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TranscriptomicsCX3CR1/Fractalkine receptor expression separates memory CD8+ T cells with distinct functional profiles (expression)
Memory T cells are important for protective immunity against infectious microorganisms. Such protection is achieved by cooperative action of memory T cell populations that differ in their tissue localization and functionality. We report on the identification of the fractalkine receptor CX3CR1 as mar...
ORGANISM(S): Mus musculus 
2016-06-10 | E-GEOD-63118 | biostudies-arrayexpress
TranscriptomicsCX3CR1/Fractalkine receptor expression separates memory CD8+ T cells with distinct functional profiles (RNA-seq)
Memory T cells are important for protective immunity against infectious microorganisms. Such protection is achieved by cooperative action of memory T cell populations that differ in their tissue localization and functionality. We report on the identification of the fractalkine receptor CX3CR1 as mar...
ORGANISM(S): Homo sapiens 
2016-06-10 | E-GEOD-63144 | biostudies-arrayexpress
ProteomicsInvestigation of cerebrum proteomic changes in CX3CR1 deficient middle aged mouse
The aging brain shows changes in microglial function, morphology, and phenotype, indicating chronic microglial activation. CX3CR1 is crucial for microglial chemotaxis, phagocytosis, and activation. However, its exact role in the aging brain is not well understood. In this study, we examined the expr...
ORGANISM(S): Mus musculus (Mouse) 
2025-07-05 | PXD058961 | Pride
Cerebrum Mouse Cx3cr1 Lc-ms/ms 
TranscriptomicsCX3CR1/Fractalkine receptor expression separates memory CD8+ T cells with distinct functional profiles
This SuperSeries is composed of the SubSeries listed below. Refer to individual Series
ORGANISM(S): Mus musculus 
2016-06-10 | E-GEOD-63147 | biostudies-arrayexpress
TranscriptomicsTranscription profile of CD103- vs CD103+ dendritic cells derived from CX3CR1+c-kit+- bone marrow cells (M1993 M2067)
We hypothesize that under homeostatic as well as inflammatory conditions circulating monocytes and/or their bone marrow-derived progenitors might contribute to the replenishment of CD103+ and CD103- DC in lymphoid and non-lymphoid compartments. To that end, bone marrow cells from CX3CR1+/gfp C57BL/6...
ORGANISM(S): Mus musculus 
2008-12-17 | E-GEOD-10882 | biostudies-arrayexpress
GenomicsTranscriptional profiling of mice decidual CX3CR1+ and CX3CR1- primed CD8 T cells
Transcriptional profiling of mice decidual CX3CR1+ and CX3CR1- primed CD8 T cells
PRJNA1495314 | ENA
GenomicsCx3cr1-deficient microglia exhibit a premature aging transcriptome
Cx3cr1-deficient microglia exhibit a premature aging transcriptome
PRJNA542087 | ENA
GenomicsCx3cr1-deficient microglia exhibit a premature aging transcriptome
Cx3cr1-deficient microglia exhibit a premature aging transcriptome
PRJNA545148 | ENA
TranscriptomicsAn abundant tissue macrophage population in the adult murine heart
GFP+CD45+CD11b+ cells were isolated from from heterozygous adult Cx3cr1-GFP/+ mouse hearts, spleens and brains by fluorescence activated cell sorting to prepare RNA for gene array analysis.
Three independently isolated populations GFP+ (CD45+CD11b+) cells for each tissue were used as replicates.
ORGANISM(S): Mus musculus 
2012-04-25 | E-MEXP-3347 | biostudies-arrayexpress
GenomicsChromatin accessibility landscapes of CX3CR1+ effector , CX3CR1- Ly108- exhausted, or Ly108+ progenitor CD8 T cells during chronic viral infection.
Chromatin accessibility landscapes of CX3CR1+ effector , CX3CR1- Ly108- exhausted, or Ly108+ progenitor CD8 T cells during chronic viral infection.
PRJNA630086 | ENA
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