Authors:
Paakkonen, K
Sauramo, S
Sarantaus, L
Vahteristo, P
Hartikainen, A
Vehmanen, P
Ignatius, J
Ollikainen, V
Kaariainen, H
Vauramo, E
Nevanlinna, H
Krahe, R
Holli, K
Kere, J
Citation: K. Paakkonen et al., Involvement of BRCA1 and BRCA2 in breast cancer in a Western Finnish sub-population, GENET EPID, 20(2), 2001, pp. 239-246
Authors:
Lahti-Domenici, J
Rapakko, K
Paakkonen, K
Allinen, M
Nevanlinna, H
Kujala, M
Huusko, P
Winqvist, R
Citation: J. Lahti-domenici et al., Exclusion of large deletions and other rearrangements in BRCA1 and BRCA2 in Finnish breast and ovarian cancer families, CANC GENET, 129(2), 2001, pp. 120-123
Authors:
Sarantaus, L
Huusko, P
Eerola, H
Launonen, V
Vehmanen, P
Rapakko, K
Gillanders, E
Syrjakoski, K
Kainu, T
Vahteristo, P
Krahe, R
Paakkonen, K
Hartikainen, J
Blomqvist, C
Lopponen, T
Holli, K
Ryynanen, M
Butzow, R
Borg, A
Arver, BW
Holmberg, E
Mannermaa, A
Kere, J
Kallioniemi, OP
Winqvist, R
Nevanlinna, H
Citation: L. Sarantaus et al., Multiple founder effects and geographical clustering of BRCA1 and BRCA2 families in Finland, EUR J HUM G, 8(10), 2000, pp. 757-763
Authors:
Rechardt, O
Elomaa, O
Vaalamo, M
Paakkonen, K
Jahkola, T
Hook-Nikanne, J
Hembry, RM
Hakkinen, L
Kere, J
Saarialho-Kere, U
Citation: O. Rechardt et al., Stromelysin-2 is upregulated during normal wound repair and is induced by cytokines, J INVES DER, 115(5), 2000, pp. 778-787
Authors:
Paakkonen, K
Sorsa, T
Drakenberg, T
Pollesello, P
Tilgmann, C
Permi, P
Heikkinen, S
Kilpelainen, I
Annila, A
Citation: K. Paakkonen et al., Conformations of the regulatory domain of cardiac troponin C examined by residual dipolar couplings, EUR J BIOCH, 267(22), 2000, pp. 6665-6672
Authors:
Balci, A
Huusko, P
Paakkonen, K
Launonen, V
Uner, A
Ekmekci, A
Winqvist, R
Citation: A. Balci et al., Mutation analysis of BRCA1 and BRCA2 in Turkish cancer families: a novel mutation BRCA2 3414de14 found in male breast cancer, EUR J CANC, 35(5), 1999, pp. 707-710
Authors:
Huusko, P
Castren, K
Launonen, V
Soini, Y
Paakkonen, K
Leisti, J
Vahakangas, K
Winqvist, R
Citation: P. Huusko et al., Germ-line TP53 mutations in Finnish cancer families exhibiting features ofthe Li-Fraumeni syndrome and negative for BRCA1 and BRCA2, CANC GENET, 112(1), 1999, pp. 9-14