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Bruno Louis

Showing results (121-130 of 125) with videos related to

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Human Molecular Genetics|January 25, 2018
Homozygous missense mutation L673P in adenylate kinase 7 (AK7) leads to primary male infertility and multiple morphological anomalies of the flagella but not to primary ciliary dyskinesiaPatrick Lorès, Charles Coutton, Elma El Khouri, et al.
Journal of Extracellular Vesicles|October 22, 2022
Proviral role of human respiratory epithelial cell-derived small extracellular vesicles in SARS-CoV-2 infectionFrançois Berry, Margot Morin-Dewaele, Amene Majidipur, et al.
American Journal of Human Genetics|November 26, 2018
Mutations in Outer Dynein Arm Heavy Chain DNAH9 Cause Motile Cilia Defects and Situs InversusMahmoud R Fassad, Amelia Shoemark, Marie Legendre, et al.
American Journal of Human Genetics|September 3, 2013
Loss-of-function mutations in RSPH1 cause primary ciliary dyskinesia with central-complex and radial-spoke defectsEsther Kott, Marie Legendre, Bruno Copin, et al.
American Journal of Human Genetics|January 25, 2020
TTC12 Loss-of-Function Mutations Cause Primary Ciliary Dyskinesia and Unveil Distinct Dynein Assembly Mechanisms in Motile Cilia Versus FlagellaLucie Thomas, Khaled Bouhouche, Marjorie Whitfield, et al.
Pageof 13

Showing results (121-130 of 125) with videos related to

Sort By:
Pageof 13
You have reached the last page of results.This site can display upto 125 results.
Human Molecular Genetics|January 25, 2018
Homozygous missense mutation L673P in adenylate kinase 7 (AK7) leads to primary male infertility and multiple morphological anomalies of the flagella but not to primary ciliary dyskinesiaPatrick Lorès, Charles Coutton, Elma El Khouri, et al.
Journal of Extracellular Vesicles|October 22, 2022
Proviral role of human respiratory epithelial cell-derived small extracellular vesicles in SARS-CoV-2 infectionFrançois Berry, Margot Morin-Dewaele, Amene Majidipur, et al.
American Journal of Human Genetics|November 26, 2018
Mutations in Outer Dynein Arm Heavy Chain DNAH9 Cause Motile Cilia Defects and Situs InversusMahmoud R Fassad, Amelia Shoemark, Marie Legendre, et al.
American Journal of Human Genetics|September 3, 2013
Loss-of-function mutations in RSPH1 cause primary ciliary dyskinesia with central-complex and radial-spoke defectsEsther Kott, Marie Legendre, Bruno Copin, et al.
American Journal of Human Genetics|January 25, 2020
TTC12 Loss-of-Function Mutations Cause Primary Ciliary Dyskinesia and Unveil Distinct Dynein Assembly Mechanisms in Motile Cilia Versus FlagellaLucie Thomas, Khaled Bouhouche, Marjorie Whitfield, et al.
Pageof 13