Spectrum of mutations in the renin-angiotensin system genes in autosomal recessive renal tubular dysgenesis von Gribouval, Olivier, Morinière, Vincent, Pawtowski, Audrey, Arrondel, Christelle, Sallinen, Satu-Leena, Saloranta, Carola, Clericuzio, Carol, Viot, Géraldine, Tantau, Julia, Blesson, Sophie, Cloarec, Sylvie, Machet, Marie Christine, Chitayat, David, Thauvin, Christelle, Laurent, Nicole, Sampson, Julian R., Bernstein, Jonathan A, Clemenson, Alix, Prieur, Fabienne, Daniel, Laurent, Levy-Mozziconacci, Annie, Lachlan, Katherine, Alessandri, Jean Luc, Cartault, François, Rivière, Jean Pierre, Picard, Nicole, Baumann, Clarisse, Delezoide, Anne Lise, Belar Ortega, Maria, Chassaing, Nicolas, Labrune, Philippe, Yu, Sui, Firth, Helen, Wellesley, Diana, Bitzan, Martin, Alfares, Ahmed, Braverman, Nancy, Krogh, Lotte, Tolmie, John, Gaspar, Harald, Doray, Bérénice, Majore, Silvia, Bonneau, Dominique, Triau, Stéphane, Loirat, Chantal, David, Albert, Bartholdi, Deborah, Peleg, Amir, Brackman, Damien, Stone, Rosario, DeBerardinis, Ralph, Corvol, Pierre, Michaud, Annie, Antignac, Corinne, Gubler, Marie Claire

Volltext

Large genomic rearrangements and germline epimutations in Lynch syndrome von Gylling, Annette, Ridanpää, Maaret, Vierimaa, Outi, Aittomäki, Kristiina, Avela, Kristiina, Kääriäinen, Helena, Laivuori, Hannele, Pöyhönen, Minna, Sallinen, Satu‐Leena, Wallgren‐Pettersson, Carina, Järvinen, Heikki J., Mecklin, Jukka‐Pekka, Peltomäki, Paivi

Volltext

Screening for BRCA1, BRCA2, CHEK2, PALB2, BRIP1, RAD50, and CDH1 mutations in high-risk Finnish BRCA1/2-founder mutation-negative breast and/or ovarian cancer individuals von Kuusisto, Kirsi M, Bebel, Aleksandra, Vihinen, Mauno, Schleutker, Johanna, Sallinen, Satu-Leena

Volltext

Genetic spectrum of hereditary neuropathies with onset in the first year of life von Baets, Jonathan, Deconinck, Tine, De Vriendt, Els, Zimo, Magdalena, Yperzeele, Laetitia, Van Hoorenbeeck, Kim, Peeters, Kristien, Spiegel, Ronen, Parman, Yesim, Ceulemans, Berten, Van Bogaert, Patrick, Pou-Serradell, Adolf, Bernert, Günther, Dinopoulos, Argirios, Auer-Grumbach, Michaela, Sallinen, Satu-Leena, Fabrizi, Gian Maria, Pauly, Fernand, Van den Bergh, Peter, Bilir, Birdal, Battaloglu, Esra, Madrid, Ricardo E., Kabzi ska, Dagmara, Kochanski, Andrzej, Topaloglu, Haluk, Miller, Geoffrey, Jordanova, Albena, Timmerman, Vincent, De Jonghe, Peter

Volltext

Absence of KLF6 gene mutations in human astrocytic tumors and cell lines von Koivisto, Pasi A., Zhang, Xiaohui, Sallinen, Satu‐Leena, Sallinen, Pauli, Helin, Heikki J., Dong, Jin‐Tang, Van Meir, Erwin G., Haapasalo, Hannu, Hyytinen, Eija‐Riitta

Volltext

Detection of human herpesvirus-6 in adult central nervous system tumors: predominance of early and late viral antigens in glial tumors von Crawford, John R., Santi, Maria Rita, Cornelison, Robbie, Sallinen, Satu-Leena, Haapasalo, Hannu, MacDonald, Tobey J.

Volltext

Cyclin D1 expression in astrocytomas is associated with cell proliferation activity and patient prognosis von Sallinen, Satu-Leena, Sallinen, Pauli K., Kononen, Juha T., Syrjäkoski, Kirsi M., Nupponen, Nina N., Rantala, Immo S., Helén, Pauli T., Helin, Heikki J., Haapasalo, Hannu K.

