Medizinische Universität Graz Austria/Österreich - Forschungsportal - Medical University of Graz

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Publikationen

Suchbegriffe: NUCLEAR PROTEINS - GENETICS , . Treffer: 45

2020

Benesch, M; Nemes, K; Neumayer, P; Hasselblatt, M; Timmermann, B; Bison, B; Ebetsberger-Dachs, G; Bourdeaut, F; Dufour, C; Biassoni, V; Morales La Madrid, A; Entz-Werle, N; Laithier, V; Quehenberger, F; Weis, S; Sumerauer, D; Siebert, R; Bens, S; Schneppenheim, R; Kool, M; Modena, P; Fouyssac, F; C Frühwald, M Spinal cord atypical teratoid/rhabdoid tumors in children: Clinical, genetic, and outcome characteristics in a representative European cohort.
Pediatr Blood Cancer. 2020; 67(1):e28022-e28022 Doi: 10.1002/pbc.28022
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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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Khan, A; Dellago, H; Terlecki-Zaniewicz, L; Karbiener, M; Weilner, S; Hildner, F; Steininger, V; Gabriel, C; Mück, C; Jansen-Dürr, P; Hacobian, A; Scheideler, M; Grillari-Voglauer, R; Schosserer, M; Grillari, J SNEVhPrp19/hPso4 Regulates Adipogenesis of Human Adipose Stromal Cells.
Stem Cell Reports. 2017; 8(1):21-29 Doi: 10.1016/j.stemcr.2016.12.001 [OPEN ACCESS]
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Planells-Palop, V; Hazazi, A; Feichtinger, J; Jezkova, J; Thallinger, G; Alsiwiehri, NO; Almutairi, M; Parry, L; Wakeman, JA; McFarlane, RJ Human germ/stem cell-specific gene TEX19 influences cancer cell proliferation and cancer prognosis.
Mol Cancer. 2017; 16(1): 84-84. Doi: 10.1186/s12943-017-0653-4 [OPEN ACCESS]
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2016

Bogen, D; Brunner, C; Walder, D; Ziegler, A; Abbasi, R; Ladenstein, RL; Noguera, R; Martinsson, T; Amann, G; Schilling, FH; Ussowicz, M; Benesch, M; Ambros, PF; Ambros, IM The genetic tumor background is an important determinant for heterogeneous MYCN-amplified neuroblastoma.
Int J Cancer. 2016; 139(1):153-163 Doi: 10.1002/ijc.30050 [OPEN ACCESS]
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2015

Berghold, VM; Gauster, M; Hemmings, DG; Moser, G; Kremshofer, J; Siwetz, M; Sundl, M; Huppertz, B Phospholipid scramblase 1 (PLSCR1) in villous trophoblast of the human placenta.
Histochem Cell Biol. 2015; 143(4):381-396 Doi: 10.1007/s00418-014-1294-y
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Haslbeck, V; Eckl, JM; Drazic, A; Rutz, DA; Lorenz, OR; Zimmermann, K; Kriehuber, T; Lindemann, C; Madl, T; Richter, K The activity of protein phosphatase 5 towards native clients is modulated by the middle- and C-terminal domains of Hsp90.
Sci Rep. 2015; 5(4):17058-17058 Doi: 10.1038/srep17058 [OPEN ACCESS]
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Wolinski, H; Hofbauer, HF; Hellauer, K; Cristobal-Sarramian, A; Kolb, D; Radulovic, M; Knittelfelder, OL; Rechberger, GN; Kohlwein, SD Seipin is involved in the regulation of phosphatidic acid metabolism at a subdomain of the nuclear envelope in yeast.
Biochim Biophys Acta. 2015; 1851(11):1450-1464 Doi: 10.1016/j.bbalip.2015.08.003 [OPEN ACCESS]
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2014

