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

Claudius Werner

Showing results (31-40 of 49) with videos related to

Pageof 5
Sort By:
American Journal of Respiratory Cell and Molecular Biology|March 20, 2015
Immunofluorescence Analysis and Diagnosis of Primary Ciliary Dyskinesia with Radial Spoke DefectsAdrien Frommer, Rim Hjeij, Niki T Loges, et al.
Thorax|December 21, 2011
Mutations of DNAH11 in patients with primary ciliary dyskinesia with normal ciliary ultrastructureMichael R Knowles, Margaret W Leigh, Johnny L Carson, et al.
American Journal of Human Genetics|November 26, 2018
Recessive DNAH9 Loss-of-Function Mutations Cause Laterality Defects and Subtle Respiratory Ciliary-Beating DefectsNiki T Loges, Dinu Antony, Ales Maver, et al.
Nature Genetics|April 22, 2014
Mutations in CCNO result in congenital mucociliary clearance disorder with reduced generation of multiple motile ciliaJulia Wallmeier, Dalal A Al-Mutairi, Chun-Ting Chen, et al.
Nature Communications|July 23, 2014
MCIDAS mutations result in a mucociliary clearance disorder with reduced generation of multiple motile ciliaMieke Boon, Julia Wallmeier, Lina Ma, et al.
The European Respiratory Journal|January 6, 2017
The international primary ciliary dyskinesia cohort (iPCD Cohort): methods and first resultsMyrofora Goutaki, Elisabeth Maurer, Florian S Halbeisen, et al.
Respiratory Research|September 20, 2019
Prevalence and course of disease after lung resection in primary ciliary dyskinesia: a cohort & nested case-control studyPanayiotis Kouis, Myrofora Goutaki, Florian S Halbeisen, et al.
Nature Genetics|May 15, 2012
CCDC103 mutations cause primary ciliary dyskinesia by disrupting assembly of ciliary dynein armsJennifer R Panizzi, Anita Becker-Heck, Victoria H Castleman, et al.
American Journal of Human Genetics|July 16, 2013
ARMC4 mutations cause primary ciliary dyskinesia with randomization of left/right body asymmetryRim Hjeij, Anna Lindstrand, Richard Francis, et al.
F1000Research|October 30, 2016
Collecting clinical data in primary ciliary dyskinesia- challenges and opportunitiesIsrael Amirav, Mary Roduta Roberts, Huda Mussaffi, et al.
Pageof 5

Showing results (31-40 of 49) with videos related to

Sort By:
Pageof 5
American Journal of Respiratory Cell and Molecular Biology|March 20, 2015
Immunofluorescence Analysis and Diagnosis of Primary Ciliary Dyskinesia with Radial Spoke DefectsAdrien Frommer, Rim Hjeij, Niki T Loges, et al.
Thorax|December 21, 2011
Mutations of DNAH11 in patients with primary ciliary dyskinesia with normal ciliary ultrastructureMichael R Knowles, Margaret W Leigh, Johnny L Carson, et al.
American Journal of Human Genetics|November 26, 2018
Recessive DNAH9 Loss-of-Function Mutations Cause Laterality Defects and Subtle Respiratory Ciliary-Beating DefectsNiki T Loges, Dinu Antony, Ales Maver, et al.
Nature Genetics|April 22, 2014
Mutations in CCNO result in congenital mucociliary clearance disorder with reduced generation of multiple motile ciliaJulia Wallmeier, Dalal A Al-Mutairi, Chun-Ting Chen, et al.
Nature Communications|July 23, 2014
MCIDAS mutations result in a mucociliary clearance disorder with reduced generation of multiple motile ciliaMieke Boon, Julia Wallmeier, Lina Ma, et al.
The European Respiratory Journal|January 6, 2017
The international primary ciliary dyskinesia cohort (iPCD Cohort): methods and first resultsMyrofora Goutaki, Elisabeth Maurer, Florian S Halbeisen, et al.
Respiratory Research|September 20, 2019
Prevalence and course of disease after lung resection in primary ciliary dyskinesia: a cohort & nested case-control studyPanayiotis Kouis, Myrofora Goutaki, Florian S Halbeisen, et al.
Nature Genetics|May 15, 2012
CCDC103 mutations cause primary ciliary dyskinesia by disrupting assembly of ciliary dynein armsJennifer R Panizzi, Anita Becker-Heck, Victoria H Castleman, et al.
American Journal of Human Genetics|July 16, 2013
ARMC4 mutations cause primary ciliary dyskinesia with randomization of left/right body asymmetryRim Hjeij, Anna Lindstrand, Richard Francis, et al.
F1000Research|October 30, 2016
Collecting clinical data in primary ciliary dyskinesia- challenges and opportunitiesIsrael Amirav, Mary Roduta Roberts, Huda Mussaffi, et al.
Pageof 5