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Julia Wallmeier

Showing results (11-20 of 31) with videos related to

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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.
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 Human Genetics|September 22, 2015
Loss-of-Function GAS8 Mutations Cause Primary Ciliary Dyskinesia and Disrupt the Nexin-Dynein Regulatory ComplexHeike Olbrich, Carolin Cremers, Niki T Loges, et al.
American Journal of Human Genetics|June 2, 2021
Mutations in TP73 cause impaired mucociliary clearance and lissencephalyJulia Wallmeier, Diana Bracht, Hessa S Alsaif, et al.
The European Respiratory Journal|December 15, 2015
An international registry for primary ciliary dyskinesiaClaudius Werner, Martin Lablans, Maximilian Ataian, et al.
American Journal of Human Genetics|August 4, 2016
TTC25 Deficiency Results in Defects of the Outer Dynein Arm Docking Machinery and Primary Ciliary Dyskinesia with Left-Right Body Asymmetry RandomizationJulia Wallmeier, Hidetaka Shiratori, Gerard W Dougherty, et al.
American Journal of Human Genetics|May 5, 2018
Mutations in C11orf70 Cause Primary Ciliary Dyskinesia with Randomization of Left/Right Body Asymmetry Due to Defects of Outer and Inner Dynein ArmsInga M Höben, Rim Hjeij, Heike Olbrich, et al.
Iscience|February 3, 2025
Pathogenic <i>KIAA0586/TALPID3</i> variants are associated with defects in primary and motile ciliaJacqueline E Taudien, Diana Bracht, Heike Olbrich, et al.
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.
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.
Pageof 4

Showing results (11-20 of 31) with videos related to

Sort By:
Pageof 4
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.
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 Human Genetics|September 22, 2015
Loss-of-Function GAS8 Mutations Cause Primary Ciliary Dyskinesia and Disrupt the Nexin-Dynein Regulatory ComplexHeike Olbrich, Carolin Cremers, Niki T Loges, et al.
American Journal of Human Genetics|June 2, 2021
Mutations in TP73 cause impaired mucociliary clearance and lissencephalyJulia Wallmeier, Diana Bracht, Hessa S Alsaif, et al.
The European Respiratory Journal|December 15, 2015
An international registry for primary ciliary dyskinesiaClaudius Werner, Martin Lablans, Maximilian Ataian, et al.
American Journal of Human Genetics|August 4, 2016
TTC25 Deficiency Results in Defects of the Outer Dynein Arm Docking Machinery and Primary Ciliary Dyskinesia with Left-Right Body Asymmetry RandomizationJulia Wallmeier, Hidetaka Shiratori, Gerard W Dougherty, et al.
American Journal of Human Genetics|May 5, 2018
Mutations in C11orf70 Cause Primary Ciliary Dyskinesia with Randomization of Left/Right Body Asymmetry Due to Defects of Outer and Inner Dynein ArmsInga M Höben, Rim Hjeij, Heike Olbrich, et al.
Iscience|February 3, 2025
Pathogenic <i>KIAA0586/TALPID3</i> variants are associated with defects in primary and motile ciliaJacqueline E Taudien, Diana Bracht, Heike Olbrich, et al.
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.
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.
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