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19 results

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Page 1
Large genomic rearrangements and germline epimutations in Lynch syndrome.
Gylling A, Ridanpää M, Vierimaa O, Aittomäki K, Avela K, Kääriäinen H, Laivuori H, Pöyhönen M, Sallinen SL, Wallgren-Pettersson C, Järvinen HJ, Mecklin JP, Peltomäki P. Gylling A, et al. Among authors: sallinen sl. Int J Cancer. 2009 May 15;124(10):2333-40. doi: 10.1002/ijc.24230. Int J Cancer. 2009. PMID: 19173287
No evidence for a genetic modifier for renal cell cancer risk in HLRCC syndrome.
Vahteristo P, Koski TA, Näätsaari L, Kiuru M, Karhu A, Herva R, Sallinen SL, Vierimaa O, Björck E, Richard S, Gardie B, Bessis D, Van Glabeke E, Blanco I, Houlston R, Senter L, Hietala M, Aittomäki K, Aaltonen LA, Launonen V, Lehtonen R. Vahteristo P, et al. Among authors: sallinen sl. Fam Cancer. 2010 Jun;9(2):245-51. doi: 10.1007/s10689-009-9312-2. Fam Cancer. 2010. PMID: 20091131
Absence of KLF6 gene mutations in human astrocytic tumors and cell lines.
Koivisto PA, Zhang X, Sallinen SL, Sallinen P, Helin HJ, Dong JT, Van Meir EG, Haapasalo H, Hyytinen ER. Koivisto PA, et al. Among authors: sallinen sl. Int J Cancer. 2004 Sep 10;111(4):642-3. doi: 10.1002/ijc.20301. Int J Cancer. 2004. PMID: 15239146 No abstract available.
Chromosome imbalances in familial gliomas detected by comparative genomic hybridization.
Paunu N, Sallinen SL, Karhu R, Miettinen H, Sallinen P, Kononen J, Laippala P, Simola KO, Helén P, Haapasalo H. Paunu N, et al. Among authors: sallinen p, sallinen sl. Genes Chromosomes Cancer. 2000 Dec;29(4):339-46. doi: 10.1002/1098-2264(2000)9999:9999<::aid-gcc1049>3.0.co;2-8. Genes Chromosomes Cancer. 2000. PMID: 11066078 Review.
Genetic aberrations in sporadic and neurofibromatosis 2 (NF2)-associated schwannomas studied by comparative genomic hybridization (CGH).
Antinheimo J, Sallinen SL, Sallinen P, Haapasalo H, Helin H, Horelli-Kuitunen N, Wessman M, Sainio M, Jääskeläinen J, Carpén O. Antinheimo J, et al. Among authors: sallinen p, sallinen sl. Acta Neurochir (Wien). 2000;142(10):1099-104; discussion 1104-5. doi: 10.1007/s007010070036. Acta Neurochir (Wien). 2000. PMID: 11129530
CHEK2 mutations in primary glioblastomas.
Sallinen SL, Ikonen T, Haapasalo H, Schleutker J. Sallinen SL, et al. J Neurooncol. 2005 Aug;74(1):93-5. doi: 10.1007/s11060-005-5953-7. J Neurooncol. 2005. PMID: 16078115 No abstract available.
19 results