Suchbegriffe: GENE DELETION - , . Treffer: 47
Sukseree, S; László, L; Gruber, F; Bergmann, S; Narzt, MS; Nagelreiter, IM; Höftberger, R; Molnár, K; Rauter, G; Birngruber, T; Larue, L; Kovacs, GG; Tschachler, E; Eckhart, L
Filamentous Aggregation of Sequestosome-1/p62 in Brain Neurons and Neuroepithelial Cells upon Tyr-Cre-Mediated Deletion of the Autophagy Gene Atg7.
Mol Neurobiol. 2018; 55(11):8425-8437
Doi: 10.1007/s12035-018-0996-x
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Abbasi, MR; Rifatbegovic, F; Brunner, C; Mann, G; Ziegler, A; Pötschger, U; Crazzolara, R; Ussowicz, M; Benesch, M; Ebetsberger-Dachs, G; Chan, GCF; Jones, N; Ladenstein, R; Ambros, IM; Ambros, PF
Impact of Disseminated Neuroblastoma Cells on the Identification of the Relapse-Seeding Clone.
Clin Cancer Res. 2017; 23(15):4224-4232
Doi: 10.1158/1078-0432.CCR-16-2082
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Themanns, M; Mueller, KM; Kessler, SM; Golob-Schwarzl, N; Mohr, T; Kaltenecker, D; Bourgeais, J; Paier-Pourani, J; Friedbichler, K; Schneller, D; Schlederer, M; Zebedin-Brandl, E; Terracciano, LM; Han, X; Kenner, L; Wagner, KU; Mikulits, W; Kozlov, AV; Heim, MH; Gouilleux, F; Haybaeck, J; Moriggl, R
Hepatic Deletion of Janus Kinase 2 Counteracts Oxidative Stress in Mice.
Sci Rep. 2016; 6(4):34719-34719
Doi: 10.1038/srep34719
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Ulz, P; Belic, J; Graf, R; Auer, M; Lafer, I; Fischereder, K; Webersinke, G; Pummer, K; Augustin, H; Pichler, M; Hoefler, G; Bauernhofer, T; Geigl, JB; Heitzer, E; Speicher, MR
Whole-genome plasma sequencing reveals focal amplifications as a driving force in metastatic prostate cancer.
Nat Commun. 2016; 7(15):12008-12008
Doi: 10.1038/ncomms12008
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Weber, J; Bao, H; Hartlmüller, C; Wang, Z; Windhager, A; Janowski, R; Madl, T; Jin, P; Niessing, D
Structural basis of nucleic-acid recognition and double-strand unwinding by the essential neuronal protein Pur-alpha.
Elife. 2016; 5(7):
Doi: 10.7554/eLife.11297
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Geiger, O; Hatzl, S; Kashofer, K; Hoefler, G; Wölfler, A; Sill, H; Zebisch, A
Deletion of SPRY4 is a frequent event in secondary acute myeloid leukemia.
Ann Hematol. 2015; 94(11):1923-1924
Doi: 10.1007/s00277-015-2445-5
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Goeritzer, M; Schlager, S; Radovic, B; Madreiter, CT; Rainer, S; Thomas, G; Lord, CC; Sacks, J; Brown, AL; Vujic, N; Obrowsky, S; Sachdev, V; Kolb, D; Chandak, PG; Graier, WF; Sattler, W; Brown, JM; Kratky, D
Deletion of CGI-58 or adipose triglyceride lipase differently affects macrophage function and atherosclerosis.
J Lipid Res. 2014; 55(12):2562-2575
Doi: 10.1194/jlr.M052613
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Lichtenegger, S; Bina, I; Roier, S; Bauernfeind, S; Keidel, K; Schild, S; Anthony, M; Reidl, J
Characterization of lactate utilization and its implication on the physiology of Haemophilus influenzae.
Int J Med Microbiol. 2014; 304(3-4): 490-498.
Doi: 10.1016/j.ijmm.2014.02.010
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Rao, S; Tortola, L; Perlot, T; Wirnsberger, G; Novatchkova, M; Nitsch, R; Sykacek, P; Frank, L; Schramek, D; Komnenovic, V; Sigl, V; Aumayr, K; Schmauss, G; Fellner, N; Handschuh, S; Glösmann, M; Pasierbek, P; Schlederer, M; Resch, GP; Ma, Y; Yang, H; Popper, H; Kenner, L; Kroemer, G; Penninger, JM
A dual role for autophagy in a murine model of lung cancer.
