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

Estelle Escudier

Showing results (31-40 of 65) with videos related to

Pageof 7
Sort By:
Journal of Clinical Medicine|May 10, 2019
Critical Evaluation of Sinonasal Disease in 64 Adults with Primary Ciliary DyskinesiaEmilie Bequignon, Laurence Dupuy, Francoise Zerah-Lancner, et al.
Journal of Clinical Medicine|September 25, 2019
Follow-Up and Management of Chronic Rhinosinusitis in Adults with Primary Ciliary Dyskinesia: Review and Experience of Our Reference CentersEmilie Bequignon, Laurence Dupuy, Virginie Escabasse, et al.
Human Molecular Genetics|November 10, 2017
Functional characterization of tektin-1 in motile cilia and evidence for TEKT1 as a new candidate gene for motile ciliopathiesRebecca Ryan, Marion Failler, Madeline Louise Reilly, et al.
The European Respiratory Journal|November 11, 2017
Infertility in an adult cohort with primary ciliary dyskinesia: phenotype-gene associationGert Jan Vanaken, Laurence Bassinet, Mieke Boon, et al.
Journal of Medical Genetics|November 28, 2019
Deep phenotyping, including quantitative ciliary beating parameters, and extensive genotyping in primary ciliary dyskinesiaSylvain Blanchon, Marie Legendre, Mathieu Bottier, et al.
Journal of Clinical Medicine|September 9, 2022
Otological Manifestations in Adults with Primary Ciliary Dyskinesia: A Controlled Radio-Clinical StudyMihaela Alexandru, Paul de Boissieu, Farida Benoudiba, et al.
Biology of Reproduction|August 19, 2007
A heterozygous mutation disrupting the SPAG16 gene results in biochemical instability of central apparatus components of the human sperm axonemeZhibing Zhang, Maimoona A Zariwala, Maha M Mahadevan, et al.
Human Mutation|April 28, 2016
Mutations in GAS8, a Gene Encoding a Nexin-Dynein Regulatory Complex Subunit, Cause Primary Ciliary Dyskinesia with Axonemal DisorganizationLudovic Jeanson, Lucie Thomas, Bruno Copin, et al.
Reproductive Biomedicine Online|September 24, 2023
Results and perinatal outcomes from 189 ICSI cycles of couples with asthenozoospermic men and flagellar defects assessed by transmission electron microscopyAngèle Boursier, Augustin Boudry, Valérie Mitchell, et al.
American Journal of Human Genetics|December 1, 2009
Loss-of-function mutations in the human ortholog of Chlamydomonas reinhardtii ODA7 disrupt dynein arm assembly and cause primary ciliary dyskinesiaPhilippe Duquesnoy, Estelle Escudier, Laetitia Vincensini, et al.
Pageof 7

Showing results (31-40 of 65) with videos related to

Sort By:
Pageof 7
Journal of Clinical Medicine|May 10, 2019
Critical Evaluation of Sinonasal Disease in 64 Adults with Primary Ciliary DyskinesiaEmilie Bequignon, Laurence Dupuy, Francoise Zerah-Lancner, et al.
Journal of Clinical Medicine|September 25, 2019
Follow-Up and Management of Chronic Rhinosinusitis in Adults with Primary Ciliary Dyskinesia: Review and Experience of Our Reference CentersEmilie Bequignon, Laurence Dupuy, Virginie Escabasse, et al.
Human Molecular Genetics|November 10, 2017
Functional characterization of tektin-1 in motile cilia and evidence for TEKT1 as a new candidate gene for motile ciliopathiesRebecca Ryan, Marion Failler, Madeline Louise Reilly, et al.
The European Respiratory Journal|November 11, 2017
Infertility in an adult cohort with primary ciliary dyskinesia: phenotype-gene associationGert Jan Vanaken, Laurence Bassinet, Mieke Boon, et al.
Journal of Medical Genetics|November 28, 2019
Deep phenotyping, including quantitative ciliary beating parameters, and extensive genotyping in primary ciliary dyskinesiaSylvain Blanchon, Marie Legendre, Mathieu Bottier, et al.
Journal of Clinical Medicine|September 9, 2022
Otological Manifestations in Adults with Primary Ciliary Dyskinesia: A Controlled Radio-Clinical StudyMihaela Alexandru, Paul de Boissieu, Farida Benoudiba, et al.
Biology of Reproduction|August 19, 2007
A heterozygous mutation disrupting the SPAG16 gene results in biochemical instability of central apparatus components of the human sperm axonemeZhibing Zhang, Maimoona A Zariwala, Maha M Mahadevan, et al.
Human Mutation|April 28, 2016
Mutations in GAS8, a Gene Encoding a Nexin-Dynein Regulatory Complex Subunit, Cause Primary Ciliary Dyskinesia with Axonemal DisorganizationLudovic Jeanson, Lucie Thomas, Bruno Copin, et al.
Reproductive Biomedicine Online|September 24, 2023
Results and perinatal outcomes from 189 ICSI cycles of couples with asthenozoospermic men and flagellar defects assessed by transmission electron microscopyAngèle Boursier, Augustin Boudry, Valérie Mitchell, et al.
American Journal of Human Genetics|December 1, 2009
Loss-of-function mutations in the human ortholog of Chlamydomonas reinhardtii ODA7 disrupt dynein arm assembly and cause primary ciliary dyskinesiaPhilippe Duquesnoy, Estelle Escudier, Laetitia Vincensini, et al.
Pageof 7