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PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, ISSN 0027-8424, 01/2019, Volume 116, Issue 3, pp. 1059 - 1064
The vast complexity of native heteromeric K+ channels is largely unexplored. Defining the composition and subunit arrangement of individual subunits in native... 
LOCALIZATION | MOLECULAR-DYNAMICS | MULTIDISCIPLINARY SCIENCES | STOICHIOMETRY | GATED ION CHANNELS | IDENTIFICATION | Kv1.2 | GROMACS | heteromeric Kv-channels | conotoxin kappaM-RIIIJ
Journal Article
Annals of the Rheumatic Diseases, ISSN 0003-4967, 06/2015, Volume 74, Issue 6, pp. 1011 - 1018
Objectives To assess the prevalence of the main causes of morbi-mortality in the antiphospholipid syndrome (APS) during a 10-year-follow-up period and to... 
Systemic Lupus Erythematosus | Antiphospholipid Syndrome | SYSTEMIC-LUPUS-ERYTHEMATOSUS | MANAGEMENT | SERIES | FOLLOW-UP | Anticardiolipin Antibodies | ARTERIAL THROMBOSIS | RHEUMATOLOGY | INTERNATIONAL CONSENSUS STATEMENT | Autoimmune Diseases | COHORT | DISEASE EXPRESSION | CLASSIFICATION CRITERIA | Antiphospholipid Antibodies | MANIFESTATIONS | Antiphospholipid Syndrome - mortality | Lupus Erythematosus, Systemic - complications | Prospective Studies | Humans | Middle Aged | Child, Preschool | Infant | Male | Lupus Erythematosus, Systemic - mortality | Antiphospholipid Syndrome - complications | Epilepsy - etiology | Infection - etiology | Pregnancy Outcome - epidemiology | Young Adult | Abortion, Spontaneous - epidemiology | Antiphospholipid Syndrome - epidemiology | Ischemic Attack, Transient - etiology | Livedo Reticularis - etiology | Aged, 80 and over | Adult | Female | Stroke - mortality | Child | Infant, Newborn | Thrombocytopenia - etiology | Fetal Growth Retardation - epidemiology | Venous Thrombosis - mortality | Infection - mortality | Premature Birth - epidemiology | Venous Thrombosis - etiology | Pregnancy | Pulmonary Embolism - mortality | Stroke - etiology | Pulmonary Embolism - etiology | Thrombosis - etiology | Adolescent | Aged | Thrombosis - mortality | Longitudinal Studies | Cohort Studies | Care and treatment | Patient outcomes | Analysis | Mortality | Risk factors | Morbidity | Antiphospholipid syndrome | Lupus | Anticoagulants | Heart attacks | Morbiditat | Case studies | Síndrome antifosfolipídica | Lupus eritematós | Malalties autoimmunitàries | Estudi de casos | Lupus erythematosus | Autoimmune diseases | Life Sciences | Human health and pathology | Rhumatology and musculoskeletal system
Journal Article
by Wood, Anew R and Esko, Tonu and Yang, Jian and Vedantam, Sailaja and Pers, Tune H and Gustafsson, Stefan and Chu, Auey Y and Estrada, Karol and Luan, Jian'an and Kutalik, Zoltán and Amin, Najaf and Buchkovich, Martin L and Croteau-Chonka, Damien C and Day, Felix R and Duan, Yanan and Fall, Tove and Fehrmann, Rudolf and Ferreira, Teresa and Jackson, Anne U and Karjalainen, Juha and Lo, Ken Sin and Locke, Adam E and Mägi, Reedik and Mihailov, Evelin and Porcu, Eleonora and Randall, Joshua C and Scherag, Ané and Vinkhuyzen, Anna A. E and Westra, Harm-Jan and Winkler, Thomas W and Workalemahu, Tsegaselassie and Zhao, Jing Hua and Absher, Devin and Albrecht, Eva and Anderson, Denise