Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Sarah Matko"'
Autor:
Marcus Odendahl, Julia Manderla, Sarah Matko, Maria Bonsack, Martin Bornhäuser, Torsten Tonn, Marc Schmitz
Publikováno v:
European Journal of Immunology. 48:1400-1411
Antigen-specific T cells isolated from healthy individuals (HIs) have shown great therapeutic potential upon adoptive transfer for the treatment of viremia in immunosuppressed patients. The lack of comprehensive data on the prevalence and characteris
Autor:
Marcus Odendahl, Madeleine Teichert, Sarah Matko, Martin Bornhäuser, Torsten Tonn, Marc Schmitz, Antje Tunger
Publikováno v:
Cytometry Part A. 91:1001-1008
The advent of novel strategies to generate leukemia-associated-antigen (LAA)-specific T cells for adoptive immunotherapies creates a demand for standardized good laboratory practice (GLP)-compliant enumeration assays to provide a secure clinical envi
Publikováno v:
Multiple Sclerosis and Related Disorders. 38:101859
Background Fingolimod (FTY) applied as treatment regimen of relapsing-remitting multiple sclerosis (RRMS) induces downregulation of sphingosine-1-phosphate receptors on the lymphocytes. As a result C C chemokine receptor type 7 (CCR7) expressing lymp
Autor:
Sarah, Matko, Julia, Manderla, Maria, Bonsack, Marc, Schmitz, Martin, Bornhauser, Torsten, Tonn, Marcus, Odendahl
Publikováno v:
European journal of immunology. 48(8)
Antigen-specific T cells isolated from healthy individuals (HIs) have shown great therapeutic potential upon adoptive transfer for the treatment of viremia in immunosuppressed patients. The lack of comprehensive data on the prevalence and characteris
Autor:
Sarah, Matko, Madeleine, Teichert, Antje, Tunger, Marc, Schmitz, Martin, Bornhauser, Torsten, Tonn, Marcus, Odendahl
Publikováno v:
Cytometry. Part A : the journal of the International Society for Analytical Cytology. 91(10)
The advent of novel strategies to generate leukemia-associated-antigen (LAA)-specific T cells for adoptive immunotherapies creates a demand for standardized good laboratory practice (GLP)-compliant enumeration assays to provide a secure clinical envi
Autor:
Cornelia S. Link, Lothar Germeroth, Denise Kühn, Elke Rücker-Braun, Martin Bornhäuser, Antje Tunger, Sevina Dietz, Marc Schmitz, Ezio Bonifacio, Falk Heidenreich, Rebekka Wehner, Michael Bachmann, Malte von Bonin, Torsten Tonn, Dirk H. Busch, Sarah Matko, Johannes Schetelig, Magdalena Nauerth, Marcus Odendahl, Anne Eugster
Publikováno v:
Leukemia & Lymphoma 58(2016)5, 1246-1249
Summary: In summary, we demonstrated that the expansion of WT1 peptide-specific CD8+ T cells by peptide-loaded MoDCs followed by streptamer-based selection represents an attractive strategy to significantly enrich such T cells prior to cloning. By us
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a334718c7e410b813bada85e453bd725
https://www.hzdr.de/publications/Publ-26305-1
https://www.hzdr.de/publications/Publ-26305-1
Publikováno v:
Zelluläre Diagnostik und Therapie ISBN: 9783110344066
Zelluläre Diagnostik und Therapie
Zelluläre Diagnostik und Therapie
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5e4cf76221e09fb0a81cfb8e9a5ea6f1
https://doi.org/10.1515/9783110344073-018
https://doi.org/10.1515/9783110344073-018
Autor:
Sarah Matko, Karl Hackmann, Andreas Rump, Evelin Schröck, Barbara Klink, Nataliya Di Donato, Eva-Maria Gerlach, Maja von der Hagen
We report about the partial de novo loss of GLRB and GRIA2 in an individual with intellectual disability (ID). No additional mutations were found in either gene. GLRB itself does not seem to be a good candidate as it causes autosomal recessive hypere
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e558a82c252fe11cfc4783d8605b4390
https://europepmc.org/articles/PMC3522202/
https://europepmc.org/articles/PMC3522202/
Publikováno v:
Blood. 126:5428-5428
While adoptive transfer of virus antigen specific T cells has shown to be effective in therapy of resistant recurrent viremia which is frequently associated with the lack of protective immunity following hematopoietic stem cell transplantation, the t
Publikováno v:
Cytotherapy. 16:S26-S27