Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Marcel Nutsua"'
Autor:
Ben Krause-Kyora, Marcel Nutsua, Lisa Boehme, Federica Pierini, Dorthe Dangvard Pedersen, Sabin-Christin Kornell, Dmitriy Drichel, Marion Bonazzi, Lena Möbus, Peter Tarp, Julian Susat, Esther Bosse, Beatrix Willburger, Alexander H. Schmidt, Jürgen Sauter, Andre Franke, Michael Wittig, Amke Caliebe, Michael Nothnagel, Stefan Schreiber, Jesper L. Boldsen, Tobias L. Lenz, Almut Nebel
Publikováno v:
Nature Communications, Vol 9, Iss 1, Pp 1-11 (2018)
Leprosy, caused by infection with Mycobacterium leprae, was common in Europe in the Middle Ages. Here, Krause-Kyora et al. analyze ancient DNA from a medieval Danish leprosarium to assemble 10 complete bacterial genomes and perform association analys
Externí odkaz:
https://doaj.org/article/8fa5ee6a3c694f099a3d3800433d8665
Autor:
Ben Krause-Kyora, Onur Özer, Almut Nebel, Joanna H. Bonczarowska, Federica Pierini, Tobias L. Lenz, Lisa Böhme, Marcel Nutsua, Andre Franke, Julian Susat
Publikováno v:
Scientific Reports
Scientific Reports, Vol 10, Iss 1, Pp 1-14 (2020)
Scientific Reports, Vol 10, Iss 1, Pp 1-14 (2020)
The highly polymorphic human leukocyte antigen (HLA) plays a crucial role in adaptive immunity and is associated with various complex diseases. Accurate analysis of HLA genes using ancient DNA (aDNA) data is crucial for understanding their role in hu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c39b7b890590d12a46196dfc37e3ff5a
https://doi.org/10.1038/s41598-020-64312-w
https://doi.org/10.1038/s41598-020-64312-w
Autor:
Annegret Fischer, Stefan Schreiber, Marcel Nutsua, Martin Petrek, Andre Franke, Britt-Sabina Petersen, Amit Kishore, Joachim Müller-Quernheim
Publikováno v:
Human Genetics. 137:705-716
Genome-wide and candidate gene studies for pulmonary sarcoidosis have highlighted several candidate variants among different populations. However, the genetic basis of functional rare variants in sarcoidosis still needs to be explored. To identify fu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8bcbc35b64ff12b68f446f7a4d5db786
https://doi.org/10.1007/s00439-018-1915-y
https://doi.org/10.1007/s00439-018-1915-y
Autor:
Federica Pierini, Ben Krause-Kyora, Andre Franke, Tobias L. Lenz, Julian Susat, Amke Caliebe, Lena Möbus, Esther Bosse, Jürgen Sauter, Sabin Christin Kornell, Jesper L. Boldsen, Lisa Boehme, Dmitriy Drichel, Dorthe Dangvard Pedersen, Marion Bonazzi, Beatrix Willburger, Michael Wittig, Alexander H. Schmidt, Stefan Schreiber, Peter Tarp, Almut Nebel, Michael Nothnagel, Marcel Nutsua
Publikováno v:
Nature Communications, Vol 9, Iss 1, Pp 1-11 (2018)
Krause-Kyora, B, Nutsua, M, Boehme, L, Pierini, F, Pedersen, D D, Kornell, S C, Drichel, D, Bonazzi, M, Möbus, L, Tarp, P, Susat, J, Bosse, E, Willburger, B, Schmidt, A H, Sauter, J, Franke, A, Wittig, M, Caliebe, A, Nothnagel, M, Schreiber, S, Boldsen, J L, Lenz, T L & Nebel, A 2018, ' Ancient DNA study reveals HLA susceptibility locus for leprosy in medieval Europeans ', Nature Communications, vol. 9, 1569 . https://doi.org/10.1038/s41467-018-03857-x
Nature Communications
