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Results: 1-14 |
Results: 14
Re: Population-based study of BRCA1 and BRCA2 mutations in 1035 unselectedFinnish breast cancer patients
Authors: Chappuis, PO Hamel, N Paradis, AJ Deschenes, J Tonin, PN Ghadirian, P Foulkes, WD
Citation: Po. Chappuis et al., Re: Population-based study of BRCA1 and BRCA2 mutations in 1035 unselectedFinnish breast cancer patients, J NAT CANC, 93(2), 2001, pp. 152-153
Microarray analysis of gene expression mirrors the biology of an ovarian cancer model
Authors: Tonin, PN Hudson, TJ Rodier, F Bossolasco, M Lee, PD Novak, J Manderson, EN Provencher, D Mes-Masson, AM
Citation: Pn. Tonin et al., Microarray analysis of gene expression mirrors the biology of an ovarian cancer model, ONCOGENE, 20(45), 2001, pp. 6617-6626
Founder BRCA1 and BRCA2 mutations in early-onset French Canadian breast cancer cases unselected for family history
Authors: Tonin, PN Perret, C Lambert, JA Paradis, AJ Kantemiroff, T Benoit, MH Martin, G Foulkes, WD Ghadirian, P
Citation: Pn. Tonin et al., Founder BRCA1 and BRCA2 mutations in early-onset French Canadian breast cancer cases unselected for family history, INT J CANC, 95(3), 2001, pp. 189-193
Haplotype analysis of BRCA2 8765delAG mutation carriers in French Canadianand Yemenite Jewish hereditary breast cancer families
Authors: Manning, AP Abelovich, D Ghadirian, P Lambert, JA Frappier, D Provencher, D Robidoux, A Peretz, T Narod, SA Mes-Masson, AM Foulkes, WD Wang, TL Morgan, K Fujiwara, TM Tonin, PN
Citation: Ap. Manning et al., Haplotype analysis of BRCA2 8765delAG mutation carriers in French Canadianand Yemenite Jewish hereditary breast cancer families, HUMAN HERED, 52(2), 2001, pp. 116-120
Mutation analysis of a Mauritian hereditary breast cancer family reveals the BRCA2 6503delTT mutation previously found to recur in different ethnic populations
Authors: Khittoo, G Manning, A Mustun, H Appadoo, J Venkatasamy, S Fagoonee, I Ghadirian, P Tonin, PN
Citation: G. Khittoo et al., Mutation analysis of a Mauritian hereditary breast cancer family reveals the BRCA2 6503delTT mutation previously found to recur in different ethnic populations, HUMAN HERED, 52(1), 2001, pp. 55-58
Genes implicated in hereditary breast cancer syndromes
Authors: Tonin, PN
Citation: Pn. Tonin, Genes implicated in hereditary breast cancer syndromes, SEM SURG ON, 18(4), 2000, pp. 281-286
High risk genes predisposing to prostate cancer development - do they exist?
Authors: Singh, R Eeles, RA Durocher, F Simard, J Edwards, S Badzioch, M Kote-Jarai, Z Teare, D Ford, D Dearnaley, D Ardern-Jones, A Murkin, A Dowe, A Shearer, R Kelly, J Labrie, F Easton, D Narod, SA Tonin, PN Foulkes, WD
Citation: R. Singh et al., High risk genes predisposing to prostate cancer development - do they exist?, PROSTATE C, 3(4), 2000, pp. 241-247
Characterization of four novel epithelial ovarian cancer cell lines
Authors: Provencher, DM Lounis, H Champoux, L Tetrault, M Manderson, EN Wang, JC Eydoux, P Savoie, R Tonin, PN Mes-Masson, AM
Citation: Dm. Provencher et al., Characterization of four novel epithelial ovarian cancer cell lines, IN VITRO-AN, 36(6), 2000, pp. 357-361
Allelotyping defines minimal imbalance at chromosomal region 17q25 in non-serous epithelial ovarian cancers
Authors: Dion, F Mes-Masson, AM Seymour, RJ Provencher, D Tonin, PN
Citation: F. Dion et al., Allelotyping defines minimal imbalance at chromosomal region 17q25 in non-serous epithelial ovarian cancers, ONCOGENE, 19(11), 2000, pp. 1466-1472
Trisomy of chromosome 10 in two cases of ovarian carcinoma
Authors: Wang, JC Mes-Masson, AM Tonin, PN Provencher, D Eydoux, P
Citation: Jc. Wang et al., Trisomy of chromosome 10 in two cases of ovarian carcinoma, CANC GENET, 118(1), 2000, pp. 65-68
Mutations in a 10-bp polyadenine repeat of transforming growth factor beta-receptor type II gene is an infrequent event in human epithelial ovarian cancer
Authors: Manderson, EN Mes-Masson, AM Provencher, D Tonin, PN
Citation: En. Manderson et al., Mutations in a 10-bp polyadenine repeat of transforming growth factor beta-receptor type II gene is an infrequent event in human epithelial ovarian cancer, CLIN GENET, 57(2), 2000, pp. 151-153
Expression of FHIT in primary cultures of human epithelial ovarian tumors and malignant ovarian ascites
Authors: Manning, AP Mes-Masson, AM Seymour, RJ Tetrault, M Provencher, DM Tonin, PN
Citation: Ap. Manning et al., Expression of FHIT in primary cultures of human epithelial ovarian tumors and malignant ovarian ascites, MOL CARCINO, 24(3), 1999, pp. 218-225
An absence of founder BRCA2 mutations in individuals with squamous cell carcinoma of the head and neck
Authors: Hamel, N Manning, A Black, MJ Tonin, PN Foulkes, WD
Citation: N. Hamel et al., An absence of founder BRCA2 mutations in individuals with squamous cell carcinoma of the head and neck, INT J CANC, 83(6), 1999, pp. 803-804
Founder BRCA1 and BRCA2 mutations in French Canadian ovarian cancer cases unselected for family history
Authors: Tonin, PN Mes-Masson, AM Narod, SA Ghadirian, P Provencher, D
Citation: Pn. Tonin et al., Founder BRCA1 and BRCA2 mutations in French Canadian ovarian cancer cases unselected for family history, CLIN GENET, 55(5), 1999, pp. 318-324
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