Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Markus Rasmussen"'
Autor:
Rebeqa Gunnarsson, Larry Mansouri, Anders Isaksson, Hanna Göransson, Nicola Cahill, Mattias Jansson, Markus Rasmussen, Jeanette Lundin, Stefan Norin, Anne Mette Buhl, Karin Ekström Smedby, Henrik Hjalgrim, Karin Karlsson, Jesper Jurlander, Christian Geisler, Gunnar Juliusson, Richard Rosenquist
Publikováno v:
Haematologica, Vol 96, Iss 8 (2011)
Background High-resolution genomic microarrays enable simultaneous detection of copy-number aberrations such as the known recurrent aberrations in chronic lymphocytic leukemia [del(11q), del(13q), del(17p) and trisomy 12], and copy-number neutral los
Externí odkaz:
https://doaj.org/article/6330c7bcd62044548d6842ccd8ff107a
Autor:
Millaray Marincevic, Nicola Cahill, Rebeqa Gunnarsson, Anders Isaksson, Mahmoud Mansouri, Hanna Göransson, Markus Rasmussen, Mattias Jansson, Fergus Ryan, Karin Karlsson, Hans-Olov Adami, Fred Davi, Jesper Jurlander, Gunnar Juliusson, Kostas Stamatopoulos, Richard Rosenquist
Publikováno v:
Haematologica, Vol 95, Iss 9 (2010)
Background The existence of multiple subsets of chronic lymphocytic leukemia expressing ‘stereotyped’ B-cell receptors implies the involvement of antigen(s) in leukemogenesis. Studies also indicate that ‘stereotypy’ may influence the clinical
Externí odkaz:
https://doaj.org/article/66d89b7e97ce4f7e8055e2586863e6d7
Autor:
Hanna Göransson, Karolina Edlund, Maria Rydåker, Markus Rasmussen, Johan Winquist, Simon Ekman, Michael Bergqvist, Andrew Thomas, Mats Lambe, Richard Rosenquist, Lars Holmberg, Patrick Micke, Johan Botling, Anders Isaksson
Publikováno v:
PLoS ONE, Vol 4, Iss 6, p e6057 (2009)
BACKGROUND: Technologies based on DNA microarrays have the potential to provide detailed information on genomic aberrations in tumor cells. In practice a major obstacle for quantitative detection of aberrations is the heterogeneity of clinical tumor
Externí odkaz:
https://doaj.org/article/683fe7d84f844ad99eb8792bef5db3cc
Autor:
Kostas Stamatopoulos, Richard Rosenquist, Fergus Ryan, Nicola Cahill, Gunnar Juliusson, Fred Davi, Karin Karlsson, Millaray Marincevic, Anders Isaksson, Hanna Göransson, Hans-Olov Adami, Rebeqa Gunnarsson, Jesper Jurlander, Mahmoud Mansouri, Markus Rasmussen, Mattias Jansson
Publikováno v:
Articles
Background The existence of multiple subsets of chronic lymphocytic leukemia expressing ‘stereotyped’ Bcell receptors implies the involvement of antigen(s) in leukemogenesis. Studies also indicate that ‘stereotypy’ may influence the clinical
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fc131ba7c99cdd8866a59bdf09cd6f15
https://doi.org/10.3324/haematol.2009.021014
https://doi.org/10.3324/haematol.2009.021014
Publikováno v:
Genome Research. 20:899-907
Noncoding RNA (ncRNA) constitutes a significant portion of the mammalian transcriptome. Emerging evidence suggests that it regulates gene expression in cis or trans by modulating the chromatin structure. To uncover the functional role of ncRNA in chr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6d471de2ede2e8e2e0f92e65f7581cf1
https://doi.org/10.1101/gr.103473.109
https://doi.org/10.1101/gr.103473.109
Autor:
Karin E. Smedby, Mattias Jansson, Nicola Cahill, Henrik Hjalgrim, Karin Karlsson, Rebeqa Gunnarsson, Jeanette Lundin, Christian H. Geisler, Markus Rasmussen, Gunnar Juliusson, Hanna Göransson, Stefan Norin, Larry Mansouri, Anders Isaksson, Anne Mette Buhl, Jesper Jurlander, Richard Rosenquist
Publikováno v:
Haematologica. 96(8)
Background High-resolution genomic microarrays enable simultaneous detection of copy-number aberrations such as the known recurrent aberrations in chronic lymphocytic leukemia [del(11q), del(13q), del(17p) and trisomy 12], and copy-number neutral los
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eb43e762ba54b06f2d591f8b99ebb63f
https://pubmed.ncbi.nlm.nih.gov/21546498
https://pubmed.ncbi.nlm.nih.gov/21546498
Autor:
Anders Isaksson, Magnus Sundström, Helgi Birgisson, Markus Rasmussen, Patrick Micke, Hanna Göransson Kultima, Johan Botling, Bengt Glimelius
Publikováno v:
Genome Biology
We describe a bioinformatic tool, Tumor Aberration Prediction Suite (TAPS), for the identification of allele-specific copy numbers in tumor samples using data from Affymetrix SNP arrays. It includes detailed visualization of genomic segment character
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::97201d1df30a4a693241cabb0dd6ba37
http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-164141
http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-164141
Autor:
Michael Bergqvist, Andrew Peter Thomas, Simon Ekman, Maria Rydåker, Mats Lambe, Patrick Micke, Johan Winquist, Anders Isaksson, Johan Botling, Markus Rasmussen, Karolina Edlund, Hanna Göransson, Richard Rosenquist, Lars Holmberg
Publikováno v:
PLoS ONE
PLoS ONE, Vol 4, Iss 6, p e6057 (2009)
PLoS ONE, Vol 4, Iss 6, p e6057 (2009)
Background Technologies based on DNA microarrays have the potential to provide detailed information on genomic aberrations in tumor cells. In practice a major obstacle for quantitative detection of aberrations is the heterogeneity of clinical tumor t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::283b0104bfc9bf1665d1d92dc7e92a08
https://pubmed.ncbi.nlm.nih.gov/19557126
https://pubmed.ncbi.nlm.nih.gov/19557126
Autor:
Rebeqa Gunnarsson, Markus Rasmussen, Richard Rosenquist, Adam Ameur, Lesley-Ann Sutton, Ulf Gyllensten, Sean D. Hooper, Anders Isaksson, Larry Mansouri
Publikováno v:
Clinical Lymphoma Myeloma and Leukemia. 11:S148-S149
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e6a18e123f6b73a7f94abdaa7aa381fc
https://doi.org/10.1016/j.clml.2011.09.013
https://doi.org/10.1016/j.clml.2011.09.013