No SMAD4 hypermethylation in colorectal cancer

por Roth, S, Laiho, P, Salovaara, R, Launonen, V, Aaltonen, L A
Publicado 2000

No evidence of microsatellite instability in bone tumours.

por Tarkkanen, M., Aaltonen, L. A., Böhling, T., Kivioja, A., Karaharju, E., Elomaa, I., Knuutila, S.
Publicado 1996

Mutation analysis of components of the Mediator kinase module in MED12 mutation-negative uterine leiomyomas

por Mäkinen, N, Heinonen, H-R, Sjöberg, J, Taipale, J, Vahteristo, P, Aaltonen, L A
Publicado 2014

Mutation analysis of aryl hydrocarbon receptor interacting protein (AIP) gene in colorectal, breast, and prostate cancers

por Georgitsi, M, Karhu, A, Winqvist, R, Visakorpi, T, Waltering, K, Vahteristo, P, Launonen, V, Aaltonen, L A
Publicado 2007

Differential expression of DHHC9 in microsatellite stable and instable human colorectal cancer subgroups

por Mansilla, F, Birkenkamp-Demtroder, K, Kruhøffer, M, Sørensen, F B, Andersen, C L, Laiho, P, Aaltonen, L A, Verspaget, H W, Ørntoft, T F
Publicado 2007

CDX2 mutations do not account for juvenile polyposis or Peutz–Jeghers syndrome and occur infrequently in sporadic colorectal cancers

por Woodford-Richens, K L, Halford, S, Rowan, A, Bevan, S, Aaltonen, L A, Wasan, H, Bicknell, D, Bodmer, W F, Houlston, R S, Tomlinson, I P M
Publicado 2001

Dysregulation of the transcription factors SOX4, CBFB and SMARCC1 correlates with outcome of colorectal cancer

por Andersen, C L, Christensen, L L, Thorsen, K, Schepeler, T, Sørensen, F B, Verspaget, H W, Simon, R, Kruhøffer, M, Aaltonen, L A, Laurberg, S, Ørntoft, T F
Publicado 2009

A missense mutation in the BRCA2 gene in three siblings with ovarian cancer.

por Roth, S., Kristo, P., Auranen, A., Shayehgi, M., Seal, S., Collins, N., Barfoot, R., Rahman, N., Klemi, P. J., Grénman, S., Sarantaus, L., Nevanlinna, H., Butzow, R., Ashworth, A., Stratton, M. R., Aaltonen, L. A.
Publicado 1998

Mutation analysis of three genes encoding novel LKB1-interacting proteins, BRG1, STRADα, and MO25α, in Peutz–Jeghers syndrome

por Alhopuro, P, Katajisto, P, Lehtonen, R, Ylisaukko-oja, S K, Näätsaari, L, Karhu, A, Westerman, A M, Wilson, J H P, de Rooij, F W M, Vogel, T, Moeslein, G, Tomlinson, I P, Aaltonen, L A, Mäkelä, T P, Launonen, V
Publicado 2005

Somatic MED12 mutations in uterine leiomyosarcoma and colorectal cancer

por Kämpjärvi, K, Mäkinen, N, Kilpivaara, O, Arola, J, Heinonen, H-R, Böhm, J, Abdel-Wahab, O, Lehtonen, H J, Pelttari, L M, Mehine, M, Schrewe, H, Nevanlinna, H, Levine, R L, Hokland, P, Böhling, T, Mecklin, J-P, Bützow, R, Aaltonen, L A, Vahteristo, P
Publicado 2012

Identification of 33 candidate oncogenes by screening for base-specific mutations

por Tuupanen, S, Hänninen, U A, Kondelin, J, von Nandelstadh, P, Cajuso, T, Gylfe, A E, Katainen, R, Tanskanen, T, Ristolainen, H, Böhm, J, Mecklin, J-P, Järvinen, H, Renkonen-Sinisalo, L, Andersen, C L, Taipale, M, Taipale, J, Vahteristo, P, Lehti, K, Pitkänen, E, Aaltonen, L A
Publicado 2014

Gene expression signatures for colorectal cancer microsatellite status and HNPCC

por Kruhøffer, M, Jensen, J L, Laiho, P, Dyrskjøt, L, Salovaara, R, Arango, D, Birkenkamp-Demtroder, K, Sørensen, F B, Christensen, L L, Buhl, L, Mecklin, J-P, Järvinen, H, Thykjaer, T, Wikman, F P, Bech-Knudsen, F, Juhola, M, Nupponen, N N, Laurberg, S, Andersen, C L, Aaltonen, L A, Ørntoft, T F
Publicado 2005

A large-scale meta-analysis to refine colorectal cancer risk estimates associated with MUTYH variants

por Theodoratou, E, Campbell, H, Tenesa, A, Houlston, R, Webb, E, Lubbe, S, Broderick, P, Gallinger, S, Croitoru, E M, Jenkins, M A, Win, A K, Cleary, S P, Koessler, T, Pharoah, P D, Küry, S, Bézieau, S, Buecher, B, Ellis, N A, Peterlongo, P, Offit, K, Aaltonen, L A, Enholm, S, Lindblom, A, Zhou, X-L, Tomlinson, I P, Moreno, V, Blanco, I, Capellà, G, Barnetson, R, Porteous, M E, Dunlop, M G, Farrington, S M
Publicado 2010

COGENT (COlorectal cancer GENeTics): an international consortium to study the role of polymorphic variation on the risk of colorectal cancer

por Tomlinson, I P M, Dunlop, M, Campbell, H, Zanke, B, Gallinger, S, Hudson, T, Koessler, T, Pharoah, P D, Niittymäkix, I, Tuupanenx, S, Aaltonen, L A, Hemminki, K, Lindblom, A, Försti, A, Sieber, O, Lipton, L, van Wezel, T, Morreau, H, Wijnen, J T, Devilee, P, Matsuda, K, Nakamura, Y, Castellví-Bel, S, Ruiz-Ponte, C, Castells, A, Carracedo, A, Ho, J W C, Sham, P, Hofstra, R M W, Vodicka, P, Brenner, H, Hampe, J, Schafmayer, C, Tepel, J, Schreiber, S, Völzke, H, Lerch, M M, Schmidt, C A, Buch, S, Moreno, V, Villanueva, C M, Peterlongo, P, Radice, P, Echeverry, M M, Velez, A, Carvajal-Carmona, L, Scott, R, Penegar, S, Broderick, P, Tenesa, A, Houlston, R S
Publicado 2010

COGENT (COlorectal cancer GENeTics): an international consortium to study the role of polymorphic variation on the risk of colorectal cancer

por Tomlinson, I P M, Dunlop, M, Campbell, H, Zanke, B, Gallinger, S, Hudson, T, Koessler, T, Pharoah, P D, Niittymäki, I, Tuupanen, S, Aaltonen, L A, Hemminki, K, Lindblom, A, Försti, A, Sieber, O, Lipton, L, van Wezel, T, Morreau, H, Wijnen, J T, Devilee, P, Matsuda, K, Nakamura, Y, Castellví-Bel, S, Ruiz-Ponte, C, Castells, A, Carracedo, A, Ho, J W C, Sham, P, Hofstra, R M W, Vodicka, P, Brenner, H, Hampe, J, Schafmayer, C, Tepel, J, Schreiber, S, Völzke, H, Lerch, M M, Schmidt, C A, Buch, S, Moreno, V, Villanueva, C M, Peterlongo, P, Radice, P, Echeverry, M M, Velez, A, Carvajal-Carmona, L, Scott, R, Penegar, S, Broderick, P, Tenesa, A, Houlston, R S
Publicado 2010