Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Andrea Inthal"'
Autor:
Dagmar Schinnerl, Marion Riebler, Angela Schumich, Sabrina Haslinger, Alice Bramböck, Andrea Inthal, Marek Nykiel, Margarita Maurer-Granofszky, Oskar A. Haas, Ulrike Pötschger, Stefan Köhrer, Karin Nebral, Michael N. Dworzak, Andishe Attarbaschi, Sabine Strehl
Publikováno v:
Blood Cancer Journal, Vol 14, Iss 1, Pp 1-5 (2024)
Externí odkaz:
https://doaj.org/article/9a38e8ba306746909e362a85dcbf2dcf
Autor:
Dagmar Schinnerl, Ester Mejstrikova, Angela Schumich, Marketa Zaliova, Klaus Fortschegger, Karin Nebral, Andishe Attarbaschi, Karel Fiser, Maximilian O. Kauer, Niko Popitsch, Sabrina Haslinger, Andrea Inthal, Barbara Buldini, Giuseppe Basso, Jean-Pierre Bourquin, Giuseppe Gaipa, Monika Brüggemann, Tamar Feuerstein, Margarita Maurer-Granofszky, Renate Panzer-Grümayer, Jan Trka, Georg Mann, Oskar A. Haas, Ondrej Hrusak, Michael N. Dworzak, Sabine Strehl
Publikováno v:
Haematologica, Vol 104, Iss 8 (2019)
Externí odkaz:
https://doaj.org/article/343859e0df1048019cf722f1f412616e
Autor:
Margit König, Renate Panzer-Grümayer, Andishe Attarbaschi, Sabrina Haslinger, Karin Nebral, Dagmar Schinnerl, Stefan Köhrer, Petra Zeitlhofer, Georg Mann, Oskar A. Haas, Andrea Inthal, Sabine Strehl, M. Reza Abbasi
Publikováno v:
Cancers
Volume 13
Issue 18
Cancers, Vol 13, Iss 4597, p 4597 (2021)
Volume 13
Issue 18
Cancers, Vol 13, Iss 4597, p 4597 (2021)
Simple Summary Array analysis is an efficient method for defining in a single experiment all genome-wide large and fine-scale copy number abnormalities, as well as their corresponding allele patterns. Based on the results of the analysis that we perf
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a3b063802176cc65b1df1f4a98ad0a8c
https://pubmed.ncbi.nlm.nih.gov/34572826
https://pubmed.ncbi.nlm.nih.gov/34572826
Autor:
Tamar Feuerstein, Klaus Fortschegger, Giuseppe Basso, Andrea Inthal, Angela Schumich, Michael Dworzak, Renate Panzer-Grümayer, Sabine Strehl, Karin Nebral, Barbara Buldini, Giuseppe Gaipa, Jean-Pierre Bourquin, Maximilian Kauer, Oskar A. Haas, Ondrej Hrusak, Karel Fiser, Jan Trka, Ester Mejstrikova, Margarita Maurer-Granofszky, Niko Popitsch, Sabrina Haslinger, Dagmar Schinnerl, Marketa Zaliova, Andishe Attarbaschi, Georg Mann, Monika Brüggemann
Publikováno v:
Haematologica. 104:e352-e355
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bdfb245d4115b7d2be794d7cef9ca8e9
https://doi.org/10.3324/haematol.2018.214353
https://doi.org/10.3324/haematol.2018.214353
Autor:
Reinhard Grausenburger, Claus Meyer, Georg Mann, Sabine Strehl, Renate Panzer-Grümayer, Reinhard Kofler, Lilian Kuster, Johannes Rainer, Andrea Inthal, Maximilian Kauer, Gerd Krapf, Oskar A. Haas, Andrew G. Hall, Markus Metzler, Gerhard Fuka, Rolf Marschalek, Jochen Harbott, Ulrike Kaindl, Lüder Hinrich Meyer
Publikováno v:
Blood. 117:2658-2667
Approximately 25% of childhood acute lymphoblastic leukemias carry the ETV6/RUNX1 fusion gene. Despite their excellent initial treatment response, up to 20% of patients relapse. To gain insight into the relapse mechanisms, we analyzed single nucleoti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::beb84b348be5a85f00fc00811fd098a4
https://doi.org/10.1182/blood-2010-03-275347
https://doi.org/10.1182/blood-2010-03-275347
Autor:
