Molecular characterization of the tumor microenvironment in breast cancer von Allinen, Minna, Beroukhim, Rameen, Cai, Li, Brennan, Cameron, Lahti-Domenici, Jaana, Huang, Haiyan, Porter, Dale, Hu, Min, Chin, Lynda, Richardson, Andrea, Schnitt, Stuart, Sellers, William R, Polyak, Kornelia

Volltext

Mutation analysis of the CHK2 gene in families with hereditary breast cancer von ALLINEN, M, HUUSKO, P, MÄNTYNIEMI, S, LAUNONEN, V, WINQVIST, R

Volltext

Evaluation of the role of Finnish ataxia-telangiectasia mutations in hereditary predisposition to breast cancer von Pylkäs, Katri, Tommiska, Johanna, Syrjäkoski, Kirsi, Kere, Juha, Gatei, Magtouf, Waddell, Nicola, Allinen, Minna, Karppinen, Sanna-Maria, Rapakko, Katrin, Kääriäinen, Helena, Aittomäki, Kristiina, Blomqvist, Carl, Mustonen, Aki, Holli, Kaija, Khanna, Kum Kum, Kallioniemi, Olli-Pekka, Nevanlinna, Heli, Winqvist, Robert

Volltext

No evidence of involvement of germline BACH1 mutations in Finnish breast and ovarian cancer families von Karppinen, S.-M., Vuosku, J., Heikkinen, K., Allinen, M., Winqvist, R.

Volltext

Nonsense-mediated decay microarray analysis identifies mutations of EPHB2 in human prostate cancer von Kallioniemi, Olli-P, Mousses, Spyro, Huusko, Pia, Ponciano-Jackson, Damaris, Wolf, Maija, Kiefer, Jeff A, Azorsa, David O, Tuzmen, Sukru, Weaver, Don, Robbins, Christiane, Moses, Tracy, Allinen, Minna, Hautaniemi, Sampsa, Chen, Yidong, Elkahloun, Abdel, Basik, Mark, Bova, G Steven, Bubendorf, Lukas, Lugli, Alessandro, Sauter, Guido, Schleutker, Johanna, Ozcelik, Hilmi, Elowe, Sabine, Pawson, Tony, Trent, Jeffrey M, Carpten, John D

Volltext

High-Resolution Analysis of Gene Copy Number Alterations in Human Prostate Cancer Using CGH on cDNA Microarrays: Impact of Copy Number on Gene Expression von Wolf, Maija, Mousses, Spyro, Hautaniemi, Sampsa, Karhu, Ritva, Huusko, Pia, Allinen, Minna, Elkahloun, Abdel, Monni, Outi, Chen, Yidong, Kallioniemi, Anne, Kallioniemi, Olli-P

Volltext

High-Resolution Analysis of Gene Copy Number Alterations in Human Prostate Cancer Using CGH on cDNA Microarrays: Impact of Copy Number on Gene Expression von Wolf, M, Mousses, S, Hautaniemi, S, Karhu, R, Huusko, P, Allinen, M, Abdel Elkahloun, Monni, O, Chen, Y, Kallioniemi, A, Kallioniemi, O-P

Volltext

ATM mutations in Finnish breast cancer patients von Allinen, M, Launonen, V, Laake, K, Jansen, L, Huusko, P, Kääriäinen, H, Børresen-Dale, A-L, Winqvist, R

Volltext

Analysis of 11q21-24 loss of heterozygosity candidate target genes in breast cancer: Indications of TSLC1 promoter hypermethylation von Allinen, Minna, Peri, Liisa, Kujala, Sonja, Lahti-Domenici, Jaana, Outila, Kati, Karppinen, Sanna-Maria, Launonen, Virpi, Winqvist, Robert

Volltext

Connexin 26 mutations and nonsyndromic hearing impairment in Northern Finland von Löppönen, Tuija, Väisänen, Marja-Leena, Luotonen, Mirja, Allinen, Minna, Uusimaa, Johanna, Lindholm, PÄIvi, Mäki-Torkko, Elina, Väyrynen, Mirja, Löppönen, Heikki, Leisti, Jaakko

Volltext

Characterization and expression of the human WNT4; lack of associated germline mutations in high—to moderate—risk breast and ovarian cancer von Peltoketo, Hellevi, Allinen, Minna, Vuosku, Jaana, Kujala, Sonja, Lundan, Tuija, Salminen, Annamari, Winqvist, Robert, Vainio, Seppo

Volltext

The role of the tumor microenvironment in breast cancer progression von Min, H, Yao, J, Allinen, M, Cai, L, Polyak, K

Volltext

The role of the tumor microenvironment in breast cancer progression von Min, H, Yao, J, Allinen, M, Cai, L, Polyak, K

Volltext

Genome-wide scanning for linkage in Finnish breast cancer families von Huusko, Pia, Juo, Suh-Hang Hank, Gillanders, Elizabeth, Sarantaus, Laura, Kainu, Tommi, Vahteristo, Pia, Allinen, Minna, Jones, MaryPat, Rapakko, Katrin, Eerola, Hannaleena, Markey, Carol, Vehmanen, Paula, Gildea, Derek, Freas-Lutz, Diane, Blomqvist, Carl, Leisti, Jaakko, Blanco, Guillermo, Puistola, Ulla, Trent, Jeffrey, Bailey-Wilson, Joan, Winqvist, Robert, Nevanlinna, Heli, Kallioniemi, Olli-P

Volltext

Germline TP53 alterations in Finnish breast cancer families are rare and occur at conserved mutation-prone sites von Rapakko, K, Allinen, M, Syrjäkoski, K, Vahteristo, P, Huusko, P, Vähäkangas, K, Eerola, H, Kainu, T, Kallioniemi, O-P, Nevanlinna, H, Winqvist, R

Volltext

Mutation analysis of the CHK2gene in families with hereditary breast cancer von Allinen, M, Huusko, P, Mäntyniemi, S, Launonen, V, Winqvist, R

Volltext

Mutation analysis of theCHK2gene in families with hereditary breast cancer von Allinen, M, Huusko, P, Mäntyniemi, S, Launonen, V, Winqvist, R

Volltext

Germline TP53mutations in Finnish breast cancer patients von Rapakko, K, Allinen, M, Syrjakoski, K, Vahteristo, P, Huusko, P, Vahakangas, K, Eerola, H, Kainu, T, Kallioniemi, O-P, Nevanlinna, H, Winqvist, R

Volltext

Germline TP53 mutations in Finnish breast cancer patients von Rapakko, K, Allinen, M, Syrjäkoski, K, Vahteristo, P, Huusko, P, Vähäkangas, K, Eerola, H, Kainu, T, Kallioniemi, O-P, Nevanlinna, H, Winqvist, R

Volltext

Exclusion of large deletions and other rearrangements in BRCA1 and BRCA2 in Finnish breast and ovarian cancer families von Lahti-Domenici, Jaana, Rapakko, Katrin, Pääkkönen, Kati, Allinen, Minna, Nevanlinna, Heli, Kujala, Marika, Huusko, Pia, Winqvist, Robert

Volltext