Medizinische Universität Graz Austria/Österreich - Forschungsportal - Medical University of Graz
Publikationen
Suchbegriffe: METHYLTRANSFERASES - GENETICS , . Treffer: 7
2018
Greif, PA; Hartmann, L; Vosberg, S; Stief, SM; Mattes, R; Hellmann, I; Metzeler, KH; Herold, T; Bamopoulos, SA; Kerbs, P; Jurinovic, V; Schumacher, D; Pastore, F; Bräundl, K; Zellmeier, E; Ksienzyk, B; Konstandin, NP; Schneider, S; Graf, A; Krebs, S; Blum, H; Neumann, M; Baldus, CD; Bohlander, SK; Wolf, S; Görlich, D; Berdel, WE; Wörmann, BJ; Hiddemann, W; Spiekermann, K
Evolution of Cytogenetically Normal Acute Myeloid Leukemia During Therapy and Relapse: An Exome Sequencing Study of 50 Patients.
Clin Cancer Res. 2018; 24(7): 1716-1726.
Doi: 10.1158/1078-0432.CCR-17-2344
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2017
Herold, T; Metzeler, KH; Vosberg, S; Hartmann, L; Jurinovic, V; Opatz, S; Konstandin, NP; Schneider, S; Zellmeier, E; Ksienzyk, B; Graf, A; Krebs, S; Blum, H; Cristina Sauerland, M; Büchner, T; Berdel, WE; Wörmann, BJ; Mansmann, U; Hiddemann, W; Bohlander, SK; Spiekermann, K; Greif, PA
Acute myeloid leukemia with del(9q) is characterized by frequent mutations of NPM1, DNMT3A, WT1 and low expression of TLE4.
Genes Chromosomes Cancer. 2017; 56(1): 75-86.
Doi: 10.1002/gcc.22418
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2016
Suárez-Calvet, M; Neumann, M; Arzberger, T; Abou-Ajram, C; Funk, E; Hartmann, H; Edbauer, D; Kremmer, E; Göbl, C; Resch, M; Bourgeois, B; Madl, T; Reber, S; Jutzi, D; Ruepp, MD; Mackenzie, IR; Ansorge, O; Dormann, D; Haass, C
Monomethylated and unmethylated FUS exhibit increased binding to Transportin and distinguish FTLD-FUS from ALS-FUS.
Acta Neuropathol. 2016; 131(4):587-604
Doi: 10.1007/s00401-016-1544-2
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2014
Bernkopf, M; Webersinke, G; Tongsook, C; Koyani, CN; Rafiq, MA; Ayaz, M; Müller, D; Enzinger, C; Aslam, M; Naeem, F; Schmidt, K; Gruber, K; Speicher, MR; Malle, E; Macheroux, P; Ayub, M; Vincent, JB; Windpassinger, C; Duba, HC
Disruption of the methyltransferase-like 23 gene METTL23 causes mild autosomal recessive intellectual disability.
Hum Mol Genet. 2014; 23(15):4015-4023
Doi: 10.1093/hmg/ddu115
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2013
Neumann, M; Heesch, S; Schlee, C; Schwartz, S; Gökbuget, N; Hoelzer, D; Konstandin, NP; Ksienzyk, B; Vosberg, S; Graf, A; Krebs, S; Blum, H; Raff, T; Brüggemann, M; Hofmann, WK; Hecht, J; Bohlander, SK; Greif, PA; Baldus, CD
Whole-exome sequencing in adult ETP-ALL reveals a high rate of DNMT3A mutations.
Blood. 2013; 121(23): 4749-4752.
Doi: 10.1182/blood-2012-11-465138
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2012
Dormann, D; Madl, T; Valori, CF; Bentmann, E; Tahirovic, S; Abou-Ajram, C; Kremmer, E; Ansorge, O; Mackenzie, IR; Neumann, M; Haass, C
Arginine methylation next to the PY-NLS modulates Transportin binding and nuclear import of FUS.
EMBO J. 2012; 31(22): 4258-4275.
Doi: 10.1038/emboj.2012.261
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Khan, MA; Rafiq, MA; Noor, A; Hussain, S; Flores, JV; Rupp, V; Vincent, AK; Malli, R; Ali, G; Khan, FS; Ishak, GE; Doherty, D; Weksberg, R; Ayub, M; Windpassinger, C; Ibrahim, S; Frye, M; Ansar, M; Vincent, JB
Mutation in NSUN2, which encodes an RNA methyltransferase, causes autosomal-recessive intellectual disability.
Am J Hum Genet. 2012; 90(5):856-863
Doi: 10.1016/j.ajhg.2012.03.023
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