Zobrazeno 1 - 10
of 64
pro vyhledávání: '"Andreas Busche"'
Autor:
Felix R Stahl, Katrin Heller, Stephan Halle, Kirsten A Keyser, Andreas Busche, Anja Marquardt, Karen Wagner, Jasmin Boelter, Yvonne Bischoff, Elisabeth Kremmer, Ramon Arens, Martin Messerle, Reinhold Förster
Publikováno v:
PLoS Pathogens, Vol 9, Iss 12, p e1003828 (2013)
Neonates, including mice and humans, are highly susceptible to cytomegalovirus (CMV) infection. However, many aspects of neonatal CMV infections such as viral cell tropism, spatio-temporal distribution of the pathogen as well as genesis of antiviral
Externí odkaz:
https://doaj.org/article/1b6b9c02372e45b19a3729b5c0d6b8e1
Autor:
Sara Rodríguez-Martín, Kai Alexander Kropp, Vanessa Wilhelmi, Vanda Juranic Lisnic, Wei Yuan Hsieh, Mathieu Blanc, Andrew Livingston, Andreas Busche, Hille Tekotte, Martin Messerle, Manfred Auer, Iain Fraser, Stipan Jonjic, Ana Angulo, Matthias J Reddehase, Peter Ghazal
Publikováno v:
PLoS Pathogens, Vol 8, Iss 8, p e1002901 (2012)
Little is known about the role of viral genes in modulating host cytokine responses. Here we report a new functional role of the viral encoded IE1 protein of the murine cytomegalovirus in sculpting the inflammatory response in an acute infection. In
Externí odkaz:
https://doaj.org/article/5b34cf90ffe1437d9285452e042e5dd5
Autor:
Marc Trimborn, Mahdi Ghani, Diego J Walther, Monika Dopatka, Véronique Dutrannoy, Andreas Busche, Franziska Meyer, Stefanie Nowak, Jean Nowak, Claus Zabel, Joachim Klose, Veronica Esquitino, Masoud Garshasbi, Andreas W Kuss, Hans-Hilger Ropers, Susanne Mueller, Charlotte Poehlmann, Ioannis Gavvovidis, Detlev Schindler, Karl Sperling, Heidemarie Neitzel
Publikováno v:
PLoS ONE, Vol 5, Iss 2, p e9242 (2010)
Mutations in the human gene MCPH1 cause primary microcephaly associated with a unique cellular phenotype with premature chromosome condensation (PCC) in early G2 phase and delayed decondensation post-mitosis (PCC syndrome). The gene encodes the BRCT-
Externí odkaz:
https://doaj.org/article/770b07381bfb4877a4b16fab25d1cd22
Autor:
Andreas Busche
Publikováno v:
Abbas Kiarostami ISBN: 9781496844910
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0432440dbc022386865665897df3fd20
https://doi.org/10.2307/jj.1866688.21
https://doi.org/10.2307/jj.1866688.21
Autor:
Erica H. Gerkes, Ingo Kurth, Beyhan Tüysüz, Isabel Filges, Martin A. Mensah, Stefan Mundlos, Susanne Markus, Luitgard Graul-Neumann, Wiebke Hülsemann, Daniel Svoboda, Manuel Holtgrewe, Nursel Elcioglu, Marie Coutelier, Almuth Caliebe, Aleksander Jamsheer, Jonas Elsner, Christopher Teller, Stefania Bigoni, Rixa Woitschach, Malte Spielmann, Inga Vater, Jakob Hertzberg, Miriam S. Reuter, Peter Krawitz, Katta M. Girisha, Deepthi De Silva, Denise Horn, André Mégarbané, André Reis, Andreas Busche, Meredith Wilson, Seval Türkmen
Publikováno v:
Human Genetics
HUMAN GENETICS, 140(8), 1229-1239. SPRINGER
HUMAN GENETICS, 140(8), 1229-1239. SPRINGER
The extensive clinical and genetic heterogeneity of congenital limb malformation calls for comprehensive genome-wide analysis of genetic variation. Genome sequencing (GS) has the potential to identify all genetic variants. Here we aim to determine th
Autor:
Chiara De Santis, Daniela Willy, Kathrin Oelmeier, Ralf Schmitz, Andreas Busche, Albrecht Röpke, Mareike Möllers
Publikováno v:
Ultraschall in der Medizin - European Journal of Ultrasound.
Autor:
Nina Bögershausen, Hannah E. Krawczyk, Rami A. Jamra, Sheng‐Jia Lin, Gökhan Yigit, Irina Hüning, Anna M. Polo, Barbara Vona, Kevin Huang, Julia Schmidt, Janine Altmüller, Johannes Luppe, Konrad Platzer, Beate B. Dörgeloh, Andreas Busche, Saskia Biskup, Marisa I. Mendes, Desiree E. C. Smith, Gajja S. Salomons, Arne Zibat, Eva Bültmann, Peter Nürnberg, Malte Spielmann, Johannes R. Lemke, Yun Li, Martin Zenker, Gaurav K. Varshney, Hauke S. Hillen, Christian P. Kratz, Bernd Wollnik
Publikováno v:
Human Mutations
Human mutation, 43(10), 1454-1471. Wiley-Liss Inc.
Human Mutation, 43(10), 1454-1471. Wiley-Liss Inc.
