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Results: 1-19 |
Results: 19
Quality of life in patients at risk of medullary thyroid carcinoma and followed by a comprehensive medical network: Trends for future evaluations
Authors: Freyer, G Ligneau, B Schlumberger, M Blandy, C Contedevolx, B Trillet-Lenoir, V Lenoir, GM Chau, N Dazord, A
Citation: G. Freyer et al., Quality of life in patients at risk of medullary thyroid carcinoma and followed by a comprehensive medical network: Trends for future evaluations, ANN ONCOL, 12(10), 2001, pp. 1461-1465
An Alu-mediated 7.1 kb deletion of BRCAI exons 8 and 9 in breast and ovarian cancer families that results in alternative splicing of exon 10
Authors: Rohlfs, EM Puget, N Graham, ML Weber, BL Garber, JE Skrzynia, C Halperin, JL Lenoir, GM Silverman, LM Mazoyer, S
Citation: Em. Rohlfs et al., An Alu-mediated 7.1 kb deletion of BRCAI exons 8 and 9 in breast and ovarian cancer families that results in alternative splicing of exon 10, GENE CHROM, 28(3), 2000, pp. 300-307
Regional methylation of the 5 ' end CpG island of BRCA1 is associated withreduced gene expression in human somatic cells
Authors: Magdinier, F Billard, LM Wittmann, G Frappart, L Benchaib, M Lenoir, GM Guerin, JF Dante, R
Citation: F. Magdinier et al., Regional methylation of the 5 ' end CpG island of BRCA1 is associated withreduced gene expression in human somatic cells, FASEB J, 14(11), 2000, pp. 1585-1594
Variable expressivity of familial medullary thyroid carcinoma (FMTC) due to a RET V804M (GTG -> ATG) mutation
Authors: Feldman, GL Edmonds, MW Ainsworth, PJ Schuffenecker, I Lenoir, GM Saxe, AW Talpos, GB Roberson, J Petrucelli, N Jackson, CE
Citation: Gl. Feldman et al., Variable expressivity of familial medullary thyroid carcinoma (FMTC) due to a RET V804M (GTG -> ATG) mutation, SURGERY, 128(1), 2000, pp. 93-98
Differential expression and subcellular localization of murine BRCA1 and BRCA1-Delta 11 isoforms in murine and human cell lines
Authors: Bachelier, R Dalla Venezia, N Mazoyer, S Frappart, L Lenoir, GM Vincent, A
Citation: R. Bachelier et al., Differential expression and subcellular localization of murine BRCA1 and BRCA1-Delta 11 isoforms in murine and human cell lines, INT J CANC, 88(4), 2000, pp. 519-524
Expression analysis of endogenous menin, the product of the multiple endocrine neoplasia type 1 gene, in cell lines and human tissues
Authors: Wautot, V Khodaei, S Frappart, L Buisson, N Baro, E Lenoir, GM Calender, A Zhang, CX Weber, G
Citation: V. Wautot et al., Expression analysis of endogenous menin, the product of the multiple endocrine neoplasia type 1 gene, in cell lines and human tissues, INT J CANC, 85(6), 2000, pp. 877-881
Screening for genomic rearrangements in families with breast and ovarian cancer identifies BRCA1 mutations previously missed by conformation-sensitive gel electrophoresis or sequencing
Authors: Unger, MA Nathanson, KL Calzone, K Antin-Ozerkis, D Shih, HA Martin, AM Lenoir, GM Mazoyer, S Weber, BL
Citation: Ma. Unger et al., Screening for genomic rearrangements in families with breast and ovarian cancer identifies BRCA1 mutations previously missed by conformation-sensitive gel electrophoresis or sequencing, AM J HU GEN, 67(4), 2000, pp. 841-850
The exon 13 duplication in the BRCA1 gene is a founder mutation present ingeographically diverse populations
Authors: Mazoyer, S Leary, J Kirk, J Fleischmann, E Wagner, T Claes, K Messiaen, L Foulkes, W Desrochers, M Simard, J Phelan, CM Kwan, E Narod, SA Vahteristo, P Nevanlinna, H Durando, X Bignon, YJ Peyrat, JP Bonnardel, C Sinilnikova, OM Puget, N Lenoir, GM Mazoyer, S Audoynaud, C Goldgar, D Maugard, C Caux, V Gad, S Stoppa-Lyonnet, D Nogues, C Lidereau, R Machavoine, C Bressac-de Paillerets, B Kuschel, B Betz, B Niederacher, D Beckmann, MW Hamann, U Gayther, SA Ponder, BAP Robinson, M Taylor, GR Bishop, T Catteau, A Solomon, E Cohen, B Steel, M Collins, N Stratton, M van der Looij, M Olah, E Miller, NJ Barton, DE Sverdlov, RS Friedman, E Radice, P Montagna, M Sensi, E Caligo, M van Eijk, R Devilee, P van der Luijt, R Heimdal, K Moller, P Borg, A Diez, O Cortes, J Domenech, M Baiget, M Osorio, A Benitez, J Borg, A Maillet, P Sappino, AP Ozdag, H Ozcelik, T Ozturk, M Rohlfs, EM Boyd, J McDermott, D Offit, K Unger, M Nathanson, K Weber, BL Sellers, TA Hampton, E Couch, FJ Neuhausen, S
Citation: S. Mazoyer et al., The exon 13 duplication in the BRCA1 gene is a founder mutation present ingeographically diverse populations, AM J HU GEN, 67(1), 2000, pp. 207-212
Co-segregation of MEN2 and Hirschsprung's disease: The same mutation of RET with both gain and loss-of-function?