Friedmacher, F; Fujiwara, N; Hofmann, AD; Takahashi, H; Gosemann, JH; Puri, P Expression of Eya1 and Six1 is decreased in distal airways of rats with experimental pulmonary hypoplasia.
J Pediatr Surg. 2014; 49(2): 301-304. Doi: 10.1016/j.jpedsurg.2013.11.043
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Pichler, M; Calin, GA Long noncoding RNA in neuroblastoma: new light on the (old) N-Myc story.
J Natl Cancer Inst. 2014; 106(7): Doi: 10.1093/jnci/dju150 [OPEN ACCESS]
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Rau, TT; Agaimy, A; Gehoff, A; Geppert, C; Jung, K; Knobloch, K; Langner, C; Lugli, A; Groenbus-Lurkin, I; Nagtegaal, ID; Rüschoff, J; Saegert, X; Sarbia, M; Schneider-Stock, R; Vieth, M; Zwarthoff, EC; Hartmann, A Defined morphological criteria allow reliable diagnosis of colorectal serrated polyps and predict polyp genetics.
Virchows Arch. 2014; 464(6):663-672 Doi: 10.1007/s00428-014-1569-7
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Thorwarth, A; Schnittert-Hübener, S; Schrumpf, P; Müller, I; Jyrch, S; Dame, C; Biebermann, H; Kleinau, G; Katchanov, J; Schuelke, M; Ebert, G; Steininger, A; Bönnemann, C; Brockmann, K; Christen, HJ; Crock, P; deZegher, F; Griese, M; Hewitt, J; Ivarsson, S; Hübner, C; Kapelari, K; Plecko, B; Rating, D; Stoeva, I; Ropers, HH; Grüters, A; Ullmann, R; Krude, H Comprehensive genotyping and clinical characterisation reveal 27 novel NKX2-1 mutations and expand the phenotypic spectrum.
J Med Genet. 2014; 51(6): 375-387. Doi: 10.1136/jmedgenet-2013-102248 [OPEN ACCESS]
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2013

Bourgeois, B; Gilquin, B; Tellier-Lebègue, C; Östlund, C; Wu, W; Pérez, J; El Hage, P; Lallemand, F; Worman, HJ; Zinn-Justin, S Inhibition of TGF-β signaling at the nuclear envelope: characterization of interactions between MAN1, Smad2 and Smad3, and PPM1A.
Sci Signal. 2013; 6(280): ra49-ra49. Doi: 10.1126/scisignal.2003411 [OPEN ACCESS]
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Dorronsoro, A; Lang, V; Jakobsson, E; Ferrin, I; Salcedo, JM; Fernández-Rueda, J; Fechter, K; Rodriguez, MS; Trigueros, C Identification of the NF-κB inhibitor A20 as a key regulator for human adipogenesis.
Cell Death Dis. 2013; 4(1):e972-e972 Doi: 10.1038/cddis.2013.494 [OPEN ACCESS]
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Pfeiffer, T; Schleuning, M; Mayer, J; Haude, KH; Tischer, J; Buchholz, S; Bunjes, D; Bug, G; Holler, E; Meyer, RG; Greinix, H; Scheid, C; Christopeit, M; Schnittger, S; Braess, J; Schlimok, G; Spiekermann, K; Ganser, A; Kolb, HJ; Schmid, C Influence of molecular subgroups on outcome of acute myeloid leukemia with normal karyotype in 141 patients undergoing salvage allogeneic stem cell transplantation in primary induction failure or beyond first relapse.
Haematologica. 2013; 98(4):518-525 Doi: 10.3324/haematol.2012.070235 [OPEN ACCESS]
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Senanayake, U; Koller, K; Pichler, M; Leuschner, I; Strohmaier, H; Hadler, U; Das, S; Hoefler, G; Guertl, B The pluripotent renal stem cell regulator SIX2 is activated in renal neoplasms and influences cellular proliferation and migration.
Hum Pathol. 2013; 44(3):336-345 Doi: 10.1016/j.humpath.2012.05.021
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Valko, PO; Gavrilov, YV; Yamamoto, M; Reddy, H; Haybaeck, J; Mignot, E; Baumann, CR; Scammell, TE Increase of histaminergic tuberomammillary neurons in narcolepsy.
Ann Neurol. 2013; 74(6):794-804 Doi: 10.1002/ana.24019
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2012

