Niini T - Search Results

1

Array comparative genomic hybridization reveals frequent alterations of G1/S checkpoint genes in undifferentiated pleomorphic sarcoma of bone.

Niini T, Lahti L, Michelacci F, Ninomiya S, Hattinger CM, Guled M, Böhling T, Picci P, Serra M, Knuutila S. Niini T, et al. Genes Chromosomes Cancer. 2011 May;50(5):291-306. doi: 10.1002/gcc.20851. Epub 2011 Jan 19. Genes Chromosomes Cancer. 2011. PMID: 21254299

2

Frequent deletion of CDKN2A and recurrent coamplification of KIT, PDGFRA, and KDR in fibrosarcoma of bone--an array comparative genomic hybridization study.

Niini T, López-Guerrero JA, Ninomiya S, Guled M, Hattinger CM, Michelacci F, Böhling T, Llombart-Bosch A, Picci P, Serra M, Knuutila S. Niini T, et al. Genes Chromosomes Cancer. 2010 Feb;49(2):132-43. doi: 10.1002/gcc.20727. Genes Chromosomes Cancer. 2010. PMID: 19862822

3

Homozygous deletions of cadherin genes in chondrosarcoma-an array comparative genomic hybridization study.

Niini T, Scheinin I, Lahti L, Savola S, Mertens F, Hollmén J, Böhling T, Kivioja A, Nord KH, Knuutila S. Niini T, et al. Cancer Genet. 2012 Nov;205(11):588-93. doi: 10.1016/j.cancergen.2012.09.007. Epub 2012 Nov 10. Cancer Genet. 2012. PMID: 23146407

4

Combined use of expression and CGH arrays pinpoints novel candidate genes in Ewing sarcoma family of tumors.

Savola S, Klami A, Tripathi A, Niini T, Serra M, Picci P, Kaski S, Zambelli D, Scotlandi K, Knuutila S. Savola S, et al. Among authors: niini t. BMC Cancer. 2009 Jan 14;9:17. doi: 10.1186/1471-2407-9-17. BMC Cancer. 2009. PMID: 19144156 Free PMC article.

5

An integrated analysis of miRNA and gene copy numbers in xenografts of Ewing's sarcoma.

Mosakhani N, Guled M, Leen G, Calabuig-Fariñas S, Niini T, Machado I, Savola S, Scotlandi K, López-Guerrero JA, Llombart-Bosch A, Knuutila S. Mosakhani N, et al. Among authors: niini t. J Exp Clin Cancer Res. 2012 Mar 20;31(1):24. doi: 10.1186/1756-9966-31-24. J Exp Clin Cancer Res. 2012. PMID: 22429812 Free PMC article.

6

AML1 gene amplification: a novel finding in childhood acute lymphoblastic leukemia.

Niini T, Kanerva J, Vettenranta K, Saarinen-Pihkala UM, Knuutila S. Niini T, et al. Haematologica. 2000 Apr;85(4):362-6. Haematologica. 2000. PMID: 10756360

7

Loss at 12p detected by comparative genomic hybridization (CGH): association with TEL-AML1 fusion and favorable prognostic features in childhood acute lymphoblastic leukemia (ALL). A multi-institutional study.

Kanerva J, Niini T, Vettenranta K, Riikonen P, Mäkipernaa A, Karhu R, Knuutila S, Saarinen-Pihkala UM. Kanerva J, et al. Among authors: niini t. Med Pediatr Oncol. 2001 Nov;37(5):419-25. doi: 10.1002/mpo.1224. Med Pediatr Oncol. 2001. PMID: 11745869

8

Overexpression of translocation-associated fusion genes of FGFRI, MYC, NPMI, and DEK, but absence of the translocations in acute myeloid leukemia. A microarray analysis.

Larramendy ML, Niini T, Elonen E, Nagy B, Ollila J, Vihinen M, Knuutila S. Larramendy ML, et al. Among authors: niini t. Haematologica. 2002 Jun;87(6):569-77. Haematologica. 2002. PMID: 12031912

9

Favorable outcome in 20-year follow-up of children with very-low-risk ALL and minimal standard therapy, with special reference to TEL-AML1 fusion.

Kanerva J, Saarinen-Pihkala UM, Niini T, Riikonen P, Möttönen M, Mäkipernaa A, Salmi TT, Vettenranta K, Knuutila S. Kanerva J, et al. Among authors: niini t. Pediatr Blood Cancer. 2004 Jan;42(1):30-5. doi: 10.1002/pbc.10417. Pediatr Blood Cancer. 2004. PMID: 14752791

10

Expression of myeloid-specific genes in childhood acute lymphoblastic leukemia - a cDNA array study.

Niini T, Vettenranta K, Hollmén J, Larramendy ML, Aalto Y, Wikman H, Nagy B, Seppänen JK, Ferrer Salvador A, Mannila H, Saarinen-Pihkala UM, Knuutila S. Niini T, et al. Leukemia. 2002 Nov;16(11):2213-21. doi: 10.1038/sj.leu.2402685. Leukemia. 2002. PMID: 12399964

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