Zobrazeno 1 - 10
of 248
pro vyhledávání: '"Romkes M"'
Autor:
Argiris, A. *, Karamouzis, M.V., Smith, R., Kotsakis, A., Gibson, M.K., Lai, S.Y., Kim, S., Branstetter, B.F., Shuai, Y., Romkes, M., Wang, L., Grandis, J.R., Ferris, R.L., Johnson, J.T., Heron, D.E.
Publikováno v:
In Annals of Oncology November 2011 22(11):2482-2488
Autor:
McKay JD, Truong T, Gaborieau V, Chabrier A, Chuang SC, Byrnes G, Zaridze D, Shangina O, Szeszenia Dabrowska N, Lissowska J, Rudnai P, Fabianova E, Bucur A, Bencko V, Holcatova I, Janout V, Foretova L, Lagiou P, Trichopoulos D, Benhamou S, Bouchardy C, Ahrens W, Merletti F, Richiardi L, Talamini R, Barzan L, Kjaerheim K, Macfarlane GJ, Macfarlane TV, Simonato L, Canova C, Agudo A, Castellsagué X, Lowry R, Conway DI, McKinney PA, Healy CM, Toner ME, Znaor A, Curado MP, Koifman S, Menezes A, Wünsch Filho V, Neto JE, Garrote LF, Boccia S, Cadoni G, Arzani D, Olshan AF, Weissler MC, Funkhouser WK, Luo J, Lubiński J, Trubicka J, Lener M, Oszutowska D, Schwartz SM, Chen C, Fish S, Doody DR, Muscat JE, Lazarus P, Gallagher CJ, Chang SC, Zhang ZF, Wei Q, Sturgis EM, Wang LE, Franceschi S, Herrero R, Kelsey KT, McClean MD, Marsit CJ, Nelson HH, Romkes M, Buch S, Nukui T, Zhong S, Lacko M, Manni JJ, Peters WH, Hung RJ, McLaughlin J, Vatten L, Njølstad I, Goodman GE, Field JK, Liloglou T, Vineis P, Clavel Chapelon F, Palli D, Tumino R, Krogh V, González CA, Quirós JR, Martínez C, Navarro C, Ardanaz E, Larrañaga N, Khaw KT, Key T, Bueno de Mesquita HB, Peeters PH, Trichopoulou A, Linseisen J, Boeing H, Hallmans G, Overvad K, Tjønneland A, Kumle M, Riboli E, Välk K, Vooder T, Metspalu A, Zelenika D, Boland A, Delepine M, Foglio M, Lechner D, Blanché H, Gut IG, Galan P, Heath S, Hashibe M, Hayes RB, Boffetta P, Lathrop M, Brennan P., PANICO, SALVATORE
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3730::c4b0be5963a7f7a22bfc465633901651
http://hdl.handle.net/11588/428718
http://hdl.handle.net/11588/428718
Autor:
Horwitz, M.S., McKay, J.D., Truong, T., Gaborieau, V., Chabrier, A., Chuang, S.-C., Byrnes, G., Zaridze, D., Shangina, O., Szeszenia-Dabrowska, N., Lissowska, J., Rudnai, P., Fabianova, E., Bucur, A., Bencko, V., Holcatova, I., Janout, V., Foretova, L., Lagiou, P., Trichopoulos, D., Benhamou, S., Bouchardy, C., Ahrens, W., Merletti, F., Richiardi, L., Talamini, R., Barzan, L., Kjaerheim, K., Macfarlane, G.J., Macfarlane, T.V., Simonato, L., Canova, C., Agudo, A., Castellsagué, X., Lowry, R., Conway, D.I., McKinney, P.A., Healy, C.M., Toner, M.E., Znaor, A., Curado, M.P., Koifman, S., Menezes, A., Wünsch-Filho, V., Neto, J.E., Garrote, L.F., Boccia, S., Cadoni, G., Arzani, D., Olshan, A.F., Weissler, M.C., Funkhouser, W.K., Luo, J., Lubiński, J., Trubicka, J., Lener, M., Oszutowska, D., Schwartz, S.M., Chen, C., Fish, S., Doody, D.R., Muscat, J.E., Lazarus, P., Gallagher, C.J., Chang, S.C., Zhang, Z.F., Wei, Q., Sturgis, E.M., Wang, L.E., Franceschi, S., Herrero, R., Kelsey, K.T., McClean, M.D., Marsit, C.J., Nelson, H.H., Romkes, M., Buch, S., Nukui, T., Zhong, S., Lacko, M., Manni, J.J., Peters, W.H.M., Hung, R.J., McLaughlin, J., Vatten, L., Njølstad, I., Goodman, G.E., Field, J.K., Liloglou, T., Vineis, P., Clavel-Chapelon, F., Palli, D., Tumino, R., Krogh, V., Panico, S., González, C.A., Quirós, J.R., Martínez, C., Navarro, C., Ardanaz, E., Larrañaga, N., Khaw, K.T., Key, T., Bueno-de-Mesquita, H. B., Peeters, P.H.M., Trichopoulou, A., Linseisen, J., Boeing, H., Hallmans, G., Overvad, K., Tjønneland, A., Kumle, M., Riboli, E., Välk, K., Vooder, T., Metspalu, A., Zelenika, D., Boland, A., Delepine, M., Foglio, M., Lechner, D., Blanché, H., Gut, I.G., Galan, P., Heath, S., Hashibe, M., Hayes, R.B., Boffetta, P., Lathrop, M., Brennan, P.