Krause-Kyora, B, Nutsua, M, Boehme, L, Pierini, F, Pedersen, D D, Kornell, S C, Drichel, D, Bonazzi, M, Möbus, L, Tarp, P, Susat, J, Bosse, E, Willburger, B, Schmidt, A H, Sauter, J, Franke, A, Wittig, M, Caliebe, A, Nothnagel, M, Schreiber, S, Boldsen, J L, Lenz, T L & Nebel, A 2018, ' Ancient DNA study reveals HLA susceptibility locus for leprosy in medieval Europeans ', Nature Communications, vol. 9, 1569 . https://doi.org/10.1038/s41467-018-03857-x
Nature Communications
Leprosy, a chronic infectious disease caused by Mycobacterium leprae (M. leprae), was very common in Europe till the 16th century. Here, we perform an ancient DNA study on medieval skeletons from Denmark that show lesions specific for lepromatous lep
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e333a6a64a990c1495262ee8b0fd63b1
https://doi.org/10.1038/s41467-018-03857-x
https://doi.org/10.1038/s41467-018-03857-x
Autor:
Juliane Muhlack, Albert Mehl, Ben Krause-Kyora, Christoph Rinne, Christof E. Dörfer, Marcel Nutsua, Katharina Fuchs
Publikováno v:
Praehistorische Zeitschrift
ZusammenfassungDas Galeriegrab von Niedertiefenbach stellt einen besonderen Befund der späten Wartberggruppe im Neolithikum der Deutschen Mittelgebirgsschwelle dar; nur hier findet sich ein in zehn Straten geborgenes Bestattungskollektiv von mindest
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b423e5c4bc55ef25ced5698dac20e182
https://www.zora.uzh.ch/id/eprint/171947/
https://www.zora.uzh.ch/id/eprint/171947/
Autor:
Wolfgang Lieb, Markus M. Nöthen, Manfred Schürmann, Sylvia Hofmann, Michael C. Iannuzzi, Joachim Müller-Quernheim, Stefan Herms, Johan Grunewald, Stefan Schreiber, Bernhard O. Boehm, Stephan Brand, Almut Nebel, Martina Sterclova, Jiri Homolka, Christian Grohé, Martin Petrek, Christian Gieger, Hansjörg Baurecht, Eva Ellinghaus, Violeta Mihailovic-Vucinic, Stefan Pabst, Andre Franke, Leonid Padyukov, Konstantin Strauch, Marcus Ronninger, Dragana Jovanovic, David Ellinghaus, Courtney G. Montgomery, Frantisek Mrazek, Marcel Nutsua, Anders Eklund, Carsten Büning, Benjamin A. Rybicki, Annegret Fischer, Juliane Winkelmann
Publikováno v:
Am. J. Respir. Crit. Care Med. 192, 727-736 (2015)
Genetic variation plays a significant role in the etiology of sarcoidosis. However, only a small fraction of its heritability has been explained so far.To define further genetic risk loci for sarcoidosis, we used the Immunochip for a candidate gene a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6f9811b1ed7008f78d891a3ba69b6cc5
https://pubmed.ncbi.nlm.nih.gov/26371809
https://pubmed.ncbi.nlm.nih.gov/26371809
Publikováno v:
Journal of Animal Science. 94:93-94
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::06627985c16e4a4aa72a0b7a401ed9d8
https://doi.org/10.2527/jas2016.94supplement493a
https://doi.org/10.2527/jas2016.94supplement493a
Autor:
Almut Nebel, Marcel Nutsua, Stefan Schreiber, Sylvia Hofmann, Annegret Fischer, Michael Nothnagel, Michael Krawczak
Publikováno v:
PLoS ONE
PLoS ONE, Vol 10, Iss 7, p e0133465 (2015)
PLoS ONE, Vol 10, Iss 7, p e0133465 (2015)
The analysis of structural variants, in particular of copy-number variations (CNVs), has proven valuable in unraveling the genetic basis of human diseases. Hence, a large number of algorithms have been developed for the detection of CNVs in SNP array
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::08dd192cfc919a3bd6964ce9e11a0b4d
https://doi.org/10.1371/journal.pone.0133465
https://doi.org/10.1371/journal.pone.0133465