Results: 1-16 |
Results: 16

Authors: Launonen, V Vierimaa, O Kiuru, M Isola, J Roth, S Pukkala, E Sistonen, P Herva, R Aaltonen, LA
Citation: V. Launonen et al., Inherited susceptibility to uterine leiomyomas and venal cell cancer, P NAS US, 98(6), 2001, pp. 3387-3392

Authors: Avizienyte, E Launonen, V Salovaara, R Kiviluoto, T Aaltonen, LA
Citation: E. Avizienyte et al., E-cadherin is not frequently mutated in hereditary gastric cancer, J MED GENET, 38(1), 2001, pp. 49-52

Authors: Loukola, A Eklin, K Laiho, P Salovaara, R Kristo, P Jarvinen, H Mecklin, JP Launonen, V Aaltonen, LA
Citation: A. Loukola et al., Microsatellite marker analysis in screening for hereditary nonpolyposis colorectal cancer (HNPCC), CANCER RES, 61(11), 2001, pp. 4545-4549

Authors: Allinen, M Huusko, P Mantyniemi, S Launonen, V Winqvist, R
Citation: M. Allinen et al., Mutation analysis of the CHK2 gene in families with hereditary breast cancer, BR J CANC, 85(2), 2001, pp. 209-212

Authors: Kiuru, M Launonen, V Hietala, M Aittomaki, K Vierimaa, O Salovaara, R Arola, J Pukkala, E Sistonen, P Herva, R Aaltonen, LA
Citation: M. Kiuru et al., Familial cutaneous leiomyomatosis is a two-hit condition associated with renal cell cancer of characteristic histopathology, AM J PATH, 159(3), 2001, pp. 825-829

Authors: Zhou, XP Woodford-Richens, K Lehtonen, R Kurose, K Aldred, M Hampel, H Launonen, V Virta, S Pilarski, R Salovaara, R Bodmer, WF Conrad, BA Dunlop, M Hodgson, SV Iwama, T Jarvinen, H Kellokumpu, I Kim, JC Leggett, B Markie, D Mecklin, JP Neale, K Phillips, R Piris, J Rozen, P Houlston, RS Aaltonen, LA Tomlinson, IPM Eng, C
Citation: Xp. Zhou et al., Germline mutations in BMPR1A/ALK3 cause a subset of cases of juvenile polyposis syndrome and of Cowden and Bannayan-Riley-Ruvalcaba syndromes, AM J HU GEN, 69(4), 2001, pp. 704-711

Authors: Sarantaus, L Huusko, P Eerola, H Launonen, V Vehmanen, P Rapakko, K Gillanders, E Syrjakoski, K Kainu, T Vahteristo, P Krahe, R Paakkonen, K Hartikainen, J Blomqvist, C Lopponen, T Holli, K Ryynanen, M Butzow, R Borg, A Arver, BW Holmberg, E Mannermaa, A Kere, J Kallioniemi, OP Winqvist, R Nevanlinna, H
Citation: L. Sarantaus et al., Multiple founder effects and geographical clustering of BRCA1 and BRCA2 families in Finland, EUR J HUM G, 8(10), 2000, pp. 757-763

Authors: Launonen, V Mannermaa, A Stenback, F Kosma, VM Puistola, U Huusko, P Anttila, M Bloigu, R Saarikoski, S Kauppila, A Winqvist, R
Citation: V. Launonen et al., Loss of heterozygosity at chromosomes 3, 6, 8, 11, 16, and 17 in ovarian cancer: correlation to clinicopathological variables, CANC GENET, 122(1), 2000, pp. 49-54

Authors: Launonen, V Avizienyte, E Loukola, A Laiho, P Salovaara, R Jarvinen, H Mecklin, JP Oku, A Shimane, M Kim, HC Kim, JC Nezu, J Aaltonen, LA
Citation: V. Launonen et al., No evidence of Peutz-Jeghers syndrome gene LKB1 involvement in left-sided colorectal carcinomas, CANCER RES, 60(3), 2000, pp. 546-548

Authors: Roth, S Laiho, P Salovaara, R Launonen, V Aaltonen, LA
Citation: S. Roth et al., No SMAD4 hypermethylation in colorectal cancer, BR J CANC, 83(8), 2000, pp. 1015-1019

Authors: Loukola, A Vilkki, S Singh, J Launonen, V Aaltonen, LA
Citation: A. Loukola et al., Germline and somatic mutation analysis of MLH3 in MSI-positive colorectal cancer, AM J PATH, 157(2), 2000, pp. 347-352

Authors: Laake, K Launonen, V Niederacher, D Gudlaugsdottir, S Seitz, S Rio, P Champeme, MH Bieche, I Birnbaum, D White, G Sztan, M Sever, N Plummer, S Osorio, A Broeks, A Huusko, P Spurr, N Borg, A Cleton-Jansen, AM van't Veer, L Benitez, J Casey, G Peterlin, B Olah, E Varley, J Bignon, YJ Scherneck, S Sigurdardottir, V Lidereau, R Eyfjord, J Beckmann, MW Winqvist, R Skovlund, E Borresen-Dale, AL
Citation: K. Laake et al., Loss of heterozygosity at 11q23.1 and survival in breast cancer: Results of a large European study, GENE CHROM, 25(3), 1999, pp. 212-221

Authors: Balci, A Huusko, P Paakkonen, K Launonen, V Uner, A Ekmekci, A Winqvist, R
Citation: A. Balci et al., Mutation analysis of BRCA1 and BRCA2 in Turkish cancer families: a novel mutation BRCA2 3414de14 found in male breast cancer, EUR J CANC, 35(5), 1999, pp. 707-710

Authors: Huusko, P Castren, K Launonen, V Soini, Y Paakkonen, K Leisti, J Vahakangas, K Winqvist, R
Citation: P. Huusko et al., Germ-line TP53 mutations in Finnish cancer families exhibiting features ofthe Li-Fraumeni syndrome and negative for BRCA1 and BRCA2, CANC GENET, 112(1), 1999, pp. 9-14

Authors: Launonen, V Laake, K Huusko, P Niederacher, D Beckmann, MW Barkardottir, RB Geirsdottir, EK Gudmundsson, J Rio, P Bignon, YJ Seitz, S Scherneck, S Bieche, I Champeme, MH Birnbaum, D White, G Varley, J Sztan, M Olah, E Osorio, A Benitez, J Spurr, N Velikonja, N Peterlin, B Borg, A Cleton-Jansen, AM Devilee, P Bloigu, R Lidereau, R Borresen-Dale, AL Winqvist, R
Citation: V. Launonen et al., European multicenter study on LOH of APOC3 at 11q23 in 766 breast cancer patients: relation to clinical variables, BR J CANC, 80(5-6), 1999, pp. 879-882

Authors: Launonen, V Stenback, F Puistola, U Bloigu, R Huusko, P Kytola, S Kauppila, A Winqvist, R
Citation: V. Launonen et al., Chromosome 11q22.3-q25 LOH in ovarian cancer: Association with a more aggressive disease course and involved subregions, GYNECOL ONC, 71(2), 1998, pp. 299-304
Risultati: 1-16 |