Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Yann Fichou

Showing results (81-90 of 96) with videos related to

Pageof 10
Sort By:
Plos One|September 27, 2013
A missense mutation in the alpha-actinin 1 gene (ACTN1) is the cause of autosomal dominant macrothrombocytopenia in a large French familyPaul Guéguen, Karen Rouault, Jian-Min Chen, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 29, 2015
Hydration water mobility is enhanced around tau amyloid fibersYann Fichou, Giorgio Schirò, François-Xavier Gallat, et al.
European Journal of Human Genetics : EJHG|August 10, 2018
Estimating the age of p.(Phe508del) with family studies of geographically distinct European populations and the early spread of cystic fibrosisPhilip Farrell, Claude Férec, Milan Macek, et al.
Acta Neuropathologica Communications|March 3, 2019
The elusive tau molecular structures: can we translate the recent breakthroughs into new targets for intervention?Yann Fichou, Youssra K Al-Hilaly, François Devred, et al.
Scientific Reports|August 17, 2016
Neutrons describe ectoine effects on water H-bonding and hydration around a soluble protein and a cell membraneGiuseppe Zaccai, Irina Bagyan, Jérôme Combet, et al.
Frontiers in Molecular Neuroscience|July 19, 2021
Structures of Pathological and Functional Amyloids and Prions, a Solid-State NMR PerspectiveAsen Daskalov, Nadia El Mammeri, Alons Lends, et al.
Journal of Applied Physics|May 12, 2011
Synthesis and characterization of core∕shell Fe(3)O(4)∕ZnSe fluorescent magnetic nanoparticlesJosé M Vargas, Amber A McBride, John B Plumley, et al.
Journal of Medical Genetics|March 13, 2020
Biallelic variants in <i>MAATS1</i> encoding CFAP91, a calmodulin-associated and spoke-associated complex protein, cause severe astheno-teratozoospermia and male infertilityGuillaume Martinez, Julie Beurois, Denis Dacheux, et al.
Human Mutation|May 28, 2019
First estimate of the scale of canonical 5' splice site GT>GC variants capable of generating wild-type transcriptsJin-Huan Lin, Xin-Ying Tang, Arnaud Boulling, et al.
Blood|January 13, 2023
Patients with Asian-type DEL can safely be transfused with RhD-positive bloodYanli Ji, Yalin Luo, Jizhi Wen, et al.
Pageof 10

Showing results (81-90 of 96) with videos related to

Sort By:
Pageof 10
Plos One|September 27, 2013
A missense mutation in the alpha-actinin 1 gene (ACTN1) is the cause of autosomal dominant macrothrombocytopenia in a large French familyPaul Guéguen, Karen Rouault, Jian-Min Chen, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 29, 2015
Hydration water mobility is enhanced around tau amyloid fibersYann Fichou, Giorgio Schirò, François-Xavier Gallat, et al.
European Journal of Human Genetics : EJHG|August 10, 2018
Estimating the age of p.(Phe508del) with family studies of geographically distinct European populations and the early spread of cystic fibrosisPhilip Farrell, Claude Férec, Milan Macek, et al.
Acta Neuropathologica Communications|March 3, 2019
The elusive tau molecular structures: can we translate the recent breakthroughs into new targets for intervention?Yann Fichou, Youssra K Al-Hilaly, François Devred, et al.
Scientific Reports|August 17, 2016
Neutrons describe ectoine effects on water H-bonding and hydration around a soluble protein and a cell membraneGiuseppe Zaccai, Irina Bagyan, Jérôme Combet, et al.
Frontiers in Molecular Neuroscience|July 19, 2021
Structures of Pathological and Functional Amyloids and Prions, a Solid-State NMR PerspectiveAsen Daskalov, Nadia El Mammeri, Alons Lends, et al.
Journal of Applied Physics|May 12, 2011
Synthesis and characterization of core∕shell Fe(3)O(4)∕ZnSe fluorescent magnetic nanoparticlesJosé M Vargas, Amber A McBride, John B Plumley, et al.
Journal of Medical Genetics|March 13, 2020
Biallelic variants in <i>MAATS1</i> encoding CFAP91, a calmodulin-associated and spoke-associated complex protein, cause severe astheno-teratozoospermia and male infertilityGuillaume Martinez, Julie Beurois, Denis Dacheux, et al.
Human Mutation|May 28, 2019
First estimate of the scale of canonical 5' splice site GT>GC variants capable of generating wild-type transcriptsJin-Huan Lin, Xin-Ying Tang, Arnaud Boulling, et al.
Blood|January 13, 2023
Patients with Asian-type DEL can safely be transfused with RhD-positive bloodYanli Ji, Yalin Luo, Jizhi Wen, et al.
Pageof 10