Authors:
Soucek, T
Rosner, M
Miloloza, A
Kubista, M
Cheadle, JP
Sampson, JR
Hengstschlager, M
Citation: T. Soucek et al., Tuberous sclerosis causing mutants of the TSC2 gene product affect proliferation and p27 expression, ONCOGENE, 20(35), 2001, pp. 4904-4909
Authors:
Hengstschlager, M
Bettelheim, D
Drahonsky, R
Deutinger, J
Bernaschek, G
Citation: M. Hengstschlager et al., Prenatal diagnosis of a de novo supernumerary marker derived from chromosome 16, PRENAT DIAG, 21(6), 2001, pp. 477-480
Authors:
Hengstschlager, M
Bettelheim, D
Rosner, M
Repa, C
Deutinger, J
Bernaschek, G
Citation: M. Hengstschlager et al., Extended prenatal survival of a non-mosaic trisomy 22 with aneuploid cytotrophoblasts, PRENAT DIAG, 21(10), 2001, pp. 897-899
Authors:
Hengstschlager, M
Holzl, G
Hengstschlager-Ottnad, E
Citation: M. Hengstschlager et al., Different regulation of c-Myc- and E2F-1-induced apoptosis during the ongoing cell cycle, ONCOGENE, 18(3), 1999, pp. 843-848
Authors:
Bauer, JW
Ortiz, S
Hengstschlager, M
Pulkkinen, L
Uitto, J
Hintner, H
Rappersberger, K
Citation: Jw. Bauer et al., Prenatal diagnosis of recessive dystrophic epidermolysis bullosa in a family at risk for recurrence by haplotype analysis of the type VII collagen gene, HAUTARZT, 50(2), 1999, pp. 121-126
Citation: T. Soucek et al., Inactivation of the cyclin-dependent kinase inhibitor p27 upon loss of thetuberous sclerosis complex gene-2, P NAS US, 95(26), 1998, pp. 15653-15658