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Svein Isungset Støves bilde

Svein Isungset Støve

Postdoktor
  • E-postSvein.Stove@uib.no
  • Telefon+47 55 58 43 49
  • Besøksadresse
    Jonas Lies vei 91
  • Postal Address
    Postboks 7804
    5020 Bergen
Tidsskriftartikler
  • Goris, Marianne; Magin, Robert S.; Foyn, Håvard; Myklebust, Line Merethe; Varland, Sylvia; Ree, Rasmus Moen; Drazic, Adrian; Bhambra, Parminder Kaur; Støve, Svein Isungset; Baumann, Markus; Haug, Bengt Erik; Marmorstein, Ronen; Arnesen, Thomas. 2018. Structural determinants and cellular environment define processed actin as the sole substrate of the N-terminal acetyltransferase NAA80. Proceedings of the National Academy of Sciences of the United States of America. 115: 4405-4410. Publisert 2018-03-26. doi: 10.1073/pnas.1719251115
  • Mc Tiernan, Nina; Støve, Svein Isungset; Aukrust, Ingvild; Mårli, Marita Torrissen; Myklebust, Line Merethe; Houge, Gunnar; Arnesen, Thomas. 2018. NAA10 dysfunction with normal NatA-complex activity in a girl with non-syndromic ID and a de novo NAA10 p.(V111G) variant - a case report. BMC Medical Genetics. 19:47: 1-9. doi: 10.1186/s12881-018-0559-z
  • Støve, Svein Isungset; Blenski, Marina; Stray-Pedersen, Asbjørg; Wierenga, Klaas J.; Jhangiani, Shalini N.; Akdemir, Zeynep Coban; Crawford, David; Mc Tiernan, Nina; Myklebust, Line Merethe; Purcarin, Gabriela; McNall-Knapp, Rene; Wadley, Alexandrea; Belmont, John W.; Kim, Jeffrey J.; Lupski, James R.; Arnesen, Thomas. 2018. A novel NAA10 variant with impaired acetyltransferase activity causes developmental delay, intellectual disability, and hypertrophic cardiomyopathy. European Journal of Human Genetics. 1-12. doi: 10.1038/s41431-018-0136-0
  • Saunier, Chloé; Støve, Svein Isungset; Popp, Bernt; Gérard, Bénédicte; Blenski, Marina; AhMew, Nicholas; de Bie, Charlotte; Goldenberg, Paula; Isidor, Bertrand; Keren, Boris; Leheup, Bruno; Lampert, Laetitia; Mignot, Cyril; Tezcan, Kamer; Mancini, Grazia M.S.; Nava, Caroline; Wasserstein, Melissa; Bruel, Ange-Line; Thevenon, Julien; Masurel, Alice; Duffourd, Yannis; Kuentz, Paul; Huet, Frédéric; Rivière, Jean-Baptiste; van Slegtenhorst, Marjon; Faivre, Laurence; Piton, Amélie; Reis, André; Arnesen, Thomas; Thauvin-Robinet, Christel; Zweier, Christiane. 2016. Expanding the phenotype associated with NAA10-related N-terminal acetylation deficiency. Human Mutation. 37: 755-764. doi: 10.1002/humu.23001
  • Støve, Svein Isungset; Magin, Robert S.; Foyn, Håvard; Haug, Bengt Erik; Marmorstein, Ronen; Arnesen, Thomas. 2016. Crystal structure of the Golgi-associated human N-alpha acetyltransferase 60 (Naa60/NatF) reveals the molecular determinants for substrate-specific acetylation. Structure. 24: 1044-1056. doi: 10.1016/j.str.2016.04.020
  • Aksnes, Henriette; Van Damme, Petra; Goris, Marianne; Starheim, Kristian K.; Marie, Michael Bruno Eric; Støve, Svein Isungset; Hoel, Camilla; Kalvik, Thomas Vikestad; Hole, Kristine; Glomnes, Nina; Furnes, Clemens; Ljostveit, Sonja; Ziegler, Mathias; Niere, Marc; Gevaert, Kris; Arnesen, Thomas. 2015. An organellar Nα-acetyltransferase, Naa60, acetylates cytosolic n termini of transmembrane proteins and maintains golgi integrity. Cell reports. 10: 1362-1374. doi: 10.1016/j.celrep.2015.01.053
  • Casey, Jillian P.; Støve, Svein Isungset; McGorrian, Catherine; Galvin, Joseph; Blenski, Marina; Dunne, Aimee; Ennis, Sean; Brett, Francesca; King, Mary D.; Arnesen, Thomas; Lynch, Sally Ann. 2015. NAA10 mutation causing a novel intellectual disability syndrome with Long QT due to N-terminal acetyltransferase impairment. Scientific Reports. 5:16022. doi: 10.1038/srep16022
  • Myklebust, Line Merethe; Støve, Svein Isungset; Arnesen, Thomas. 2015. Naa10 in development and disease. OncoTarget. 6: 34041-34042. doi: 10.18632/oncotarget.5867
  • Myklebust, Line Merethe; Van Damme, Petra; Støve, Svein Isungset; Dörfel, Max J; Abboud, Angèle; Kalvik, Thomas Vikestad; Grauffel, Cédric; Jonckheere, Veronique; Wu, Yiyang; Swensen, Jeffrey; Kaasa, Hanna; Liszczak, Glen; Marmorstein, Ronen; Reuter, Nathalie; Lyon, Gholson J; Gevaert, Kris; Arnesen, Thomas. 2015. Biochemical and cellular analysis of Ogden syndrome reveals downstream Nt-acetylation defects. Human Molecular Genetics. 24: 1956-1976. doi: 10.1093/hmg/ddu611
  • Popp, Bernt; Støve, Svein Isungset; Endele, Sabine; Myklebust, Line Merethe; Hoyer, Juliane; Sticht, Heinrich; Azzarello-Burri, Silvia; Rauch, Anita; Arnesen, Thomas; Reis, Andre. 2015. De novo missense mutations in the NAA10 gene cause severe non-syndromic developmental delay in males and females. European Journal of Human Genetics. 23: 602-609. doi: 10.1038/ejhg.2014.150
  • Van Damme, Petra; Støve, Svein Isungset; Glomnes, Nina; Gevaert, Kris; Arnesen, Thomas. 2014. A Saccharomyces cerevisiae model reveals in vivo functional impairment of the Ogden syndrome N-terminal acetyltransferase NAA10 Ser37Pro mutant. Molecular & Cellular Proteomics. 13: 2031-2041. doi: 10.1074/mcp.M113.035402
  • Foyn, Håvard; Van Damme, Petra; Støve, Svein Isungset; Glomnes, Nina; Evjenth, Rune Henrik; Gevaert, Kris; Arnesen, Thomas. 2013. Protein N-terminal acetyltransferases act as N-terminal propionyltransferases in vitro and in vivo. Molecular & Cellular Proteomics. 12: 42-54. doi: 10.1074/mcp.M112.019299
Rapporter/avhandlinger
  • Støve, Svein Isungset. 2015. Functional analysis of Na-acetyltransferase 10(NAA10) variants identified in patients with genetic disorders. University of Bergen.

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