Andishe Attarbaschi, Georg Mann, Margit König, Sabrina Haslinger, Karin Nebral, Oskar A. Haas, Sabine Strehl, Andrea Inthal, Renate Panzer-Grümayer
Publikováno v:
Blood. 132:4082-4082
Background: The detailed definition of causative genomic alterations is not only an indispensable prerequisite for the predictive and prognostic subdivision of childhood acute lymphoblastic leukemia (ALL) but increasingly also one, on which individua
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::24ec8764c5340476b84dbf73d2cd2869
https://doi.org/10.1182/blood-2018-99-115761
https://doi.org/10.1182/blood-2018-99-115761
Autor:
Annette Neubüser, Heiko Peters, Mitsushiro Nakatomi, Alisa Fuchs, Andrea Inthal, David Herrmann, Shuofei Cheng
Publikováno v:
Developmental Dynamics. 239:2860-2874
Mutations in the gene encoding the T-box transcription factor TBX22 cause X-linked cleft palate and ankyloglossia in humans. Here we show that Tbx22 expression during facial and palatal development is regulated by FGF and BMP signaling. Our results d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6890be8e3c5670422dc4c76b92c0cc14
https://doi.org/10.1002/dvdy.22421
https://doi.org/10.1002/dvdy.22421
Autor:
Helmut Gadner, Herbert Pichler, Andrea Inthal, Michael Dworzak, Martin Schrappe, Felix Niggli, Andrea Teigler-Schlegel, Georg Mann, Jochen Harbott, Margit König, Renate Panzer-Grümayer, Daniela Krehan, Andishe Attarbaschi, Oskar A. Haas, Sabine Strehl, Anja Möricke, Karin Nebral, Dasa Janousek
Publikováno v:
British journal of haematology. 149(1)
The presence of a dicentric chromosome dic(9;20) has been reported to have an unfavourable prognosis in children with B-cell precursor acute lymphoblastic leukaemia (BCP-ALL). As outcome may be influenced by type and composition of treatment, we anal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::62f2eb94d30aa2a8b3ce350822ade05b
https://pubmed.ncbi.nlm.nih.gov/20067563
https://pubmed.ncbi.nlm.nih.gov/20067563
Autor:
Michael Dworzak, Dasa Janousek, Ulrike Pötschger, Sabine Strehl, Andishe Attarbaschi, Andrea Inthal, Georg Mann, Markus Pisecker, Oskar A. Haas, Renate Panzer-Grümayer, Martin Schrappe, Helmut Gadner, Reinhard Ullmann
Publikováno v:
British journal of haematology. 148(2)
Summary TLX3 expression (TLX3+) in childhood T-cell acute lymphoblastic leukaemia (T-ALL) seems to be associated with a poor prognosis when treated with regimens that lack early and/or late re-intensification therapy elements. Because such elements a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ec700749aedf794cfbff11a95256756e
https://pubmed.ncbi.nlm.nih.gov/19821827
https://pubmed.ncbi.nlm.nih.gov/19821827
Autor:
Gerd Krapf, Ruth Joas, Gerhard Fuka, Dominik Beck, E. Renate Panzer-Grümayer, Georg Mann, Andrea Inthal, Lukas Orel, Max O. Kauer
Publikováno v:
Clinical cancer research : an official journal of the American Association for Cancer Research. 14(22)
Purpose: We explored the mechanisms leading to the distinct overexpression of EPOR as well as the effects of EPO signaling on ETV6/RUNX1-positive acute lymphoblastic leukemias. Experimental Design: ETV6/RUNX1-expressing model cell lines and leukemic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a66c00e546d45272991a32612b95ee17
https://pubmed.ncbi.nlm.nih.gov/19010836
https://pubmed.ncbi.nlm.nih.gov/19010836