Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Jana Kminkova"'
Autor:
Lesley-Ann Sutton, Emma Young, Panagiotis Baliakas, Anastasia Hadzidimitriou, Theodoros Moysiadis, Karla Plevova, Davide Rossi, Jana Kminkova, Evangelia Stalika, Lone Bredo Pedersen, Jitka Malcikova, Andreas Agathangelidis, Zadie Davis, Larry Mansouri, Lydia Scarfò, Myriam Boudjoghra, Alba Navarro, Alice F. Muggen, Xiao-Jie Yan, Florence Nguyen-Khac, Marta Larrayoz, Panagiotis Panagiotidis, Nicholas Chiorazzi, Carsten Utoft Niemann, Chrysoula Belessi, Elias Campo, Jonathan C. Strefford, Anton W. Langerak, David Oscier, Gianluca Gaidano, Sarka Pospisilova, Frederic Davi, Paolo Ghia, Kostas Stamatopoulos, Richard Rosenquist
Publikováno v:
Haematologica, Vol 101, Iss 8 (2016)
We report on markedly different frequencies of genetic lesions within subsets of chronic lymphocytic leukemia patients carrying mutated or unmutated stereotyped B-cell receptor immunoglobulins in the largest cohort (n=565) studied for this purpose. B
Externí odkaz:
https://doaj.org/article/565f9a6095ed413e91b042f8d0c0b812
Autor:
Veronika Navrkalova, Ludmila Sebejova, Jana Zemanova, Jana Kminkova, Blanka Kubesova, Jitka Malcikova, Marek Mraz, Jana Smardova, Sarka Pavlova, Michael Doubek, Yvona Brychtova, David Potesil, Veronika Nemethova, Jiri Mayer, Sarka Pospisilova, Martin Trbusek
Publikováno v:
Haematologica, Vol 98, Iss 7 (2013)
ATM abnormalities are frequent in chronic lymphocytic leukemia and represent an important prognostic factor. Sole 11q deletion does not result in ATM inactivation by contrast to biallelic defects involving mutations. Therefore, the analysis of ATM mu
Externí odkaz:
https://doaj.org/article/7151e415765547daba8ee5a8ed2e6964
Autor:
Marta Larrayoz, Panagiotis Panagiotidis, Theodoros Moysiadis, Evangelia Stalika, Kostas Stamatopoulos, Alba Navarro, Šárka Pospíšilová, Xiao-Jie Yan, Chrysoula Belessi, Jitka Malčíková, Florence Nguyen-Khac, Frederic Davi, Richard Rosenquist, Lesley-Ann Sutton, Lone Bredo Pedersen, Nicholas Chiorazzi, Karla Plevová, Gianluca Gaidano, Panagiotis Baliakas, Lydia Scarfò, Emma Young, Andreas Agathangelidis, Paolo Ghia, Anton W. Langerak, Carsten Utoft Niemann, Davide Rossi, Jonathan C. Strefford, Elias Campo, Alice F. Muggen, Myriam Boudjoghra, Larry Mansouri, Jana Kminkova, Anastasia Hadzidimitriou, Zadie Davis, David Oscier
Publikováno v:
Haematologica, 101(8), 959-967. Ferrata Storti Foundation
Dipòsit Digital de la UB
Universidad de Barcelona
Recercat. Dipósit de la Recerca de Catalunya
instname
Haematologica
Haematologica, Ferrata Storti Foundation, 2016, 101 (8), pp.959-967. ⟨10.3324/haematol.2016.141812⟩
Haematologica, 2016, 101 (8), pp.959-967. ⟨10.3324/haematol.2016.141812⟩
Dipòsit Digital de la UB
Universidad de Barcelona
Recercat. Dipósit de la Recerca de Catalunya
instname
Haematologica
Haematologica, Ferrata Storti Foundation, 2016, 101 (8), pp.959-967. ⟨10.3324/haematol.2016.141812⟩
Haematologica, 2016, 101 (8), pp.959-967. ⟨10.3324/haematol.2016.141812⟩
on behalf of ERIC, the European Research Initiative on CLL; International audience; We report on markedly different frequencies of genetic lesions within subsets of chronic lymphocytic leukemia patients carrying mutated or unmutated stereotyped B-cel
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::94c934a33f8ed965a68fdb04d50f4544
http://www.haematologica.org/content/101/8/959.full.pdf
http://www.haematologica.org/content/101/8/959.full.pdf
Autor:
Kostas Stamatopoulos, Achilles Anagnostopoulos, Karin E. Smedby, Diego Cortese, Neus Villamor, Alba Navarro, C. Belessi, La. Sutton, E. Minga, Larry Mansouri, Gianluca Gaidano, Eugen Tausch, Paolo Ghia, Richard Rosenquist, Veronika Navrkalová, Šárka Pospíšilová, Jana Kminkova, Julio Delgado, Anastasia Hadzidimitriou, Lydia Scarfò, Gunnar Juliusson, Andreas Agathangelidis, Davide Rossi, Jonathan C. Strefford, Zadie Davis, Antonios M. Makris, Matthew J. J. Rose-Zerilli, David Oscier, Stephan Stilgenbauer, Panagiotis Baliakas, Elias Campo, Barbara Kantorová, Marta Larrayoz, Evangelia Stalika
