Search Results - "FIORETOS, T" :: K.UTB vyhledávací portál | TBU Library Retrieval Portal

The genomic landscape of high hyperdiploid childhood acute lymphoblastic leukemia

The genomic landscape of high hyperdiploid childhood acute lymphoblastic leukemia

by Paulsson, Kajsa, Lilljebjörn, Henrik, Biloglav, Andrea, Olsson, Linda, Rissler, Marianne, Castor, Anders, Barbany, Gisela, Fogelstrand, Linda, Nordgren, Ann, Sjögren, Helene, Fioretos, Thoas, Johansson, Bertil
Published in Nature genetics (01.06.2015)

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Interleukin 4 induces apoptosis of acute myeloid leukemia cells in a Stat6-dependent manner

Interleukin 4 induces apoptosis of acute myeloid leukemia cells in a Stat6-dependent manner

by Peña-Martínez, P, Eriksson, M, Ramakrishnan, R, Chapellier, M, Högberg, C, Orsmark-Pietras, C, Richter, J, Andersson, A, Fioretos, T, Järås, M
Published in Leukemia (01.03.2018)

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Implementing precision medicine in a regionally organized healthcare system in Sweden

Implementing precision medicine in a regionally organized healthcare system in Sweden

by Fioretos, Thoas, Wirta, Valtteri, Cavelier, Lucia, Berglund, Eva, Friedman, Mikaela, Akhras, Michael, Botling, Johan, Ehrencrona, Hans, Engstrand, Lars, Helenius, Gisela, Fagerqvist, Therese, Gisselsson, David, Gruvberger-Saal, Sofia, Gyllensten, Ulf, Heidenblad, Markus, Höglund, Kina, Jacobsson, Bo, Johansson, Maria, Johansson, Åsa, Soller, Maria Johansson, Landström, Maréne, Larsson, Pär, Levin, Lars-Åke, Lindstrand, Anna, Lovmar, Lovisa, Lyander, Anna, Melin, Malin, Nordgren, Ann, Nordmark, Gunnel, Mölling, Paula, Palmqvist, Lars, Palmqvist, Richard, Repsilber, Dirk, Sikora, Per, Stenmark, Bianca, Söderkvist, Peter, Stranneheim, Henrik, Strid, Tobias, Wheelock, Craig E., Wadelius, Mia, Wedell, Anna, Edsjö, Anders, Rosenquist, Richard
Published in Nature medicine (2022)

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Microarray-based classification of a consecutive series of 121 childhood acute leukemias: prediction of leukemic and genetic subtype as well as of minimal residual disease status

Microarray-based classification of a consecutive series of 121 childhood acute leukemias: prediction of leukemic and genetic subtype as well as of minimal residual disease status

by ANDERSSON, A, RITZ, C, BEHRENDTZ, M, HÖGLUND, M, JOHANSSON, B, FIORETOS, T, LINDGREN, D, EDEN, P, LASSEN, C, HELDRUP, J, OLOFSSON, T, RADE, J, FONTES, M, PORWIT-MACDONALD, A
Published in Leukemia (01.06.2007)

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RNA-seq identifies clinically relevant fusion genes in leukemia including a novel MEF2D/CSF1R fusion responsive to imatinib

RNA-seq identifies clinically relevant fusion genes in leukemia including a novel MEF2D/CSF1R fusion responsive to imatinib

by Lilljebjörn, H, Ågerstam, H, Orsmark-Pietras, C, Rissler, M, Ehrencrona, H, Nilsson, L, Richter, J, Fioretos, T
Published in Leukemia (01.04.2014)

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Impact of malignant stem cell burden on therapy outcome in newly diagnosed chronic myeloid leukemia patients

Impact of malignant stem cell burden on therapy outcome in newly diagnosed chronic myeloid leukemia patients

by Mustjoki, S, Richter, J, Barbany, G, Ehrencrona, H, Fioretos, T, Gedde-Dahl, T, Gjertsen, B T, Hovland, R, Hernesniemi, S, Josefsen, D, Koskenvesa, P, Dybedal, I, Markevärn, B, Olofsson, T, Olsson-Strömberg, U, Rapakko, K, Thunberg, S, Stenke, L, Simonsson, B, Porkka, K, Hjorth-Hansen, H
Published in Leukemia (01.07.2013)

