Potential role of a navigator gene NAV3 in colorectal cancer von Carlsson, E, Ranki, A, Sipilä, L, Karenko, L, Abdel-Rahman, W M, Ovaska, K, Siggberg, L, Aapola, U, Ässämäki, R, Häyry, V, Niiranen, K, Helle, M, Knuutila, S, Hautaniemi, S, Peltomäki, P, Krohn, K

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Molecular cytogenetics in the study of cutaneous T-cell lymphomas (CTCL) von Karenko, L., Hahtola, S., Ranki, A.

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Chromosomal abnormalities in relation to clinical disease in patients with cutaneous T-cell lymphoma: a 5-year follow-up study von Karenko, L., Sarna, S., Kähkönen, M., Ranki, A.

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Allelic variants in genes associated with hereditary periodic fever syndromes as susceptibility factors for reactive systemic AA amyloidosis von Aganna, E, Hawkins, P N, Ozen, S, Pettersson, T, Bybee, A, McKee, S A, Lachmann, H J, Karenko, L, Ranki, A, Bakkaloglu, A, Besbas, N, Topaloglu, R, Hoffman, H M, Hitman, G A, Woo, P, McDermott, M F

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Proapoptotic and antiapoptotic markers in cutaneous T-cell lymphoma skin infiltrates and lymphomatoid papulosis von Nevala, H., Karenko, L., Väkevä, L., Ranki, A.

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Germline Mutations in the Extracellular Domains of the 55 kDa TNF Receptor, TNFR1, Define a Family of Dominantly Inherited Autoinflammatory Syndromes von McDermott, Michael F, Aksentijevich, Ivona, Galon, Jérôme, McDermott, Elizabeth M, Ogunkolade, B.William, Centola, Michael, Mansfield, Elizabeth, Gadina, Massimo, Karenko, Leena, Pettersson, Tom, McCarthy, John, Frucht, David M, Aringer, Martin, Torosyan, Yelizaveta, Teppo, Anna-Maija, Wilson, Meredith, Karaarslan, H.Mehmet, Wan, Ying, Todd, Ian, Wood, Geryl, Schlimgen, Ryan, Kumarajeewa, Thisum R, Cooper, Sheldon M, Vella, John P, Amos, Christopher I, Mulley, John, Quane, Kathleen A, Molloy, Michael G, Ranki, Annamari, Powell, Richard J, Hitman, Graham A, O’Shea, John J, Kastner, Daniel L

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The genetic background of tumour necrosis factor receptor-associated periodic syndrome and other systemic autoinflammatory disorders von Stjernberg-Salmela, S, Ranki, A, Karenko, L, Pettersson, T

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Primary cutaneous T-cell lymphomas show a deletion or translocation affecting NAV3, the human UNC-53 homologue von KARENKO, Leena, HAHTOLA, Sonja, PESONEN, Maria, NEVALA, Hanna, NUPPONEN, Nina, SIHTO, Harri, KREBS, Inge, POUSTKA, Annemarie, ROSZKIEWICZ, Jadwiga, SAKSELA, Kalle, PETERSON, Pärt, VISAKORPI, Tapio, PÄIVINEN, Suvi, RANKI, Annamari, KARHU, Ritva, SYRJÄ, Sanna, KÄHKÖNEN, Marketta, NEDOSZYTKO, Boguslaw, KYTÖLÄ, Soili, YING ZHOU, BLAZEVIC, Vesna

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A novel tumour necrosis factor receptor mutation in a Finnish family with periodic fever syndrome von Stjernberg-Salmela, S, Pettersson, T, Karenko, L, Blazevic, V, Nevala, H, Pitkänen, S, Peterson, P, Ranki, A

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376 POSTER NAV3–anovel cancer biomarker von Sipilä, L, Karenko, L, Siggberg, L, Abdel-Rahman, W, Helle, M, Häyry, V, Knuutila, S, Peltomäki, P, Ranki, A, Krohn, K

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366 POSTER NAV3 gene aberrations in colorectal cancer target signalling pathways associated with inflammation and the progression of cancer von Carlsson, E, Ovaska, K, Sipilä, L, Helle, M, Abdel-Rahman, W, Karenko, L, Peltomäki, P, Hautaniemi, S, Krohn, K, Ranki, A

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Comment on: Low TNF-induced NF- B and p38 phosphorylation levels in leucocytes in tumour necrosis factor receptor-associated periodic syndrome: reply von Stjernberg-Salmela, S., Ranki, A., Karenko, L., Siitonen, S., Mustonen, H., Puolakkainen, P., Sarna, S., Pettersson, T., Repo, H.

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Low TNF-induced NF- B and p38 phosphorylation levels in leucocytes in tumour necrosis factor receptor-associated periodic syndrome von Stjernberg-Salmela, S., Ranki, A., Karenko, L., Siitonen, S., Mustonen, H., Puolakkainen, P., Sarna, S., Pettersson, T., Repo, H.

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Chromosomal Abnormalities in Cutaneous T-Cell Lymphoma and in Its Premalignant Conditions as Detected by G-Banding and Interphase Cytogenetic Methods von Karenko, Leena, Hyytinen, Eija, Sarna, Seppo, Ranki, Annamari

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Notable Losses at Specific Regions of Chromosomes 10q and 13q in the Sézary Syndrome Detected by Comparative Genomic Hybridization

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Notable Losses at Specific Regions of Chromosomes 10q and 13q in the Sézary Syndrome Detected by Comparative Genomic Hybridization von Karenko, Leena, Kähkönen, Marketta, Hyytinen, Eija-Riitta, Lindlöf, Mikael, Ranki, Annamari

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Cellular Coincidence of Clonal T Cell Receptor Rearrangements and Complex Clonal Chromosomal Aberrations—A Hallmark of Malignancy in Cutaneous T Cell Lymphoma von Marcus Muche, J., Karenko, Leena, Gellrich, Sylke, Karhu, Ritva, Kytölä, Soili, Kähkönen, Marketta, Lukowsky, Ansgar, Sterry, Wolfram, Ranki, Annamari

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Chromosomally Clonal T Cells in the Skin, Blood, or Lymph Nodes of Two Sezary Syndrome Patients Express CD45RA, CD45RO, CDw150, and Interleukin-4, but no Interleukin-2 or Interfero... von Karenko, Leena, Nevala, Hanna, Raatikainen, Maria, Ranki, Annamari, Franssila, Kaarle

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409 POSTER Identification of novel candidate genes for targeted therapy of primary cutaneous T-cell lymphomas von Ranki, A., Hahtola, S., Tuomela, S., Burghart, E., Elo, L., Karenko, L., Krohn, K., Lahesmaa, R., Monni, O., Klein, C.

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Identification of chromosomal regions amplified or deleted in Sézary syndrome von Karenko, L., Kähkönen, M., Hyytinen, E., Ranki, A.

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