and Baron, Jeffrey and Beekman, Marian and Demirkan, Ayse and Ehret, Georg B and Feenstra, Bjarke and Feitosa, Mary F and Fischer, Krista and Fraser, Ross M and Goel, Anuj and Gong, Jian and Justice, Anne E and Kanoni, Stavroula and Kleber, Marcus E and Kristiansson, Kati and Lim, Unhee and Lotay, Vaneet and Lui, Julian C and Mangino, Massimo and Mateo Leach, Irene and Medina-Gomez, Carolina and Nalls, Michael A and Nyholt, Dale R and Palmer, Cameron D and Pasko, Dorota and Pechlivanis, Sonali and Prokopenko, Inga and Ried, Janina S and Ripke, Stephan and Shungin, Dmitry and Stancáková, Alena and Strawbridge, Rona J and Sung, Yun Ju and Tanaka, Toshiko and Teumer, Alexander and Trompet, Stella and van der Laan, Sander W and van Setten, Jessica and van Vliet-Ostaptchouk, Jana V and Wang, Zhaoming and Yengo, Loïc and Zhang, Weihua and Afzal, Uzma and Arnlöv, Johan and Arscott, Gillian M and Bandinelli, Stefania and Barrett, Amy and Bellis, Claire and Bennett, Amanda J and Berne, Christian and Blüher, Matthias and Bolton, Jennifer L and Böttcher, Yvonne and Boyd, Heather A and Bruinenberg, Marcel and Buckley, Brendan M and Buyske, Steven and Caspersen, Ida H and Chines, Peter S and Clarke, Robert and Claudi-Boehm, Simone and Cooper, Matthew and Daw, E. Warwick and de Jong, Pim A and Deelen, Joris and Delgado, Graciela and ... and PAGE Consortium and MIGen Consortium and LifeLines Cohort Study and Elect Med Records & Genom eMERGE C and Electronic Medical Records and Genomics (eMEMERGEGE) Consortium and PAGEGE Consortium and The MIGen Consortium and The PAGE Consortium and The Electronic Medical Records and Genomics (eMERGE) Consortium and The LifeLines Cohort Study and Högskolan Dalarna and Akademin Utbildning, hälsa och samhälle and Medicinsk vetenskap
Nature genetics, ISSN 1061-4036, 2014, Volume 46, Issue 11, pp. 1173 - 1186
Journal Article
Nature Biotechnology, ISSN 1087-0156, 2007, Volume 25, Issue 2, pp. 221 - 231
Journal Article
Proceedings of the National Academy of Sciences, ISSN 0027-8424, 01/2019, Volume 116, Issue 3, pp. 1059 - 1064
The vast complexity of native heteromeric K+ channels is largely unexplored. Defining the composition and subunit arrangement of individual subunits in native... 
Biological Sciences | Kv1.2 | heteromeric Kv-channels | conotoxin kappaM-RIIIJ
Journal Article
by Zheng, Hou-Feng and Forgetta, Vincenzo and Hsu, Yi-Hsiang and Estrada, Karol and Rosello-Diez, Alberto and Leo, Paul J and Dahia, Chitra L and Park-Min, Kyung Hyun and Tobias, Jonathan H and Kooperberg, Charles and Kleinman, Aaron and Styrkarsdottir, Unnur and Liu, Ching-Ti and Uggla, Charlotta and Evans, Daniel S and Nielson, Carrie M and Walter, Klaudia and Pettersson-Kymmer, Ulrika and Mccarthy, Shane and Eriksson, Joel and Kwan, Tony and Jhamai, Mila and Trajanoska, Katerina and Memari, Yasin and Min, Josine and Huang, Jie and Danecek, Petr and Wilmot, Beth and Li, Rui and Chou, Wen-Chi and Mokry, Lauren E and Moayyeri, Alireza and Claussnitzer, Melina and Cheng, Chia-Ho and Cheung, Warren and Medina-Gómez, Carolina and Ge, Bing and Chen, Shu-Huang and Choi, Kwangbom and Oei, Ling and Fraser, James and Kraaij, Robert and Hibbs, Matthew A and Gregson, Celia L and Paquette, Denis