Resultados de búsqueda - Anders Lundmark
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1
Allele-specific gene expression patterns in primary leukemic cells reveal regulation of gene expression by CpG site methylation por Lili Milani, Anders Lundmark, Jessica Nordlund, Anna Kiialainen, Trond Flægstad, Guđmundur Jónmundsson, Jukka Kanerva, Kjeld Schmiegelow, Kevin L. Gunderson, Gudmar Lönnerholm, Ann‐Christine Syvänen
Publicado 2008Artigo -
2
DNA methylation for subtype classification and prediction of treatment outcome in patients with childhood acute lymphoblastic leukemia por Lili Milani, Anders Lundmark, Anna Kiialainen, Jessica Nordlund, Trond Flægstad, Erik Forestier, Mats Heyman, Guđmundur Jónmundsson, Jukka Kanerva, Kjeld Schmiegelow, Stefan Söderhäll, Mats G. Gustafsson, Gudmar Lönnerholm, Ann‐Christine Syvänen
Publicado 2009Artigo -
3
Deep targeted sequencing in pediatric acute lymphoblastic leukemia unveils distinct mutational patterns between genetic subtypes and novel relapse-associated genes por C. Lindqvist, Anders Lundmark, Jessica Nordlund, Eva Freyhult, Diana Ekman, Jonas Carlsson Almlöf, Amanda Raine, Elin Övernäs, Jonas Abrahamsson, Britt-Marie Frost, Dan Grandér, Mats Heyman, Josefine Palle, Erik Forestier, Gudmar Lönnerholm, Eva Berglund, Ann-Christine Syvänen
Publicado 2016Artigo -
4
Interferon regulatory factor 5 (IRF5) gene variants are associated with multiple sclerosis in three distinct populations por Guðrún Kristjánsdóttir, Johanna K. Sandling, Alessandro Bonetti, Izaura M. Roos, Lili Milani, Chao Wang, Sigrun Gustafsdottir, Snævar Sigurðsson, Anders Lundmark, Pentti J. Tienari, Keijo Koivisto, Irina Elovaara, Tuula Pirttilä, Mauri Reunanen, L. Peltonen, Janna Saarela, Jan Hillert, Tomas Olsson, Ulf Landegren, Antonio Alcina, Óscar Fernández, Laura Leyva, María del Mar López-Guerrero, Miguel Lucas, Guillermo Izquierdo, Fuencisla Matesanz, A-C Syvänen
Publicado 2008Artigo -
5
Large-scale association analysis identifies new risk loci for coronary artery disease por Panos Deloukas, Stavroula Kanoni, Christina Willenborg, Martin Farrall, Themistocles L. Assimes, John R. Thompson, Erik Ingelsson, Danish Saleheen, Jeanette Erdmann, Benjamin A. Goldstein, Kathleen Stirrups, Inke R. König, Jean‐Baptiste Cazier, Åsa Johansson, Alistair S. Hall, Jong‐Young Lee, Cristen J. Willer, John C. Chambers, Tõnu Esko, Lasse Folkersen, Anuj Goel, Elin Grundberg, Aki S. Havulinna, Weang-Kee Ho, Jemma C. Hopewell, Niclas Eriksson, Marcus E. Kleber, Kati Kristiansson, Per Lundmark, Leo‐Pekka Lyytikäinen, Suzanne Rafelt, Dmitry Shungin, Rona J. Strawbridge, Guðmar Þorleifsson, Emmi Tikkanen, Natalie Van Zuydam, Benjamin F. Voight, Lindsay L. Waite, Weihua Zhang, Andreas Ziegler, Devin Absher, David Altshuler, Anthony J. Balmforth, Inês Barroso, Peter S. Braund, Christof Burgdorf, Xueling Sim, David Cox, Maria Dimitriou, Ron Do, Alex S. F. Doney, NourEddine El Mokhtari, Per Eriksson, Krista Fischer, Pierre Fontanillas, Anders Franco‐Cereceda, Bruna Gigante, Per‐Henrik Groop, Stefan Gustafsson, Jörg Hager, Göran Hallmans, Bok-Ghee Han, Sarah Hunt, Hyun Min Kang, Thomas Illig, Thorsten Kessler, Joshua Knowles, Genovefa Kolovou, Johanna Kuusisto, Claudia Langenberg, Cordelia Langford, Karin Leander, Marja‐Liisa Lokki, Anders Lundmark, Mark I. McCarthy, Christa Meisinger, Olle Melander, Evelin Mihailov, Seraya Maouche, Andrew D. Morris, Martina Müller‐Nurasyid, Kjell Nikus, John F. Peden, Nigel W. Rayner, Asif Rasheed, Silke Rosinger, Deborah C. Rubin, Moritz Rumpf, Arne Schäfer, Mohan U. Sivananthan, Ci Song, Alexandre F.R. Stewart, Sian-Tsung Tan, Guðmundur Þorgeirsson, C. Ellen van der Schoot, Peter J. Wagner, George A. Wells, Philipp S. Wild, Tsun-Po Yang, Philippe Amouyel
Publicado 2012Artigo
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Materias Relacionadas
Biology
Gene
Genetics
Medicine
Genotype
Single-nucleotide polymorphism
Allele
CpG site
DNA methylation
Gene expression
Methylation
Acute lymphocytic leukemia
Allele frequency
Biochemistry
Bioinformatics
CAD
Candidate gene
Coronary artery disease
Disease
Environmental health
Family medicine
Genetic association
Genome-wide association study
Genotyping
Haplotype
Heritability
IRF5
IRF7
Indel
Interferon regulatory factors