Zobrazeno 1 - 10
of 37
pro vyhledávání: '"Stefan Imreh"'
Autor:
Behrooz Torabi Moghadam, Noémi Nagy, Karolina Bukowska-Strakova, Ulf Gyllensten, Vilmantas Giedraitis, Erin Oerton, Edyta Rychlicka-Buniowska, Łukasz Bełch, Lars Forsberg, Hanna Davies, Jarosław Baran, Jessica Nordlund, Stefan Enroth, Åsa Johansson, Maciej Siedlar, Tomasz Grodzicki, Kazimierz Weglarczyk, Alicja Klich-Rączka, Lena Kilander, Jan P. Dumanski, Alicja Jozkowicz, Marcus Danielsson, John R. B. Perry, Janusz Ryś, Arkadiusz Piotrowski, Stefan Imreh, Janusz Jaszczyński, Jonas Mattisson, Martin Ingelsson, Adam Ameur, Paweł Olszewski, Piotr Chlosta, Jonatan Halvardson, Aleksandra Ambicka, Marcin Przewoźnik
Publikováno v:
Cellular and Molecular Life Sciences
Funder: Kjell och Märta Beijers Stiftelse (SE)
Funder: Hjärnfonden; doi: http://dx.doi.org/10.13039/501100003792
Funder: Cancerfonden; doi: http://dx.doi.org/10.13039/501100002794
Funder: Vetenskapsrådet; doi: http://dx.doi.org/10.1
Funder: Hjärnfonden; doi: http://dx.doi.org/10.13039/501100003792
Funder: Cancerfonden; doi: http://dx.doi.org/10.13039/501100002794
Funder: Vetenskapsrådet; doi: http://dx.doi.org/10.1
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f215d3561c3c224d4a6e35ac682f5329
https://ruj.uj.edu.pl/xmlui/handle/item/274018
https://ruj.uj.edu.pl/xmlui/handle/item/274018
Publikováno v:
bioRxiv
Publikováno v:
Journal of Cell Science.
This Publisher's Note updates and replaces the Expression of Concern ([doi: 10.1242/jcs.205559][1]) relating to the article ‘Chromosomal breaks during mitotic catastrophe trigger γH2AX–ATM–p53-mediated apoptosis’ by Gabriela Imreh, Helin Vak
Autor:
Stefan C. Müller, Maria Kost-Alimova, Stefan Imreh, George Klein, Eva Darai-Ramqvist, Agneta Sandlund
Publikováno v:
Genome Research. 18:370-379
We have previously found that the borders of evolutionarily conserved chromosomal regions often coincide with tumor-associated deletion breakpoints within human 3p12-p22. Moreover, a detailed analysis of a frequently deleted region at 3p21.3 (CER1) s
Publikováno v:
Oncogene. 27:1218-1230
To better understand the dual, tumour-suppressive and tumour-promoting function of transforming growth factor-beta (TGFbeta), we analysed mammary epithelial NMuMG cells in response to short and long-term TGFbeta exposure. NMuMG cells became prolifera
Autor:
Maria Kost-Alimova, Stefan Imreh
Publikováno v:
Seminars in Cancer Biology. 17:19-30
Chromosome deletions do abound in cancer and are detected in certain regions in a non-random manner. Although their relevance remains elusive, it is a general agreement that segmental losses provide the cell with selective growth advantage. Consequen
Autor:
Stefan Imreh, Sabine Mai
Publikováno v:
Seminars in Cancer Biology. 17:1-4
Autor:
Stefan Imreh, Gabor G. Kovacs, György Fekete, Irén Haltrich, George Klein, M. Dobos, Maria Kost-Alimova
Publikováno v:
Cancer Genetics and Cytogenetics. 172:54-60
We examined chromosome 3 in 32 childhood acute lymphoblastic leukemia (ALL) bone marrow samples. Using interphase multipoint FISH (mp-FISH), which was developed by our group, with 42 chromosome 3-specific probes, we detected clonal chromosome 3 aberr
Autor:
Irén Haltrich, Dezső David, Lígia S. Almeida, Giovanna Valentini, György Fekete, Carlos Araújo, Stefan Imreh, Maristella Maggi
Publikováno v:
JIMD Reports ISBN: 9783662474662
Acessível em: www.ncbi.nlm.nih.gov/pmc/articles/pmid/25814383/ Carriers of cytogenetically similar, apparentlybalanced familial chromosome translocations not alwaysexhibit the putative translocation-associated disease phenotype.Additional genetic de
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b9a086ed62b3ea10532b007a8fd7a0f3
https://doi.org/10.1007/8904_2015_427
https://doi.org/10.1007/8904_2015_427
Autor:
György Fekete, Irén Haltrich, Maria Kost-Alimova, Gabor G. Kovacs, Stefan Imreh, George Klein
Publikováno v:
European Journal of Haematology. 76:124-133
We detected non-random 3p losses and 3q gains on well-determined regions in both murine and human tumors using a microcell hybrid-based model system called ‘elimination test’. We suggest that these are general malignancy-associated aberrations no