Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Jens Warfsmann"'
Autor:
Manuel Delgado Caceres, Katharina Angerpointner, Michael Galler, Dasheng Lin, Philipp A. Michel, Christoph Brochhausen, Xin Lu, Adithi R. Varadarajan, Jens Warfsmann, Richard Stange, Volker Alt, Christian G. Pfeifer, Denitsa Docheva
Publikováno v:
Cell Death and Disease, Vol 12, Iss 11, Pp 1-13 (2021)
Abstract Heterotopic ossification (HO) represents a common problem after tendon injury with no effective treatment yet being developed. Tenomodulin (Tnmd), the best-known mature marker for tendon lineage cells, has important effects in tendon tissue
Externí odkaz:
https://doaj.org/article/9c34c922da0345759afc57f0147bba83
Autor:
Melanie Werner-Klein, Ana Grujovic, Christoph Irlbeck, Milan Obradović, Martin Hoffmann, Huiqin Koerkel-Qu, Xin Lu, Steffi Treitschke, Cäcilia Köstler, Catherine Botteron, Kathrin Weidele, Christian Werno, Bernhard Polzer, Stefan Kirsch, Miodrag Gužvić, Jens Warfsmann, Kamran Honarnejad, Zbigniew Czyz, Giancarlo Feliciello, Isabell Blochberger, Sandra Grunewald, Elisabeth Schneider, Gundula Haunschild, Nina Patwary, Severin Guetter, Sandra Huber, Brigitte Rack, Nadia Harbeck, Stefan Buchholz, Petra Rümmele, Norbert Heine, Stefan Rose-John, Christoph A. Klein
Publikováno v:
Nature Communications, Vol 11, Iss 1, Pp 1-18 (2020)
Metastatic dissemination in breast cancer patients occurs early in malignant transformation, raising questions about how disseminated cancer cells (DCC) progress at distant sites. Here, the authors show that DCCs in bone marrow are activated via IL6-
Externí odkaz:
https://doaj.org/article/852fb79d2cfa456b923be4f3ce115b15
Autor:
Jessica I. Hoell, Jens Warfsmann, Felix Distelmaier, Arndt Borkhardt, Gisela Janßen, Michaela Kuhlen
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 13, Iss 1, Pp 1-7 (2018)
Abstract Background Our objective was to evaluate children with metabolic diseases in paediatric palliative home care (PPC) and the process of decision-making. This study was conducted as single-centre retrospective cohort study of patients in the ca
Externí odkaz:
https://doaj.org/article/3eae427a7ab5457b8c404e6377df3f2b
Autor:
Sadra Bakhshandeh, Hubert M. Taïeb, Adithi R. Varadarajan, Susanna M. Lissek, Sarah M. Hücker, Xin Lu, Daniela S. Garske, Sarah A. E. Young, Jörg Contzen, Manfred Gossen, Stefan Kirsch, Jens Warfsmann, Kamran Honarnejad, Christoph A. Klein, Amaia Cipitria
Resected tumors frequently relapse with distant metastasis, despite systemic treatment. Cellular quiescence has been identified as an important mechanism underlying such drug resistance enabling late relapse. Nonetheless, hurdles associated with dete
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::82a24605666b1a7b87c30e6988c35238
https://doi.org/10.1101/2023.01.25.525382
https://doi.org/10.1101/2023.01.25.525382
Autor:
André Franken, Annika Kraemer, Alicia Sicking, Meike Watolla, Mahdi Rivandi, Liwen Yang, Jens Warfsmann, Bernhard M. Polzer, Thomas W. P. Friedl, Franziska Meier-Stiegen, Nikolas H. Stoecklein, Davut Dayan, Sabine Riethdorf, Volkmar Mueller, Klaus Pantel, André Koch, Andreas D. Hartkopf, Natalia Krawczyk, Eugen Ruckhaeberle, Dieter Niederacher, Tanja Fehm, Hans Neubauer
Background Circulating tumour cells (CTCs) are mainly enriched based on the epithelial cell adhesion molecule (EpCAM). Although it was shown that an EpCAM low-expressing CTC fraction is not captured by such approaches, knowledge about its prognostic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2135e5daa3637915ae372f9de7c8d8b5
https://publica.fraunhofer.de/handle/publica/441437
https://publica.fraunhofer.de/handle/publica/441437
Autor:
Anja Kathrin Wege, Eva‐Maria Rom‐Jurek, Paul Jank, Carsten Denkert, Peter Ugocsai, Christine Solbach, Jens‐Uwe Blohmer, Bruno Sinn, Marion Mackelenbergh, Volker Möbus, Andreas Trumpp, Elisabetta Marangoni, Nicole Pfarr, Christoph Irlbeck, Jens Warfsmann, Bernhard Polzer, Florian Weber, Olaf Ortmann, Sibylle Loibl, Valentina Vladimirova, Gero Brockhoff
