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pro vyhledávání: '"Katalin Benedek"'
Publikováno v:
Chromosome Research. 12:777-785
Previous work has demonstrated that chromosome 11 is trisomic or shows a duplicated region encompassing the E1/E2 band of chromosome 11 in 90% of v-abl/myc-induced plasmacytomas (Wiener et al. 1995). In the present report, we have studied BALB/c PreB
Autor:
A G dos Santos Silva, S Lacoste, G Williams, M Lowbeer, Amanda Guffei, Marie Henriksson, George Klein, Sabine Mai, Katalin Benedek, Emilia Wiechec
Publikováno v:
Lacoste, S, Wiechec, E, Dos Santos Silva, A G, Guffei, A, Williams, G, Lowbeer, M, Benedek, K, Henriksson, M, Klein, G & Mai, S 2010, ' Chromosomal rearrangements after ex vivo Epstein-Barr virus (EBV) infection of human B cells ', Oncogene, vol. 29, no. 4, pp. 503-15 . https://doi.org/10.1038/onc.2009.359
Lacoste, S, Wiechec, E, Dos Santos Silva, AG, Guffei, A, Williams, G, Lowbeer, M, Benedek, K, Henriksson, M, Klein, G & Mai, S 2009, ' Chromosomal rearrangements after ex vivo Epstein-Barr virus (EBV) infection of human B cells. ', Oncogene .
Lacoste, S, Wiechec, E, Dos Santos Silva, AG, Guffei, A, Williams, G, Lowbeer, M, Benedek, K, Henriksson, M, Klein, G & Mai, S 2009, ' Chromosomal rearrangements after ex vivo Epstein-Barr virus (EBV) infection of human B cells. ', Oncogene .
The Epstein–Barr virus (EBV) is carried by more than 90% of the adult world population and has been implicated in several human malignancies. Its ability to induce unlimited in vitro proliferation of B cells is frequently used to generate lymphobla
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d474c77ac582effc9fe6ab40ae569381
https://pure.au.dk/portal/da/publications/chromosomal-rearrangements-after-ex-vivo-epsteinbarr-virus-ebv-infection-of-human-b-cells(3ca80da5-7a53-4d06-b4cc-cefc13b44472).html
https://pure.au.dk/portal/da/publications/chromosomal-rearrangements-after-ex-vivo-epsteinbarr-virus-ebv-infection-of-human-b-cells(3ca80da5-7a53-4d06-b4cc-cefc13b44472).html
Publikováno v:
Cytotechnology. 44(3)
Characterization of genetic disorders in humans and animal models requires identification of chromosomal aberrations. However, identifying fine deletions or insertion in metaphase chromosomes has been always a challenge due to limitations of resoluti
Publikováno v:
Cytotechnology; Mar2004, Vol. 44 Issue 3, p143-149, 7p