Publikováno v:
Leukemia
Through the European Research Initiative on chronic lymphocytic leukemia (CLL) (ERIC), we screened 3490 patients with CLL for mutations within the NOTCH1 (n=3334), SF3B1 (n=2322), TP53 (n=2309), MYD88 (n=1080) and BIRC3 (n=919) genes, mainly at diagn
Autor:
Richard Rosenquist, Lesley-Ann Sutton, Davide Rossi, Paolo Ghia, Lydia Scarfò, Andreas Agathangelidis, Gianluca Gaidano, Šárka Pospíšilová, Jana Kminkova, Anastasia Hadzidimitriou, Kostas Stamatopoulos, Panagiotis Baliakas
Publikováno v:
Blood
Genome surveys have offered a comprehensive view of the genetic landscape of chronic lymphocytic leukemia (CLL), identifying several recurrently mutated genes, including myeloid differentiation primary response 88 (MYD88). The predominant mutation co
Autor:
Zadie Davis, David Oscier, Lydia Scarfò, Andreas Agathangelidis, Gianluca Gaidano, Lesley-Ann Sutton, Jitka Malčíková, Šárka Pospíšilová, Kostas Stamatopoulos, Davide Rossi, Jonathan C. Strefford, Diego Cortese, Neus Villamor, Karin E. Smedby, Eugen Tausch, Eva Minga, Gunnar Juliusson, Julio Delgado, Stephan Stilgenbauer, Larry Mansouri, Jana Kminkova, Karla Plevová, Anastasia Hadzidimitriou, Paolo Ghia, Alba Navarro, Antonios M Makris, Richard Rosenquist, Elias Campo, Chrysoula Belessi, Evangelia Stalika, Marta Larrayoz
Publikováno v:
Blood. 122:1614-1614
In chronic lymphocytic leukemia (CLL), genomic aberrations identify subgroups of patients with distinct treatment outcomes. In particular, patients with deletion of chromosome 17p and/or TP53 gene mutations have inferior prognosis with standard thera
Autor:
Jitka Malčíková, Tobias Rausch, Jiri Mayer, Marek Mráz, Šárka Pospíšilová, Veronika Navrkalová, Boris Tichy, Karla Plevová, Vladimir Benes, Michael Doubek, Jana Kminkova, Yvona Brychtová
Publikováno v:
Blood. 120:3895-3895
Abstract 3895 Background Unique miRNA expression signature is associated with CLL prognostic factors and disease progression (Calin et al., 2005; Mraz et al., 2009), and thus contributes to CLL pathogenesis. The mechanism through which miRNA expressi
Autor:
Jana Kminkova, Ludmila Šebejová, Martin Trbušek, Jiri Mayer, Jana Zemanová, Michael Doubek, Blanka Kubešová, Yvona Brychtová, Veronika Navrkalová, Šárka Pospíšilová, Jana Šmardová
Publikováno v:
Blood. 120:3902-3902
Abstract 3902 Abnormalities of ATM gene are frequent in chronic lymphocytic leukemia (CLL) patients and represent important predictive and prognostic factor. ATM defects are commonly assessed through monitoring of 11q deletion (11q-) using I-FISH. Ho
Autor:
Martin Trbušek, Katerina Stano-Kozubik, Michael Doubek, Karol Pál, Ludmila Šebejová, Lin Wu, Barbara Kantorová, Nancy Patten, Jana Kminkova, Sim Truong, Barbora Dvorakova, Nikola Tom, Veronika Navrkalová, Šárka Pospíšilová, Jiri Mayer, Boris Tichy, Jitka Malčíková, Jana Šmardová
Publikováno v:
Blood. 120:3911-3911
Abstract 3911 Background The adverse prognostic significance of p53 aberrations (gene deletion at locus 17p13.1 and/or TP53 mutations) has been already proven in chronic lymphocytic leukemia (CLL). In contrast to the standardized examination of the g
Autor:
Martin Trbušek, Jana Kminkova, Yvona Brychtová, Marek Mráz, Ludmila Šebejová, Veronika Navrkalová, Šárka Pospíšilová, Jitka Malčíková, Blanka Kubešová, Michael Doubek, Jiri Mayer, Jana Šmardová, Veronika Némethová, Jana Zemanová, David Potesil, Šárka Pavlová
Publikováno v:
Haematologica
ATM abnormalities are frequent in chronic lymphocytic leukemia and represent an important prognostic factor. Sole 11q deletion does not result in ATM inactivation by contrast to biallelic defects involving mutations. Therefore, the analysis of ATM mu