and Hofman, Albert and Wibom, Carl and Tranah, Gregory J and Marshall, Mhairi and Gardiner, Brooke B and Cremin, Katie and Auer, Paul and Hsu, Li and Ring, Sue and Tung, Joyce Y and Thorleifsson, Gudmar and Enneman, Anke W and van Schoor, Natasja M and de Groot, Lisette C. P. G. M and van der Velde, Nathalie and Melin, Beatrice and Kemp, John P and Christiansen, Claus and Sayers, Aian and Zhou, Yanhua and Calderari, Sophie and van Rooij, Jeroen and Carlson, Chris and Peters, Ulrike and Berlivet, Soizik and Dostie, Josée and Uitterlinden, Ane G and Williams, Stephen R and Farber, Charles and Grinberg, Daniel and LaCroix, Anea Z and Haessler, Jeff and Chasman, Daniel I and Giulianini, Franco and Rose, Lynda M and Ridker, Paul M and Eisman, John A and Nguyen, Tuan V and Center, Jacqueline R and Nogues, Xavier and Garcia-Giralt, Natalia and Launer, Lenore L and Gudnason, Vilmunder and Mellström, Dan and Vandenput, Liesbeth and Amin, Najaf and van Duijn, Cornelia M and Karlsson, Magnus K and Ljunggren, Östen and Svensson, Olle and Hallmans, Göran and Rousseau, François and Giroux, Sylvie and Bussière, Johanne and Arp, Pascal P and ... and AOGC Consortium and UK10K Consortium and Medicinska fakulteten and Institutionen för strålningsvetenskaper and Umeå universitet and Institutionen för folkhälsa och klinisk medicin and Institutionen för farmakologi och klinisk neurovetenskap and Farmakologi and Enheten för biobanksforskning and Näringsforskning and Institutionen för kirurgisk och perioperativ vetenskap
Nature, ISSN 0028-0836, 2015, Volume 526, Issue 7571, pp. 112 - +
The extent to which low-frequency (minor allele frequency (MAF) between 1-5%) and rare (MAF <= 1%) variants contribute to complex traits and disease in the... 
WIDE ASSOCIATION LOCI | MINERAL DENSITY | METAANALYSIS | VARIANTS | GENE | ENGRAILED-1 | MULTIDISCIPLINARY SCIENCES | MOUSE | HUMAN-DISEASES | COMPLEX TRAITS | OSTEOPOROSIS | European Continental Ancestry Group - genetics | Gene Frequency - genetics | Genetic Predisposition to Disease - genetics | Genomics | Humans | Genotype | Bone Density - genetics | Sequence Analysis, DNA | Europe - ethnology | Fractures, Bone - genetics | Genome, Human - genetics | Homeodomain Proteins - genetics | Exome - genetics | Animals | Wnt Proteins - genetics | Bone and Bones - metabolism | Female | Genetic Variation - genetics | Mice | Disease Models, Animal | Quantitative trait loci | Fractures | Bones | Genetic aspects | Nucleotide sequencing | Identification and classification | Density | Methods | DNA sequencing | Proteins | Studies | Osteoporosis | Ethnicity | Population | Bone density | Genomes | Neck | Meta-analysis | Malalties | Aspectes genètics | Ossos | Hälsovetenskaper | Folkhälsovetenskap, global hälsa, socialmedicin och epidemiologi | Medical and Health Sciences | Medicin och hälsovetenskap | Public Health, Global Health, Social Medicine and Epidemiology | Health Sciences | HNE Voeding en Gezondheid in de Levenscyclus | Wereldvoeding | VLAG | Chair Nutrition and Health over the Lifecourse | Global Nutrition | HNE Nutrition and Health over the Lifecourse
Journal Article
Lancet, The, ISSN 0140-6736, 2016, Volume 388, Issue 10055, pp. 1995 - 2003
Journal Article