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Julia Wallmeier

Showing results (21-30 of 31) with videos related to

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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.
International Journal of Molecular Sciences|July 27, 2022
miR449 Protects Airway Regeneration by Controlling AURKA/HDAC6-Mediated Ciliary DisassemblyMerit Wildung, Christian Herr, Dietmar Riedel, et al.
Human Mutation|November 1, 2020
Loss of CBY1 results in a ciliopathy characterized by features of Joubert syndromeDaniel Epting, Lokuliyange D S Senaratne, Elisabeth Ott, et al.
F1000Research|October 30, 2016
Collecting clinical data in primary ciliary dyskinesia- challenges and opportunitiesIsrael Amirav, Mary Roduta Roberts, Huda Mussaffi, et al.
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.
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|October 22, 2019
De Novo Mutations in FOXJ1 Result in a Motile Ciliopathy with Hydrocephalus and Randomization of Left/Right Body AsymmetryJulia Wallmeier, Diana Frank, Amelia Shoemark, 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.
Science (New York, N.Y.)|April 25, 2024
Ciliopathy patient variants reveal organelle-specific functions for TUBB4B in axonemal microtubulesDaniel O Dodd, Sabrina Mechaussier, Patricia L Yeyati, et al.
Pageof 4

Showing results (21-30 of 31) with videos related to

Sort By:
Pageof 4
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.
International Journal of Molecular Sciences|July 27, 2022
miR449 Protects Airway Regeneration by Controlling AURKA/HDAC6-Mediated Ciliary DisassemblyMerit Wildung, Christian Herr, Dietmar Riedel, et al.
Human Mutation|November 1, 2020
Loss of CBY1 results in a ciliopathy characterized by features of Joubert syndromeDaniel Epting, Lokuliyange D S Senaratne, Elisabeth Ott, et al.
F1000Research|October 30, 2016
Collecting clinical data in primary ciliary dyskinesia- challenges and opportunitiesIsrael Amirav, Mary Roduta Roberts, Huda Mussaffi, et al.
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.
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|October 22, 2019
De Novo Mutations in FOXJ1 Result in a Motile Ciliopathy with Hydrocephalus and Randomization of Left/Right Body AsymmetryJulia Wallmeier, Diana Frank, Amelia Shoemark, 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.
Science (New York, N.Y.)|April 25, 2024
Ciliopathy patient variants reveal organelle-specific functions for TUBB4B in axonemal microtubulesDaniel O Dodd, Sabrina Mechaussier, Patricia L Yeyati, et al.
Pageof 4