao Wu, Wen-Bin Zou, et al.
Chemical Reviews|March 11, 2024
Molecular Crowding: The History and Development of a Scientific ParadigmCaterina Alfano, Yann Fichou, Klaus Huber, et al.
Neurogenetics|October 7, 2009
Revisiting the phenotype associated with FOXG1 mutations: two novel cases of congenital Rett variantNadia Bahi-Buisson, Juliette Nectoux, Benoit Girard, et al.
Pageof 10

Showing results (61-70 of 96) with videos related to

Sort By:
Pageof 10
Transfusion|March 17, 2012
Weak D caused by a founder deletion in the RHD geneYann Fichou, Jian-Min Chen, Cédric Le Maréchal, et al.
Transfusion|June 10, 2021
Missense RHD single nucleotide variants induce weakened D antigen expression by altering splicing and/or protein expressionLoann Raud, Marlène Le Tertre, Léonie Vigneron, et al.
Journal of Lipid Research|April 8, 2026
The impact of charge on chlorpromazine interaction with lipid membranesAna Gorse, Nicolò Paracini, Marion Mathelié-Guinlet, et al.
Transfusion|December 12, 2012
Establishment of a medium-throughput approach for the genotyping of RHD variants and report of nine novel rare allelesYann Fichou, Cédric Le Maréchal, Déborah Jamet, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 13, 2018
Cofactors are essential constituents of stable and seeding-active tau fibrilsYann Fichou, Yanxian Lin, Jennifer N Rauch, et al.
Blood Transfusion = Trasfusione Del Sangue|November 13, 2018
Comprehensive phenotypic and molecular investigation of RhD and RhCE variants in Moroccan blood donorsHouria El Housse, Mariam El Wafi, Zainab Ouabdelmoumene, et al.
Blood Transfusion = Trasfusione Del Sangue|February 5, 2024
First investigation of RH gene polymorphism in patients with sickle cell disease and associated blood donors in Cameroon, Central AfricaJeanne Manga Messina Mbeti, Caroline Bénech, Françoise Ngo Sack, et al.
Frontiers in Genetics|August 23, 2021
Splicing Outcomes of 5' Splice Site GT>GC Variants That Generate Wild-Type Transcripts Differ Significantly Between Full-Length and Minigene Splicing AssaysJin-Huan Lin, Hao Wu, Wen-Bin Zou, et al.
Chemical Reviews|March 11, 2024
Molecular Crowding: The History and Development of a Scientific ParadigmCaterina Alfano, Yann Fichou, Klaus Huber, et al.
Neurogenetics|October 7, 2009
Revisiting the phenotype associated with FOXG1 mutations: two novel cases of congenital Rett variantNadia Bahi-Buisson, Juliette Nectoux, Benoit Girard, et al.
Pageof 10