检索结果 - Snævar Sigurðsson

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  1. 1
    Detection of Skin Cancer by Classification of Raman Spectra

    Detection of Skin Cancer by Classification of Raman Spectra 由 Snævar Sigurðsson, Peter A. Philipsen, Lars Kai Hansen, Jan Larsen, Monika Gniadecka, Hans Christian Wulf

    出版 2004
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  2. 2
    The Non-Antibacterial Effects of Azithromycin and Other Macrolides on the Bronchial Epithelial Barrier and Cellular Differentiation

    The Non-Antibacterial Effects of Azithromycin and Other Macrolides on the Bronchial Epithelial Barrier and Cellular Differentiation 由 Árni Ásbjarnarson, Jon Pétur Joelsson, Fridrik Runar Gardarsson, Snævar Sigurðsson, Michael J. Parnham, Jennifer Kricker, Þórarinn Guðjónsson

    出版 2025
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  3. 3
    Structural basis for the inhibitory efficacy of efavirenz (DMP‐266), MSC194 and PNU142721 towards the HIV‐1 RT K103N mutant

    Structural basis for the inhibitory efficacy of efavirenz (DMP‐266), MSC194 and PNU142721 towards the HIV‐1 RT K103N mutant 由 Jimmy Lindberg, Snævar Sigurðsson, Seved Löwgren, Hans O. Andersson, Christer Sahlberg, Rolf Noréen, K. Fridborg, Hong Zhang, Torsten Unge

    出版 2002
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  4. 4
    Genetic variants and disease‐associated factors contribute to enhanced interferon regulatory factor 5 expression in blood cells of patients with systemic lupus erythematosus

    Genetic variants and disease‐associated factors contribute to enhanced interferon regulatory factor 5 expression in blood cells of patients with systemic lupus erythematosus 由 Di Feng, R. Stone, Maija‐Leena Eloranta, Niquiche Sangster‐Guity, Gunnel Nordmark, Snævar Sigurðsson, Chuan Wang, Gunnar V. Alm, Ann‐Christine Syvänen, Lars Rönnblom, Betsy Barnes

    出版 2010
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  5. 5
    Fine-mapping and mutation analysis of TRPM1: a candidate gene for leopard complex (LP) spotting and congenital stationary night blindness in horses

    Fine-mapping and mutation analysis of TRPM1: a candidate gene for leopard complex (LP) spotting and congenital stationary night blindness in horses 由 Rebecca R. Bellone, George W. Forsyth, Tosso Leeb, Sheila Archer, Snævar Sigurðsson, Freyja Imsland, Evan Mauceli, Martina Engensteiner, Ernest Bailey, Lynne S Sandmeyer, Bruce H Grahn, Kerstin Lindblad‐Toh, Claire M. Wade

    出版 2010
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  6. 6
    An insertion deletion polymorphism in the Interferon Regulatory Factor 5 (IRF5) gene confers risk of inflammatory bowel diseases

    An insertion deletion polymorphism in the Interferon Regulatory Factor 5 (IRF5) gene confers risk of inflammatory bowel diseases 由 Vinciane Dideberg, Guðrún Kristjánsdóttir, Lili Milani, Cécile Libioulle, Snævar Sigurðsson, Édouard Louis, A.-C. Wiman, Séverine Vermeire, Paul Rutgeerts, Jacques Bélaïche, Denis Franchimont, A. Van Gossum, Vincent Bours, A-C Syvänen

    出版 2007
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  7. 7
    Candidate genes and functional noncoding variants identified in a canine model of obsessive-compulsive disorder

    Candidate genes and functional noncoding variants identified in a canine model of obsessive-compulsive disorder 由 Ruqi Tang, Hyun Ji Noh, Dongqing Wang, Snævar Sigurðsson, Ross Swofford, Michele Perloski, Margaret Duxbury, Edward E. Patterson, Julie M. Albright, Marta G. Castelhano, Adam Auton, Adam R. Boyko, Guoping Feng, Kerstin Lindblad‐Toh, Elinor K. Karlsson

