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Yann Fichou

Showing results (51-60 of 96) with videos related to

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American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|May 21, 2009
Epileptic encephalopathy in a girl with an interstitial deletion of Xp22 comprising promoter and exon 1 of the CDKL5 geneNadia Bahi-Buisson, Benoit Girard, Agnes Gautier, et al.
Transfusion Medicine and Hemotherapy : Offizielles Organ Der Deutschen Gesellschaft Fur Transfusionsmedizin Und Immunhamatologie|June 22, 2018
RHD-Positive Alleles among D- C/E+ Individuals from IndiaSwati S Kulkarni, Harita Gogri, Disha Parchure, et al.
Journal of Molecular Biology|December 6, 2020
Liquid-Liquid Phase Separation of Tau Driven by Hydrophobic Interaction Facilitates Fibrillization of TauYanxian Lin, Yann Fichou, Andrew P Longhini, et al.
Transfusion|September 29, 2011
Variant screening of the RHD gene in a large cohort of subjects with D phenotype ambiguity: report of 17 novel rare allelesYann Fichou, Cédric Le Maréchal, Laurence Bryckaert, et al.
Transfusion|November 16, 2022
Molecular and serological analysis of the D variant in the Chinese population and identification of seven novel RHD allelesJizhi Wen, Shuangshuang Jia, Zhen Wang, et al.
Transfusion|February 27, 2018
Molecular basis of weak D expression in the Indian population and report of a novel, predominant variant RHD alleleYann Fichou, Disha Parchure, Harita Gogri, et al.
Transfusion|January 31, 2022
The novel c.634+4A>G splicing variant in RHCE results in weak C and e antigen expression in a pregnant woman originated from JapanCynthia Restivo, Myriam Le Bras, Pierre-Antoine Deguigne, et al.
Blood Transfusion = Trasfusione Del Sangue|July 18, 2022
From the investigation of RHD-CE hybrid genes to the recognition of RHCE variants and RHD zygosity. Expanding the analysis by QMPSF in Brazilian donors and in patients with sickle cell diseaseTatiane A de Paula Vendrame, Carine P Arnoni, Flavia R M Latini, et al.
Human Mutation|February 1, 2011
A missense mutation within the fork-head domain of the forkhead box G1 Gene (FOXG1) affects its nuclear localizationTangui Le Guen, Yann Fichou, Juliette Nectoux, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 30, 2016
A ring-shaped conduit connects the mother cell and forespore during sporulation in Bacillus subtilisChristopher D A Rodrigues, Xavier Henry, Emmanuelle Neumann, et al.
Pageof 10

Showing results (51-60 of 96) with videos related to

Sort By:
Pageof 10
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|May 21, 2009
Epileptic encephalopathy in a girl with an interstitial deletion of Xp22 comprising promoter and exon 1 of the CDKL5 geneNadia Bahi-Buisson, Benoit Girard, Agnes Gautier, et al.
Transfusion Medicine and Hemotherapy : Offizielles Organ Der Deutschen Gesellschaft Fur Transfusionsmedizin Und Immunhamatologie|June 22, 2018
RHD-Positive Alleles among D- C/E+ Individuals from IndiaSwati S Kulkarni, Harita Gogri, Disha Parchure, et al.
Journal of Molecular Biology|December 6, 2020
Liquid-Liquid Phase Separation of Tau Driven by Hydrophobic Interaction Facilitates Fibrillization of TauYanxian Lin, Yann Fichou, Andrew P Longhini, et al.
Transfusion|September 29, 2011
Variant screening of the RHD gene in a large cohort of subjects with D phenotype ambiguity: report of 17 novel rare allelesYann Fichou, Cédric Le Maréchal, Laurence Bryckaert, et al.
Transfusion|November 16, 2022
Molecular and serological analysis of the D variant in the Chinese population and identification of seven novel RHD allelesJizhi Wen, Shuangshuang Jia, Zhen Wang, et al.
Transfusion|February 27, 2018
Molecular basis of weak D expression in the Indian population and report of a novel, predominant variant RHD alleleYann Fichou, Disha Parchure, Harita Gogri, et al.
Transfusion|January 31, 2022
The novel c.634+4A>G splicing variant in RHCE results in weak C and e antigen expression in a pregnant woman originated from JapanCynthia Restivo, Myriam Le Bras, Pierre-Antoine Deguigne, et al.
Blood Transfusion = Trasfusione Del Sangue|July 18, 2022
From the investigation of RHD-CE hybrid genes to the recognition of RHCE variants and RHD zygosity. Expanding the analysis by QMPSF in Brazilian donors and in patients with sickle cell diseaseTatiane A de Paula Vendrame, Carine P Arnoni, Flavia R M Latini, et al.
Human Mutation|February 1, 2011
A missense mutation within the fork-head domain of the forkhead box G1 Gene (FOXG1) affects its nuclear localizationTangui Le Guen, Yann Fichou, Juliette Nectoux, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 30, 2016
A ring-shaped conduit connects the mother cell and forespore during sporulation in Bacillus subtilisChristopher D A Rodrigues, Xavier Henry, Emmanuelle Neumann, et al.
Pageof 10