TCR activation mimics CD127lowPD-1high phenotype and functional alterations of T lymphocytes from septic shock patients
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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1364-8535
- Extent
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Online-Ressource
- Language
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Englisch
- Notes
-
online resource.
- Bibliographic citation
-
TCR activation mimics CD127lowPD-1high phenotype and functional alterations of T lymphocytes from septic shock patients ; volume:23 ; number:1 ; day:17 ; month:4 ; year:2019 ; pages:1-14 ; date:12.2019
Critical care ; 23, Heft 1 (17.4.2019), 1-14, 12.2019
- Creator
-
Mouillaux, Julie
Allam, Camille
Gossez, Morgane
Uberti, Thomas
Delwarde, Benjamin
Hayman, Jack
Rimmelé, Thomas
Textoris, Julien
Monneret, Guillaume
Peronnet, Estelle
Venet, Fabienne
- Contributor
-
SpringerLink (Online service)
- DOI
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10.1186/s13054-018-2305-5
- URN
-
urn:nbn:de:101:1-2019051123160505972806
- Rights
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
14.08.2025, 10:51 AM CEST
Data provider
This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Mouillaux, Julie
- Allam, Camille
- Gossez, Morgane
- Uberti, Thomas
- Delwarde, Benjamin
- Hayman, Jack
- Rimmelé, Thomas
- Textoris, Julien
- Monneret, Guillaume
- Peronnet, Estelle
- Venet, Fabienne
- SpringerLink (Online service)
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Chronic TCR-MHC (self)-interactions limit the functional potential of TCR affinity-increased CD8 T lymphocytes
Recognition of renal cell carcinoma by CD8+ and CD4+ TCR-engineered T lymphocytes
Molecular alterations in the TCR signaling pathway in patients with aplastic anemia
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TcR
Effects of desialyation on TCR-cross-linking and antigen sensitivity of CD8 positive T lymphocytes
Globally shared TCR repertoires within the tumor-infiltrating lymphocytes of patients with metastatic gynecologic cancer
P71. Adoptive transfer of TCR gene-transduced lymphocytes targeting MAGE-A4 for refractory esophageal cancer
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