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Claudius Werner

Showing results (11-20 of 49) with videos related to

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Pediatric Research|January 14, 2016
Effect of TH2 cytokines and interferon gamma on beat frequency of human respiratory ciliaJoerg Grosse-Onnebrink, Claudius Werner, Niki Tomas Loges, et al.
The Pediatric Infectious Disease Journal|October 1, 2019
Acinetobacter baumannii Is a Risk Factor for Lower Respiratory Tract Infections in Children and Adolescents With a TracheostomyJoerg Grosse-Onnebrink, Johanna Rudloff, Christina Kessler, et al.
Human Reproduction (Oxford, England)|September 17, 2015
Ciliary function and motor protein composition of human fallopian tubesJohanna Raidt, Claudius Werner, Tabea Menchen, et al.
The European Respiratory Journal|September 5, 2014
Ciliary beat pattern and frequency in genetic variants of primary ciliary dyskinesiaJohanna Raidt, Julia Wallmeier, Rim Hjeij, et al.
Human Mutation|December 16, 2014
Mutations in CCDC11, which encodes a coiled-coil containing ciliary protein, causes situs inversus due to dysmotility of monocilia in the left-right organizerVijayashankaranarayanan Narasimhan, Rim Hjeij, Shubha Vij, et al.
Journal of Medical Genetics|April 26, 2020
TRAPγ-CDG shows asymmetric glycosylation and an effect on processing of proteins required in higher organismsSabine Dittner-Moormann, Charles Marques Lourenco, Janine Reunert, et al.
Annals of the American Thoracic Society|February 24, 2022
Limitations of Nasal Nitric Oxide Measurement for Diagnosis of Primary Ciliary Dyskinesia with Normal UltrastructureJohanna Raidt, Henrike Krenz, Johannes Tebbe, et al.
BMC Pulmonary Medicine|July 25, 2016
Study protocol, rationale and recruitment in a European multi-centre randomized controlled trial to determine the efficacy and safety of azithromycin maintenance therapy for 6 months in primary ciliary dyskinesiaHelene E Kobbernagel, Frederik F Buchvald, Eric G Haarman, et al.
Human Mutation|January 19, 2016
Systematic Analysis of CCNO Variants in a Defined Population: Implications for Clinical Phenotype and Differential DiagnosisIsrael Amirav, Julia Wallmeier, Niki T Loges, et al.
American Journal of Respiratory Cell and Molecular Biology|September 24, 2019
<i>SPEF2-</i> and <i>HYDIN</i>-Mutant Cilia Lack the Central Pair-associated Protein SPEF2, Aiding Primary Ciliary Dyskinesia DiagnosticsSandra Cindrić, Gerard W Dougherty, Heike Olbrich, et al.
Pageof 5

Showing results (11-20 of 49) with videos related to

Sort By:
Pageof 5
Pediatric Research|January 14, 2016
Effect of TH2 cytokines and interferon gamma on beat frequency of human respiratory ciliaJoerg Grosse-Onnebrink, Claudius Werner, Niki Tomas Loges, et al.
The Pediatric Infectious Disease Journal|October 1, 2019
Acinetobacter baumannii Is a Risk Factor for Lower Respiratory Tract Infections in Children and Adolescents With a TracheostomyJoerg Grosse-Onnebrink, Johanna Rudloff, Christina Kessler, et al.
Human Reproduction (Oxford, England)|September 17, 2015
Ciliary function and motor protein composition of human fallopian tubesJohanna Raidt, Claudius Werner, Tabea Menchen, et al.
The European Respiratory Journal|September 5, 2014
Ciliary beat pattern and frequency in genetic variants of primary ciliary dyskinesiaJohanna Raidt, Julia Wallmeier, Rim Hjeij, et al.
Human Mutation|December 16, 2014
Mutations in CCDC11, which encodes a coiled-coil containing ciliary protein, causes situs inversus due to dysmotility of monocilia in the left-right organizerVijayashankaranarayanan Narasimhan, Rim Hjeij, Shubha Vij, et al.
Journal of Medical Genetics|April 26, 2020
TRAPγ-CDG shows asymmetric glycosylation and an effect on processing of proteins required in higher organismsSabine Dittner-Moormann, Charles Marques Lourenco, Janine Reunert, et al.
Annals of the American Thoracic Society|February 24, 2022
Limitations of Nasal Nitric Oxide Measurement for Diagnosis of Primary Ciliary Dyskinesia with Normal UltrastructureJohanna Raidt, Henrike Krenz, Johannes Tebbe, et al.
BMC Pulmonary Medicine|July 25, 2016
Study protocol, rationale and recruitment in a European multi-centre randomized controlled trial to determine the efficacy and safety of azithromycin maintenance therapy for 6 months in primary ciliary dyskinesiaHelene E Kobbernagel, Frederik F Buchvald, Eric G Haarman, et al.
Human Mutation|January 19, 2016
Systematic Analysis of CCNO Variants in a Defined Population: Implications for Clinical Phenotype and Differential DiagnosisIsrael Amirav, Julia Wallmeier, Niki T Loges, et al.
American Journal of Respiratory Cell and Molecular Biology|September 24, 2019
<i>SPEF2-</i> and <i>HYDIN</i>-Mutant Cilia Lack the Central Pair-associated Protein SPEF2, Aiding Primary Ciliary Dyskinesia DiagnosticsSandra Cindrić, Gerard W Dougherty, Heike Olbrich, et al.
Pageof 5