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Suchbegriffe: CHROMOSOME 18, . Treffer: 10


Hofving, T; Arvidsson, Y; Almobarak, B; Inge, L; Pfragner, R; Persson, M; Stenman, G; Kristiansson, E; Johanson, V; Nilsson, O The neuroendocrine phenotype, genomic profile and therapeutic sensitivity of GEPNET cell lines.
ENDOCR-RELAT CANCER. 2018; 25(3): 367-380. [OPEN ACCESS]
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Nieser, M; Henopp, T; Brix, J; Stoß, L; Sitek, B; Naboulsi, W; Anlauf, M; Schlitter, AM; Klöppel, G; Gress, T; Moll, R; Bartsch, DK; Heverhagen, AE; Knoefel, WT; Kaemmerer, D; Haybaeck, J; Fend, F; Sperveslage, J; Sipos, B Loss of Chromosome 18 in Neuroendocrine Tumors of the Small Intestine: The Enigma Remains.
Neuroendocrinology. 2017; 104(3):302-312
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Pfragner, R; Behmel, A; Höger, H; Beham, A; Ingolic, E; Stelzer, I; Svejda, B; Moser, VA; Obenauf, AC; Siegl, V; Haas, O; Niederle, B Establishment and characterization of three novel cell lines - P-STS, L-STS, H-STS - derived from a human metastatic midgut carcinoid.
ANTICANCER RES. 2009; 29(6): 1951-1961. [OPEN ACCESS]
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Vincent, JB; Noor, A; Windpassinger, C; Gianakopoulos, PJ; Schwarzbraun, T; Alfred, SE; Stachowiak, B; Scherer, SW; Roberts, W; Wagner, K; Kroisel, PM; Petek, E Characterization of a de novo translocation t(5;18)(q33.1;q12.1) in an autistic boy identifies a breakpoint close to SH3TC2, ADRB2, and HTR4 on 5q, and within the desmocollin gene cluster on 18q.
Am J Med Genet B Neuropsychiatr Genet. 2009; 150B(6):817-826
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Meins, M; Bohm, D; Grossmann, A; Herting, E; Fleckenstein, B; Fauth, C; Speicher, MR; Schindler, R; Zoll, B; Bartels, I; Burfeind, P First non-mosaic case of isopseudodicentric chromosome 18 (psu idic(18)(pter -> q22.1 :: q22.1 -> pter) is associated with multiple congenital anomalies reminiscent of trisomy 18 and 18q-syndrome
AM J MED GENET PART A 2004 : 58-64.
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Cremer, M; Küpper, K; Wagler, B; Wizelman, L; von Hase, J; Weiland, Y; Kreja, L; Diebold, J; Speicher, MR; Cremer, T Inheritance of gene density-related higher order chromatin arrangements in normal and tumor cell nuclei.
J Cell Biol. 2003; 162(5):809-820 [OPEN ACCESS]
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Petek, E; Pertl, B; Tschernigg, M; Bauer, M; Mayr, J; Wagner, K; Kroisel, PM Characterisation of a 19-year-old long-term survivor with Edwards syndrome.
Genet Couns. 2003; 14(2):239-244 (- Case Report)
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Dahlman, I; Wallström, E; Weissert, R; Storch, M; Kornek, B; Jacobsson, L; Linington, C; Luthman, H; Lassmann, H; Olsson, T Linkage analysis of myelin oligodendrocyte glycoprotein-induced experimental autoimmune encephalomyelitis in the rat identifies a locus controlling demyelination on chromosome 18.
HUM MOL GENET. 1999; 8(12): 2183-2190. [OPEN ACCESS]
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Cerroni, L; Volkenandt, M; Rieger, E; Soyer, HP; Kerl, H bcl-2 protein expression and correlation with the interchromosomal 14;18 translocation in cutaneous lymphomas and pseudolymphomas.
J Invest Dermatol. 1994; 102(2):231-235 [OPEN ACCESS]
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Bakhshi, A; Wright, JJ; Graninger, W; Seto, M; Owens, J; Cossman, J; Jensen, JP; Goldman, P; Korsmeyer, SJ Mechanism of the t(14;18) chromosomal translocation: structural analysis of both derivative 14 and 18 reciprocal partners.
Proc Natl Acad Sci U S A. 1987; 84(8):2396-2400 [OPEN ACCESS]
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