Որոնման արդյունքները - Heymut Omran
- Ցուցադրվում են 1 - 20 արդյունքները 91
- Գնացեք Հաջորդ էջ
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The role of cilia for hydrocephalus formation Julia Wallmeier, Marlene Dallmayer, Heymut Omran
Հրապարակվել է 2022Revisão -
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The Emerging Genetics of Primary Ciliary Dyskinesia Maimoona A. Zariwala, Heymut Omran, Thomas W. Ferkol
Հրապարակվել է 2011Revisão -
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Primary ciliary dyskinesia in the genomics age Jane S. Lucas, Stephanie D. Davis, Heymut Omran, Amelia Shoemark
Հրապարակվել է 2019Revisão -
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U1 snRNA-mediated gene therapeutic correction of splice defects caused by an exceptionally mild BBS mutation F Schmid, Esther Glaus, Daniel Barthelmes, Manfred Fliegauf, Harald Gaspar, Gudrun Nürnberg, Peter Nürnberg, Heymut Omran, Wolfgang Berger, John Neidhardt
Հրապարակվել է 2011Artigo -
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First Reported Nosocomial Outbreak of Severe Acute Respiratory Syndrome Coronavirus 2 in a Pediatric Dialysis Unit Vera Schwierzeck, Jens König, Joachim Kühn, Alexander Mellmann, Carlos L. Correa-Martínez, Heymut Omran, Martin Konrad, Thomas Kaiser, Stefanie Kampmeier
Հրապարակվել է 2020Artigo -
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Mutation of <i>serine/threonine protein kinase 36</i> ( <i>STK36</i> ) causes primary ciliary dyskinesia with a central pair defect Christine Edelbusch, Sandra Cindrić, Gerard W. Dougherty, Niki T. Loges, Heike Olbrich, Joseph Rivlin, Julia Wallmeier, Petra Pennekamp, Israel Amirav, Heymut Omran
Հրապարակվել է 2017Artigo -
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<i>Cyclin O</i> ( <i>Ccno</i> ) functions during deuterosome‐mediated centriole amplification of multiciliated cells Maja C. Funk, Agata Bera, Tabea Menchen, Georg Kuales, Kerstin Thriene, Soeren S. Lienkamp, Jörn Dengjel, Heymut Omran, Marcus Frank, Sebastian J. Arnold
Հրապարակվել է 2015Artigo -
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Next generation massively parallel sequencing of targeted exomes to identify genetic mutations in primary ciliary dyskinesia: Implications for application to clinical testing Jonathan S. Berg, James P. Evans, Margaret W. Leigh, Heymut Omran, Chris Bizon, Ketan K. Mane, Michael R. Knowles, Karen E. Weck, Maimoona A. Zariwala
Հրապարակվել է 2011Artigo -
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Identification of a New Gene Locus for Adolescent Nephronophthisis, on Chromosome 3q22 in a Large Venezuelan Pedigree Heymut Omran, Carmen Fernández, Martin Jung, Karsten Häffner, Bernardo Fargier, Aminta Villaquiran, Rüdiger Waldherr, Norbert Gretz, M. Brandis, Franz Rüschendorf, André Reis, Friedhelm Hildebrandt
Հրապարակվել է 2000Artigo -
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Ciliary beat pattern and frequency in genetic variants of primary ciliary dyskinesia Johanna Raidt, Julia Wallmeier, Rim Hjeij, Jörg Große Onnebrink, Petra Pennekamp, Niki T. Loges, Heike Olbrich, Karsten Häffner, Gerard W. Dougherty, Heymut Omran, Claudius Werner
Հրապարակվել է 2014Artigo -
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Motility of efferent duct cilia aids passage of sperm cells through the male reproductive system Isabella Aprea, Tabea Nöthe-Menchen, Gerard W. Dougherty, Johanna Raidt, Niki T. Loges, Thomas Kaiser, Julia Wallmeier, Heike Olbrich, Timo Strünker, Sabine Kliesch, Petra Pennekamp, Heymut Omran
Հրապարակվել է 2021Artigo
Որոնման գործիքներ:
Առնչվող խորագիր
Biology
Genetics
Medicine
Gene
Cilium
Lung
Bronchiectasis
Primary ciliary dyskinesia
Internal medicine
Cell biology
Motile cilium
Flagellum
Microtubule
Phenotype
Dynein
Mutation
Pathology
Anatomy
Axoneme
Intraflagellar transport
Ciliogenesis
Ciliopathy
Disease
Ciliopathies
Mutant
Situs inversus
Dynein ATPase
Dyskinesia
Kartagener Syndrome
Parkinson's disease