检索结果 - Myklebust, Line M

Receptor for activated C-kinase (RACK1) plays a central role in Ras-mediated signal transduction 由 Lillehaug, Johan R, Myklebust, Line M, Raae, Arnt, Bjørndal, Bodil

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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 由 McTiernan, Nina, Støve, Svein Isungset, Aukrust, Ingvild, Mårli, Marita Torrisen, Myklebust, Line M., Houge, Gunnar, Arnesen, Thomas

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LEDGF/p75 has increased expression in blasts from chemotherapy-resistant human acute myelogenic leukemia patients and protects leukemia cells from apoptosis in vitro 由 Huang, Tien-sheng, Myklebust, Line M, Kjarland, Endre, Gjertsen, Bjørn Tore, Pendino, Frederic, Bruserud, Øystein, Døskeland, Stein Ove, Lillehaug, Johan R

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De novo missense mutations in the NAA10 gene cause severe non-syndromic developmental delay in males and females 由 Popp, Bernt, Støve, Svein I, Endele, Sabine, Myklebust, Line M, Hoyer, Juliane, Sticht, Heinrich, Azzarello-Burri, Silvia, Rauch, Anita, Arnesen, Thomas, Reis, André

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A Role for Human N-alpha Acetyltransferase 30 (Naa30) in Maintaining Mitochondrial Integrity 由 Van Damme, Petra, Kalvik, Thomas V., Starheim, Kristian K., Jonckheere, Veronique, Myklebust, Line M., Menschaert, Gerben, Varhaug, Jan Erik, Gevaert, Kris, Arnesen, Thomas

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Structural determinants and cellular environment define processed actin as the sole substrate of the N-terminal acetyltransferase NAA80 由 Goris, Marianne, Magin, Robert S., Foyn, Håvard, Myklebust, Line M., Varland, Sylvia, Ree, Rasmus, Drazic, Adrian, Bhambra, Parminder, Støve, Svein I., Baumann, Markus, Haug, Bengt Erik, Marmorstein, Ronen, Arnesen, Thomas

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Downregulation of N-terminal acetylation triggers ABA-mediated drought responses in Arabidopsis 由 Linster, Eric, Stephan, Iwona, Bienvenut, Willy V., Maple-Grødem, Jodi, Myklebust, Line M., Huber, Monika, Reichelt, Michael, Sticht, Carsten, Geir Møller, Simon, Meinnel, Thierry, Arnesen, Thomas, Giglione, Carmela, Hell, Rüdiger, Wirtz, Markus

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Biochemical and cellular analysis of Ogden syndrome reveals downstream Nt-acetylation defects 由 Myklebust, Line M., Van Damme, Petra, Støve, Svein I., Dörfel, Max J., Abboud, Angèle, Kalvik, Thomas V., Grauffel, Cedric, Jonckheere, Veronique, Wu, Yiyang, Swensen, Jeffrey, Kaasa, Hanna, Liszczak, Glen, Marmorstein, Ronen, Reuter, Nathalie, Lyon, Gholson J., Gevaert, Kris, Arnesen, Thomas

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A novel NAA10 variant with impaired acetyltransferase activity causes developmental delay, intellectual disability, and hypertrophic cardiomyopathy 由 Støve, Svein Isungset, Blenski, Marina, Stray-Pedersen, Asbjørg, Wierenga, Klaas J., Jhangiani, Shalini N., Akdemir, Zeynep Coban, Crawford, David, McTiernan, Nina, Myklebust, Line M., Purcarin, Gabriela, McNall-Knapp, Rene, Wadley, Alexandrea, Belmont, John W., Kim, Jeffrey J., Lupski, James R, Arnesen, Thomas

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