Zobrazeno 1 - 10
of 64
pro vyhledávání: '"Veli, Kairisto"'
Autor:
Fabio Efficace, Francois-Xavier Mahon, Johan Richter, Alfonso Piciocchi, Marta Cipriani, Franck Emmanuel Nicolini, Henrik Hjorth-Hansen, Antonio Almeida, Jeroen J. W. M. Janssen, Jiri Mayer, Perttu Koskenvesa, Panayiotis Panayiotidis, Ulla Olsson-Strömberg, Joaquín Martinez-Lopez, Philippe Rousselot, Hanne Vestergaard, Hans Ehrencrona, Veli Kairisto, Katerina Machova Polakova, Satu Mustjoki, Marc Berger, Andreas Hochhaus, Markus Pfirrmann, Susanne Saussele
Publikováno v:
HemaSphere, Vol 7, p e0972454 (2023)
Externí odkaz:
https://doaj.org/article/a078e335813f413cb617882efe61628c
Autor:
Markus Pfirrmann, Francois-Xavier Mahon, Stéphanie Dulucq, Andreas Hochhaus, Panayiotis Panayiotidis, Antonio Almeida, Jiri Mayer, Henrik Hjorth-Hansen, Jeroen J. W. M. Janssen, Satu Mustjoki, Joaquín Martinez-Lopez, Hanne Vestergaard, Hans Ehrencrona, Veli Kairisto, Kateřina Machová Poláková, Franck Emmanuel Nicolini, Wolf-Karsten Hofmann, Joëlle Guilhot, Susanne Saussele, Johan Richter
Publikováno v:
HemaSphere, Vol 7, p e230884b (2023)
Externí odkaz:
https://doaj.org/article/f21cdde0c6114e2fb555ae09f10c9dbe
Autor:
Ning Wang, Vladislav Lysenkov, Katri Orte, Veli Kairisto, Juhani Aakko, Sofia Khan, Laura L Elo
Publikováno v:
PLoS Computational Biology, Vol 18, Iss 2, p e1009269 (2022)
Insertions and deletions (indels) in human genomes are associated with a wide range of phenotypes, including various clinical disorders. High-throughput, next generation sequencing (NGS) technologies enable the detection of short genetic variants, su
Externí odkaz:
https://doaj.org/article/a437cab2e4244fe1ade8f6b8eae33a05
Autor:
Iiris Ukkola, Pirjo Nummela, Mia Kero, Hanna Tammio, Jenni Tuominen, Veli Kairisto, Markku Kallajoki, Caj Haglund, Päivi Peltomäki, Soili Kytölä, Ari Ristimäki
Publikováno v:
Virchows Archiv : an international journal of pathology. 480(4)
Gene fusions can act as oncogenic drivers and offer targets for cancer therapy. Since fusions are rare in colorectal cancer (CRC), their universal screening seems impractical. Our aim was to investigate gene fusions in 62 CRC cases with deficient MLH
Autor:
Sofia Khan, Katri Orte, Vladislav Lysenkov, Ning Wang, Juhani Aakko, Veli Kairisto, Laura L. Elo
Insertions and deletions (indels) in human genomes are associated with a wide range of phenotypes, including various clinical disorders. High-throughput, next generation sequencing (NGS) technologies enable detection of short genetic variants, such a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::032f8776eed7705173ce3fec2a43d878
https://doi.org/10.1101/2021.07.15.452444
https://doi.org/10.1101/2021.07.15.452444
Autor:
Sofia Khan, Vladislav Lysenkov, Katri Orte, Laura Elo, Ning Wang, Juhani Aakko, Veli Kairisto
Publikováno v:
PLoS computational biology. 18(2)
Insertions and deletions (indels) in human genomes are associated with a wide range of phenotypes, including various clinical disorders. High-throughput, next generation sequencing (NGS) technologies enable the detection of short genetic variants, su
Autor:
Anna Kreutzman, Peter Rohon, Edgar Faber, Karel Indrak, Vesa Juvonen, Veli Kairisto, Jaroslava Voglová, Marjatta Sinisalo, Emília Flochová, Jukka Vakkila, Petteri Arstila, Kimmo Porkka, Satu Mustjoki
Publikováno v:
PLoS ONE, Vol 6, Iss 8, p e23022 (2011)
Before the era of tyrosine kinase inhibitors (TKIs), interferon-alpha (IFN-α) was the treatment of choice in chronic myeloid leukemia (CML). Curiously, some IFN-α treated patients were able to discontinue therapy without disease progression. The ai
Externí odkaz:
https://doaj.org/article/6dd371f4b6b64bb396523e3f23e118ab
Autor:
Tuija Lundán, Vesa Juvonen, Martin C. Mueller, Satu Mustjoki, Taina Lakkala, Veli Kairisto, Andreas Hochhaus, Sakari Knuutila, Kimmo Porkka
Publikováno v:
Haematologica, Vol 93, Iss 2 (2008)
