Expression of IL‐7Rα and KLRG1 defines functionally distinct CD8 + T‐cell populations in humans

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Location: Deutsche Nationalbibliothek Frankfurt am Main

Extent: Online-Ressource

Language: Englisch

Bibliographic citation: Expression of IL‐7Rα and KLRG1 defines functionally distinct CD8 + T‐cell populations in humans ; volume:49 ; number:5 ; year:2019 ; pages:694-708 ; extent:15
European journal of immunology ; 49, Heft 5 (2019), 694-708 (gesamt 15)

Creator: Remmerswaal, Ester B. M.
Hombrink, Pleun
Nota, Benjamin
Pircher, Hanspeter
ten Berge, Ineke J. M.
van Lier, René A. W.
van Aalderen, Michiel C.

DOI: 10.1002/eji.201847897

URN: urn:nbn:de:101:1-2022072108515798370999

Rights: Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.

Last update: 15.08.2025, 7:19 AM CEST

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Remmerswaal, Ester B. M.
Hombrink, Pleun
Nota, Benjamin
Pircher, Hanspeter
ten Berge, Ineke J. M.
van Lier, René A. W.
van Aalderen, Michiel C.

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Expression of IL‐7R[alpha] and KLRG1 defines functionally distinct CD8+ T-cell populations in humans

CD4 T-cell help sustains distinct subpopulations in functional and dysfunctional CD8 T-cell responses.

TOX defines the degree of CD8+ T cell dysfunction in distinct phases of chronic HBV infection

SLAMF7 defines subsets of human effector CD8 T cells

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FGFR1 expression defines clinically distinct subtypes in pancreatic cancer

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Functionally distinct IFN‐γ + IL‐17A + Th cells in experimental autoimmune uveitis: T‐cell heterogeneity, migration, and steroid response

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Immunopathology caused by impaired CD8+ T‐cell responses

Immunopathology caused by impaired CD8 + T‐cell responses

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Expression of IL‐7Rα and KLRG1 defines functionally distinct CD8 + T‐cell populations in humans

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Other Objects (12)

Expression of IL‐7R[alpha] and KLRG1 defines functionally distinct CD8+ T-cell populations in humans

CD4 T-cell help sustains distinct subpopulations in functional and dysfunctional CD8 T-cell responses.

TOX defines the degree of CD8+ T cell dysfunction in distinct phases of chronic HBV infection

SLAMF7 defines subsets of human effector CD8 T cells

T-cell receptor avidity of polyclonal CD8+ T-cell populations

Lmo2 expression defines tumor cell identity during T‐cell leukemogenesis

FGFR1 expression defines clinically distinct subtypes in pancreatic cancer

Unbiased phenotypic identification of functionally distinct hematopoietic progenitors

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EWSR1-BEND2 fusion defines an epigenetically distinct subtype of astroblastoma

Immunopathology caused by impaired CD8+ T‐cell responses

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Expression of IL‐7R[alpha] and KLRG1 defines functionally distinct CD8+ T-cell populations in humans

CD4 T-cell help sustains distinct subpopulations in functional and dysfunctional CD8 T-cell responses.

TOX defines the degree of CD8+ T cell dysfunction in distinct phases of chronic HBV infection

SLAMF7 defines subsets of human effector CD8 T cells

T-cell receptor avidity of polyclonal CD8+ T-cell populations

Lmo2 expression defines tumor cell identity during T‐cell leukemogenesis

FGFR1 expression defines clinically distinct subtypes in pancreatic cancer

Unbiased phenotypic identification of functionally distinct hematopoietic progenitors

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EWSR1-BEND2 fusion defines an epigenetically distinct subtype of astroblastoma

Immunopathology caused by impaired CD8+ T‐cell responses

Immunopathology caused by impaired CD8 + T‐cell responses

Expression of IL‐7R[alpha] and KLRG1 defines functionally distinct CD8+ T-cell populations in humans

CD4 T-cell help sustains distinct subpopulations in functional and dysfunctional CD8 T-cell responses.

TOX defines the degree of CD8+ T cell dysfunction in distinct phases of chronic HBV infection

SLAMF7 defines subsets of human effector CD8 T cells

T-cell receptor avidity of polyclonal CD8+ T-cell populations

Lmo2 expression defines tumor cell identity during T‐cell leukemogenesis

FGFR1 expression defines clinically distinct subtypes in pancreatic cancer

Unbiased phenotypic identification of functionally distinct hematopoietic progenitors

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EWSR1-BEND2 fusion defines an epigenetically distinct subtype of astroblastoma

Immunopathology caused by impaired CD8+ T‐cell responses

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