Genome-wide association studies (GWAS) have been successful in identifying common genetic variation involved in susceptibility to etiologically complex disease. We conducted a GWAS to identify common genetic variation involved in susceptibility to up
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=core_ac_uk__::98b988ee6fc9ebc81c48b54fdc4bdaba
https://eprints.gla.ac.uk/51692/4/51692.pdf
https://eprints.gla.ac.uk/51692/4/51692.pdf
Autor:
McKay, James D., Truong, Therese, Gaborieau, V, Chabrier, Amelie, Chuang, Shu-Chun, Byrnes, G, Zaridze, D, Shangina, O, Szeszenia-Dabrowska, N, Lissowska, Jolanta, Rudnai, P, Fabianova, E, Bucur, A, Bencko, V, Holcatova, I, Janout, V, Foretova, L, Lagiou, Pagona, Trichopoulos, Dimitrios, Benhamou, S, Ahrens, Wolfgang, Bouchardy, C, Merletti, F, Richiardi, L, Talamini, R, Simonato, L, Barzan, L, Kjærheim, Kristina, Macfarlane, G, Agudo, Antonio, Macfarlane, Tatiana V., Canova, C, Castellsague, X, Conway, DI, Lowry, R, Healy, CM, McKinney, PA, Toner, ME, Znaor, A, Menezes, A, Curado, MP, Koifman, S, Neto, JE, Wünsch-Filho, V, Boccia, S, Arzani, D, Garrote, LF, Cadoni, G, Olshan, AF, Weissler, MC, Luo, JC, Funkhouser, WK, Lubinski, Jan, Lener, M, Trubicka, J, Schwartz, SM, Oszutowska, D, Doody, DR, Chen, C, Fish, S, Lazarus, P, Muscat, JE, Gallagher, CJ, Zhang, Zuo-Feng, Chang, SC, Wei, QY, Sturgis, EM, Franceschi, S, Kelsey, KT, Wang, LE, Herrero, R, Marsit, CJ, McClean, MD, Romkes, M, Nelson, HH, Buch, S, Nukui, T, Zhong, SL, Lacko, M, Manni, JJ, McLaughlin, J, Hung, RJ, Peters, WHM, Vatten, Lars Johan, Njølstad, Inger, Goodman, GE, Field, JK, Palli, D, Liloglou, T, Clavel-Chapelon, F, Vineis, P, Krogh, V, Tumino, R, Panico, S, Martinez, Carmen, Gonzalez, CA, Quiros, JR, Navarro, C, Larranaga, N, Khaw, KT, Ardanaz, E, Key, T, Peeters, PHM, Bueno-De-Mesquita, H. Bas, Boeing, H, Overvad, K, Trichopoulou, A, Linseisen, J, Hallmans, G, Tjønneland, Anne, Riboli, Elio, Kumle, Merethe, Valk, K, Voodern, Tonu, Metspalu, Andres, Boland, A, Zelenika, D, Delepine, M, Foglio, M, Lechner, D, Blanché, Hélène, Gut, Ivo G., Galan, P, Hashibe, Mia, Heath, Simon, Hayes, Richard B., Lathrop, Mark, Boffetta, Paolo, Brennan, Paul
Publikováno v:
PLoS Genetics (2011) 7(3): e1001333.
