Hasil Pencarian - Heymut Omran

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  1. 1
    Current and Future Treatments in Primary Ciliary Dyskinesia

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

    Diterbitkan 2021-09-01
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  2. 2
    Novel pathogenic variants of DNAH5 associated with clinical and genetic spectra of primary ciliary dyskinesia in an Arab population

    Novel pathogenic variants of DNAH5 associated with clinical and genetic spectra of primary ciliary dyskinesia in an Arab population oleh Dalal A. Al-Mutairi, Basel H. Alsabah, Petra Pennekamp, Heymut Omran

    Diterbitkan 2024-07-01
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  3. 3
    A novel hypomorphic allele of Spag17 causes primary ciliary dyskinesia phenotypes in mice

    A novel hypomorphic allele of Spag17 causes primary ciliary dyskinesia phenotypes in mice oleh Zakia Abdelhamed, Marshall Lukacs, Sandra Cindric, Heymut Omran, Rolf W. Stottmann

    Diterbitkan 2020-10-01
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  4. 4
    Mucociliary Wnt signaling promotes cilia biogenesis and beating

    Mucociliary Wnt signaling promotes cilia biogenesis and beating oleh Carina Seidl, Fabio Da Silva, Kaiqing Zhang, Kai Wohlgemuth, Heymut Omran, Christof Niehrs

    Diterbitkan 2023-03-01
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  5. 5
    Correction: A novel hypomorphic allele of Spag17 causes primary ciliary dyskinesia phenotypes in mice

    Correction: A novel hypomorphic allele of Spag17 causes primary ciliary dyskinesia phenotypes in mice oleh Zakia Abdelhamed, Marshall Lukacs, Sandra Cindric, Saima Ali, Heymut Omran, Rolf W. Stottmann

    Diterbitkan 2021-01-01
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  6. 6
    Molecular defects in primary ciliary dyskinesia are associated with agenesis of the frontal and sphenoid paranasal sinuses and chronic rhinosinusitis

    Molecular defects in primary ciliary dyskinesia are associated with agenesis of the frontal and sphenoid paranasal sinuses and chronic rhinosinusitis oleh Andre Schramm, Johanna Raidt, Anika Gross, Maik Böhmer, Achim Georg Beule, Heymut Omran

    Diterbitkan 2023-10-01
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  7. 7
    Identification of a novel founder variant in DNAI2 cause primary ciliary dyskinesia in five consanguineous families derived from a single tribe descendant of Arabian Peninsula

    Identification of a novel founder variant in DNAI2 cause primary ciliary dyskinesia in five consanguineous families derived from a single tribe descendant of Arabian Peninsula oleh Dalal A. Al-Mutairi, Basel H. Alsabah, Bashar A. Alkhaledi, Petra Pennekamp, Heymut Omran

    Diterbitkan 2022-10-01
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  8. 8
    Target discovery screens using pooled shRNA libraries and next-generation sequencing: A model workflow and analytical algorithm.

    Target discovery screens using pooled shRNA libraries and next-generation sequencing: A model workflow and analytical algorithm. oleh Christiane Schaefer, Nikhil Mallela, Jochen Seggewiß, Birgit Lechtape, Heymut Omran, Uta Dirksen, Eberhard Korsching, Jenny Potratz

    Diterbitkan 2018-01-01
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  9. 9
    Extracorporeal Membrane Oxygenation in Children With Cancer or Hematopoietic Cell Transplantation: Single-Center Experience in 20 Consecutive Patients

    Extracorporeal Membrane Oxygenation in Children With Cancer or Hematopoietic Cell Transplantation: Single-Center Experience in 20 Consecutive Patients oleh Jenny C. Potratz, Sarah Guddorf, Martina Ahlmann, Maria Tekaat, Claudia Rossig, Heymut Omran, Katja Masjosthusmann, Andreas H. Groll

    Diterbitkan 2021-04-01
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  10. 10
    Crisponi syndrome/cold-induced sweating syndrome type 2: Reprogramming of CS/CISS2 individual derived fibroblasts into three clones of one iPSC line

