Search research articles
Contact Us
Filters
Showing results (21-30 of 31) with videos related to
Page
of 4
Sort By:
Nature Communications
|
July 23, 2014
MCIDAS mutations result in a mucociliary clearance disorder with reduced generation of multiple motile cilia
Mieke 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 Disassembly
Merit Wildung, Christian Herr, Dietmar Riedel, et al.
Human Mutation
|
November 1, 2020
Loss of CBY1 results in a ciliopathy characterized by features of Joubert syndrome
Daniel Epting, Lokuliyange D S Senaratne, Elisabeth Ott, et al.
F1000Research
|
October 30, 2016
Collecting clinical data in primary ciliary dyskinesia- challenges and opportunities
Israel 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 Complexes
Gerard 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 practices
Revital 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 Asymmetry
Julia 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 arms
Michael 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 module
Gerard 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 microtubules
Daniel O Dodd, Sabrina Mechaussier, Patricia L Yeyati, et al.
Page
of 4
Search research articles
Search
Showing results (21-30 of 31) with videos related to
Sort By:
Page
of 4
Nature Communications
|
July 23, 2014
MCIDAS mutations result in a mucociliary clearance disorder with reduced generation of multiple motile cilia
Mieke 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 Disassembly
Merit Wildung, Christian Herr, Dietmar Riedel, et al.
Human Mutation
|
November 1, 2020
Loss of CBY1 results in a ciliopathy characterized by features of Joubert syndrome
Daniel Epting, Lokuliyange D S Senaratne, Elisabeth Ott, et al.
F1000Research
|
October 30, 2016
Collecting clinical data in primary ciliary dyskinesia- challenges and opportunities
Israel 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 Complexes
Gerard 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 practices
Revital 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 Asymmetry
Julia 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 arms
Michael 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 module
Gerard 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 microtubules
Daniel O Dodd, Sabrina Mechaussier, Patricia L Yeyati, et al.
Page
of 4