Zobrazeno 1 - 10
of 25
pro vyhledávání: '"Renate, Marschon"'
Autor:
Theodora Malli, Melanie Rammer, Sabrina Haslinger, Jonathan Burghofer, Sonja Burgstaller, Hans-Christian Boesmueller, Renate Marschon, Wolfgang Kranewitter, Martin Erdel, Sabine Deutschbauer, Gerald Webersinke
Publikováno v:
Molecular Cytogenetics, Vol 11, Iss 1, Pp 1-9 (2018)
Abstract Background Translocations of the IGH locus on 14q32.3 are present in about 8% of patients with chronic lymphocytic leukemia (CLL) and contribute to leukemogenesis by deregulating the expression of the IGH-partner genes. Identification of the
Externí odkaz:
https://doaj.org/article/9caff90d8fc94d6c995c5338a0baf292
Autor:
Klaus Geissler, Eva Jäger, Agnes Barna, Michael Gurbisz, Renate Marschon, Temeida Graf, Thomas Nösslinger, Michael Pfeilstöcker, Sigrid Machherndl‐Spandl, Reinhard Stauder, Armin Zebisch, Heinz Sill, Leopold Öhler, Rajko Kusec, Gregor Hoermann, Peter Valent
Publikováno v:
European Journal of Haematology. 109:50-57
Background: A multistep pathogenesis of myeloid leukemia including mutations in epigenetic, spliceosome, and signaling genes has been recently demonstrated in a preclinical model but is poorly validated in patients. ----- Methods: Clinical, phenotypi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0b6c4e7bfff274d3c74b05de741e98cf
https://doi.org/10.1111/ejh.13768
https://doi.org/10.1111/ejh.13768
Autor:
Ernst Ulsperger, Elmir Graf, Reinhard Stauder, Eva Jäger, Klaus Geissler, Heinz Tüchler, Josef Thaler, Ulrich Germing, Peter Valent, Ansgar Weltermann, Christoph Geissler, Sonja Heibl, Renate Marschon, Agnes Barna, Armin Zebisch, Michael Pfeilstöcker, Leopold Öhler, Rajko Kusec, Otto Zach, Bruno Schneeweiss, Michael Gurbisz, Temeida Graf, Peter Bettelheim, Heinz Sill, Sigrid Machherndl-Spandl, Gerald Webersinke, Gregor Hoermann, Thomas Nösslinger
Publikováno v:
European Journal of Haematology
In older patients with chronic myelomonocytic leukaemia (CMML) and limited life expectancy due to age and or comorbidities, it is particularly important to consider the risk of transformation for individualised treatment decisions. There is limited i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0499bf4bc452a507e0fef47b6ab23a47
http://europepmc.org/articles/PMC8480146
http://europepmc.org/articles/PMC8480146
Autor:
Paul Knöbl, Elmir Graf, Gerald Webersinke, Ulrich Germing, Heinz Sill, Andreas L. Petzer, Renate Marschon, Sigrid Machherndl-Spandl, Klaus Geissler, Peter Valent, Thomas Nösslinger, Peter Bettelheim, Ilse Schwarzinger, Leopold Öhler, Heinz Tüchler, Bruno Schneeweiss, Gregor Hoermann, Ulrich Jäger, Sonja Heibl, Jörg Berger, Agnes Barna, Bernhard Doleschal, Thamer Sliwa, Felix Keil, Harald Esterbauer, Josef Thaler, Ansgar Weltermann, Reinhard Stauder, Bojana Borjan, Temeida Graf, Regina Reisner, Michael Gurbisz, Otto Zach, Eva Jäger, Ruth Jilch, Rajko Kusec, Ernst Ulsperger, Armin Zebisch, Michael Pfeilstöcker, Christoph Geissler, Wolfgang R. Sperr
Publikováno v:
Wiener Klinische Wochenschrift
Summary In the Austrian biodatabase for chronic myelomonocytic leukemia (ABCMML) clinicolaboratory real-life data have been captured from 606 CMML patients from 14 different hospitals over the last 30 years. It is the only large biodatabase worldwide
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::40ccc6eb5b700b55d2c63b6be6a2bc89
https://doi.org/10.1007/s00508-019-1526-1
https://doi.org/10.1007/s00508-019-1526-1
Autor:
Renate Marschon, Martin Erdel, Hans-Christian Boesmueller, Sabrina Haslinger, Gerald Webersinke, Jonathan Burghofer, Wolfgang Kranewitter, Melanie Rammer, Sabine Deutschbauer, Theodora Malli, Sonja Burgstaller
Publikováno v:
Molecular Cytogenetics
Molecular Cytogenetics, Vol 11, Iss 1, Pp 1-9 (2018)
Molecular Cytogenetics, Vol 11, Iss 1, Pp 1-9 (2018)
