Zobrazeno 1 - 10
of 128
pro vyhledávání: '"Marie Jarošová"'
Autor:
Eva Ondroušková, Michaela Bohúnová, Kristýna Závacká, Patrik Čech, Petra Šmuhařová, Miroslav Boudný, Martina Oršulová, Anna Panovská, Lenka Radová, Michael Doubek, Karla Plevová, Marie Jarošová
Publikováno v:
Frontiers in Oncology, Vol 12 (2022)
Chronic lymphocytic leukemia (CLL) with cytogenetics findings, such as complex karyotype and deletions of TP53 or ATM, is associated with adverse clinical outcomes. Additional chromosomal abnormalities further stratify patients into groups with diver
Externí odkaz:
https://doaj.org/article/9874afffb5374bcba126ff413f2cbae2
Autor:
Hana Klamová, Kateřina Machová Poláková, Jan Mužík, Zdeněk Ráčil, Daniela Žáčková, Kateřina Steinerová, Michal Karas, Edgar Faber, Eva Demečková, Zuzana Michalovičová‐Sninská, Jaroslava Voglová, Ľudmila Demitrovičová, Eva Mikušková, Elena Tóthová, Juraj Chudej, Imrich Markuljak, Eduard Cmunt, Jana Moravcová, Dana Dvořáková, Kyra Michalová, Marie Jarošová, Markéta Marková Šťastná, Petr Cetkovský, Ladislav DuŠek, Vladimír Koza, Marek Trněný, Karel Indrák
Publikováno v:
Cancer Medicine, Vol 2, Iss 2, Pp 216-225 (2013)
Abstract We evaluated responses to the treatment and long‐term outcomes of chronic myeloid leukemia patients treated with imatinib as first‐line treatment in routine clinical setting from two countries with centralized tyrosine kinase inhibitors
Externí odkaz:
https://doaj.org/article/3352c3f69ea544aab068556ac3c96068
Autor:
Martin Stork, Eva Ondrouskova, Michaela Bohunova, Ivanna Boichuk, Dominik Fric, Zdenek Adam, Marta Krejci, Viera Sandecka, Zdenka Knechtova, Lenka Radova, Zuzana Jelinkova, Tatana Adlerova, Milan Krticka, Vladimir Nekuda, Marek Borsky, Sabina Sevcikova, Marie Jarosova, Ludek Pour
Publikováno v:
Blood Cancer Journal, Vol 14, Iss 1, Pp 1-3 (2024)
Externí odkaz:
https://doaj.org/article/5aea7f2816d842e89d6116072aa074df
Autor:
František Folber, Cyril Šálek, Jan M. Horáček, Jiri Mayer, Michael Doubek, Jiri Stika, Stepan Hrabovsky, Zuzana Vrzalová, Šárka Pospíšilová, Hana Jelínková, Veronika Navrkalová, Marie Jarošová, Jiri Martenek
Publikováno v:
Acta Oncologica. 60:760-770
BCR-ABL1-like acute lymphoblastic leukemia (ALL) is a high-risk disease with a complex genomic background. Though extensively studied, data on the frequency and mutual associations of present mutat...
