Zobrazeno 1 - 10
of 46
pro vyhledávání: '"ARLTS1"'
Publikováno v:
Hereditary Cancer in Clinical Practice, Vol 15, Iss 1, Pp 1-8 (2017)
Abstract Adenosine diphosphate (ADP)-ribosylation factor-like tumour suppressor gene 1(ARLTS1) might be associated with an increased risk of several types of familial cancers. However, previous studies have shown that cancer susceptibility is not com
Externí odkaz:
https://doaj.org/article/6e77b73b31a44dd5a98bbdbb338b0d5f
Akademický článek
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Autor:
Li Xuchen, Gast Andreas, Rudnai Peter, Gurzau Eugene, Koppova Kvetoslava, Hemminki Kari, Kumar Rajiv
Publikováno v:
Hereditary Cancer in Clinical Practice, Vol 5, Iss 1, Pp 25-29 (2007)
Abstract Polymorphisms in the ARLTS1 gene, a member of the Ras super-family, have been associated with susceptibility in different cancer types. The involvement of the gene in apoptotic signalling motivated us to study the role of ARLTS1 polymorphic
Externí odkaz:
https://doaj.org/article/cc13a8ad12624472aeca24ca96f9fb79
Akademický článek
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Publikováno v:
The Journal of Biological Chemistry
ADP-ribosylation factor-like GTPase 11 (ARL11) is a cancer-predisposing gene that has remained functionally uncharacterized to date. In this study, we report that ARL11 is endogenously expressed in mouse and human macrophages and regulates their acti
Publikováno v:
Hereditary Cancer in Clinical Practice
Hereditary Cancer in Clinical Practice, Vol 15, Iss 1, Pp 1-8 (2017)
Hereditary Cancer in Clinical Practice, Vol 15, Iss 1, Pp 1-8 (2017)
Adenosine diphosphate (ADP)-ribosylation factor-like tumour suppressor gene 1(ARLTS1) might be associated with an increased risk of several types of familial cancers. However, previous studies have shown that cancer susceptibility is not completely c
Autor:
Siltanen, Sanna
Eturauhassyöpä on miesten yleisin syöpä teollistuneissa maissa, myös Suomessa, ja se aiheuttaa toiseksi eniten miesten syöpäkuolemia. Vaikka eturauhassyöpä on hyvin yleinen sairaus, sen syntyyn vaikuttavat syyt ja riskitekijät tunnetaan vie
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______4853::7538a493d579e826148352f66c982531
https://trepo.tuni.fi/handle/10024/68248
https://trepo.tuni.fi/handle/10024/68248
Akademický článek
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K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
Manuela Ferracin, Calin Dan Dumitru, Massimo Negrini, Devjani Chatterjee, Jens Overgaard, Laura Z. Rassenti, George A. Calin, Donna Neuberg, Francesca Romana Mauro, Guido Bernardi, Hansjuerg Alder, Vlad Herlea, Hideaki Mabuchi, Andrew K. Godwin, Raffaele Baffa, Carlo M. Croce, Masayoshi Shimizu, Florencia Bullrich, Shashi Rattan, Benjamin Movsas, Lise Lotte Hansen, Gustavo Baldassarre, Alfredo Fusco, Guillaume Dighiero, Chang Gong Liu, Giandomenico Russo, Francesco Trapasso, Masaki Mori, Sai Yendamuri, Takeshi Shiraishi, Thomas J. Kipps
Publikováno v:
Aarhus University
Calin, G A, Trapasso, F, Shimizu, M, Dumitru, C D, Yendamuri, S, Godwin, A K, Ferracin, M, Bernardi, G, Chatterjee, D, Baldassarre, G, Rattan, S, Alder, H, Mabuchi, H, Shiraishi, T, Hansen, L L, Overgaard, J, Herlea, V, Mauro, F R, Dighiero, G, Movsas, B, Rassenti, L, Kipps, T, Baffa, R, Fusco, A, Mori, M, Russo, G, Liu, C-G, Neuberg, D, Bullrich, F, Negrini, M & Croce, C M 2005, ' Familial cancer associated with a polymorphism in ARLTS1 ', The New England Journal of Medicine, vol. 352, no. 16, pp. 1667-76 . https://doi.org/10.1056/NEJMoa042280
Calin, G A, Trapasso, F, Shimizu, M, Dumitru, C D, Yendamuri, S, Godwin, A K, Ferracin, M, Bernardi, G, Chatterjee, D, Baldassarre, G, Rattan, S, Alder, H, Mabuchi, H, Shiraishi, T, Hansen, L L, Overgaard, J, Herlea, V, Mauro, F R, Dighiero, G, Movsas, B, Rassenti, L, Kipps, T, Baffa, R, Fusco, A, Mori, M, Russo, G, Liu, C-G, Neuberg, D, Bullrich, F, Negrini, M & Croce, C M 2005, ' Familial cancer associated with a polymorphism in ARLTS1 ', N. Engl. J. Med., vol. 352, no. 16, pp. 1667-1676 .
Calin, G A, Trapasso, F, Shimizu, M, Dumitru, C D, Yendamuri, S, Godwin, A K, Ferracin, M, Bernardi, G, Chatterjee, D, Baldassarre, G, Rattan, S, Alder, H, Mabuchi, H, Shiraishi, T, Hansen, L L, Overgaard, J, Herlea, V, Mauro, F R, Dighiero, G, Movsas, B, Rassenti, L, Kipps, T, Baffa, R, Fusco, A, Mori, M, Russo, G, Liu, C-G, Neuberg, D, Bullrich, F, Negrini, M & Croce, C M 2005, ' Familial cancer associated with a polymorphism in ARLTS1 ', The New England Journal of Medicine, vol. 352, no. 16, pp. 1667-76 . https://doi.org/10.1056/NEJMoa042280
Calin, G A, Trapasso, F, Shimizu, M, Dumitru, C D, Yendamuri, S, Godwin, A K, Ferracin, M, Bernardi, G, Chatterjee, D, Baldassarre, G, Rattan, S, Alder, H, Mabuchi, H, Shiraishi, T, Hansen, L L, Overgaard, J, Herlea, V, Mauro, F R, Dighiero, G, Movsas, B, Rassenti, L, Kipps, T, Baffa, R, Fusco, A, Mori, M, Russo, G, Liu, C-G, Neuberg, D, Bullrich, F, Negrini, M & Croce, C M 2005, ' Familial cancer associated with a polymorphism in ARLTS1 ', N. Engl. J. Med., vol. 352, no. 16, pp. 1667-1676 .
The finding of hemizygous or homozygous deletions at band 14 on chromosome 13 in a variety of neoplasms suggests the presence of a tumor-suppressor locus telomeric to the RB1 gene. METHODS: We studied samples from 216 patients with various types of s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::505c4eda23cf0a6fe2dd5100d5aef95c
http://hdl.handle.net/11392/1199730
http://hdl.handle.net/11392/1199730