Background Translocations of the IGH locus on 14q32.3 are present in about 8% of patients with chronic lymphocytic leukemia (CLL) and contribute to leukemogenesis by deregulating the expression of the IGH-partner genes. Identification of these genes
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c95665c56913744e56e598f7dfc3c1a8
http://europepmc.org/articles/PMC5765657
http://europepmc.org/articles/PMC5765657
Autor:
Gerald Webersinke, Wolfgang Kranewitter, Ingrid Simonitsch-Klupp, Peter Valent, Sabine Deutschbauer, Veronika Buxhofer-Ausch, Holger Rumpold, Melanie Rammer, Theodora Malli, Martin Erdel, Kirsten Muellner-Ammer, Thomas Birkner, Renate Marschon, Christian Sebesta
Publikováno v:
Genes, Chromosomes and Cancer. 55:60-68
Myeloid and lymphoid neoplasms with fibroblast growth factor receptor 1 (FGFR1) abnormalities, also known as 8p11 myeloproliferative syndrome (EMS), represent rare and aggressive disorders, associated with chromosomal aberrations that lead to the fus
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::33d15a78b716e061fcd7b3f3bb93b4aa
https://doi.org/10.1002/gcc.22311
https://doi.org/10.1002/gcc.22311
Autor:
Theodora, Malli, Veronika, Buxhofer-Ausch, Melanie, Rammer, Martin, Erdel, Wolfgang, Kranewitter, Holger, Rumpold, Renate, Marschon, Sabine, Deutschbauer, Ingrid, Simonitsch-Klupp, Peter, Valent, Kirsten, Muellner-Ammer, Christian, Sebesta, Thomas, Birkner, Gerald, Webersinke
Publikováno v:
Genes, chromosomescancer. 55(1)
Myeloid and lymphoid neoplasms with fibroblast growth factor receptor 1 (FGFR1) abnormalities, also known as 8p11 myeloproliferative syndrome (EMS), represent rare and aggressive disorders, associated with chromosomal aberrations that lead to the fus
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::51f024c346f48950a4a5d0dfd56ef123
https://pubmed.ncbi.nlm.nih.gov/26391436
https://pubmed.ncbi.nlm.nih.gov/26391436
Autor:
Wolfgang Kranewitter, Sabine Deutschbauer, Renate Marschon, Evita Diel, Hans-Christoph Duba, Gerald Webersinke, Barbara Güenther, Johanna M Kralik, Martin Erdel, Doris Mueller, Theodora Malli
Publikováno v:
American journal of medical genetics. Part A. (12)
Here, we report on a male patient with developmental delay, speech impairment, mild dysmorphic features, and borderline intellectual disability, bearing a de novo balanced t(5;6)(q11;q25.3). By combining FISH and long distance inverse PCR, we identif
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8f573b20561c648379e686de7936caef
https://pubmed.ncbi.nlm.nih.gov/25250687
https://pubmed.ncbi.nlm.nih.gov/25250687
Autor:
Sophie Haitchi-Petnehazy, Tanja Fehm, Hans Bösmüller, Margit Klier-Richter, Wolfgang Stummvoll, Renate Marschon, Annette Staebler, Gerald Webersinke, Irina Bonzheim, Falko Fend, Franz Roithmeier
Publikováno v:
Virchows Archiv : an international journal of pathology. 459(2)
Intratumoral immune cells and ERCC1 expression are likely to play a role in the response of ovarian carcinoma to chemotherapy, but their impact on therapy outcome is still unclear. Therefore, 41 cases of optimally resected high grade serous ovarian c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c68bf07ef575f51b040a193d70c41d2a
https://pubmed.ncbi.nlm.nih.gov/21713364
https://pubmed.ncbi.nlm.nih.gov/21713364
Autor:
Gertraud Tschurtschenthaler, Holger Rumpold, Gerald Webersinke, Renate Marschon, Kurt Wiesinger, Martin Erdel, Johanna M Kralik, Hans Boesmueller, Wolfgang Kranewitter, Andreas L. Petzer
Publikováno v:
Diagnostic Pathology, Vol 6, Iss 1, p 19 (2011)
Diagnostic Pathology
Diagnostic Pathology
Background Characterization of novel fusion genes in acute leukemia is important for gaining information about leukemia genesis. We describe the characterization of a new ETV6 fusion gene in acute myeloid leukemia (AML) FAB M0 as a result of an uncom
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c5199379eb8709ad3253a1609cf4cc36
http://www.diagnosticpathology.org/content/6/1/19
http://www.diagnosticpathology.org/content/6/1/19