Volltext

Chromosome imbalances in familial gliomas detected by comparative genomic hybridization von Paunu, Niina, Sallinen, Satu-Leena, Karhu, Ritva, Miettinen, Helena, Sallinen, Pauli, Kononen, Juha, Laippala, Pekka, Simola, Kalle O.J., Helén, Pauli, Haapasalo, Hannu

Volltext

No evidence for a genetic modifier for renal cell cancer risk in HLRCC syndrome von Vahteristo, Pia, Koski, Taru A., Näätsaari, Laura, Kiuru, Maija, Karhu, Auli, Herva, Riitta, Sallinen, Satu-Leena, Vierimaa, Outi, Björck, Erik, Richard, Stéphane, Gardie, Betty, Bessis, Didier, Van Glabeke, Emmanuel, Blanco, Ignacio, Houlston, Richard, Senter, Leigha, Hietala, Marja, Aittomäki, Kristiina, Aaltonen, Lauri A., Launonen, Virpi, Lehtonen, Rainer

Volltext

CHEK2 mutations in primary glioblastomas von SALLINEN, Satu-Leena, IKONEN, Tarja, HAAPASALO, Hannu, SCHLEUTKER, Johanna

Volltext

Increased expression of telomerase RNA component is associated with increased cell proliferation in human astrocytomas von Sallinen, P, Miettinen, H, Sallinen, SL, Haapasalo, H, Helin, H, Kononen, J

Volltext

Accumulation of genetic changes is associated with poor prognosis in grade II astrocytomas von Sallinen, SL, Sallinen, P, Haapasalo, H, Kononen, J, Karhu, R, Helen, P, Isola, J

Volltext

Identification of differentially expressed genes in human gliomas by DNA microarray and tissue chip techniques von SALLINEN, Satu-Leena, SALLINEN, Pauli K, HAAPASALO, Hannu K, HELIN, Heikki J, HELEN, Pauli T, SCHRAML, Peter, KALLIONIEMI, Olli-P, KONONEN, Juha

Volltext

Abstract 1844: No evidence for genetic factor increasing renal cell cancer risk in Hereditary Leiomyomatosis and Renal Cell Cancer syndrome von Koski, Taru A., Vahteristo, Pia, Näätsaari, Laura, Kiuru, Maija, Karhu, Auli, Herva, Riitta, Sallinen, Satu-Leena, Vierimaa, Outi, Björck, Erik, Richard, Stéphane, Gardie, Betty, Bessis, Didier, Glabeke, Emmanuel Van, Blanco, Ignacio, Houlston, Richard, Senter, Leigha, Hietala, Marja, Aittomäki, Kristiina, Aaltonen, Lauri A., Launonen, Virpi, Lehtonen, Rainer

Volltext

Spectrum of mutations in the renin-angiotensin system genes in autosomal recessive renal tubular dysgenesis von Gribouval, Olivier, Morinière, Vincent, Pawtowski, Audrey, Arrondel, Christelle, Sallinen, Satu-Leena, Saloranta, Carola, Clericuzio, Carol, Viot, Géraldine, Tantau, Julia, Blesson, Sophie, Cloarec, Sylvie, Machet, Marie Christine, Chitayat, David, Thauvin, Christelle, Laurent, Nicole, Sampson, Julian R, Bernstein, Jonathan A, Clemenson, Alix, Prieur, Fabienne, Daniel, Laurent, Levy-Mozziconacci, Annie, Lachlan, Katherine, Alessandri, Jean Luc, Cartault, François, Rivière, Jean Pierre, Picard, Nicole, Baumann, Clarisse, Delezoide, Anne Lise, Belar Ortega, Maria, Chassaing, Nicolas, Labrune, Philippe, Yu, Sui, Firth, Helen, Wellesley, Diana, Bitzan, Martin, Alfares, Ahmed, Braverman, Nancy, Krogh, Lotte, Tolmie, John, Gaspar, Harald, Doray, Bérénice, Majore, Silvia, Bonneau, Dominique, Triau, Stéphane, Loirat, Chantal, David, Albert, Bartholdi, Deborah, Peleg, Amir, Brackman, Damien, Stone, Rosario, Deberardinis, Ralph, Corvol, Pierre, Michaud, Annie, Antignac, Corinne, Gubler, Marie Claire

Volltext

Arm-specific multicolor fluorescence in situ hybridization reveals widespread chromosomal instability in glioma cell lines von Sallinen, Satu-Leena, Sallinen, Pauli, Ahlstedt-Soini, Minna, Haapasalo, Hannu, Helin, Heikki, Isola, Jorma, Karhu, Ritva

Volltext