Zobrazeno 1 - 10
of 58
pro vyhledávání: '"Anita Becker"'
Autor:
Anita Becker
Transesterification is an organic reaction in which the organic group R′′ of an ester is exchanged with another organic group R′ of an alcohol according to a mechanism called alcoholysis. In this compilation, the authors address the way the tra
Autor:
Thomas Ferkol, Dinu Antony, Heymut Omran, Peadar G. Noone, Christopher O'Callaghan, Scott D. Sagel, Heike Olbrich, Richard D. Emes, Michael R. Knowles, Claire Hogg, Jane S. Lucas, Maimoona A. Zariwala, Whitney E. Wolf, Ann Dewar, Peter J. Scambler, Robert Wilson, M. Leigh Anne Daniels, Anita Becker-Heck, Martine Jaspers, Hannah M. Mitchison, Andrew Rutman, Niki T. Loges, Amelia Shoemark, Mark Jorissen, Theresa Taylor‐Cox, Margaret Rosenfeld, Mitra Forouhan, Patricia Goggin, Abhijit Dixit, Claire L. Jackson, Miriam Schmidts, Alexandros Onoufriadis, Margaret W. Leigh, Eddie M. K. Chung
Publikováno v:
Human Mutation. 34:462-472
Primary ciliary dyskinesia (PCD) is a genetically heterogeneous disorder caused by cilia and sperm dysmotility. About 12% of cases show perturbed 9+2 microtubule cilia structure and inner dynein arm (IDA) loss, historically termed ‘radial spoke def
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c849926e67223df945bafad97f26b9fa
https://doi.org/10.1002/humu.22261
https://doi.org/10.1002/humu.22261
Publikováno v:
Orvosi Hetilap. 152:437-442
An effective control of healthcare-associated infections is not realized without an intensive participation of microbiologic activities. Authors present the model of a centre for healthcare-associated infection control established in 2008 at Semmelwe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6abb3392c016ed8d2f8f46f8f5688fa8
https://doi.org/10.1556/oh.2011.29062
https://doi.org/10.1556/oh.2011.29062
Autor:
Rebecca D. Burdine, Gyorgy Baktai, Lee Niswander, Richard Reinhardt, Jessica Sullivan-Brown, Heike Olbrich, Heymut Omran, Kathryn V. Anderson, Andrew Pollock, June K. Marthin, Robert Geisler, Judith Horvath, Manfred Fliegauf, Karsten Haeffner, Anita Becker-Heck, Niki T. Loges, Irene E. Zohn, Kim G. Nielsen, Jason C. McSheene, Kari Baker Lenhart, Noriko Okabe
Publikováno v:
Nature Genetics. 43:79-84
Primary ciliary dyskinesia (PCD) is a genetically heterogeneous autosomal recessive disorder characterized by recurrent infections of the respiratory tract associated with the abnormal function of motile cilia. Approximately half of individuals with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fe0dc3c265ae0d5362cdc4add59af92b
https://doi.org/10.1038/ng.727
https://doi.org/10.1038/ng.727
Autor:
Christina Reinhard, Gudrun Nürnberg, Anita Becker-Heck, Richard Reinhardt, Niki T. Loges, Hanswalter Zentgraf, Margaret W. Leigh, H. Seithe, Maimoona A. Zariwala, Heymut Omran, Andreas Kispert, Angelina Heer, Miriam Schmidts, Heike Olbrich, Michael R. Knowles, Karsten Häffner, Peter Nürnberg
Publikováno v:
The American Journal of Human Genetics. 85:883-889
Genetic defects affecting motility of cilia and flagella cause chronic destructive airway disease, randomization of left-right body asymmetry, and, frequently, male infertility in primary ciliary dyskinesia (PCD). The most frequent defects involve ou
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::59dd04ac9c3398ddd6bb8215d7c59f2a
https://doi.org/10.1016/j.ajhg.2009.10.018
https://doi.org/10.1016/j.ajhg.2009.10.018
Autor:
