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Claudius Werner

Showing results (41-50 of 49) with videos related to

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American Journal of Respiratory Cell and Molecular Biology|February 25, 2016
DNAH11 Localization in the Proximal Region of Respiratory Cilia Defines Distinct Outer Dynein Arm ComplexesGerard W Dougherty, Niki T Loges, Judith A Klinkenbusch, et al.
The European Respiratory Journal|November 13, 2016
European Respiratory Society guidelines for the diagnosis of primary ciliary dyskinesiaJane S Lucas, Angelo Barbato, Samuel A Collins, et al.
Respiratory Medicine|October 4, 2016
Primary ciliary dyskinesia in Israel: Prevalence, clinical features, current diagnosis and management practicesRevital Abitbul, Israel Amirav, Hannah Blau, et al.
American Journal of Human Genetics|September 6, 2014
CCDC151 mutations cause primary ciliary dyskinesia by disruption of the outer dynein arm docking complex formationRim Hjeij, Alexandros Onoufriadis, Christopher M Watson, et al.
Archives of Disease in Childhood. Fetal and Neonatal Edition|June 29, 2019
Active perinatal care of preterm infants in the German Neonatal NetworkAlexander Humberg, Christoph Härtel, Tanja K Rausch, et al.
Nature Genetics|July 23, 2013
DYX1C1 is required for axonemal dynein assembly and ciliary motilityAarti Tarkar, Niki T Loges, Christopher E Slagle, et al.
American Journal of Human Genetics|September 24, 2013
Mutations in SPAG1 cause primary ciliary dyskinesia associated with defective outer and inner dynein armsMichael R Knowles, Lawrence E Ostrowski, Niki T Loges, et al.
Nature Communications|November 3, 2020
CFAP45 deficiency causes situs abnormalities and asthenospermia by disrupting an axonemal adenine nucleotide homeostasis moduleGerard W Dougherty, Katsutoshi Mizuno, Tabea Nöthe-Menchen, et al.
American Journal of Human Genetics|July 30, 2013
ZMYND10 is mutated in primary ciliary dyskinesia and interacts with LRRC6Maimoona A Zariwala, Heon Yung Gee, Małgorzata Kurkowiak, et al.
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Showing results (41-50 of 49) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 49 results.
American Journal of Respiratory Cell and Molecular Biology|February 25, 2016
DNAH11 Localization in the Proximal Region of Respiratory Cilia Defines Distinct Outer Dynein Arm ComplexesGerard W Dougherty, Niki T Loges, Judith A Klinkenbusch, et al.
The European Respiratory Journal|November 13, 2016
European Respiratory Society guidelines for the diagnosis of primary ciliary dyskinesiaJane S Lucas, Angelo Barbato, Samuel A Collins, et al.
Respiratory Medicine|October 4, 2016
Primary ciliary dyskinesia in Israel: Prevalence, clinical features, current diagnosis and management practicesRevital Abitbul, Israel Amirav, Hannah Blau, et al.
American Journal of Human Genetics|September 6, 2014
CCDC151 mutations cause primary ciliary dyskinesia by disruption of the outer dynein arm docking complex formationRim Hjeij, Alexandros Onoufriadis, Christopher M Watson, et al.
Archives of Disease in Childhood. Fetal and Neonatal Edition|June 29, 2019
Active perinatal care of preterm infants in the German Neonatal NetworkAlexander Humberg, Christoph Härtel, Tanja K Rausch, et al.
Nature Genetics|July 23, 2013
DYX1C1 is required for axonemal dynein assembly and ciliary motilityAarti Tarkar, Niki T Loges, Christopher E Slagle, et al.
American Journal of Human Genetics|September 24, 2013
Mutations in SPAG1 cause primary ciliary dyskinesia associated with defective outer and inner dynein armsMichael R Knowles, Lawrence E Ostrowski, Niki T Loges, et al.
Nature Communications|November 3, 2020
CFAP45 deficiency causes situs abnormalities and asthenospermia by disrupting an axonemal adenine nucleotide homeostasis moduleGerard W Dougherty, Katsutoshi Mizuno, Tabea Nöthe-Menchen, et al.
American Journal of Human Genetics|July 30, 2013
ZMYND10 is mutated in primary ciliary dyskinesia and interacts with LRRC6Maimoona A Zariwala, Heon Yung Gee, Małgorzata Kurkowiak, et al.
Pageof 5