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

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Publikationen

Suchbegriffe: GENETIC HETEROGENEITY - , . Treffer: 12

2017

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 (- Case Report) [OPEN ACCESS]
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El-Heliebi, A; Kashofer, K; Fuchs, J; Jahn, SW; Viertler, C; Matak, A; Sedlmayr, P; Hoefler, G Visualization of tumor heterogeneity by in situ padlock probe technology in colorectal cancer.
Histochem Cell Biol. 2017; 148(2):105-115 [OPEN ACCESS]
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Lohberger, B; Stuendl, N; Leithner, A; Rinner, B; Sauer, S; Kashofer, K; Liegl-Atzwanger, B Establishment of a novel cellular model for myxofibrosarcoma heterogeneity.
Sci Rep. 2017; 7(9):44700-44700 [OPEN ACCESS]
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Sheffield, NC; Pierron, G; Klughammer, J; Datlinger, P; Schönegger, A; Schuster, M; Hadler, J; Surdez, D; Guillemot, D; Lapouble, E; Freneaux, P; Champigneulle, J; Bouvier, R; Walder, D; Ambros, IM; Hutter, C; Sorz, E; Amaral, AT; de Álava, E; Schallmoser, K; Strunk, D; Rinner, B; Liegl-Atzwanger, B; Huppertz, B; Leithner, A; de Pinieux, G; Terrier, P; Laurence, V; Michon, J; Ladenstein, R; Holter, W; Windhager, R; Dirksen, U; Ambros, PF; Delattre, O; Kovar, H; Bock, C; Tomazou, EM DNA methylation heterogeneity defines a disease spectrum in Ewing sarcoma.
Nat Med. 2017; 23(3):386-395 [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 [OPEN ACCESS]
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Khan, MA; Mohan, S; Zubair, M; Windpassinger, C Homozygosity mapping identified a novel protein truncating mutation (p.Ser100Leufs*24) of the BBS9 gene in a consanguineous Pakistani family with Bardet Biedl syndrome.
BMC Med Genet. 2016; 17(6): 10-10. [OPEN ACCESS]
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Stanta, G; Jahn, SW; Bonin, S; Hoefler, G Tumour heterogeneity: principles and practical consequences.
Virchows Arch. 2016; 469(4):371-384
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2012

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 [OPEN ACCESS]
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2011

Lanktree, MB; Guo, Y; Murtaza, M; Glessner, JT; Bailey, SD; Onland-Moret, NC; Lettre, G; Ongen, H; Rajagopalan, R; Johnson, T; Shen, H; Nelson, CP; Klopp, N; Baumert, J; Padmanabhan, S; Pankratz, N; Pankow, JS; Shah, S; Taylor, K; Barnard, J; Peters, BJ; Maloney, CM; Lobmeyer, MT; Stanton, A; Zafarmand, MH; Romaine, SP; Mehta, A; van Iperen, EP; Gong, Y; Price, TS; Smith, EN; Kim, CE; Li, YR; Asselbergs, FW; Atwood, LD; Bailey, KM; Bhatt, D; Bauer, F; Behr, ER; Bhangale, T; Boer, JM; Boehm, BO; Bradfield, JP; Brown, M; Braund, PS; Burton, PR; Carty, C; Chandrupatla, HR; Chen, W; Connell, J; Dalgeorgou, C; Boer, Ad; Drenos, F; Elbers, CC; Fang, JC; Fox, CS; Frackelton, EC; Fuchs, B; Furlong, CE; Gibson, Q; Gieger, C; Goel, A; Grobbee, DE; Hastie, C; Howard, PJ; Huang, GH; Johnson, WC; Li, Q; Kleber, ME; Klein, BE; Klein, R; Kooperberg, C; Ky, B; Lacroix, A; Lanken, P; Lathrop, M; Li, M; Marshall, V; Melander, O; Mentch, FD; Meyer, NJ; Monda, KL; Montpetit, A; Murugesan, G; Nakayama, K; Nondahl, D; Onipinla, A; Rafelt, S; Newhouse, SJ; Otieno, FG; Patel, SR; Putt, ME; Rodriguez, S; Safa, RN; Sawyer, DB; Schreiner, PJ; Simpson, C; Sivapalaratnam, S; Srinivasan, SR; Suver, C; Swergold, G; Sweitzer, NK; Thomas, KA; Thorand, B; Timpson, NJ; Tischfield, S; Tobin, M; Tomaszewski, M; Tomaszweski, M; Verschuren, WM; Wallace, C; Winkelmann, B; Zhang, H; Zheng, D; Zhang, L; Zmuda, JM; Clarke, R; Balmforth, AJ; Danesh, J; Day, IN; Schork, NJ; de Bakker, PI; Delles, C; Duggan, D; Hingorani, AD; Hirschhorn, JN; Hofker, MH; Humphries, SE; Kivimaki, M; Lawlor, DA; Kottke-Marchant, K; Mega, JL; Mitchell, BD; Morrow, DA; Palmen, J; Redline, S; Shields, DC; Shuldiner, AR; Sleiman, PM; Smith, GD; Farrall, M; Jamshidi, Y; Christiani, DC; Casas, JP; Hall, AS; Doevendans, PA; Christie, JD; Berenson, GS; Murray, SS; Illig, T; Dorn, GW; Cappola, TP; Boerwinkle, E; Sever, P; Rader, DJ; Reilly, MP; Caulfield, M; Talmud, PJ; Topol, E; Engert, JC; Wang, K; Dominiczak, A; Hamsten, A; Curtis, SP; Silverstein, RL; Lange, LA; Sabatine, MS; Trip, M; Saleheen, D; Peden, JF; Cruickshanks, KJ; März, W; O'Connell, JR; Klungel, OH; Wijmenga, C; Maitland-van der Zee, AH; Schadt, EE; Johnson, JA; Jarvik, GP; Papanicolaou, GJ; Hugh Watkins on behalf of PROCARDIS; Grant, SF; Munroe, PB; North, KE; Samani, NJ; Koenig, W; Gaunt, TR; Anand, SS; van der Schouw, YT; Meena Kumari on behalf of the Whitehall II Study and the WHII 50K Group; Soranzo, N; Fitzgerald, GA; Reiner, A; Hegele, RA; Hakonarson, H; Keating, BJ Meta-analysis of Dense Genecentric Association Studies Reveals Common and Uncommon Variants Associated with Height.
Am J Hum Genet. 2011; 88(1):6-18 [OPEN ACCESS]
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2007

Kelly, H; Molony, CM; Darlow, JM; Pirker, ME; Yoneda, A; Green, AJ; Puri, P; Barton, DE A genome-wide scan for genes involved in primary vesicoureteric reflux.
J Med Genet. 2007; 44(11): 710-717. [OPEN ACCESS]
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2005

Cauza, E; Hanusch-Enserer, U; Bischof, M; Spak, M; Kostner, K; Tammaa, A; Dunky, A; Ferenci, P Increased C282Y heterozygosity in gestational diabetes.
Fetal Diagn Ther. 2005; 20(5):349-354
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2001

Eller, P; Föger, B; Gander, R; Sauper, T; Lechleitner, M; Finkenstedt, G; Patsch, JR Wolfram syndrome: a clinical and molecular genetic analysis.
J Med Genet. 2001; 38(11):E37-E37 [OPEN ACCESS]
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