doi: 10.1371/jo
doi: 10.1371/jo
Externí odkaz:
https://hdl.handle.net/10037/4033
Autor:
McKay, J.D., Truong, T., Gaborieau, V., Chabrier, A., Chuang, S.C., Byrnes, G., Zaridze, D., Shangina, O., Szeszenia-Dabrowska, N., Lissowska, J., Rudnai, P., Fabianova, E., Bucur, A., Bencko, V., Holcatova, I., Janout, V., Foretova, L., Lagiou, P., Trichopoulos, D., Benhamou, S., Bouchardy, C., Ahrens, W., Merletti, F., Richiardi, L., Talamini, R., Barzan, L., Kjaerheim, K., Macfarlane, G.J., Macfarlane, T.V., Simonato, L., Canova, C., Agudo, A., Castellsague, X., Lowry, R., Conway, D.I., McKinney, P.A., Healy, C.M., Toner, M.E., Znaor, A., Curado, M.P., Koifman, S., Menezes, A., Wunsch-Filho, V., Neto, J.E., Garrote, L.F., Boccia, S., Cadoni, G., Arzani, D., Olshan, A.F., Weissler, M.C., Funkhouser, W.K., Luo, J., Lubinski, J., Trubicka, J., Lener, M., Oszutowska, D., Schwartz, S.M., Chen, C., Fish, S., Doody, D.R., Muscat, J.E., Lazarus, P., Gallagher, C.J., Chang, S.C., Zhang, Z.F., Wei, Q., Sturgis, E.M., Wang, L.E., Franceschi, S., Herrero, R., Kelsey, K.T., McClean, M.D., Marsit, C.J., Nelson, H.H., Romkes, M., Buch, S., Nukui, T., Zhong, S., Lacko, M., Manni, J.J., Peters, W.H.M., Hung, R.J., McLaughlin, J., Vatten, L., Njolstad, I., Goodman, G.E., Field, J.K., Liloglou, T., Vineis, P., Clavel-Chapelon, F., Palli, D., Tumino, R., Krogh, V., Panico, S., Gonzalez, C.A., Quiros, J.R., Martinez, C., Navarro, C, Ardanaz, E., Larrañaga, N.
Publikováno v:
Plos Genetics, 7, e1001333-e1001333
Genome-wide association studies (GWAS) have been successful in identifying common genetic variation involved in susceptibility to etiologically complex disease. We conducted a GWAS to identify common genetic variation involved in susceptibility to up
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=narcis______::65fb4daacad5d51534ef26293fe380e9
http://hdl.handle.net/2066/96576
http://hdl.handle.net/2066/96576
Background: Sequence variants located at 15q25 have been associated with lung cancer and propensity to smoke. We recently reported an association between rs16969968 and risk of upper aerodigestive tract (UADT) cancers (oral cavity, oropharynx, hypoph
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::e22c66c94b453268d6aec6be5d2da7a0
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3111630
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3111630
Autor:
Garte, S., Gaspari, L., Alexandrie, A. K., Ambrosone, C., Autrup, H., Autrup, J. L., Baranova, H., Bathum, L., Benhamou, S., Boffetta, P., Bouchardy, C., Breskvar, K., Brockmoller, J., Cascorbi, I., Clapper, M. L., Coutelle, C., Daly, A., Omo, M., Dolzan, V., Dresler, C. M., Fryer, A., Haugen, A., Hein, D. W., Hildesheim, A., Hirvonen, A., Hsieh, L. L., Ingelman-Sundberg, M., Kalina, I., Kang, D., Kihara, M., Kiyohara, C., Kremers, P., Lazarus, P., Le Marchand, L., Lechner, M. C., Lieshout, E. M., Stephanie London, Manni, J. J., Maugard, C. M., Morita, S., Nazar-Stewart, V., Noda, K., Oda, Y., Parl, F. F., Pastorelli, R., Persson, I., Peters, W. H., Rannug, A., Rebbeck, T., Risch, A., Roelandt, L., Romkes, M., Ryberg, D., Salagovic, J., Schoket, B., Seidegard, J., Shields, P. G., Sim, E., Sinnet, D., Strange, R. C., Stucker, I., Sugimura, H., To-Figueras, J., Vineis, P., Yu, M. C., Taioli, E.
Publikováno v:
Garte, S, Gaspari, L, Alexandrie, A-K, Ambrosone, C, Autrup, H, Autrup, J, Baranova, H, Bathum, L, Benhamou, S, Boffetta, P, Bouchardy, C, Breskvar, K, Brockmoller, J, Cascorbi, I, Clapper, M L, Coutelle, C, Daly, A, Dell'Omo, M, Dolzan, V, Dresler, C M, Fryer, A, Haugen, A, Hein, D W, Hildesheim, A, Hirvonen, A, Hsieh, L-L, Ingelman-Sundberg, M, Kalina, I, Kang, D, Kihara, M, Kiyohara, C, Kremers, P, Lazarus, P, Le Marchand, L L, Lechner, M C, van Lieshout, E M M, London, S, Manni, J J, Maugard, C M, Morita, S, Nazar-Stewart, V, Noda, K, Oda, Y, Parl, F F, Pastorelli, R, Persson, I, Peters, W H M, Rannug, A, Rebbeck, T, Risch, A, Roelandt, L, Romkes, M, Ryberg, D, Salagovic, J, Schoket, B, Seidegard, J, Shields, P G, Sim, E, Sinnet, D, Strange, R C, Stucker, I, Sugimura, H, To-Figueras, J, Vineis, P, Yu, M C & Taioli, E 2001, ' Metabolic gene polymorphism frequencies in control populations ', Cancer Epidemiology, Biomarkers & Prevention, vol. 10, no. 12, pp. 1239-1248 .