Bolan Linghu, Pierre Saint-Mezard, Fan Yang, Marion Delous, Anita Becker-Heck, Joseph D. Szustakowski, Fabrizio C. Serluca, Jan Halbritter, Alexandre Benmerah, Mohammed Zarhrate, Rebecca Ryan, Albane A. Bizet, Elisabeth Cassuto, Kristina Weber, Esben Lorentzen, Marie-Christine Lasbennes, Neveen A. Soliman Elshakhs, Philippe Dubot, Sophie Saunier, Patrick Nitschke, Pauline Krug, Andreas W. Sailer, Edward J. Oakeley, Corinne Antignac, Emilie Filhol, Rémi Salomon, José Sahel, Friedhelm Hildebrandt, Meriem Garfa-Traore, Marie-Claire Gubler, Iain A. Drummond, Tewis Bouwmeester, Salah-Dine Chibout, Lucile Pinson
Publikováno v:
NATURE COMMUNICATIONS
Aarhus University
Nature Communications
Nature Communications, 2015, 6 (1), pp.8666. ⟨10.1038/ncomms9666⟩
Aarhus University
Nature Communications
Nature Communications, 2015, 6 (1), pp.8666. ⟨10.1038/ncomms9666⟩
Ciliopathies are a large group of clinically and genetically heterogeneous disorders caused by defects in primary cilia. Here we identified mutations in TRAF3IP1 (TNF Receptor-Associated Factor Interacting Protein 1) in eight patients from five famil
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ad14ead313b33ec20a078dda76896f88
https://hdl.handle.net/11858/00-001M-0000-0029-331E-611858/00-001M-0000-0029-3320-F
https://hdl.handle.net/11858/00-001M-0000-0029-331E-611858/00-001M-0000-0029-3320-F
Autor:
Anita Becker
Manchmal spreche ich mit Gott: Jeden Morgen wird es hell. Manchmal scheint die Sonne, aber oft verdunkeln die Wolken ihre hellen Strahlen und doch nimmt der Tag seinen Lauf. Oft wissen wir, dass uns schöne Tage erwarten. Unsere Erwartungen werden ni
Autor:
M Forouhan, Dinu Antony, Heymut Omran, Patricia Goggin, Amelia Shoemark, Anita Becker-Heck, Mellisa Dixon, E. M K Chung, Hannah M. Mitchison, C. Hogg, Christopher O'Callaghan, Alexandros Onoufriadis, Claire L. Jackson, Miriam Schmidts, Jane S. Lucas, Heike Olbrich
Publikováno v:
Cilia, Vol 1, Iss Suppl 1, p P1 (2012)
Europe PubMed Central
Cilia
Europe PubMed Central
Cilia
Primary ciliary dyskinesia (PCD) is a genetically heterogeneous inherited disorder characterised by recurrent respiratory tract infections, bronchiectasis and subfertility which arises from cilia/sperm dysmotility associated with axonemal ultrastruct
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e37bbba0c9e916173935f84da07a158f
https://doaj.org/article/8f0b4fb1d8fd49ab86378b00869ed110
https://doaj.org/article/8f0b4fb1d8fd49ab86378b00869ed110
Cilia are highly conserved organelles extending from almost every cell type of the human body. Their core structure, the axoneme, consists of nine doublet microtubules composed of α- and β-tubulin. Cilia can be divided into two classes, motile and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5f9dbfc26c3481cf1f64eb052b1a5783
https://doi.org/10.1016/b978-0-12-382004-4.10024-x
https://doi.org/10.1016/b978-0-12-382004-4.10024-x
Autor:
Scott D. Sagel, Kenneth N. Olivier, Susan L. Minnix, Johnny L. Carson, Miriam Schmidts, Heike Olbrich, Maimoona A. Zariwala, Milan J. Hazucha, Michael C. Armstrong, Margaret W. Leigh, Sharon D. Dell, Niki Tomas Loges, Kimberlie A. Burns, Adriana Lori, Stephanie D. Davis, Anita Becker-Heck, Margaret Rosenfeld, Thomas W. Ferkol, Heymut Omran, Claudius Werner, Michael R. Knowles
Publikováno v:
Thorax. 67(5)
Rationale Primary ciliary dyskinesia (PCD) is an autosomal recessive, genetically heterogeneous disorder characterised by oto-sino-pulmonary disease and situs abnormalities (Kartagener syndrome) due to abnormal structure and/or function of cilia. Mos
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::979bdd5bdb6772560efb79a707eee8fa
https://pubmed.ncbi.nlm.nih.gov/22232363
https://pubmed.ncbi.nlm.nih.gov/22232363