    出版 2014
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  8. 8
    A STAT4 risk allele is associated with ischaemic cerebrovascular events and anti-phospholipid antibodies in systemic lupus erythematosus

    A STAT4 risk allele is associated with ischaemic cerebrovascular events and anti-phospholipid antibodies in systemic lupus erythematosus 由 Elisabet Svenungsson, Jan-Ακε Gustafsson, Dag Leonard, Johanna K. Sandling, Iva Gunnarsson, Gunnel Nordmark, Andreas Jönsen, Anders Bengtsson, G Sturfelt, Solbritt Rantapää‐Dahlqvist, Kerstin Elvin, Ulf Sundin, Sophie Garnier, Julia F. Simard, Snævar Sigurðsson, Leonid Padyukov, Ann-Christine Syvänen, Lars Rönnblom

    出版 2009
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  9. 9
    Comprehensive evaluation of the genetic variants of interferon regulatory factor 5 (IRF5) reveals a novel 5 bp length polymorphism as strong risk factor for systemic lupus erythematosus

    Comprehensive evaluation of the genetic variants of interferon regulatory factor 5 (IRF5) reveals a novel 5 bp length polymorphism as strong risk factor for systemic lupus erythema... 由 Snævar Sigurðsson, Harald H.H. Göring, Gudlaug Kristjansdottir, Lili Milani, Gunnel Nordmark, Johanna K. Sandling, Maija‐Leena Eloranta, Di Feng, Niquiche Sangster‐Guity, Iva Gunnarsson, Elisabet Svenungsson, Gunnar Sturfelt, Andreas Jönsen, Lennart Truedsson, Betsy Barnes, Gunnar V. Alm, Lars Rönnblom, Ann-Christine Syvänen

    出版 2007
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  10. 10
    Rare mutations associating with serum creatinine and chronic kidney disease

    Rare mutations associating with serum creatinine and chronic kidney disease 由 Garðar Sveinbjörnsson, Evgenia Mikaelsdottir, Runólfur Pálsson, Ólafur S. Indridason, Hilma Hólm, Áslaug Jónasdóttir, Agnar Helgason, Snævar Sigurðsson, Aðalbjörg Jónasdóttir, Ásgeir Sigurðsson, Guðmundur I. Eyjólfsson, Ólöf Sigurðardóttir, Ólafur Þ. Magnússon, Augustine Kong, Gísli Másson, Patrick Sulem, Ísleifur Ólafsson, Unnur Þorsteinsdóttir, Daníel F. Guðbjartsson, Kāri Stefánsson

    出版 2014
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  11. 11
    Polymorphisms in the Tyrosine Kinase 2 and Interferon Regulatory Factor 5 Genes Are Associated with Systemic Lupus Erythematosus

    Polymorphisms in the Tyrosine Kinase 2 and Interferon Regulatory Factor 5 Genes Are Associated with Systemic Lupus Erythematosus 由 Snævar Sigurðsson, Gunnel Nordmark, Harald H.H. Göring, Katarina Lindroos, Ann-Christin Wiman, Gunnar Sturfelt, Andreas Jönsen, Solbritt Rantapää‐Dahlqvist, Bozena Möller, Juha Kere, Sari Koskenmies, Elisabeth Widén, Maija‐Leena Eloranta, Heikki Julkunen, Helga Kristjánsdóttir, Kristján Steinsson, Gunnar V. Alm, Lars Rönnblom, Ann‐Christine Syvänen

    出版 2005
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  12. 12
    A risk haplotype of STAT4 for systemic lupus erythematosus is over-expressed, correlates with anti-dsDNA and shows additive effects with two risk alleles of IRF5

