Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Susanne, Jabar"'
Autor:
Shunya Ohmura, Aruna Marchetto, Martin F. Orth, Jing Li, Susanne Jabar, Andreas Ranft, Endrit Vinca, Katharina Ceranski, Martha J. Carreño-Gonzalez, Laura Romero-Pérez, Fabienne S. Wehweck, Julian Musa, Felix Bestvater, Maximilian M. L. Knott, Tilman L. B. Hölting, Wolfgang Hartmann, Uta Dirksen, Thomas Kirchner, Florencia Cidre-Aranaz, Thomas G. P. Grünewald
Publikováno v:
Molecular Cancer, Vol 20, Iss 1, Pp 1-7 (2021)
Externí odkaz:
https://doaj.org/article/e5b2afe00395468698e4d825cb3744ab
Autor:
Giuseppina Sannino, Aruna Marchetto, Andreas Ranft, Susanne Jabar, Constanze Zacherl, Rebeca Alba-Rubio, Stefanie Stein, Fabienne S. Wehweck, Merve M. Kiran, Tilman L.B. Hölting, Julian Musa, Laura Romero-Pérez, Florencia Cidre-Aranaz, Maximilian M.L. Knott, Jing Li, Heribert Jürgens, Ana Sastre, Javier Alonso, Willian Da Silveira, Gary Hardiman, Julia S. Gerke, Martin F. Orth, Wolfgang Hartmann, Thomas Kirchner, Shunya Ohmura, Uta Dirksen, Thomas G.P. Grünewald
Publikováno v:
EBioMedicine, Vol 47, Iss , Pp 156-162 (2019)
Background: Up to 30–40% of Ewing sarcoma (EwS) patients with non-metastatic disease develop local or metastatic relapse within a time span of 2–10 years. This is in part caused by the absence of prognostic biomarkers that can identify high-risk
Externí odkaz:
https://doaj.org/article/519688e9d40c4215ae075d85d43e55cd
Autor:
Pethő, Sebastian Fuest, Christoph Post, Sebastian T. Balbach, Susanne Jabar, Ilka Neumann, Sandra Schimmelpfennig, Sarah Sargin, Elke Nass, Thomas Budde, Sareetha Kailayangiri, Bianca Altvater, Andreas Ranft, Wolfgang Hartmann, Uta Dirksen, Claudia Rössig, Albrecht Schwab, Zoltán
Publikováno v:
Cancers; Volume 14; Issue 19; Pages: 4819
Ewing sarcoma (EwS) is a rare and highly malignant bone tumor occurring mainly in childhood and adolescence. Physiologically, the bone is a central hub for Ca2+ homeostasis, which is severely disturbed by osteolytic processes in EwS. Therefore, we ai
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=multidiscipl::abd41282a4b4508e18133efd0d8903b5
Autor:
Thomas Kirchner, Shunya Ohmura, Florencia Cidre-Aranaz, Uta Dirksen, Martin F. Orth, Katharina Ceranski, Julian Musa, Laura Romero-Pérez, Thomas G. P. Grunewald, Tilman L B Hölting, Susanne Jabar, Aruna Marchetto, Jing Li, Endrit Vinca, Felix Bestvater, Martha J. Carreño-Gonzalez, Maximilian M. L. Knott, Wolfgang Hartmann, Andreas Ranft, Fabienne S. Wehweck
Publikováno v:
Molecular Cancer, Vol 20, Iss 1, Pp 1-7 (2021)
Molecular Cancer
Molecular Cancer
PurposeEwing sarcoma (EwS) is a highly aggressive bone- or soft tissue-associated malignancy mostly affecting children, adolescents, and young adults. Although multimodal therapies have strongly improved patients’ overall survival over the past dec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6b450b5b37f0e16903413a4de90e1967
https://doaj.org/article/e5b2afe00395468698e4d825cb3744ab
https://doaj.org/article/e5b2afe00395468698e4d825cb3744ab
Autor:
Uwe Thiel, Sebastian J. Schober, Ingo Einspieler, Andreas Kirschner, Melanie Thiede, David Schirmer, Katja Gall, Franziska Blaeschke, Oxana Schmidt, Susanne Jabar, Andreas Ranft, Rebeca Alba Rubío, Uta Dirksen, Thomas G. P. Grunewald, Poul H. Sorensen, Günther H. S. Richter, Irene Teichert von Lüttichau, Dirk H. Busch, Stefan E. G. Burdach
Publikováno v:
OncoImmunology, Vol 6, Iss 5 (2017)
Background: Chondromodulin-I (CHM1) sustains malignancy in Ewing sarcoma (ES). Refractory ES carries a dismal prognosis and patients with bone marrow (BM) metastases do not survive irrespective of therapy. We assessed HLA-A*02:01/CHM1-specific allore
Externí odkaz:
https://doaj.org/article/3cc9a9d7f65440adbaafa92d0d5289d0
Autor:
Stefan K. Zöllner, Katja L. Kauertz, Isabelle Kaiser, Maximilian Kerkhoff, Christiane Schaefer, Madita Tassius, Susanne Jabar, Heribert Jürgens, Ruth Ladenstein, Thomas Kühne, Lianne M. Haveman, Michael Paulussen, Andreas Ranft, Uta Dirksen
Publikováno v:
Cancers; Volume 14; Issue 23; Pages: 5935