Nat Commun. 2014; 5(5):3056-3056
Doi: 10.1038/ncomms4056
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Shenje, LT; Andersen, P; Uosaki, H; Fernandez, L; Rainer, PP; Cho, GS; Lee, DI; Zhong, W; Harvey, RP; Kass, DA; Kwon, C
Precardiac deletion of Numb and Numblike reveals renewal of cardiac progenitors.
Elife. 2014; 3(5):e02164-e02164
Doi: 10.7554/eLife.02164
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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
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Wong, WW; Vince, JE; Lalaoui, N; Lawlor, KE; Chau, D; Bankovacki, A; Anderton, H; Metcalf, D; O'Reilly, L; Jost, PJ; Murphy, JM; Alexander, WS; Strasser, A; Vaux, DL; Silke, J
cIAPs and XIAP regulate myelopoiesis through cytokine production in an RIPK1- and RIPK3-dependent manner.
Blood. 2014; 123(16):2562-2572
Doi: 10.1182/blood-2013-06-510743
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Chitraju, C; Trötzmüller, M; Hartler, J; Wolinski, H; Thallinger, GG; Haemmerle, G; Zechner, R; Zimmermann, R; Köfeler, HC; Spener, F
The impact of genetic stress by ATGL deficiency on the lipidome of lipid droplets from murine hepatocytes.
J Lipid Res. 2013; 54(8):2185-2194
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Murali, R; Wiesner, T; Scolyer, RA
Tumours associated with BAP1 mutations.
Pathology. 2013; 45(2):116-126
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Bassler, J; Klein, I; Schmidt, C; Kallas, M; Thomson, E; Wagner, MA; Bradatsch, B; Rechberger, G; Strohmaier, H; Hurt, E; Bergler, H;
The Conserved Bud20 Zinc Finger Protein Is a New Component of the Ribosomal 60S Subunit Export Machinery.
MOL CELL BIOL. 2012; 32(24): 4898-4912.
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Fried, I; Wölfler, A; Quehenberger, F; Hoefler, G; Sill, H; Zebisch, A
Mutations inDNMT3A and loss of RKIP are independent events in acute monocytic leukemia.
Haematologica. 2012; 97(12):1936-1937
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Carmona-Gutiérrez, D; Bauer, MA; Ring, J; Knauer, H; Eisenberg, T; Büttner, S; Ruckenstuhl, C; Reisenbichler, A; Magnes, C; Rechberger, GN; Birner-Gruenberger, R; Jungwirth, H; Fröhlich, KU; Sinner, F; Kroemer, G; Madeo, F
The propeptide of yeast cathepsin D inhibits programmed necrosis.
Cell Death Dis. 2011; 2(16):e161-e161
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Horvath, SE; Wagner, A; Steyrer, E; Daum, G
Metabolic link between phosphatidylethanolamine and triacylglycerol metabolism in the yeast Saccharomyces cerevisiae.
Biochim Biophys Acta. 2011; 1811(12): 1030-1037.
Doi: 10.1016/j.bbalip.2011.08.007
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Zung, A; Petek, E; Ben-Zeev, B; Schwarzbraun, T; Ben-Yehoshua, SJ
MODY type 2 in Greig cephalopolysyndactyly syndrome (GCPS) as part of a contiguous gene deletion syndrome.
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Connerth, M; Czabany, T; Wagner, A; Zellnig, G; Leitner, E; Steyrer, E; Daum, G
Oleate inhibits steryl ester synthesis and causes liposensitivity in yeast.
J Biol Chem. 2010; 285(35): 26832-26841.
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Fröhlich, LF; Mrakovcic, M; Steinborn, R; Chung, UI; Bastepe, M; Jüppner, H
Targeted deletion of the Nesp55 DMR defines another Gnas imprinting control region and provides a mouse model of autosomal dominant PHP-Ib.
Proc Natl Acad Sci U S A. 2010; 107(20): 9275-9280.
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Köse, O; Zimmerhackl, LB; Jungraithmayr, T; Mache, C; Nürnberger, J
New treatment options for atypical hemolytic uremic syndrome with the complement inhibitor eculizumab.
Semin Thromb Hemost. 2010; 36(6):669-672
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Vikstrom, I; Carotta, S; Lüthje, K; Peperzak, V; Jost, PJ; Glaser, S; Busslinger, M; Bouillet, P; Strasser, A; Nutt, SL; Tarlinton, DM
Mcl-1 is essential for germinal center formation and B cell memory.
Science. 2010; 330(6007):1095-1099
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Begus-Nahrmann, Y; Lechel, A; Obenauf, AC; Nalapareddy, K; Peit, E; Hoffmann, E; Schlaudraff, F; Liss, B; Schirmacher, P; Kestler, H; Danenberg, E; Barker, N; Clevers, H; Speicher, MR; Rudolph, KL
p53 deletion impairs clearance of chromosomal-instable stem cells in aging telomere-dysfunctional mice.