    A risk haplotype of STAT4 for systemic lupus erythematosus is over-expressed, correlates with anti-dsDNA and shows additive effects with two risk alleles of IRF5 由 Snævar Sigurðsson, Gunnel Nordmark, Sophie Garnier, Elin Grundberg, Tony Kwan, Ola Nilsson, Maija‐Leena Eloranta, Iva Gunnarsson, Elisabet Svenungsson, Gunnar Sturfelt, Anders Bengtsson, Andreas Jönsen, Lennart Truedsson, Solbritt Rantapää‐Dahlqvist, Catharina Eriksson, G. Alm, H.H.H. Göring, Tomi Pastinen, A-C Syvänen, L. Ronnblom

    出版 2008
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  13. 13
    Identification of Genomic Regions Associated with Phenotypic Variation between Dog Breeds using Selection Mapping

    Identification of Genomic Regions Associated with Phenotypic Variation between Dog Breeds using Selection Mapping 由 Amaury Vaysse, Abhirami Ratnakumar, Thomas Derrien, Erik Axelsson, Gerli Pielberg, Snævar Sigurðsson, Tove Fall, Eija H. Seppälä, Mark S. Hansen, Cindy Lawley, Elinor K. Karlsson, Danika L. Bannasch, Carles Vilà, Hannes Lohi, Francis Galibert, Merete Fredholm, Jens Häggström, Åke Hedhammar, Catherine André, Kerstin Lindblad‐Toh, Christophe Hitte, Matthew T. Webster

    出版 2011
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  14. 14
    Canine Hereditary Ataxia in Old English Sheepdogs and Gordon Setters Is Associated with a Defect in the Autophagy Gene Encoding RAB24

    Canine Hereditary Ataxia in Old English Sheepdogs and Gordon Setters Is Associated with a Defect in the Autophagy Gene Encoding RAB24 由 Caryline Agler, Dahlia M. Nielsen, Ganokon Urkasemsin, Andrew Singleton, Noriko Tonomura, Snævar Sigurðsson, Ruqi Tang, Keith E. Linder, Sampath Arepalli, Dena G. Hernandez, Kerstin Lindblad‐Toh, Joyce van de Leemput, Alison A. Motsinger‐Reif, Dennis P. O’Brien, Jerold S. Bell, Tonya Harris, Steven J. Steinberg, Natasha J. Olby

    出版 2014
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  15. 15
    A candidate gene study of the type I interferon pathway implicates IKBKE and IL8 as risk loci for SLE

    A candidate gene study of the type I interferon pathway implicates IKBKE and IL8 as risk loci for SLE 由 Johanna K. Sandling, Sophie Garnier, Snævar Sigurðsson, Chuan Wang, Gunnel Nordmark, Iva Gunnarsson, Elisabet Svenungsson, Leonid Padyukov, Gunnar Sturfelt, Andreas Jönsen, Anders A Bengtsson, Lennart Truedsson, Catharina Eriksson, Solbritt Rantapää‐Dahlqvist, Anders Mälarstig, Rona J. Strawbridge, Anders Hamsten, Lindsey A. Criswell, Robert Graham, Timothy W. Behrens, Maija‐Leena Eloranta, Gunnar V. Alm, Lars Rönnblom, Ann‐Christine Syvänen

    出版 2010
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  16. 16
    Sequence variants in ARHGAP15, COLQ and FAM155A associate with diverticular disease and diverticulitis

    Sequence variants in ARHGAP15, COLQ and FAM155A associate with diverticular disease and diverticulitis 由 Snævar Sigurðsson, Kristjan F. Alexandersson, Patrick Sulem, Bjarke Feenstra, Steinunn Guðmundsdóttir, Gísli H. Halldórsson, Sigurgeir Ólafsson, Ásgeir Sigurðsson, Þórunn Rafnar, Thorgeir E. Thorgeirsson, Erik Sørensen, Andreas Nordholm‐Carstensen, Jakob Burcharth, Jens Rikardt Andersen, Henrik Jørgensen, Emma Possfelt-Møller, Henrik Ullum, Guðmar Þorleifsson, Gísli Másson, Unnur Þorsteinsdóttir, Mads Melbye, Daníel F. Guðbjartsson, Tryggvi Stefánsson, Ingileif Jónsdóttir, Kāri Stefánsson

