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Heymut Omran

Showing results (11-20 of 208) with videos related to

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Pediatric Nephrology (Berlin, Germany)|February 21, 2007
Nephrocystin and ciliary defects not only in the kidney?Christian von Schnakenburg, Manfred Fliegauf, Heymut Omran
Cardiology in the Young|July 28, 2022
Amiodarone-sirolimus interaction in a neonate with tuberous sclerosis complexDaniel Ebrahimi-Fakhari, Hans G Kehl, Heymut Omran
Annual Review of Physiology|October 25, 2006
Genetic defects in ciliary structure and functionMaimoona A Zariwala, Michael R Knowles, Heymut Omran
Current Opinion in Pulmonary Medicine|September 15, 2025
Primary ciliary dyskinesia phenotypes and correlation with genotypeAmjad Horani, Wallace Wee, Heymut Omran, et al.
Proceedings of the American Thoracic Society|September 20, 2011
The emerging genetics of primary ciliary dyskinesiaMaimoona A Zariwala, Heymut Omran, Thomas W Ferkol
Genes & Development|June 18, 2014
Multicilin drives centriole biogenesis via E2f proteinsLina Ma, Ian Quigley, Heymut Omran, et al.
Annals of Neurology|January 26, 2005
Autosomal recessive rippling muscle disease with homozygous CAV3 mutationsChristian Kubisch, Uwe-Peter Ketelsen, Ingrid Goebel, et al.
Journal of Pediatric Hematology/Oncology|August 18, 2017
Successful Extracorporeal Life Support in a Pediatric Hematopoietic Stem Cell Transplant Recipient With Periengraftment Respiratory FailureJenny Potratz, Martina Ahlmann, Claudia Rössig, et al.
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.
International Journal of Molecular Sciences|September 28, 2021
Current and Future Treatments in Primary Ciliary DyskinesiaTamara Paff, Heymut Omran, Kim G Nielsen, et al.
Pageof 21

Showing results (11-20 of 208) with videos related to

Sort By:
Pageof 21
Pediatric Nephrology (Berlin, Germany)|February 21, 2007
Nephrocystin and ciliary defects not only in the kidney?Christian von Schnakenburg, Manfred Fliegauf, Heymut Omran
Cardiology in the Young|July 28, 2022
Amiodarone-sirolimus interaction in a neonate with tuberous sclerosis complexDaniel Ebrahimi-Fakhari, Hans G Kehl, Heymut Omran
Annual Review of Physiology|October 25, 2006
Genetic defects in ciliary structure and functionMaimoona A Zariwala, Michael R Knowles, Heymut Omran
Current Opinion in Pulmonary Medicine|September 15, 2025
Primary ciliary dyskinesia phenotypes and correlation with genotypeAmjad Horani, Wallace Wee, Heymut Omran, et al.
Proceedings of the American Thoracic Society|September 20, 2011
The emerging genetics of primary ciliary dyskinesiaMaimoona A Zariwala, Heymut Omran, Thomas W Ferkol
Genes & Development|June 18, 2014
Multicilin drives centriole biogenesis via E2f proteinsLina Ma, Ian Quigley, Heymut Omran, et al.
Annals of Neurology|January 26, 2005
Autosomal recessive rippling muscle disease with homozygous CAV3 mutationsChristian Kubisch, Uwe-Peter Ketelsen, Ingrid Goebel, et al.
Journal of Pediatric Hematology/Oncology|August 18, 2017
Successful Extracorporeal Life Support in a Pediatric Hematopoietic Stem Cell Transplant Recipient With Periengraftment Respiratory FailureJenny Potratz, Martina Ahlmann, Claudia Rössig, et al.
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.
International Journal of Molecular Sciences|September 28, 2021
Current and Future Treatments in Primary Ciliary DyskinesiaTamara Paff, Heymut Omran, Kim G Nielsen, et al.
Pageof 21