Scopus-Elsevier
Cancer Epidemiology, Biomarkers & Prevention, 10, 1239-48
Cancer Epidemiology, Biomarkers & Prevention, 10, 12, pp. 1239-48
ResearcherID
Scopus-Elsevier
Cancer Epidemiology, Biomarkers & Prevention, 10, 1239-48
Cancer Epidemiology, Biomarkers & Prevention, 10, 12, pp. 1239-48
ResearcherID
Item does not contain fulltext Using the International Project on Genetic Susceptibility to Environmental Carcinogens (GSEC) database containing information on over 15,000 control (noncancer) subjects, the allele and genotype frequencies for many of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::50d65a4a000e08102cd99494ec202137
https://pure.au.dk/portal/da/publications/metabolic-gene-polymorphism-frequencies-in-control-populations(ed04a5b0-983e-11da-bee9-02004c4f4f50).html
https://pure.au.dk/portal/da/publications/metabolic-gene-polymorphism-frequencies-in-control-populations(ed04a5b0-983e-11da-bee9-02004c4f4f50).html
Autor:
Garte, S, Gaspari, L, Alexandrie, Ak, Ambrosone, C, Autrup, H, Autrup, Jl, Baranova, H, Bathum, L, Benhamou, S, Boffetta, P, Bouchardy, C, Breskvar, K, Brockmoller, J, Cascorbi, I, Clapper, Ml, Coutelle, C, Daly, A, Dell'Omo, Marco, Dolzan, V, Dresler, Cm, Fryer, A, Haugen, A, Hein, Dw, Hildesheim, A, Hirvonen, A, Hsieh, Ll, Ingelman, Sundberg, M, Kalina, I, Kang, D, Kihara, M, Kiyohara, C, Kremers, P, Lazarus, P, LE MARCHAND, L, Lechner, Mc, VAN LIESHOUT EM, London, S, Manni, Jj, Maugard, Cm, Morita, S, NAZAR STEWART, V, Noda, K, Oda, Y, Parl, Ff, Pastorelli, R, Persson, I, Peters, Wh, Rannug, A, Rebbeck, T, Risch, A, Roelandt, L, Romkes, M, Ryberg, D, Salagovic, J, Schoket, B, Seidegard, J, Shields, Pg, Sim, E, Sinnet, D, Strange, Rc, Stücker, I, Sugimura, H, TO FIGUERAS, J, Vineis, P, Yu, Mc, Taioli, E.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3982::7479ca41a3725aec659938eb8f3d769a
http://hdl.handle.net/11391/113029
http://hdl.handle.net/11391/113029
Autor:
Romkes, M, Marcus, PM, Hayes, RB, Vineis, P, Garcia-Closas, M, Caporaso, NE, Autrup, H, Branch, RA, Brockmoller, J, Ishizaki, T, Karakaya, AE, Ladero, JM, Mommsen, S, Okkels, H, Roots, I, Rothman, N
Publikováno v:
Marcus, P M, Hayes, R B, Vineis, P, Carcia-Closas, M, Caporaso, N E, Autrup, H, Branch, R A, Brockmöller, J, Ishizaki, T, Karakaya, A E, Ladero, J M, Mommsen, S, Okkels, H, Romkes, M, Roots, I & Rothman, N 2000, ' Cigarette Smoking, N-Acetyltransferase 2 Acetylation Status, and Bladder Cancer Risk : A Case-Series Meta-analysis of a Gene-Environment Interaction ', Cancer Epidemiology, Biomarkers & Prevention, vol. 9, no. 5, pp. 461-467 .
Tobacco use is an established cause of bladder cancer. The ability to detoxify aromatic amines, which are present in tobacco and are potent bladder carcinogens, is compromised in persons with the N-acetyltransferase 2 slow acetylation polymorphism. T
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::02e9fdf174e08077893e55a16e20d02b
https://pure.au.dk/portal/da/publications/cigarette-smoking-nacetyltransferase-2-acetylation-status-and-bladder-cancer-risk(f3e5f820-983e-11da-bee9-02004c4f4f50).html
https://pure.au.dk/portal/da/publications/cigarette-smoking-nacetyltransferase-2-acetylation-status-and-bladder-cancer-risk(f3e5f820-983e-11da-bee9-02004c4f4f50).html