Autor:
Martin Spacek, Šárka Pospíšilová, Daniel Lysák, Lukas Smolej, Martin Simkovic, Tomas Papajik, Renata Urbanova, Martin Brejcha, Michal Doubek, Marie Jarošová
Publikováno v:
Transfuze a hematologie dnes. 27:91-106
Autor:
Hana Palova, Anirban Das, Petra Pokorna, Viera Bajciova, Zdenek Pavelka, Marta Jezova, Karol Pal, Jose R. Dimayacyac, Logine Negm, Lucie Stengs, Vanessa Bianchi, Klara Vejmelkova, Kristyna Noskova, Marie Jarosova, Sona Mejstrikova, Peter Mudry, Michal Kyr, Tomas Merta, Pavel Tinka, Klara Drabova, Stefania Aulicka, Robin Jugas, Uri Tabori, Ondrej Slaby, Jaroslav Sterba
Publikováno v:
npj Precision Oncology, Vol 8, Iss 1, Pp 1-9 (2024)
Abstract Constitutional mismatch repair deficiency (CMMRD) is a rare syndrome characterized by an increased incidence of cancer. It is caused by biallelic germline mutations in one of the four mismatch repair genes (MMR) genes: MLH1, MSH2, MSH6, or P
Externí odkaz:
https://doaj.org/article/b0a2950947714c9188792348f38d31f7
Autor:
Marie Jarošová, Heidi Mocikova, Jan Oppelt, Leos Kren, Vít Procházka, Katerina Machova Polakova, Pavel Burda, Olaf Merkel, Katerina Cerna, Robert Pytlik, Ana-Iris Schiefer, Marek Trneny, Lenka Zlamalikova, Martin Trbušek, Ján Deván, Lenka Kruzova, Ingrid Simonitsch-Klupp, Václav Šeda, Sonali Sharma, Zuzana Prouzová, Andrea Janíková, Katerina Musilova, Andrew G. Evans, Gabriela Pavlasova, Clive S. Zent, Jiri Mayer, Kvetoslava Liskova, Andrea Marečková, Christoph Kornauth, Marek Mráz
Publikováno v:
Blood. 132:2389-2400
Follicular lymphoma (FL) is a common indolent B-cell malignancy with a variable clinical course. An unfavorable event in its course is histological transformation to a high-grade lymphoma, typically diffuse large B-cell lymphoma. Recent studies show
Autor:
Donald Yergeau, Marry M. van den Heuvel-Eibrink, Sanne Noort, Lei Shi, Charikleia Kelaidi, Jeffrey E. Rubnitz, Yanling Liu, Tanja A. Gruber, Stephanie Nance, C. Michel Zwaan, Jing Ma, Franco Locatelli, Yuanyuan Wang, Maarten Fornerod, Heather L. Mulder, Jeffery M. Klco, Martina Pigazzi, Esther A. Obeng, Guangchun Song, Jennifer Kamens, Sharyn D. Baker, James R. Downing, Stanley Pounds, John Easton, Tamara Lamprecht, Michael P. Walsh, Marie Jarošová, Sophia Polychronopoulou, Dirk Reinhardt, Henrik Hasle, Jinghui Zhang, Jatinder K. Lamba, Jacquelyn Myers, Yu Liu
Publikováno v:
Fornerod, M, Ma, J, Noort, S, Liu, Y, Walsh, M P, Shi, L, Nance, S, Liu, Y, Wang, Y, Song, G, Lamprecht, T, Easton, J, Mulder, H L, Yergeau, D, Myers, J, Kamens, J L, Obeng, E A, Pigazzi, M, Jarosova, M, Kelaidi, C, Polychronopoulou, S, Lamba, J K, Baker, S D, Rubnitz, J E, Reinhardt, D, van den Heuvel-Eibrink, M M, Locatelli, F, Hasle, H, Klco, J M, Downing, J R, Zhang, J, Pounds, S, Zwaan, C M & Gruber, T A 2021, ' Integrative Genomic Analysis of Pediatric Myeloid-Related Acute Leukemias Identifies Novel Subtypes and Prognostic Indicators ', Blood cancer discovery, vol. 2, no. 6, pp. 586-599 . https://doi.org/10.1158/2643-3230.BCD-21-0049
Blood Cancer Discovery
Blood Cancer Discovery
Integrating somatic mutation analysis and gene expression profiling distinguishes pediatric AML subtypes with differential prognoses and clinical risks.
