检索结果 - Heymut Omran

Refine Results
  1. 1
    The role of cilia for hydrocephalus formation

    The role of cilia for hydrocephalus formation 由 Julia Wallmeier, Marlene Dallmayer, Heymut Omran

    出版 2022
    获取全文 获取全文
    Revisão
    加到收藏夹
    Saved in:
  2. 2
    Diagnosis and management of primary ciliary dyskinesia

    Diagnosis and management of primary ciliary dyskinesia 由 Claudius Werner, Jörg Große Onnebrink, Heymut Omran

    出版 2015
    获取全文 获取全文
    Artigo
    加到收藏夹
    Saved in:
  3. 3
    The Emerging Genetics of Primary Ciliary Dyskinesia

    The Emerging Genetics of Primary Ciliary Dyskinesia 由 Maimoona A. Zariwala, Heymut Omran, Thomas W. Ferkol

    出版 2011
    获取全文
    Revisão
    加到收藏夹
    Saved in:
  4. 4
    Multicilin drives centriole biogenesis via E2f proteins

    Multicilin drives centriole biogenesis via E2f proteins 由 Lina Ma, Ian K. Quigley, Heymut Omran, Chris Kintner

    出版 2014
    获取全文 获取全文
    Artigo
    加到收藏夹
    Saved in:
  5. 5
    Primary ciliary dyskinesia in the genomics age

    Primary ciliary dyskinesia in the genomics age 由 Jane S. Lucas, Stephanie D. Davis, Heymut Omran, Amelia Shoemark

    出版 2019
    获取全文
    Revisão
    加到收藏夹
    Saved in:
  6. 6
    Current and Future Treatments in Primary Ciliary Dyskinesia

    Current and Future Treatments in Primary Ciliary Dyskinesia 由 Tamara Paff, Heymut Omran, Kim G. Nielsen, Eric G. Haarman

    出版 2021
    获取全文 获取全文
    Revisão
    加到收藏夹
    Saved in:
  7. 7
    Nuclear Factor I X Deficiency Causes Brain Malformation and Severe Skeletal Defects

    Nuclear Factor I X Deficiency Causes Brain Malformation and Severe Skeletal Defects 由 Katrin Driller, Axel Pagenstecher, Markus Uhl, Heymut Omran, Ansgar Berlis, Albert Gründer, Albrecht E. Sippel

    出版 2007
    获取全文
    Artigo
    加到收藏夹
    Saved in:
  8. 8
    Tyrosine kinase 2 is not limiting human antiviral type III interferon responses

    Tyrosine kinase 2 is not limiting human antiviral type III interferon responses 由 Sebastian Fuchs, Petra Kaiser‐Labusch, Julia Bank, Sandra Ammann, Anja Kolb‐Kokocinski, Christine Edelbusch, Heymut Omran, Stephan Ehl

    出版 2016
    获取全文
    Artigo
    加到收藏夹
    Saved in:
  9. 9
    Diagnostic Role of Immunofluorescence Analysis in Primary Ciliary Dyskinesia-Suspected Individuals

    Diagnostic Role of Immunofluorescence Analysis in Primary Ciliary Dyskinesia-Suspected Individuals 由 Elif Karakoç, Rim Hjeij, Zeynep Bengisu Kaya, Nagehan Emiralioğlu, Dilber Ademhan Tural, Pergin Atilla, Uğur Özçelik, Heymut Omran

    出版 2025
    获取全文
    Artigo
    加到收藏夹
    Saved in:
  10. 10
    Ciliary function and motor protein composition of human fallopian tubes

    Ciliary function and motor protein composition of human fallopian tubes 由 Johanna Raidt, Claudius Werner, Tabea Menchen, Gerard W. Dougherty, Heike Olbrich, Niki T. Loges, Ralf Schmitz, Petra Pennekamp, Heymut Omran

    出版 2015
    获取全文 获取全文
    Artigo
    加到收藏夹
    Saved in:
  11. 11
    Consensus nomenclature for dyneins and associated assembly factors

    Consensus nomenclature for dyneins and associated assembly factors 由 Bryony Braschi, Heymut Omran, George B. Witman, Gregory J. Pazour, K. Kevin Pfister, Elspeth A. Bruford, Stephen M. King

    出版 2022
    获取全文
    Artigo
    加到收藏夹
    Saved in:
  12. 12
    Mislocalization of DNAH5 and DNAH9 in Respiratory Cells from Patients with Primary Ciliary Dyskinesia