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IL1RAP expression as a measure of leukemic stem cell burden at diagnosis of chronic myeloid leukemia predicts therapy outcome

IL1RAP expression as a measure of leukemic stem cell burden at diagnosis of chronic myeloid leukemia predicts therapy outcome

by Landberg, N, Hansen, N, Askmyr, M, Ågerstam, H, Lassen, C, Rissler, M, Hjorth-Hansen, H, Mustjoki, S, Järås, M, Richter, J, Fioretos, T
Published in Leukemia (01.01.2016)

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Feasibility to use whole-genome sequencing as a sole diagnostic method to detect genomic aberrations in pediatric B-cell acute lymphoblastic leukemia

Feasibility to use whole-genome sequencing as a sole diagnostic method to detect genomic aberrations in pediatric B-cell acute lymphoblastic leukemia

by Rezayee, Fatemah, Eisfeldt, Jesper, Skaftason, Aron, Öfverholm, Ingegerd, Sayyab, Shumaila, Syvänen, Ann Christine, Maqbool, Khurram, Lilljebjörn, Henrik, Johansson, Bertil, Olsson-Arvidsson, Linda, Pietras, Christina Orsmark, Staffas, Anna, Palmqvist, Lars, Fioretos, Thoas, Cavelier, Lucia, Fogelstrand, Linda, Nordlund, Jessica, Wirta, Valtteri, Rosenquist, Richard, Barbany, Gisela
Published in Frontiers in oncology (2023)

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Molecular characterization of early-stage bladder carcinomas by expression profiles, FGFR3 mutation status, and loss of 9q

Molecular characterization of early-stage bladder carcinomas by expression profiles, FGFR3 mutation status, and loss of 9q

by LINDGREN, D, LIEDBERG, F, ANDERSSON, A, CHEBIL, G, GUDJONSSON, S, BORG, A, MANSSON, W, FIORETOS, T, HÖGLUND, M
Published in Oncogene (27.04.2006)

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Relapsed childhood high hyperdiploid acute lymphoblastic leukemia: presence of preleukemic ancestral clones and the secondary nature of microdeletions and RTK-RAS mutations

Relapsed childhood high hyperdiploid acute lymphoblastic leukemia: presence of preleukemic ancestral clones and the secondary nature of microdeletions and RTK-RAS mutations

by Davidsson, J, Paulsson, K, Lindgren, D, Lilljebjörn, H, Chaplin, T, Forestier, E, Andersen, M K, Nordgren, A, Rosenquist, R, Fioretos, T, Young, B D, Johansson, B
Published in Leukemia (01.05.2010)

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Whole-exome sequencing of pediatric acute lymphoblastic leukemia

Whole-exome sequencing of pediatric acute lymphoblastic leukemia

by Lilljebjörn, H, Rissler, M, Lassen, C, Heldrup, J, Behrendtz, M, Mitelman, F, Johansson, B, Fioretos, T
Published in Leukemia (01.07.2012)

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High-resolution genome-wide array-based comparative genome hybridization reveals cryptic chromosome changes in AML and MDS cases with trisomy 8 as the sole cytogenetic aberration

High-resolution genome-wide array-based comparative genome hybridization reveals cryptic chromosome changes in AML and MDS cases with trisomy 8 as the sole cytogenetic aberration

by PAULSSON, K, HEIDENBLAD, M, STRÖMBECK, B, STAAF, J, JÖNSSON, G, BORG, A, FIORETOS, T, JOHANSSON, B
Published in Leukemia (01.05.2006)

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Molecular Signatures in Childhood Acute Leukemia and Their Correlations to Expression Patterns in Normal Hematopoietic Subpopulations

Molecular Signatures in Childhood Acute Leukemia and Their Correlations to Expression Patterns in Normal Hematopoietic Subpopulations

by Anna Andersson, Tor Olofsson, David Lindgren, Nilsson, Björn, Cecilia Ritz, Patrik Edén, Carin Lassen, Johan Råde, Magnus Fontes, Helena Mörse, Jesper Heldrup, Mikael Behrendtz, Mitelman, Felix, Höglund, Mattias, Johansson, Bertil, Thoas Fioretos
Published in Proceedings of the National Academy of Sciences - PNAS (27.12.2005)