    Crisponi syndrome/cold-induced sweating syndrome type 2: Reprogramming of CS/CISS2 individual derived fibroblasts into three clones of one iPSC line oleh Insa Buers, Lara Schöning, Niki Tomas Loges, Yvonne Nitschke, Inga Marlena Höben, Albrecht Röpke, Laura Crisponi, Heymut Omran, Frank Rutsch

    Diterbitkan 2020-07-01
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  11. 11
    Primary Ciliary Dyskinesia Associated Disease-Causing Variants in <i>CCDC39</i> and <i>CCDC40</i> Cause Axonemal Absence of Inner Dynein Arm Heavy Chains DNAH1, DNAH6, and DNAH7

    Primary Ciliary Dyskinesia Associated Disease-Causing Variants in <i>CCDC39</i> and <i>CCDC40</i> Cause Axonemal Absence of Inner Dynein Arm Heavy Chains DNAH1, DNAH6, and DNAH7 oleh Alina Wilken, Inga Marlena Höben, Alexander Wolter, Niki Tomas Loges, Heike Olbrich, Isabella Aprea, Bernd Dworniczak, Johanna Raidt, Heymut Omran

    Diterbitkan 2024-07-01
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  12. 12
    Generation of induced pluripotent stem cell lines from a Crisponi/Cold induced sweating syndrome type 1 individual

    Generation of induced pluripotent stem cell lines from a Crisponi/Cold induced sweating syndrome type 1 individual oleh Lara Schöning, Niki Tomas Loges, Yvonne Nitschke, Inga Marlena Höben, Albrecht Röpke, Laura Crisponi, Heymut Omran, Frank Rutsch, Insa Buers

    Diterbitkan 2020-07-01
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  13. 13
    Registries and collaborative studies for primary ciliary dyskinesia in Europe

    Registries and collaborative studies for primary ciliary dyskinesia in Europe oleh Cristina Ardura-Garcia, Myrofora Goutaki, Siobhán B. Carr, Suzanne Crowley, Florian S. Halbeisen, Kim G. Nielsen, Petra Pennekamp, Johanna Raidt, Guillaume Thouvenin, Panayiotis K. Yiallouros, Heymut Omran, Claudia E. Kuehni

    Diterbitkan 2020-05-01
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  14. 14
    Defects in the cytoplasmic assembly of axonemal dynein arms cause morphological abnormalities and dysmotility in sperm cells leading to male infertility.

    Defects in the cytoplasmic assembly of axonemal dynein arms cause morphological abnormalities and dysmotility in sperm cells leading to male infertility. oleh Isabella Aprea, Johanna Raidt, Inga Marlena Höben, Niki Tomas Loges, Tabea Nöthe-Menchen, Petra Pennekamp, Heike Olbrich, Thomas Kaiser, Luisa Biebach, Frank Tüttelmann, Judit Horvath, Maria Schubert, Claudia Krallmann, Sabine Kliesch, Heymut Omran

    Diterbitkan 2021-02-01
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  15. 15
    Biallelic Variants in <i>MNS1</i> Are Associated with Laterality Defects and Respiratory Involvement

    Biallelic Variants in <i>MNS1</i> Are Associated with Laterality Defects and Respiratory Involvement oleh Rim Hjeij, Joseph Leslie, Hoda Rizk, Bernd Dworniczak, Heike Olbrich, Johanna Raidt, Sebastian Felix Nepomuk Bode, Alice Gardham, Karen Stals, Mohammad Al-Haggar, Engy Osman, Andrew Crosby, Tarek Eldesoky, Emma Baple, Heymut Omran

    Diterbitkan 2024-06-01
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  16. 16
    International BEAT-PCD consensus statement for infection prevention and control for primary ciliary dyskinesia in collaboration with ERN-LUNG PCD Core Network and patient representatives

    International BEAT-PCD consensus statement for infection prevention and control for primary ciliary dyskinesia in collaboration with ERN-LUNG PCD Core Network and patient represent... oleh June K. Marthin, Jane S. Lucas, Mieke Boon, Carmen Casaulta, Suzanne Crowley, Damien M.S. Destouches, Ernst Eber, Amparo Escribano, Eric Haarman, Claire Hogg, Bernard Maitre, Gemma Marsh, Vendula Martinu, Antonio Moreno-Galdó, Huda Mussaffi, Heymut Omran, Petr Pohunek, Bernhard Rindlisbacher, Phil Robinson, Deborah Snijders, Woolf T. Walker, Panayiotis Yiallouros, Helle Krogh Johansen, Kim G. Nielsen