    出版 2017
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  17. 17
    Interferon regulatory factor 5 (IRF5) gene variants are associated with multiple sclerosis in three distinct populations

    Interferon regulatory factor 5 (IRF5) gene variants are associated with multiple sclerosis in three distinct populations 由 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

    出版 2008
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  18. 18
    Genome-wide analyses implicate 33 loci in heritable dog osteosarcoma, including regulatory variants near CDKN2A/B

    Genome-wide analyses implicate 33 loci in heritable dog osteosarcoma, including regulatory variants near CDKN2A/B 由 Elinor K. Karlsson, Snævar Sigurðsson, Emma Ivansson, Rachael Thomas, Ingegerd Elvers, Jason Wright, Cédric Howald, Noriko Tonomura, Michele Perloski, Ross Swofford, Tara Biagi, Sarah Fryc, Nathan Anderson, Céline Courtay-Cahen, Lisa Youell, Sally L. Ricketts, Sarah Mandlebaum, Patricio Rivera, Henrik von Euler, William C. Kisseberth, Cheryl A. London, Eric S. Lander, Guillermo Couto, Kenine E. Comstock, Mike Starkey, Jaime F. Modiano, Matthew Breen, Kerstin Lindblad‐Toh

    出版 2013
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  19. 19
    Three functional variants of IFN regulatory factor 5 ( <i>IRF5</i> ) define risk and protective haplotypes for human lupus

    Three functional variants of IFN regulatory factor 5 ( <i>IRF5</i> ) define risk and protective haplotypes for human lupus 由 Robert Graham, Chieko Kyogoku, Snævar Sigurðsson, Irina Vlasova-St. Louis, Leela Davies, Emily C. Baechler, Robert M. Plenge, Thearith Koeuth, Ward Ortmann, Geoffrey Hom, Jason W. Bauer, Clarence Gillett, Noël P. Burtt, Deborah S. Cunninghame Graham, Robert C. Onofrio, Michelle Petri, Iva Gunnarsson, Elisabet Svenungsson, Lars Rönnblom, Gunnel Nordmark, Peter K. Gregersen, Kathy L. Moser, Patrick M. Gaffney, Lindsey A. Criswell, Timothy J. Vyse, Ann-Christine Syvänen, Paul R. Bohjanen, Mark J. Daly, Timothy W. Behrens, David Altshuler

    出版 2007
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  20. 20
    A homozygous loss-of-function mutation leading to CYBC1 deficiency causes chronic granulomatous disease

    A homozygous loss-of-function mutation leading to CYBC1 deficiency causes chronic granulomatous disease 由 Gudny A. Arnadottir, Gudmundur L. Norddahl, Steinunn Guðmundsdóttir, Arna B. Agustsdottir, Snævar Sigurðsson, Brynjar Ö. Jensson, Kristbjörg Bjarnadóttir, Fannar Theódórs, Stefania Benónísdóttir, Erna V. Ivarsdottir, Ásmundur Oddsson, Ragnar P. Kristjansson, Gerald Sulem, Kristjan F. Alexandersson, Thorhildur Juliusdottir, Kjartan R. Guðmundsson, Jona Saemundsdottir, Aðalbjörg Jónasdóttir, Áslaug Jónasdóttir, Ásgeir Sigurðsson, Paolo Manzanillo, Sigurjón A. Guðjónsson, Guðmundur Á. Þórisson, Ólafur Þ. Magnússon, Gísli Másson, Kjartan B. Örvar, Hilma Hólm, Sigurður Björnsson, Reynir Arngrı́msson, Daníel F. Guðbjartsson, Unnur Þorsteinsdóttir, Ingileif Jónsdóttir, Ásgeir Haraldsson, Patrick Sulem, Kāri Stefánsson

    出版 2018
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