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Science (New York, N.Y.)|October 12, 2019
Genetic regulatory variation in populations informs transcriptome analysis in rare diseasePejman Mohammadi, Stephane E Castel, Beryl B Cummings, et al.
Cancer Research|October 9, 2012
Oxidative stress-regulated lentiviral TK/GCV gene therapy for lung cancer treatmentHanna M Leinonen, Anna-Kaisa Ruotsalainen, Ann-Marie Määttä, et al.
American Journal of Human Genetics|August 5, 2005
Mitochondrial DNA polymerase W748S mutation: a common cause of autosomal recessive ataxia with ancient European originAnna H Hakonen, Silja Heiskanen, Vesa Juvonen, et al.
The American Journal of Gastroenterology|February 27, 2007
Prevalence of CARD15/NOD2 mutations in Caucasian healthy peopleJean-Pierre Hugot, Isabelle Zaccaria, Juleen Cavanaugh, et al.
Nature Communications|June 24, 2017
Ezrin enhances line tension along transcellular tunnel edges via NMIIa driven actomyosin cable formationCaroline Stefani, David Gonzalez-Rodriguez, Yosuke Senju, et al.
Tissue Antigens|October 19, 2012
Association study of FUT2 (rs601338) with celiac disease and inflammatory bowel disease in the Finnish populationA S Parmar, N Alakulppi, P Paavola-Sakki, et al.
Nutrition, Metabolism, and Cardiovascular Diseases : NMCD|April 20, 2010
Association of the FTO gene variant (rs9939609) with cardiovascular disease in men with abnormal glucose metabolism--the Finnish Diabetes Prevention StudyT Lappalainen, M Kolehmainen, U S Schwab, et al.
Cardiovascular Research|January 24, 2013
The absence of macrophage Nrf2 promotes early atherogenesisAnna-Kaisa Ruotsalainen, Matias Inkala, Mervi E Partanen, et al.
Current Biology : CB|October 5, 2021
SHANK3 conformation regulates direct actin binding and crosstalk with Rap1 signalingSiiri I Salomaa, Mitro Miihkinen, Elena Kremneva, et al.
Annals of Medicine|April 26, 2016
Preeclampsia does not share common risk alleles in 9p21 with coronary artery disease and type 2 diabetesTea Kaartokallio, A Inkeri Lokki, Hanna Peterson, et al.
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