OA Förderung 2022 Ewing sarcoma (EwS) is the second most common bone and soft tissue tumor, affecting primarily adolescents and young adults. Patients with secondary EwS are excluded from risk stratification in several studies and therefore do not b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d6ab11fa69c06daddc4f8898e748d850
https://pubmed.ncbi.nlm.nih.gov/36497417
https://pubmed.ncbi.nlm.nih.gov/36497417
Autor:
Sebastian, Fuest, Christoph, Post, Sebastian T, Balbach, Susanne, Jabar, Ilka, Neumann, Sandra, Schimmelpfennig, Sarah, Sargin, Elke, Nass, Thomas, Budde, Sareetha, Kailayangiri, Bianca, Altvater, Andreas, Ranft, Wolfgang, Hartmann, Uta, Dirksen, Claudia, Rössig, Albrecht, Schwab, Zoltán, Pethő
Publikováno v:
Cancers. 14(19)
Ewing sarcoma (EwS) is a rare and highly malignant bone tumor occurring mainly in childhood and adolescence. Physiologically, the bone is a central hub for Ca
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ae6c6fd1cff43de8a149076b77313f7f
https://pubmed.ncbi.nlm.nih.gov/36230742
https://pubmed.ncbi.nlm.nih.gov/36230742
Autor:
Andreas Ranft, Stefanie Stein, Martin F. Orth, Thomas Kirchner, Julia S. Gerke, Maximilian M. L. Knott, Shunya Ohmura, Florencia Cidre-Aranaz, Tilman L. B. Hoelting, Uta Dirksen, Javier Alonso, Willian Da Silveira, Aruna Marchetto, Jing Li, Wolfgang Hartmann, Thomas G. P. Grunewald, Julian Musa, Rebeca Alba-Rubio, Ana Sastre, Laura Romero-Pérez, Susanne Jabar, Giuseppina Sannino, Gary Hardiman, Merve M. Kiran, Fabienne S. Wehweck, Constanze Zacherl, Heribert Jürgens
Publikováno v:
Repisalud
Instituto de Salud Carlos III (ISCIII)
EBioMedicine
Instituto de Salud Carlos III (ISCIII)
EBioMedicine
BACKGROUND: Up to 30-40% of Ewing sarcoma (EwS) patients with non-metastatic disease develop local or metastatic relapse within a time span of 2-10 years. This is in part caused by the absence of prognostic biomarkers that can identify high-risk pati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::604e81a7ef2fd3c74ab81186da29b3b7
https://doi.org/10.1016/j.ebiom.2019.08.002
https://doi.org/10.1016/j.ebiom.2019.08.002
Autor:
Stefan Burdach, I. Kazantsev, Andreas Ranft, Katja Gall, Susanne Jabar, A. Prete, Angela Wawer, Sebastian J. Schober, Michael Merker, Uta Dirksen, Hendrik Gassmann, I. von Lüttichau, Peter Bader, Peter Lang, Uwe Thiel, E. Koscielniak, T Klingebiel, B. Gruhn, B. Afanasyev, Rupert Handgretinger, Miguel Angel Diaz, Heribert Jürgens, Marek Ussowicz
Publikováno v:
Bone Marrow Transplantation
Patients with advanced Ewing sarcoma (AES) carry a poor prognosis. Retrospectively, we analyzed 66 AES patients treated with allogeneic stem cell transplantation (allo-SCT) receiving HLA-mismatched (group A, n = 39) versus HLA-matched grafts (group B
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5f1f6bbbb1f1de5db61ecb0fb2eb21e2
https://mediatum.ub.tum.de/doc/1704376/document.pdf
https://mediatum.ub.tum.de/doc/1704376/document.pdf
Autor:
Christian Vokuhl, Gunhild Mechtersheimer, Eva Wardelmann, Daniel Schrimpf, Wolfgang Hartmann, Andreas von Deimling, Felix Sahm, Uta Dirksen, Melanie Bewerunge-Hudler, Daniel Baumhoer, Iver Petersen, Uta Flucke, Susanne Jabar, Damian Stichel, Manel Esteller, Andreas Ranft, Marcel Trautmann, Stefan M. Pfister, Manfred Gessler, David E. Reuss, Christian Koelsche, Marcel Kool, Thomas Klingebiel, Stefan Fröhling, Cristina R. Antonescu, David T.W. Jones
Publikováno v:
Modern Pathology, 31, 8, pp. 1246-1256
Dipòsit Digital de la UB
Universidad de Barcelona
Mod Pathol
Modern Pathology, 31, 1246-1256
Dipòsit Digital de la UB
Universidad de Barcelona
Mod Pathol
Modern Pathology, 31, 1246-1256
Undifferentiated solid tumors with small blue round cell histology and expression of CD99 mostly resemble Ewing sarcoma. However, they also may include other tumors such as mesenchymal chondrosarcoma, synovial sarcoma, or small cell osteosarcoma. Def
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2f9d1125f2908a929b435fe05743f01f
https://doi.org/10.1038/s41379-018-0045-3
https://doi.org/10.1038/s41379-018-0045-3