Authors:
Holzinger, A
Maier, EM
Buck, C
Mayerhofer, PU
Kappler, M
Haworth, JC
Moroz, SP
Hadorn, HB
Sadler, JE
Roscher, AA
Citation: A. Holzinger et al., Mutations in the proenteropeptidase gene are the molecular cause of congenital enteropeptidase deficiency, AM J HU GEN, 70(1), 2002, pp. 20-25
Authors:
Bache, M
Oehlmann, S
Meye, A
Bartel, F
Kappler, M
Wurl, P
Schmidt, H
Rath, FW
Dunst, J
Taubert, H
Citation: M. Bache et al., Radiosensitization in sarcoma cell lines with a p53 missense mutation correlates with prevention of irradiation G2/M arrest but not with induction ofapoptosis, ONCOL REP, 8(5), 2001, pp. 1007-1011
Authors:
Kappler, M
Kohler, T
Kampf, C
Diestelkotter, P
Wurl, P
Schmitz, M
Bartel, F
Lautenschlager, C
Rieber, EP
Schmidt, H
Bache, M
Taubert, H
Meye, A
Citation: M. Kappler et al., Increased survivin transcript levels: An independent negative predictor ofsurvival in soft tissue sarcoma patients, INT J CANC, 95(6), 2001, pp. 360-363
Authors:
Bartel, F
Meye, A
Wurl, P
Kappler, M
Bache, M
Lautenschlager, C
Grunbaum, U
Schmidt, H
Taubert, H
Citation: F. Bartel et al., Amplification of the MDM2 gene, but not expression of splice variants of MDM2 mRNA, is associated with prognosis in soft tissue sarcoma, INT J CANC, 95(3), 2001, pp. 168-175
Authors:
Taubert, H
Kappler, M
Meye, A
Bartel, F
Schlott, T
Lautenschlager, C
Bache, M
Schmidt, H
Wurl, P
Citation: H. Taubert et al., A MboII polymorphism in exon 11 of the human MDM2 gene occuring in normal blood donors and in soft tissue sarcoma patients: an indication for an increased cancer susceptibility?, MUT RES-F M, 456(1-2), 2000, pp. 39-44