Zobrazeno 1 - 10
of 55
pro vyhledávání: '"Barbara Plaimauer"'
Autor:
Paolo Rossato, Enrica Federti, Alessandro Matte, Helmut Glantschnig, Fabio Canneva, Maria Schuster, Sogue Coulibaly, Gerald Schrenk, Dirk Voelkel, Michael Dockal, Barbara Plaimauer, Immacolata Andolfo, Achille Iolascon, Hanspeter Rottensteiner, Herbert Gritsch, Friedrich Scheiflinger, Werner Hoellriegl, Lucia De Franceschi
Publikováno v:
Haematologica, Vol 107, Iss 11 (2022)
Sickle cell disease (SCD) is an inherited red blood cell disorder that occurs worldwide. Acute vaso-occlusive crisis is the main cause of hospitalization in patients with SCD. There is growing evidence that inflammatory vasculopathy plays a key role
Externí odkaz:
https://doaj.org/article/8c70e0b3cd1f416b96b51f9736f32503
Autor:
Silvia Ferrari, Kristina Palavra, Bernadette Gruber, Johanna A. Kremer Hovinga, Paul Knöbl, Claudine Caron, Caroline Cromwell, Louis Aledort, Barbara Plaimauer, Peter L. Turecek, Hanspeter Rottensteiner, Friedrich Scheiflinger
Publikováno v:
Haematologica, Vol 99, Iss 4 (2014)
Anti-ADAMTS13 autoantibodies are the main cause of acquired thrombotic thrombocytopenic purpura. Binding of these antibodies to ADAMTS13 eventually results in the formation of antigen-antibody immune complexes. Circulating ADAMTS13-specific immune co
Externí odkaz:
https://doaj.org/article/6088089c03124975a2c1d1ed3b9c8981
Publikováno v:
BioTechniques, Vol 23, Iss 5, Pp 882-888 (1997)
A control template for a competitive nested primer PCR of the HIV-1 gag region was constructed. This construct shares the primer recognition sequences with the wildtype template and yields a 97-bp fragment after amplification (wild-type: 115 bp). To
Externí odkaz:
https://doaj.org/article/6cf5b4231f524db185430d0f08199e55
Publikováno v:
BioTechniques, Vol 21, Iss 3, Pp 480-484 (1996)
A quantitative multiple competitive PCR (QMC-PCR) for determination of DNA copy numbers is described. Four competitive DNA templates for the env region of HIV-1 were constructed with sizes longer (187 and 163 bp) or shorter (122 and 105 bp) than the
Externí odkaz:
https://doaj.org/article/7e0c4210cecf4ca28b38d5ff180e90ad
Autor:
Birgit K. Seyfried, Friedrich Scheiflinger, Barbara Plaimauer, X. Long Zheng, Christian Fiedler, Stefan Kaufmann, Hanspeter Rottensteiner, Jing-fei Dong
Publikováno v:
Journal of Thrombosis and Haemostasis
Background ADAMTS13, a plasma metalloprotease, cleaves von Willebrand factor (VWF) to regulate its function. Additionally, ADAMTS13 is thought to regulate lateral association of VWF multimers to form fibrillar structures through its free thiols. Obje
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3d223ddd6eb626937e35558731fd8938
http://europepmc.org/articles/PMC6916347
http://europepmc.org/articles/PMC6916347
Autor:
Peter Matthiessen, Hanspeter Rottensteiner, Friedrich Scheiflinger, Barbara Kink, Stephan Hann, Barbara Plaimauer, Anna Rathgeb, Stefan Kaufmann
Publikováno v:
Journal of Thrombosis and Haemostasis
Background The catalytic domain of ADAMTS13 possesses one Zn2+ and up to three putative Ca2+ binding sites and can be inactivated by chelating agents. Although replenishment with an appropriate metallic cation is thought to restore the enzyme's prote
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c0536c7f296a58ce056edcd474c23c46
https://doi.org/10.1111/jth.14440
https://doi.org/10.1111/jth.14440
Autor:
Peter Turecek, Barbara Plaimauer, H Gritsch, I.M. Lang, Adelheid Panzenboeck, Roela Sadushi-Kolici
Publikováno v:
European Heart Journal. 39
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7f5e2bf59d80f55b91cf678b13cf6f81
https://doi.org/10.1093/eurheartj/ehy565.p1621
https://doi.org/10.1093/eurheartj/ehy565.p1621
Autor:
Alexandra Schiviz, Barbara Plaimauer, W. Höllriegl, F. Scheiflinger, Hanspeter Rottensteiner, Stefan Kaufmann
Publikováno v:
Journal of Thrombosis and Haemostasis. 13:2053-2062
SummaryBackground Acquired thrombotic thrombocytopenic purpura (TTP) is caused by an autoantibody-mediated deficiency of the von Willebrand factor-cleaving protease ADAMTS-13. Acute episodes of the disease are treated with a combination of immunosupp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e8cea0e822c8b43469e4d8dc5905954b
https://doi.org/10.1111/jth.13137
https://doi.org/10.1111/jth.13137
Autor:
Hanspeter Rottensteiner, Alexandra Schiviz, Simon F. De Meyer, Claudia Tersteeg, Barbara Plaimauer, Friedrich Scheiflinger, Karen Vanhoorelbeke
Publikováno v:
Arteriosclerosis, Thrombosis, and Vascular Biology. 35:2336-2342
Objective— The metalloprotease ADAMTS13 (a disintegrin and metalloproteinase with a thrombospondin type 1 motif, member 13) regulates the size of von Willebrand factor multimers. A deficiency in ADAMTS13 activity is associated with the life-threate
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::40aa7ec13702371a40c56e127d73c0a5
https://doi.org/10.1161/atvbaha.115.306014
https://doi.org/10.1161/atvbaha.115.306014
Autor:
Ayami Isonishi, Yoshihiro Fujimura, Charles L. Bennett, Barbara Plaimauer, Masanori Matsumoto, Friedrich Scheiflinger
Publikováno v:
Transfusion. 55:2321-2330
BACKGROUND Plasma exchange (PE) is the first-line treatment for primary acquired thrombotic thrombocytopenic purpura (aTTP) with severe deficiency of ADAMTS13 activity (ADAMTS13:AC). Some patients are poor responders to PE, raising concern over multi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9ff01f179972137e1995b8e1811efdcf
https://doi.org/10.1111/trf.13182
https://doi.org/10.1111/trf.13182