Hasil Pencarian - Per Marits
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FOXP3 promoter demethylation reveals the committed Treg population in humans. oleh Peter C J Janson, Malin E Winerdal, Per Marits, Magnus Thörn, Rolf Ohlsson, Ola Winqvist
Diterbitkan 2008-01-01
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Case report: IKZF1-related early-onset CID is expected to be missed in TREC-based SCID screening but can be identified by determination of KREC levels oleh Christofer Äng, Christofer Äng, Rolf H. Zetterström, Rolf H. Zetterström, Kim Ramme, Kim Ramme, Emma Axelsen, Per Marits, Mikael Sundin, Mikael Sundin
Diterbitkan 2023-09-01
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Eleven percent intact PGM3 in a severely immunodeficient patient with a novel splice-site mutation, a case report oleh Karin E. Lundin, Qing Wang, Abdulrahman Hamasy, Per Marits, Mehmet Uzunel, Valtteri Wirta, Ann-Charlotte Wikström, Anders Fasth, Olov Ekwall, C.I. Edvard Smith
Diterbitkan 2018-08-01
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First Year of TREC-Based National SCID Screening in Sweden oleh Christina Göngrich, Olov Ekwall, Mikael Sundin, Nicholas Brodszki, Anders Fasth, Per Marits, Sam Dysting, Susanne Jonsson, Michela Barbaro, Anna Wedell, Ulrika von Döbeln, Rolf H. Zetterström
Diterbitkan 2021-08-01
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Drug Tolerant Anti-drug Antibody Assay for Infliximab Treatment in Clinical Practice Identifies Positive Cases Earlier oleh Nastya Kharlamova, Nastya Kharlamova, Christina Hermanrud, Christina Hermanrud, Nicky Dunn, Nicky Dunn, Malin Ryner, Malin Ryner, Karen Hambardzumyan, Nancy Vivar Pomiano, Per Marits, Inger Gjertsson, Saedis Saevarsdottir, Saedis Saevarsdottir, Rille Pullerits, Rille Pullerits, Anna Fogdell-Hahn, Anna Fogdell-Hahn
Diterbitkan 2020-07-01
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Increased CD4+ T cell lineage commitment determined by CpG methylation correlates with better prognosis in urinary bladder cancer patients oleh Emma Ahlén Bergman, Ciputra Adijaya Hartana, Markus Johansson, Ludvig B. Linton, Sofia Berglund, Martin Hyllienmark, Christian Lundgren, Benny Holmström, Karin Palmqvist, Johan Hansson, Farhood Alamdari, Ylva Huge, Firas Aljabery, Katrine Riklund, Malin E. Winerdal, David Krantz, A. Ali Zirakzadeh, Per Marits, Louise K. Sjöholm, Amir Sherif, Ola Winqvist
Diterbitkan 2018-08-01
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Integration of whole genome sequencing into a healthcare setting: high diagnostic rates across multiple clinical entities in 3219 rare disease patients oleh Henrik Stranneheim, Kristina Lagerstedt-Robinson, Måns Magnusson, Malin Kvarnung, Daniel Nilsson, Nicole Lesko, Martin Engvall, Britt-Marie Anderlid, Henrik Arnell, Carolina Backman Johansson, Michela Barbaro, Erik Björck, Helene Bruhn, Jesper Eisfeldt, Christoph Freyer, Giedre Grigelioniene, Peter Gustavsson, Anna Hammarsjö, Maritta Hellström-Pigg, Erik Iwarsson, Anders Jemt, Mikael Laaksonen, Sara Lind Enoksson, Helena Malmgren, Karin Naess, Magnus Nordenskjöld, Mikael Oscarson, Maria Pettersson, Chiara Rasi, Adam Rosenbaum, Ellika Sahlin, Eliane Sardh, Tommy Stödberg, Bianca Tesi, Emma Tham, Håkan Thonberg, Virpi Töhönen, Ulrika von Döbeln, Daphne Vassiliou, Sofie Vonlanthen, Ann-Charlotte Wikström, Josephine Wincent, Ola Winqvist, Anna Wredenberg, Sofia Ygberg, Rolf H. Zetterström, Per Marits, Maria Johansson Soller, Ann Nordgren, Valtteri Wirta, Anna Lindstrand, Anna Wedell
Diterbitkan 2021-03-01
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