Bögershausen, N, Krawczyk, H E, Jamra, R A, Lin, S-J, Yigit, G K, Hüning, I, Polo, A M, Vona, B, Huang, K, Schmidt, J, Altmüller, J, Luppe, J, Platzer, K, Dörgeloh, B B, Busche, A, Biskup, S, Mendes, M I, Smith, D E C, Salomons, G S, Zibat, A, Bültmann, E, Nürnberg, P, Spielmann, M, Lemke, J R, Li, Y, Zenker, M, Varshney, G K, Hillen, H S, Kratz, C P & Wollnik, B 2022, ' WARS1 and SARS1 : Two tRNA synthetases implicated in autosomal recessive microcephaly ', Human Mutation, vol. 43, no. 10, pp. 1454-1471 . https://doi.org/10.1002/humu.24430
Human mutation, 43(10), 1454-1471. Wiley-Liss Inc.
Human Mutation, 43(10), 1454-1471. Wiley-Liss Inc.
Bögershausen, N, Krawczyk, H E, Jamra, R A, Lin, S-J, Yigit, G K, Hüning, I, Polo, A M, Vona, B, Huang, K, Schmidt, J, Altmüller, J, Luppe, J, Platzer, K, Dörgeloh, B B, Busche, A, Biskup, S, Mendes, M I, Smith, D E C, Salomons, G S, Zibat, A, Bültmann, E, Nürnberg, P, Spielmann, M, Lemke, J R, Li, Y, Zenker, M, Varshney, G K, Hillen, H S, Kratz, C P & Wollnik, B 2022, ' WARS1 and SARS1 : Two tRNA synthetases implicated in autosomal recessive microcephaly ', Human Mutation, vol. 43, no. 10, pp. 1454-1471 . https://doi.org/10.1002/humu.24430
Aminoacylation of tRNA is a key step in protein biosynthesis, carried out by highly specific aminoacyl-tRNA synthetases (ARS). ARS have been implicated in autosomal dominant and autosomal recessive human disorders. Autosomal dominant variants in tryp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::85935df54049d5375dcb05087f17d26d
https://hdl.handle.net/21.11116/0000-000B-2BDE-C21.11116/0000-000B-2BE0-8
https://hdl.handle.net/21.11116/0000-000B-2BDE-C21.11116/0000-000B-2BE0-8
Autor:
Eva Christina Prott, Angelo Selicorni, Cristina Gervasini, Axel Bohring, Alma Kuechler, Mark B. Mallozzi, Emanuele Agolini, Alisha Wilkens, Heiko Reutter, Barbara Mikat, Giuseppe Zampino, Yorck Hellenbroich, Eva Rossier, Denise Horn, Carolina Baquero-Montoya, Roberta Onesimo, Yiran Guo, Hakon Hakonarson, Chiara Leoni, Elaine H. Zackai, Yun Li, Dagmar Wieczorek, Frank J. Kaiser, Milena Mariani, Andreas Busche, Birgit Zirn, Andreas Dalski, Sally Ann Lynch, Livija Medne, Nuria C. Bramswig, Beate Albrecht, Donatella Milani, Xilma R. Ortiz-Gonzalez, Ilaria Parenti, Matthew A Deardorff, A. Micheil Innes, Britta Hanker, Irina Huening, Gabriele Gillessen-Kaesbach, Peter Wieacker
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::902404dcbdaa40403724acccee7e7a22
https://doi.org/10.1111/cge.13977/v2/response1
https://doi.org/10.1111/cge.13977/v2/response1
Autor:
Carolina Baquero-Montoya, Heiko Reutter, Andreas Busche, Yiran Guo, A. Micheil Innes, Alisha Wilkens, Nuria C. Bramswig, Donatella Milani, Denise Horn, Birgit Zirn, Roberta Onesimo, Beate Albrecht, Alma Kuechler, Sally Ann Lynch, Xilma R. Ortiz-Gonzalez, Irina Hüning, Britta Hanker, Cristina Gervasini, Matthew A. Deardorff, Giuseppe Zampino, Gabriele Gillessen-Kaesbach, Peter Wieacker, Livija Medne, Andreas Dalski, Chiara Leoni, Milena Mariani, Eva Christina Prott, Barbara Mikat, Yorck Hellenbroich, Axel Bohring, Ilaria Parenti, Eva Rossier, Elaine H. Zackai, Angelo Selicorni, Dagmar Wieczorek, Emanuele Agolini, Mark B. Mallozzi, Frank J. Kaiser, Hakon Hakonarson, Yun Li
Publikováno v:
Clinical geneticsREFERENCES. 100(2)
Mutations affecting the transcriptional regulator ANKRD11 are mainly associated with the multisystem developmental disorder known as KBG syndrome, but have also been identified in individuals with Cornelia de Lange syndrome (CdLS) and other developme
Autor:
Antje Schwinger, Andreas Büscher, Gerald Willms, Nahne-Alina Knizia, Josefine Hirschler, Constance Stegbauer, Nathalie Englert, Lara Peters, Hakim A. Bayarassou, Leonie Mallmann
Publikováno v:
BMJ Open, Vol 14, Iss 3 (2024)
Introduction An increasing number of tracheotomised and/or ventilated patients with high-cost out-of-hospital intensive care needs and, at the same time, a decreasing number of healthcare professionals inevitably lead to challenges in the care of thi
Externí odkaz:
https://doaj.org/article/f8e1662376234a9aa027a55ed65a86de