Nat Genet. 2009; 41(10): 1138-1143.
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Molecular determinants of the coupling between STIM1 and Orai channels: differential activation of Orai1-3 channels by a STIM1 coiled-coil mutant.
J Biol Chem. 2009; 284(32): 21696-21706.
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Fine-mapping chromosomal loss at 9p21: correlation with prognosis in primary cutaneous diffuse large B-cell lymphoma, leg type.
J INVEST DERMATOL. 2009; 129(5): 1149-1155.
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Wiesner, T; Obenauf, AC; Geigl, JB; Vallant, EM; Speicher, MR; Fink-Puches, R; Kerl, H; Cerroni, L
9p21 deletion in primary cutaneous large B-cell lymphoma, leg type, may escape detection by standard FISH assays.
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Cabanski, M; Steinmüller, M; Marsh, LM; Surdziel, E; Seeger, W; Lohmeyer, J
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Dacic, S; Kothmaier, H; Land, S; Shuai, Y; Halbwedl, I; Morbini, P; Murer, B; Comin, C; Galateau-Salle, F; Demirag, F; Zeren, H; Attanoos, R; Gibbs, A; Cagle, P; Popper, H
Prognostic significance of p16/cdkn2a loss in pleural malignant mesotheliomas.
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Göhler, A; Xiong, G; Paulsen, S; Trentmann, G; Maser, E
Testosterone-inducible regulator is a kinase that drives steroid sensing and metabolism in Comamonas testosteroni.
J Biol Chem. 2008; 283(25):17380-17390
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Wultsch, T; Painsipp, E; Shahbazian, A; Mitrovic, M; Edelsbrunner, M; Lazdunski, M; Waldmann, R; Holzer, P
Deletion of the acid-sensing ion channel ASIC3 prevents gastritis-induced acid hyperresponsiveness of the stomach-brainstem axis.
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Endonuclease G regulates budding yeast life and death.
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Eller, P; Kaser, S; Lhotta, K; Edghill, EL; Ellard, S; Ebenbichler, C; Patsch, JR
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Bloethner, S; Hemminki, K; Thirumaran, RK; Chen, B; Mueller-Berghaus, J; Ugurel, S; Schadendorf, D; Kumar, R
Differences in global gene expression in melanoma cell lines with and without homozygous deletion of the CDKN2A locus genes.
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Schäfer, E; Weger, M; Birgül, T; Renner, W; Stanger, O; Steinbrugger, I; Schmut, O; Temmel, W; Haas, A
Angiotensin-converting enzyme insertion/deletion polymorphism and retinal artery occlusion.
Acta Ophthalmol Scand. 2006; 84(3):305-308
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Mai, G; Bucher, P; Morel, P; Mei, J; Bosco, D; Andres, A; Mathe, Z; Wekerle, T; Berney, T; Bühler, LH
Role of CD40-CD154 pathway in the rejection of concordant and discordant xenogeneic islets.
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Wieser, R; Fritz, B; Ullmann, R; Müller, I; Galhuber, M; Storlazzi, CT; Ramaswamy, A; Christiansen, H; Shimizu, N; Rehder, H
Novel rearrangement of chromosome band 22q11.2 causing 22q11 microdeletion syndrome-like phenotype and rhabdoid tumor of the kidney.
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Thromb Haemost. 2004; 91(1):76-79
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Petek, E; Jenne, DE; Smolle, J; Binder, B; Lasinger, W; Windpassinger, C; Wagner, K; Kroisel, PM; Kehrer-Sawatzki, H
Mitotic recombination mediated by the JJAZF1 (KIAA0160) gene causing somatic mosaicism and a new type of constitutional NF1 microdeletion in two children of a mosaic female with only few manifestations.
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Worel, N; Greinix, H; Ackermann, J; Kaufmann, H; Urbauer, E; Höcker, P; Gisslinger, H; Lechner, K; Kalhs, P; Drach, J
Deletion of chromosome 13q14 detected by fluorescence in situ hybridization has prognostic impact on survival after high-dose therapy in patients with multiple myeloma.
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Imprinting centre deletions in two PWS families: implications for diagnostic testing and genetic counseling.
Clin Genet. 2000; 58(4):284-290
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Functions of c-Jun in liver and heart development.
J Cell Biol. 1999; 145(5):1049-1061
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Autoimmune-thrombocytopenia and SLE in a patient with 5q-anomaly and deletion of the c-fms oncogene.
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