ArticleMethods in molecular biology (Clifton, N.J.)2013
Generation of bone marrow and fetal liver chimeric mice.
Article in Methods in molecular biology (Clifton, N.J.), 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.
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Who cites it
12 citing papers in PubMed.
- Hematopoietic EphA4 deficiency alters microglial heterogeneity and improves chronic spatial memory after brain injury.Scientific reports · 2025Article
- Microglia express Tie2 in a longitudinal imaging study of acute neural injury in mice.Molecular biology of the cell · 2025Article
- MicroRNAs regulate alveolar macrophage homeostasis and its function in lung fibrosis.Frontiers in immunology · 2025Article
- Skull bone marrow-derived immune cells infiltrate the injured cerebral cortex and exhibit anti-inflammatory properties.Brain, behavior, and immunity · 2025Article
- Conditional Deletion of EphA4 on Cx3cr1-Expressing Microglia Fails to Influence Histopathological Outcome and Blood Brain Barrier Disruption Following Brain Injury.Frontiers in molecular neuroscience · 2021Article
- A truncating mutation in the autophagy gene UVRAG drives inflammation and tumorigenesis in mice.Nature communications · 2019Article
- Rejection of adoptively transferred Eµ-TCL1 chronic lymphocytic leukemia cells in C57BL/6 substrains or knockout mouse lines.Leukemia · 2019Article
- Crk Adaptor Proteins Regulate NK Cell Expansion and Differentiation during Mouse Cytomegalovirus Infection.Journal of immunology (Baltimore, Md. : 1950) · 2018Article
- Article
- NLRP3 tyrosine phosphorylation is controlled by protein tyrosine phosphatase PTPN22.The Journal of clinical investigation · 2016Article
- The NLRP1 inflammasome attenuates colitis and colitis-associated tumorigenesis.Journal of immunology (Baltimore, Md. : 1950) · 2015Article
- Caspase-11 attenuates gastrointestinal inflammation and experimental colitis pathogenesis.American journal of physiology. Gastrointestinal and liver physiology · 2015Article
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Authors and funding
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Abstract
The creation of bone marrow and fetal liver chimeric mice has proven to be a valuable tool in the field of immunology. Chimeric mice are used to study the contribution of various cell types of hematopoietic versus non-hematopoietic origin in the course of an immune response. In this chapter, we describe a detailed method to obtain bone marrow or fetal liver chimeric mice and assess the efficiency of donor cells to repopulate the hematopoietic compartment of recipient mice.
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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.