Genomic characterization of pediatric patients with acute myeloid leukemia (AML) has led to
Genomic characterization of pediatric patients with acute myeloid leukemia (AML) has led to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6001997a3dced2a8310c0a75e26e1c37
https://hdl.handle.net/10807/228320
https://hdl.handle.net/10807/228320
Autor:
Clemens Mellink, Šárka Pospíšilová, Paolo Ghia, Constantine S. Tam, Mar Bellido, Marie Jarošová, Richard Rosenquist, Eva van den Berg, Jacqueline Schoumans, Claudia Haferlach, Lotta Hansson, Zadie Davis, Blanca Espinet, Anna Puiggros, David Oscier, Eric Eldering, Marian Stevens-Kroef, Jonathan C. Strefford, Panagiotis Baliakas, Karla Plevová, Ana E. Rodríguez-Vicente, Alexander C. Leeksma, Kostas Stamatopoulos, Rebeqa Gunnarsson, Pino J Poddighe, Anne Marie van der Kevie-Kersemaekers, Arnon P. Kater, Meaghan Wall, Florence Nguyen-Khac, Theodoros Moysiadis, Anders Österborg, Anh Nhi Tran, Larry Mansouri, Ilaria Scarpelli, Hidde Posthuma, Gisela Barbany, Loic Ysebaert, Helen Parker
Publikováno v:
Digital.CSIC. Repositorio Institucional del CSIC
instname
Haematologica, 105(5). Ferrata Storti Foundation
Haematologica, 106, 87-97
Haematologica, vol. 106, no. 1, pp. 87-97
Haematologica, 106(1), 87-97. FERRATA STORTI FOUNDATION
Haematologica, 106, 1, pp. 87-97
Leeksma, A C, Baliakas, P, Moysiadis, T, Puiggros, A, Plevova, K, van der Kevie-Kersemaekers, A M, Posthuma, H, Rodriguez-Vicente, A E, Tran, A N, Barbany, G, Mansouri, L, Gunnarsson, R, Parker, H, van den Berg, E, Bellido, M, Davis, Z, Wall, M, Scarpelli, I, Österborg, A, Hansson, L, Jarosova, M, Ghia, P, Poddighe, P, Espinet, B, Pospisilova, S, Tam, C, Ysebaert, L, Nguyen-Khac, F, Oscier, D, Haferlach, C, Schoumans, J, Stevens-Kroef, M, Eldering, E, Stamatopoulos, K, Rosenquist, R, Strefford, J C, Mellink, C, Kater, A P & ERIC, the European Research Initiative on CLL 2020, ' Genomic arrays identify high-risk chronic lymphocytic leukemia with genomic complexity : A multi-center study ', Haematologica, vol. 105, no. 5 . https://doi.org/10.3324/HAEMATOL.2019.239947
Haematologica
instname
Haematologica, 105(5). Ferrata Storti Foundation
Haematologica, 106, 87-97
Haematologica, vol. 106, no. 1, pp. 87-97
Haematologica, 106(1), 87-97. FERRATA STORTI FOUNDATION
Haematologica, 106, 1, pp. 87-97
Leeksma, A C, Baliakas, P, Moysiadis, T, Puiggros, A, Plevova, K, van der Kevie-Kersemaekers, A M, Posthuma, H, Rodriguez-Vicente, A E, Tran, A N, Barbany, G, Mansouri, L, Gunnarsson, R, Parker, H, van den Berg, E, Bellido, M, Davis, Z, Wall, M, Scarpelli, I, Österborg, A, Hansson, L, Jarosova, M, Ghia, P, Poddighe, P, Espinet, B, Pospisilova, S, Tam, C, Ysebaert, L, Nguyen-Khac, F, Oscier, D, Haferlach, C, Schoumans, J, Stevens-Kroef, M, Eldering, E, Stamatopoulos, K, Rosenquist, R, Strefford, J C, Mellink, C, Kater, A P & ERIC, the European Research Initiative on CLL 2020, ' Genomic arrays identify high-risk chronic lymphocytic leukemia with genomic complexity : A multi-center study ', Haematologica, vol. 105, no. 5 . https://doi.org/10.3324/HAEMATOL.2019.239947
Haematologica
Complex karyotype (CK) identified by chromosome-banding analysis (CBA) has shown prognostic value in chronic lymphocytic leukemia (CLL). Genomic arrays offer high-resolution genome-wide detection of copy-number alterations (CNAs) and could therefore
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3075b2a6908d0109aebb0114832e447c
http://hdl.handle.net/10261/222849
http://hdl.handle.net/10261/222849
Autor:
Mihal, Marian Hajduch, Helena Urbankova, Eva Klásková, Jirina Zapletalova, Marie Jarošová, Petr, Horwitz Ms, Jana Volejnikova
Publikováno v:
Biomedical Papers, Vol 162, Iss 1, Pp 65-70 (2018)
Background: Leri-Weill syndrome (LWS) ranks among conditions with short stature homeobox gene (SHOX) haploinsufficiency. Data on possible association of SHOX aberrations with malignant diseases are scarce. Methods and Results: We report a unique case