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Gain-of-Function SAMD9L Mutations Cause a Syndrome of Cytopenia, Immunodeficiency, Myelodysplastic Syndrome and Neurological Symptoms

Gain-of-Function SAMD9L Mutations Cause a Syndrome of Cytopenia, Immunodeficiency, Myelodysplastic Syndrome and Neurological Symptoms

by Tesi, B, Davidsson, J, Voss, M, Rahikkala, E, Holmes, T, Chiang, S, Komulainen-Ebrahim, J, Kokkonen, H, Bryder, D, Fioretos, T, Henter, J.I, Möttönen, M, Niinimäki, R, Nilsson, L, Pronk, C.J, Uusimaa, J, Moilanen, J, Tedgård, U, Cammenga, J, Bryceson, Y
Published in LEUKEMIA RESEARCH (2017)

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Journal Article Conference Proceeding

SOCS2 is dispensable for BCR/ABL1-induced chronic myeloid leukemia-like disease and for normal hematopoietic stem cell function

SOCS2 is dispensable for BCR/ABL1-induced chronic myeloid leukemia-like disease and for normal hematopoietic stem cell function

by Hansen, N, Ågerstam, H, Wahlestedt, M, Landberg, N, Askmyr, M, Ehinger, M, Rissler, M, Lilljebjörn, H, Johnels, P, Ishiko, J, Melo, J V, Alexander, W S, Bryder, D, Järås, M, Fioretos, T
Published in Leukemia (01.01.2013)

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Journal Article

Evidence for a single-step mechanism in the origin of hyperdiploid childhood acute lymphoblastic leukemia

Evidence for a single-step mechanism in the origin of hyperdiploid childhood acute lymphoblastic leukemia

by Paulsson, Kajsa, Mörse, Helena, Fioretos, Thoas, Behrendtz, Mikael, Strömbeck, Bodil, Johansson, Bertil
Published in Genes chromosomes & cancer (01.10.2005)

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BRAF mutations are very rare in B- and T-cell pediatric acute lymphoblastic leukemias

BRAF mutations are very rare in B- and T-cell pediatric acute lymphoblastic leukemias

by Davidsson, J, Lilljebjörn, H, Panagopoulos, I, Fioretos, T, Johansson, B
Published in Leukemia (01.08.2008)

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Journal Article

Combined high-resolution array-based comparative genomic hybridization and expression profiling of ETV6/RUNX1-positive acute lymphoblastic leukemias reveal a high incidence of cryptic Xq duplications and identify several putative target genes within the commonly gained region

Combined high-resolution array-based comparative genomic hybridization and expression profiling of ETV6/RUNX1-positive acute lymphoblastic leukemias reveal a high incidence of cryptic Xq duplications and identify several putative target genes within the commonly gained region

by LILLJEBJÖRN, H, HEIDENBLAD, M, NILSSON, B, LASSEN, C, HORVAT, A, HELDRUP, J, BEHRENDTZ, M, JOHANSSON, B, ANDERSSON, A, FIORETOS, T
Published in Leukemia (01.10.2007)

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Journal Article

Deregulation of the Wilms' tumour gene 1 protein (WT1) by BCR ABL1 mediates resistance to imatinib in human leukaemia cells

Deregulation of the Wilms' tumour gene 1 protein (WT1) by BCR ABL1 mediates resistance to imatinib in human leukaemia cells

by SVENSSON, E, VIDOVIC, K, LASSEN, C, RICHTER, J, OLOFSSON, T, FIORETOS, T, GULLBERG, U
Published in Leukemia (01.12.2007)

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Journal Article

Modeling chronic myeloid leukemia in immunodeficient mice reveals expansion of aberrant mast cells and accumulation of pre-B cells

Modeling chronic myeloid leukemia in immunodeficient mice reveals expansion of aberrant mast cells and accumulation of pre-B cells

by Askmyr, M, Ågerstam, H, Lilljebjörn, H, Hansen, N, Karlsson, C, von Palffy, S, Landberg, N, Högberg, C, Lassen, C, Rissler, M, Richter, J, Ehinger, M, Järås, M, Fioretos, T
Published in Blood cancer journal (New York) (12.12.2014)

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