Laimer, D; Dolznig, H; Kollmann, K; Vesely, PW; Schlederer, M; Merkel, O; Schiefer, AI; Hassler, MR; Heider, S; Amenitsch, L; Thallinger, C; Staber, PB; Simonitsch-Klupp, I; Artaker, M; Lagger, S; Turner, SD; Pileri, S; Piccaluga, PP; Valent, P; Messana, K; Landra, I; Weichhart, T; Knapp, S; Shehata, M; Todaro, M; Sexl, V; Höfler, G; Piva, R; Medico, E; Ruggeri, BA; Cheng, M; Eferl, R; Egger, G; Penninger, JM; Jaeger, U; Moriggl, R; Inghirami, G; Kenner, L PDGFR blockade is a rational and effective therapy for NPM-ALK-driven lymphomas.
Nat Med. 2012; 18(11):1699-1704 Doi: 10.1038/nm.2966 [OPEN ACCESS]
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Quarrell, OW; Handley, O; O'Donovan, K; Dumoulin, C; Ramos-Arroyo, M; Biunno, I; Bauer, P; Kline, M; Landwehrmeyer, GB; European Huntington’s Disease Network Discrepancies in reporting the CAG repeat lengths for Huntington's disease.
Eur J Hum Genet. 2012; 20(1): 20-26. Doi: 10.1038/ejhg.2011.136 [OPEN ACCESS]
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2011

Schrama, D; Scherer, D; Schneider, M; Zapatka, M; Bröcker, EB; Schadendorf, D; Ugurel, S; Kumar, R; Becker, JC ERCC5 p.Asp1104His and ERCC2 p.Lys751Gln Polymorphisms Are Independent Prognostic Factors for the Clinical Course of Melanoma.
J Invest Dermatol. 2011; 131(6):1280-1290 Doi: 10.1038/jid.2011.35 [OPEN ACCESS]
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2010

Houlden, H; Schneider, SA; Paudel, R; Melchers, A; Schwingenschuh, P; Edwards, M; Hardy, J; Bhatia, KP THAP1 mutations (DYT6) are an additional cause of early-onset dystonia.
Neurology. 2010; 74(10): 846-850. Doi: 10.1212/WNL.0b013e3181d5276d [OPEN ACCESS]
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Pannicke, U; Hönig, M; Schulze, I; Rohr, J; Heinz, GA; Braun, S; Janz, I; Rump, EM; Seidel, MG; Matthes-Martin, S; Soerensen, J; Greil, J; Stachel, DK; Belohradsky, BH; Albert, MH; Schulz, A; Ehl, S; Friedrich, W; Schwarz, K The most frequent DCLRE1C (ARTEMIS) mutations are based on homologous recombination events.
Hum Mutat. 2010; 31(2):197-207 Doi: 10.1002/humu.21168
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Schmetterer, KG; Seidel, MG; Körmöczi, U; Rottal, A; Schwarz, K; Matthes-Martin, S; Steinberger, P; Pickl, WF Two newly diagnosed HLA class II-deficient patients identified by rapid vector-based complementation analysis reveal discoordinate invariant chain expression levels.
Int Arch Allergy Immunol. 2010; 152(4):390-400 Doi: 10.1159/000288292
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Soehn, AS; Franck, T; Biskup, S; Giaime, E; Melle, C; Rott, R; Cebo, D; Kalbacher, H; Ott, E; Pahnke, J; Meitinger, T; Krüger, R; Gasser, T; Berg, D; von Eggeling, F; Engelender, S; da Costa, CA; Riess, O Periphilin is a novel interactor of synphilin-1, a protein implicated in Parkinson's disease.
Neurogenetics. 2010; 11(2):203-215 Doi: 10.1007/s10048-009-0215-z
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Villar, V; Kocic, J; Bugarski, D; Jovcic, G; Santibanez, JF SKIP is required for TGF-β1-induced epithelial mesenchymal transition and migration in transformed keratinocytes.
FEBS Lett. 2010; 584(22):4586-4592 Doi: 10.1016/j.febslet.2010.10.020 [OPEN ACCESS]
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2009

