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Results: 1-7 |
Results: 7
Functional analysis of BRCA1 C-terminal missense mutations identified in breast and ovarian cancer families
Authors: Vallon-Christersson, J Cayanan, C Haraldsson, K Loman, N Bergthorsson, JT Brondum-Nielsen, K Gerdes, AM Moller, P Kristoffersson, U Olsson, H Borg, A Monteiro, ANA
Citation: J. Vallon-christersson et al., Functional analysis of BRCA1 C-terminal missense mutations identified in breast and ovarian cancer families, HUM MOL GEN, 10(4), 2001, pp. 353-360
BRCA1 and BRCA2 mutation status and cancer family history of Danish women affected with multifocal or bilateral breast cancer at a young age
Authors: Bergthorsson, JT Ejlertsen, B Olsen, JH Borg, A Nielsen, KV Barkardottir, RB Klausen, S Mouridsen, HT Winther, K Fenger, K Niebuhr, A Harboe, TL Niebuhr, E
Citation: Jt. Bergthorsson et al., BRCA1 and BRCA2 mutation status and cancer family history of Danish women affected with multifocal or bilateral breast cancer at a young age, J MED GENET, 38(6), 2001, pp. 361-368
The effect of mismatch repair deficiency on tumourigenesis; microsatelliteinstability affecting genes containing short repeated sequences
Authors: Johannsdottir, JT Jonasson, JG Bergthorsson, JT Amundadottir, L Magnusson, J Egilsson, V Ingvarsson, S
Citation: Jt. Johannsdottir et al., The effect of mismatch repair deficiency on tumourigenesis; microsatelliteinstability affecting genes containing short repeated sequences, INT J ONCOL, 16(1), 2000, pp. 133-139
Analysis of HPC1, HPCX, and PCaP in Icelandic hereditary prostate cancer
Authors: Bergthorsson, JT Johannesdottir, G Arason, A Benediktsdottir, KR Agnarsson, BA Bailey-Wilson, JE Gillanders, E Smith, J Trent, J Barkardottir, RS
Citation: Jt. Bergthorsson et al., Analysis of HPC1, HPCX, and PCaP in Icelandic hereditary prostate cancer, HUM GENET, 107(4), 2000, pp. 372-375
Somatic deletions in hereditary breast cancers implicate 13q21 as a putative novel breast cancer susceptibility locus
Authors: Kainu, T Juo, SHH Desper, R Schaffer, AA Gillanders, E Rozenblum, E Freas-Lutz, D Weaver, D Stephan, D Bailey-Wilson, J Kallioniemi, OP Tirkkonen, M Syrjakoski, K Kuukasjarvi, T Koivisto, P Karhu, R Holli, K Arason, A Johannesdottir, G Bergthorsson, JT Johannsdottir, H Egilsson, V Barkardottir, RB Johannsson, O Haraldsson, K Sandberg, T Holmberg, E Gronberg, H Olsson, H Borg, A Vehmanen, P Eerola, H Heikkila, P Pyrhonen, S Nevanlinna, H
Citation: T. Kainu et al., Somatic deletions in hereditary breast cancers implicate 13q21 as a putative novel breast cancer susceptibility locus, P NAS US, 97(17), 2000, pp. 9603-9608
Mutations of the BRCA1 and BRCA2 genes in Danish patients diagnosed at young age with multi-centric or bilateral breast cancer
Authors: Bergthorsson, JT Winther, K Fenger, K Niebuhr, A Klausen, S Borg, A Harboe, T Ejlertsen, B Niebuhr, E
Citation: Jt. Bergthorsson et al., Mutations of the BRCA1 and BRCA2 genes in Danish patients diagnosed at young age with multi-centric or bilateral breast cancer, DIS MARKER, 15(1-3), 1999, pp. 94-94
Replication error in colorectal carcinoma: Association with loss of heterozygosity at mismatch repair loci and clinicopathological variables
Authors: Johannsdottir, JT Bergthorsson, JT Gretarsdottir, S Kristjansson, AK Ragnarsson, G Jonasson, JG Egilsson, V Ingvarsson, S
Citation: Jt. Johannsdottir et al., Replication error in colorectal carcinoma: Association with loss of heterozygosity at mismatch repair loci and clinicopathological variables, ANTICANC R, 19(3A), 1999, pp. 1821-1826
Risultati: 1-7 |