Background Recently, an International Scale was proposed for standardizing BCR-ABL transcript measurements and reporting in the assessment of minimal residual disease by real-time quantitative polymerase chain reaction (RQ-PCR). Here we present the s
Externí odkaz:
https://doaj.org/article/f184cadaa0a64359b303c05e9692b1af
Autor:
Jonas Abrahamsson, Hans Beier Ommen, Helen Vålerhaugen, Kirsi Jahnukainen, Birgitte Lausen, Linda Fogelstrand, Sofie Johansson Alm, Christiane Walter, Bernward Zeller, Veli Kairisto, Nils von Neuhoff, Dirk Reinhardt, Henrik Hasle, Charlotte Guldborg Nyvold, Kristian Løvvik Juul-Dam
Publikováno v:
Juul-Dam, K L, Ommen, H B, Nyvold, C G, Walter, C, Vålerhaugen, H, Kairisto, V, Abrahamsson, J, Alm, S J, Jahnukainen, K, Lausen, B, Reinhardt, D, Zeller, B, von Neuhoff, N, Fogelstrand, L & Hasle, H 2020, ' Measurable residual disease assessment by qPCR in peripheral blood is an informative tool for disease surveillance in childhood acute myeloid leukaemia ', British Journal of Haematology, vol. 190, no. 2, pp. 198-208 . https://doi.org/10.1111/bjh.16560
Løvvik Juul-Dam, K, Ommen, H B, Nyvold, C G, Walter, C, Vålerhaugen, H, Kairisto, V, Abrahamsson, J, Johansson Alm, S, Jahnukainen, K, Lausen, B, Reinhardt, D, Zeller, B, Von Neuhoff, N, Fogelstrand, L & Hasle, H 2018, ' Measurable Residual Disease Assessment By qPCR in Peripheral Blood Is an Informative Tool for Disease Surveillance in Childhood Acute Myeloid Leukemia ', American Society of Hematology: 60th Annual Meeting (ASH), San Diego, USA, 29/11/2018-04/12/2018 . < https://ash.confex.com/ash/2018/webprogram/Paper119642.html >
Løvvik Juul-Dam, K, Ommen, H B, Nyvold, C G, Walter, C, Vålerhaugen, H, Kairisto, V, Abrahamsson, J, Johansson Alm, S, Jahnukainen, K, Lausen, B, Reinhardt, D, Zeller, B, Von Neuhoff, N, Fogelstrand, L & Hasle, H 2018, ' Measurable Residual Disease Assessment By qPCR in Peripheral Blood Is an Informative Tool for Disease Surveillance in Childhood Acute Myeloid Leukemia ', Blood, vol. 132, no. Suppl. 1 . https://doi.org/10.1182/blood-2018-99-119642
Løvvik Juul-Dam, K, Ommen, H B, Nyvold, C G, Walter, C, Vålerhaugen, H, Kairisto, V, Abrahamsson, J, Johansson Alm, S, Jahnukainen, K, Lausen, B, Reinhardt, D, Zeller, B, Von Neuhoff, N, Fogelstrand, L & Hasle, H 2018, ' Measurable Residual Disease Assessment By qPCR in Peripheral Blood Is an Informative Tool for Disease Surveillance in Childhood Acute Myeloid Leukemia ', American Society of Hematology: 60th Annual Meeting (ASH), San Diego, USA, 29/11/2018-04/12/2018 . < https://ash.confex.com/ash/2018/webprogram/Paper119642.html >
Løvvik Juul-Dam, K, Ommen, H B, Nyvold, C G, Walter, C, Vålerhaugen, H, Kairisto, V, Abrahamsson, J, Johansson Alm, S, Jahnukainen, K, Lausen, B, Reinhardt, D, Zeller, B, Von Neuhoff, N, Fogelstrand, L & Hasle, H 2018, ' Measurable Residual Disease Assessment By qPCR in Peripheral Blood Is an Informative Tool for Disease Surveillance in Childhood Acute Myeloid Leukemia ', Blood, vol. 132, no. Suppl. 1 . https://doi.org/10.1182/blood-2018-99-119642
Background: Relapse remains a serious event and main obstacle to permanent cure in childhood acute myeloid leukemia (AML). Reduction of measurable/minimal residual disease (MRD) assessed by real-time quantitative PCR (qPCR) during therapy is predicti
Autor:
Eliisa Löyttyniemi, Maija Itälä-Remes, Taru Varila, Otto Kauko, Urpu Salmenniemi, Eleonora Makela, Jukka Westermarck, Veli Kairisto
Despite of extensive genetic analysis of acute myeloid leukemia (AML), we still do not understand comprehensively mechanism that promote disease relapse from standard chemotherapy. Based on recent indications for non-genomic inhibition of tumor suppr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e8c0c9ce33caf8a77527510f8bbef202
https://doi.org/10.1101/693705
https://doi.org/10.1101/693705