Authors: Takahashi, M Iwashita, T Santoro, M Lyonnet, S Lenoir, GM Billaud, M
Citation: M. Takahashi et al., Co-segregation of MEN2 and Hirschsprung's disease: The same mutation of RET with both gain and loss-of-function?, HUM MUTAT, 13(4), 1999, pp. 331-336
Two distinct mutations of the RET receptor causing Hirschsprung's disease impair the binding of signalling effecters to a multifunctional docking site
Authors: Geneste, O Bidaud, C De Vita, G Hofstra, RMW Tartare-Deckert, S Buys, CHCM Lenoir, GM Santoro, M Billaud, M
Citation: O. Geneste et al., Two distinct mutations of the RET receptor causing Hirschsprung's disease impair the binding of signalling effecters to a multifunctional docking site, HUM MOL GEN, 8(11), 1999, pp. 1989-1999
BRCA1 expression during prenatal development of the human mammary gland
Authors: Magdinier, F Dalla Venezia, N Lenoir, GM Frappart, L Dante, R
Citation: F. Magdinier et al., BRCA1 expression during prenatal development of the human mammary gland, ONCOGENE, 18(27), 1999, pp. 4039-4043
Psychosocial impact of genetic testing in familial medullary-thyroid carcinoma: A multicentric pilot-evaluation
Authors: Freyer, G Dazord, A Schlumberger, M Conte-Devolx, B Ligneau, B Trillet-Lenoir, V Lenoir, GM
Citation: G. Freyer et al., Psychosocial impact of genetic testing in familial medullary-thyroid carcinoma: A multicentric pilot-evaluation, ANN ONCOL, 10(1), 1999, pp. 87-95
Germline brca2 sequence variants in patients with ocular melanoma
Authors: Sinilnikova, OM Egan, KM Quinn, JL Boutrand, L Lenoir, GM Stoppa-Lyonnet, D Desjardins, L Levy, C Goldgar, D Gragcoudas, ES
Citation: Om. Sinilnikova et al., Germline brca2 sequence variants in patients with ocular melanoma, INT J CANC, 82(3), 1999, pp. 325-328
Screening for germ-line rearrangements and regulatory mutations in BRCA1 led to the identification of four new deletions
Authors: Puget, N Stoppa-Lyonnet, D Sinilnikova, OM Pages, S Lynch, HT Lenoir, GM Mazoyer, S
Citation: N. Puget et al., Screening for germ-line rearrangements and regulatory mutations in BRCA1 led to the identification of four new deletions, CANCER RES, 59(2), 1999, pp. 455-461
An Alu-mediated 6-kb duplication in the BRCA1 gene: A new founder mutation?
Authors: Puget, N Sinilnikova, OM Stoppa-Lyonnet, D Audoynaud, C Pages, S Lynch, HT Goldgar, D Lenoir, GM Mazoyer, S
Citation: N. Puget et al., An Alu-mediated 6-kb duplication in the BRCA1 gene: A new founder mutation?, AM J HU GEN, 64(1), 1999, pp. 300-302
Down-regulation of BRCA1 in human sporadic breast cancer; analysis of DNA methylation patterns of the putative promoter region
Authors: Magdinier, F Ribieras, S Lenoir, GM Frappart, L Dante, R
Citation: F. Magdinier et al., Down-regulation of BRCA1 in human sporadic breast cancer; analysis of DNA methylation patterns of the putative promoter region, ONCOGENE, 17(24), 1998, pp. 3169-3176
Dual effect on the RET receptor of MEN 2 mutations affecting specific extracytoplasmic cysteines
Authors: Chappuis-Flament, S Pasini, A De Vita, G Segouffin-Cariou, C Fusco, A Attie, T Lenoir, GM Santoro, M Billaud, M
Citation: S. Chappuis-flament et al., Dual effect on the RET receptor of MEN 2 mutations affecting specific extracytoplasmic cysteines, ONCOGENE, 17(22), 1998, pp. 2851-2861
RET, hereditary cancers and congenital malformation: A deregulation model of a tyrosine kinase receptor in human pathology
Authors: Pasini, A Chappuis-Flament, S Geneste, O Fournier, L Schuffenecker, I Michiels, FM Feunteun, J Pelet, A Lyonnet, S De Vita, G Santoro, M Lenoir, GM Giraud, S Billaud, M
Citation: A. Pasini et al., RET, hereditary cancers and congenital malformation: A deregulation model of a tyrosine kinase receptor in human pathology, EUROCANCER 98, 1998, pp. 95-96
Implication of germline BRCA2 gene mutations for the occurrence of ocular melanoma and pancreatic cancer
Authors: Serova-Sinilnikova, O Egan, K Boutrand, L Stoppa-Lyonnet, D Desjardins, L Levy, C Bignon, YJ Lasset, C Haguenauer, O Goldgar, D Lenoir, GM
Citation: O. Serova-sinilnikova et al., Implication of germline BRCA2 gene mutations for the occurrence of ocular melanoma and pancreatic cancer, EUROCANCER 98, 1998, pp. 113-114
Risultati: 1-19 |