Tracking distinct microglia subpopulations with photoconvertible Dendra2 in vivo
- Standort
-
Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
-
1742-2094
- Umfang
-
Online-Ressource
- Sprache
-
Englisch
- Anmerkungen
-
online resource.
- Erschienen in
-
Tracking distinct microglia subpopulations with photoconvertible Dendra2 in vivo ; volume:18 ; number:1 ; day:15 ; month:10 ; year:2021 ; pages:1-13 ; date:12.2021
Journal of neuroinflammation ; 18, Heft 1 (15.10.2021), 1-13, 12.2021
- Urheber
-
Miller, Eric B.
Karlen, Sarah J.
Ronning, Kaitryn E.
Burns, Marie E.
- Beteiligte Personen und Organisationen
-
SpringerLink (Online service)
- DOI
-
10.1186/s12974-021-02285-x
- URN
-
urn:nbn:de:101:1-2021122921370429179486
- Rechteinformation
-
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
-
15.08.2025, 07:32 MESZ
Datenpartner
Dieses Objekt wird bereitgestellt von:
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Beteiligte
- Miller, Eric B.
- Karlen, Sarah J.
- Ronning, Kaitryn E.
- Burns, Marie E.
- SpringerLink (Online service)
Ähnliche Objekte (12)
Distribution and prognostic impact of microglia/macrophage subpopulations in gliomas
Distribution and prognostic impact of microglia/macrophage subpopulations in gliomas
Cytokine profiling in active and quiescent SLE reveals distinct patient subpopulations
Transcriptionally defined amygdala subpopulations play distinct roles in innate social behaviors
Tracking and ablating subpopulations of epiblast cells in the chick embryo
Single‐cell transcriptomics reveals distinct inflammation‐induced microglia signatures
Single‐cell transcriptomics reveals distinct inflammation‐induced microglia signatures
Functionally distinct and selectively phosphorylated GPCR subpopulations co-exist in a single cell
Inflammation leads to distinct populations of extracellular vesicles from microglia
Chimeric GPCRs mimic distinct signaling pathways and modulate microglia responses
Computational identification of surface markers for isolating distinct subpopulations from heterogeneous cancer cell populations
Influenza A virus reassortment in mammals gives rise to genetically distinct within-host subpopulations
Distribution and prognostic impact of microglia/macrophage subpopulations in gliomas
Distribution and prognostic impact of microglia/macrophage subpopulations in gliomas
Cytokine profiling in active and quiescent SLE reveals distinct patient subpopulations
Transcriptionally defined amygdala subpopulations play distinct roles in innate social behaviors
Tracking and ablating subpopulations of epiblast cells in the chick embryo
Single‐cell transcriptomics reveals distinct inflammation‐induced microglia signatures
Single‐cell transcriptomics reveals distinct inflammation‐induced microglia signatures
Functionally distinct and selectively phosphorylated GPCR subpopulations co-exist in a single cell
Inflammation leads to distinct populations of extracellular vesicles from microglia
Chimeric GPCRs mimic distinct signaling pathways and modulate microglia responses
Computational identification of surface markers for isolating distinct subpopulations from heterogeneous cancer cell populations
Influenza A virus reassortment in mammals gives rise to genetically distinct within-host subpopulations
Distribution and prognostic impact of microglia/macrophage subpopulations in gliomas
Distribution and prognostic impact of microglia/macrophage subpopulations in gliomas
Cytokine profiling in active and quiescent SLE reveals distinct patient subpopulations
Transcriptionally defined amygdala subpopulations play distinct roles in innate social behaviors
Tracking and ablating subpopulations of epiblast cells in the chick embryo
Single‐cell transcriptomics reveals distinct inflammation‐induced microglia signatures
Single‐cell transcriptomics reveals distinct inflammation‐induced microglia signatures
Functionally distinct and selectively phosphorylated GPCR subpopulations co-exist in a single cell
Inflammation leads to distinct populations of extracellular vesicles from microglia
Chimeric GPCRs mimic distinct signaling pathways and modulate microglia responses
Computational identification of surface markers for isolating distinct subpopulations from heterogeneous cancer cell populations