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

Julia Wallmeier

Showing results (1-10 of 31) with videos related to

Pageof 4
Sort By:
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|April 26, 2022
The role of cilia for hydrocephalus formationJulia Wallmeier, Marlene Dallmayer, Heymut Omran
The Clinical Respiratory Journal|March 4, 2017
DYNC2H1 mutation causes Jeune syndrome and recurrent lung infections associated with ciliopathyNagehan Emiralioglu, Julia Wallmeier, Heike Olbrich, et al.
Presse Medicale (Paris, France : 1983)|July 29, 2023
Primary ciliary dyskinesiaJohanna Raidt, Niki Tomas Loges, Heike Olbrich, et al.
European Archives of Oto-Rhino-Laryngology : Official Journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : Affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery|July 24, 2010
ENT manifestations in patients with primary ciliary dyskinesia: prevalence and significance of otorhinolaryngologic co-morbiditiesJ Ulrich Sommer, Kerstin Schäfer, Heymut Omran, et al.
Nature Reviews. Disease Primers|September 18, 2020
Motile ciliopathiesJulia Wallmeier, Kim G Nielsen, Claudia E Kuehni, et al.
Human Mutation|May 26, 2017
Mutation of serine/threonine protein kinase 36 (STK36) causes primary ciliary dyskinesia with a central pair defectChristine Edelbusch, Sandra Cindrić, Gerard W Dougherty, 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.
Circulation. Genomic and Precision Medicine|October 23, 2019
Randomization of Left-right Asymmetry and Congenital Heart Defects: The Role of <i>DNAH5</i> in Humans and MiceTabea Nöthe-Menchen, Julia Wallmeier, Petra Pennekamp, et al.
Molecular Human Reproduction|February 9, 2021
Motility of efferent duct cilia aids passage of sperm cells through the male reproductive systemIsabella Aprea, Tabea Nöthe-Menchen, Gerard W Dougherty, 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.
Pageof 4

Showing results (1-10 of 31) with videos related to

Sort By:
Pageof 4
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|April 26, 2022
The role of cilia for hydrocephalus formationJulia Wallmeier, Marlene Dallmayer, Heymut Omran
The Clinical Respiratory Journal|March 4, 2017
DYNC2H1 mutation causes Jeune syndrome and recurrent lung infections associated with ciliopathyNagehan Emiralioglu, Julia Wallmeier, Heike Olbrich, et al.
Presse Medicale (Paris, France : 1983)|July 29, 2023
Primary ciliary dyskinesiaJohanna Raidt, Niki Tomas Loges, Heike Olbrich, et al.
European Archives of Oto-Rhino-Laryngology : Official Journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : Affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery|July 24, 2010
ENT manifestations in patients with primary ciliary dyskinesia: prevalence and significance of otorhinolaryngologic co-morbiditiesJ Ulrich Sommer, Kerstin Schäfer, Heymut Omran, et al.
Nature Reviews. Disease Primers|September 18, 2020
Motile ciliopathiesJulia Wallmeier, Kim G Nielsen, Claudia E Kuehni, et al.
Human Mutation|May 26, 2017
Mutation of serine/threonine protein kinase 36 (STK36) causes primary ciliary dyskinesia with a central pair defectChristine Edelbusch, Sandra Cindrić, Gerard W Dougherty, 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.
Circulation. Genomic and Precision Medicine|October 23, 2019
Randomization of Left-right Asymmetry and Congenital Heart Defects: The Role of <i>DNAH5</i> in Humans and MiceTabea Nöthe-Menchen, Julia Wallmeier, Petra Pennekamp, et al.
Molecular Human Reproduction|February 9, 2021
Motility of efferent duct cilia aids passage of sperm cells through the male reproductive systemIsabella Aprea, Tabea Nöthe-Menchen, Gerard W Dougherty, 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.
Pageof 4