Sollner, S; Schober, M; Wagner, A; Prem, A; Lorkova, L; Palfey, BA; Groll, M; Macheroux, P Quinone reductase acts as a redox switch of the 20S yeast proteasome.
EMBO Rep. 2009; 10(1): 65-70. Doi: 10.1038/embor.2008.218 [OPEN ACCESS]
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Vilkin, A; Niv, Y; Nagasaka, T; Morgenstern, S; Levi, Z; Fireman, Z; Fuerst, F; Goel, A; Boland, CR Microsatellite instability, MLH1 promoter methylation, and BRAF mutation analysis in sporadic colorectal cancers of different ethnic groups in Israel.
Cancer. 2009; 115(4):760-769 Doi: 10.1002/cncr.24019 [OPEN ACCESS]
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2008

Pasqualucci, L; Li, S; Meloni, G; Schnittger, S; Gattenlohner, S; Liso, A; Di Ianni, M; Martelli, MP; Pescarmona, E; Foa, R; Haferlach, T; Skoda, RC; Falini, B NPM1-mutated acute myeloid leukaemia occurring in JAK2-V617F+ primary myelofibrosis: de-novo origin?
Leukemia. 2008; 22(7):1459-1463 Doi: 10.1038/sj.leu.2405093 (- Case Report) [OPEN ACCESS]
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2007

Rohkamm, B; Reilly, MM; Lochmuller, H; Schlotter-Weigel, B; Barisic, N; Schols, L; Laura, M; Janecke, AR; Miltenberger-Miltenyi, G; John, E; Fischer, C; Grill, F; Wakeling, W; Davis, M; Pieber, TR; Auer-Grumbach, M; Nicholson, G; Pareyson, D Further evidence for genetic heterogeneity of distal HMN type V, CMT2 with predominant hand involvement and Silver syndrome.
J NEUROL SCI. 2007; 263(1-2): 100-106. Doi: 10.1016/j.jns.2007.06.047 [OPEN ACCESS]
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2006

Brücher, BL; Geddert, H; Langner, C; Höfler, H; Fink, U; Siewert, JR; Sarbia, M Hypermethylation of hMLH1, HPP1, p14(ARF), p16(INK4A) and APC in primary adenocarcinomas of the small bowel.
Int J Cancer. 2006; 119(6): 1298-1302. Doi: 10.1002/ijc.21990 [OPEN ACCESS]
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Yazdani-Biuki, B; Brickmann, K; Wohlfahrt, K; Mueller, T; März, W; Renner, W; Gutjahr, M; Langsenlehner, U; Krippl, P; Wascher, TC; Paulweber, B; Graninger, W; Brezinschek, HP The MHC2TA -168A>G gene polymorphism is not associated with rheumatoid arthritis in Austrian patients.
Arthritis Res Ther. 2006; 8(4):R97-R97 Doi: 10.1186/ar1974 [OPEN ACCESS]
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2005

Geier, A; Zollner, G; Dietrich, CG; Wagner, M; Fickert, P; Denk, H; van Rooijen, N; Matern, S; Gartung, C; Trauner, M Cytokine-independent repression of rodent Ntcp in obstructive cholestasis.
Hepatology. 2005; 41(3):470-477 Doi: 10.1002/hep.20594 [OPEN ACCESS]
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Quehenberger, F; Vasen, HF; van Houwelingen, HC Risk of colorectal and endometrial cancer for carriers of mutations of the hMLH1 and hMSH2 gene: correction for ascertainment.
J Med Genet. 2005; 42(6):491-496 Doi: 10.1136/jmg.2004.024299 [OPEN ACCESS]
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Schmidt, HH MYST3/CREBBP (MOZ/CBP) and CREBBP/MYST3 (CBP/MOZ) transcripts in AML with t(8;16)(p11;p13).
Genes Chromosomes Cancer. 2005; 42(2):207-208 Doi: 10.1002/gcc.20112
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2004