    Diterbitkan 2021-08-01
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  17. 17
    Access to medicines for rare diseases: beating the drum for primary ciliary dyskinesia

    Access to medicines for rare diseases: beating the drum for primary ciliary dyskinesia oleh Suzanne Crowley, Inês Azevedo, Mieke Boon, Andrew Bush, Ernst Eber, Eric Haarman, Bulent Karadag, Karsten Kötz, Margaret Leigh, Antonio Moreno-Galdó, Huda Mussaffi, Kim G. Nielsen, Heymut Omran, Jean-François Papon, Petr Pohunek, Kostas Priftis, Bernhard Rindlisbacher, Francesca Santamaria, Arunas Valiulis, Michal Witt, Panayiotis Yiallouros, Zorica Zivkovic, Claudia E. Kuehni, Jane S. Lucas

    Diterbitkan 2020-09-01
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  18. 18
    Homozygous loss-of-function mutations in MNS1 cause laterality defects and likely male infertility.

    Homozygous loss-of-function mutations in MNS1 cause laterality defects and likely male infertility. oleh Asaf Ta-Shma, Rim Hjeij, Zeev Perles, Gerard W Dougherty, Ibrahim Abu Zahira, Stef J F Letteboer, Dinu Antony, Alaa Darwish, Dorus A Mans, Sabrina Spittler, Christine Edelbusch, Sandra Cindrić, Tabea Nöthe-Menchen, Heike Olbrich, Friederike Stuhlmann, Isabella Aprea, Petra Pennekamp, Niki T Loges, Oded Breuer, Avraham Shaag, Azaria J J T Rein, Elif Yilmaz Gulec, Alper Gezdirici, Revital Abitbul, Nael Elias, Israel Amirav, Miriam Schmidts, Ronald Roepman, Orly Elpeleg, Heymut Omran

    Diterbitkan 2018-08-01
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  19. 19
    Collecting clinical data in primary ciliary dyskinesia- challenges and opportunities [version 2; referees: 2 approved]

    Collecting clinical data in primary ciliary dyskinesia- challenges and opportunities [version 2; referees: 2 approved] oleh Israel Amirav, Mary Roduta Roberts, Huda Mussaffi, Avigdor Mandelberg, Yehudah Roth, Revital Abitbul, Anthony Luder, Hannah Blau, Soliman Alkrinawi, Micha Aviram, Marta Ben-Ami, Moshe Rotschild, Lea Bentur, David Shoseyov, Malena Cohen-Cymberknoh, Eitan Kerem, Avraham Avital, Chaim Springer, Avigdor Hevroni, Husein Dabbah, Arnon Elizur, Elie Picard, Shmuel Goldberg, Joseph Rivlin, Galit Livnat, Moran Lavie, Nael Alias, Ruth Soferman, Heike Olbrich, Johanna Raidt, Julia Wallmeier, Claudius Werner, Niki T. Loges, Heymut Omran

    Diterbitkan 2016-10-01
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  20. 20
    Collecting clinical data in primary ciliary dyskinesia- challenges and opportunities [version 1; referees: 2 approved]

    Collecting clinical data in primary ciliary dyskinesia- challenges and opportunities [version 1; referees: 2 approved] oleh Israel Amirav, Mary Roduta Roberts, Huda Mussaffi, Avigdor Mandelberg, Yehudah Roth, Revital Abitbul, Anthony Luder, Hannah Blau, Soliman Alkrinawi, Micha Aviram, Marta Ben-Ami, Moshe Rotschild, Lea Bentur, David Shoseyov, Malena Cohen-Cymberknoh, Eitan Kerem, Avraham Avital, Chaim Springer, Avigdor Hevroni, Husein Dabbah, Arnon Elizur, Elie Picard, Shmuel Goldberg, Joseph Rivlin, Galit Livnat, Moran Lavie, Nael Alias, Ruth Soferman, Heike Olbrich, Johanna Raidt, Julia Wallmeier, Claudius Werner, Niki T. Loges, Heymut Omran

    Diterbitkan 2016-08-01
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