Publikováno v:
International journal of cancerREFERENCES. 150(8)
Estrogen receptor-positive breast cancer is a highly prevalent but heterogeneous disease among women. Advanced molecular stratification is required to enable individually most efficient treatments based on relevant prognostic and predictive biomarker
Autor:
Elisabeth Schneider, Steffi Treitschke, Sandra Grunewald, Severin Guetter, Isabell Blochberger, Stefan Rose-John, Melanie Werner-Klein, Miodrag Gužvić, Ana Grujovic, Norbert Heine, Jens Warfsmann, Catherine Botteron, Christian Werno, Nadia Harbeck, Cäcilia Köstler, Huiqin Koerkel-Qu, Milan Obradovic, Brigitte Rack, Bernhard Polzer, Kathrin Weidele, Martin Hoffmann, Petra Rümmele, Xin Lu, Giancarlo Feliciello, Sandra Huber, Nina Patwary, Stefan Buchholz, Stefan Kirsch, Gundula Haunschild, Kamran Honarnejad, Zbigniew T. Czyz, Christoph Klein, Christoph Irlbeck
Publikováno v:
Nature Communications
Nature Communications, Vol 11, Iss 1, Pp 1-18 (2020)
Nature Communications, Vol 11, Iss 1, Pp 1-18 (2020)
Although thousands of breast cancer cells disseminate and home to bone marrow until primary surgery, usually less than a handful will succeed in establishing manifest metastases months to years later. To identify signals that support survival or outg
Autor:
Huiqin Koerkel-Qu, Sandra Grunewald, Stefan Rose-John, Stefan Kirsch, Melanie Werner-Klein, Martin Hoffmann, Severin Guetter, Isabell Blochberger, Catherine Botteron, Elisabeth Schneider, Petra Ruemmele, Miodrag Guzvic, Stefan Buchholz, Gundula Haunschild, Kamran Honarnejad, Christoph Klein, Christoph Irlbeck, Nina Patwary, Sandra Huber, Caecilia Koestler, Kathrin Weidele, Ana Grujovic, Milan Obradovic, Zbigniew T. Czyz, Steffie Treitschke, Norbert Heine, Xin Lu, Jens Warfsmann, Bernhard Polzer, Christian Werno
Although thousands of breast cancer cells disseminate and home to bone marrow until primary surgery, usually less than a handful will succeed in establishing manifest metastases months to years later. To identify signals that support survival or outg
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a6e8f731ee4d130ef1923858cc0248cb
https://doi.org/10.1101/2020.05.28.121145
https://doi.org/10.1101/2020.05.28.121145
Autor:
Michaela Kuhlen, G. Janßen, Jens Warfsmann, Jessica I. Hoell, Felix Distelmaier, Arndt Borkhardt
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 13, Iss 1, Pp 1-7 (2018)
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases
Background Our objective was to evaluate children with metabolic diseases in paediatric palliative home care (PPC) and the process of decision-making. This study was conducted as single-centre retrospective cohort study of patients in the care of a l
Autor:
Yuan Zhuang, Dirk Brenner, Verena Keitel, Haifeng C. Xu, Philipp A. Lang, Ertan Mayatepek, Diran Herebian, Mohamed S. Taha, Prashant V. Shinde, Klaus Pfeffer, Karl S. Lang, Kristina Behnke, Balamurugan Sundaram, Dieter Häussinger, Jens Warfsmann, Jelena Vasilevska, Aleksandra A. Pandyra, Mohammad Reza Ahmadian, Jessica I. Hoell, Dagmar Wieczorek, Jun Huang, Arndt Borkhardt
Publikováno v:
Zhuang, Y, Xu, H C, Shinde, P V, Warfsmann, J, Vasilevska, J, Sundaram, B, Behnke, K, Huang, J, Hoell, J I, Borkhardt, A, Pfeffer, K, Taha, M S, Herebian, D, Mayatepek, E, Brenner, D, Ahmadian, M R, Keitel, V, Wieczorek, D, Häussinger, D, Pandyra, A A, Lang, K S & Lang, P A 2020, ' Fragile X mental retardation protein protects against tumour necrosis factor-mediated cell death and liver injury ', Gut, vol. 69, no. 1, pp. 133-145 . https://doi.org/10.1136/gutjnl-2019-318215
ObjectiveThe Fragile X mental retardation (FMR) syndrome is a frequently inherited intellectual disability caused by decreased or absent expression of the FMR protein (FMRP). Lack of FMRP is associated with neuronal degradation and cognitive dysfunct