Runte, M; Kroisel, PM; Gillessen-Kaesbach, G; Varon, R; Horn, D; Cohen, MY; Wagstaff, J; Horsthemke, B; Buiting, K SNURF-SNRPN and UBE3A transcript levels in patients with Angelman syndrome.
HUM GENET. 2004; 114(6): 553-561. Doi: 10.1007/s00439-004-1104-z
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Schmidt, HH; Strehl, S; Thaler, D; Strunk, D; Sill, H; Linkesch, W; Jäger, U; Sperr, W; Greinix, HT; König, M; Emberger, W; Haas, OA RT-PCR and FISH analysis of acute myeloid leukemia with t(8;16)(p11;p13) and chimeric MOZ and CBP transcripts: breakpoint cluster region and clinical implications.
Leukemia. 2004; 18(6):1115-1121 Doi: 10.1038/sj.leu.2403353 (- Case Report) [OPEN ACCESS]
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2003

Fragaki, K; Ferrua, B; Mograbi, B; Waldispuhl, J; Kubar, J A novel Leishmania infantum nuclear phosphoprotein Lepp12 which stimulates IL1-beta synthesis in THP-1 transfectants.
BMC MICROBIOL. 2003; 3(2): 7-7. Doi: 10.1186/1471-2180-3-7 [OPEN ACCESS]
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Kerbl, R; Urban, CE; Ambros, IM; Dornbusch, HJ; Schwinger, W; Lackner, H; Ladenstein, R; Strenger, V; Gadner, H; Ambros, PF Neuroblastoma mass screening in late infancy: insights into the biology of neuroblastic tumors.
J Clin Oncol. 2003; 21(22):4228-4234 Doi: 10.1200/JCO.2003.10.168 [OPEN ACCESS]
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2002

Behrends, U; Jandl, T; Golbeck, A; Lechner, B; Muller-Weihrich, S; Schmid, I; Till, H; Berthold, F; Voltz, R; Mautner, JM Novel products of the HUD, HUC, NNP-1 and alpha-internexin genes identified by autologous antibody screening of a pediatric neuroblastoma library
Int J Cancer. 2002; 100(6):669-677 Doi: 10.1002/ijc.10550
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Fiedler, B; Lohmann, SM; Smolenski, A; Linnemuller, S; Pieske, B; Schroder, F; Molkentin, JD; Drexler, H; Wollert, KC Inhibition of calcineurin-NFAT hypertrophy signaling by cGMP-dependent protein kinase type I in cardiac myocytes.
Proc Natl Acad Sci U S A. 2002; 99(17):11363-11368 Doi: 10.1073/pnas.162100799 [OPEN ACCESS]
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Morerio, C; Calvari, V; Rosanda, C; Porta, S; Gambini, C; Panarello, C XY female with a dysgerminoma and no mutation in the coding sequence of the SRY gene.
Cancer Genet Cytogenet. 2002; 136(1):58-61 Doi: 10.1016%2FS0165-4608%2801%2900662-8 (- Case Report)
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2001

Stover, C; Gradl, G; Jentsch, I; Speicher, MR; Wieser, R; Schwaeble, W cDNA cloning, chromosome assignment, and genomic structure of a human gene encoding a novel member of the RBM family.
Cytogenet Cell Genet. 2001; 92(3-4):225-230 Doi: 10.1159/000056908
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2000

Gierens, H; Nauck, M; Roth, M; Schinker, R; Schürmann, C; Scharnagl, H; Neuhaus, G; Wieland, H; März, W Interleukin-6 stimulates LDL receptor gene expression via activation of sterol-responsive and Sp1 binding elements.
ARTERIOSCLER THROMB VASC BIOL 2000 20: 1777-1783. Doi: 10.1161/01.ATV.20.7.1777 [OPEN ACCESS]
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Staebler, A; Lax, SF; Ellenson, LH Altered expression of hMLH1 and hMSH2 protein in endometrial carcinomas with microsatellite instability.
Hum Pathol. 2000; 31(3):354-358 Doi: 10.1016/S0046-8177(00)80250-6
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1999

Auner, HW; Olipitz, W; Hoefler, G; Bodner, C; Konrad, D; Crevenna, R; Linkesch, W; Sill, H Mutational analysis of the DNA mismatch repair gene hMLH1 in myeloid leukaemias.
Br J Haematol. 1999; 106(3):706-708 Doi: 10.1046%2Fj.1365-2141.1999.01595.x [OPEN ACCESS]
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