    Mislocalization of DNAH5 and DNAH9 in Respiratory Cells from Patients with Primary Ciliary Dyskinesia 由 Manfred Fliegauf, Heike Olbrich, Judit Horváth, Johannes H. Wildhaber, Maimoona A. Zariwala, Marcus P. Kennedy, Michael R. Knowles, Heymut Omran

    出版 2005
    获取全文
    Artigo
    加到收藏夹
    Saved in:
  13. 13
    U1 snRNA-mediated gene therapeutic correction of splice defects caused by an exceptionally mild BBS mutation

    U1 snRNA-mediated gene therapeutic correction of splice defects caused by an exceptionally mild BBS mutation 由 F Schmid, Esther Glaus, Daniel Barthelmes, Manfred Fliegauf, Harald Gaspar, Gudrun Nürnberg, Peter Nürnberg, Heymut Omran, Wolfgang Berger, John Neidhardt

    出版 2011
    获取全文
    Artigo
    加到收藏夹
    Saved in:
  14. 14
    First Reported Nosocomial Outbreak of Severe Acute Respiratory Syndrome Coronavirus 2 in a Pediatric Dialysis Unit

    First Reported Nosocomial Outbreak of Severe Acute Respiratory Syndrome Coronavirus 2 in a Pediatric Dialysis Unit 由 Vera Schwierzeck, Jens König, Joachim Kühn, Alexander Mellmann, Carlos L. Correa-Martínez, Heymut Omran, Martin Konrad, Thomas Kaiser, Stefanie Kampmeier

    出版 2020
    获取全文 获取全文
    Artigo
    加到收藏夹
    Saved in:
  15. 15
    Mutation of <i>serine/threonine protein kinase 36</i> ( <i>STK36</i> ) causes primary ciliary dyskinesia with a central pair defect

    Mutation of <i>serine/threonine protein kinase 36</i> ( <i>STK36</i> ) causes primary ciliary dyskinesia with a central pair defect 由 Christine Edelbusch, Sandra Cindrić, Gerard W. Dougherty, Niki T. Loges, Heike Olbrich, Joseph Rivlin, Julia Wallmeier, Petra Pennekamp, Israel Amirav, Heymut Omran

    出版 2017
    获取全文
    Artigo
    加到收藏夹
    Saved in:
  16. 16
    <i>Cyclin O</i> ( <i>Ccno</i> ) functions during deuterosome‐mediated centriole amplification of multiciliated cells

    <i>Cyclin O</i> ( <i>Ccno</i> ) functions during deuterosome‐mediated centriole amplification of multiciliated cells 由 Maja C. Funk, Agata Bera, Tabea Menchen, Georg Kuales, Kerstin Thriene, Soeren S. Lienkamp, Jörn Dengjel, Heymut Omran, Marcus Frank, Sebastian J. Arnold

    出版 2015
    获取全文
    Artigo
    加到收藏夹
    Saved in:
  17. 17
    Next generation massively parallel sequencing of targeted exomes to identify genetic mutations in primary ciliary dyskinesia: Implications for application to clinical testing

    Next generation massively parallel sequencing of targeted exomes to identify genetic mutations in primary ciliary dyskinesia: Implications for application to clinical testing 由 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

    出版 2011
    获取全文 获取全文
    Artigo
    加到收藏夹
    Saved in:
  18. 18
    Identification of a New Gene Locus for Adolescent Nephronophthisis, on Chromosome 3q22 in a Large Venezuelan Pedigree

    Identification of a New Gene Locus for Adolescent Nephronophthisis, on Chromosome 3q22 in a Large Venezuelan Pedigree 由 Heymut Omran, Carmen Fernández, Martin Jung, Karsten Häffner, Bernardo Fargier, Aminta Villaquiran, Rüdiger Waldherr, Norbert Gretz, M. Brandis, Franz Rüschendorf, André Reis, Friedhelm Hildebrandt

    出版 2000
    获取全文
    Artigo
    加到收藏夹
    Saved in:
  19. 19
    Ciliary beat pattern and frequency in genetic variants of primary ciliary dyskinesia

    Ciliary beat pattern and frequency in genetic variants of primary ciliary dyskinesia 由 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

    出版 2014
    获取全文 获取全文
    Artigo
    加到收藏夹
    Saved in:
  20. 20
    Motility of efferent duct cilia aids passage of sperm cells through the male reproductive system

    Motility of efferent duct cilia aids passage of sperm cells through the male reproductive system 由 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

    出版 2021
    获取全文 获取全文
    Artigo
    加到收藏夹
    Saved in:

检索工具: