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Results suggest that TP63 (show TP63 ELISA Kits) rs7631358 G > A and CSF1R rs10079250 A > G may affect the risk and prognosis of lung cancer in never-smoking females.
study, therefore, provided insights into the sequence-structure-function relationships of the M-CSF (show CSF1 ELISA Kits)/c-FMS interaction and of ligand/receptor tyrosine kinase (show RET ELISA Kits) interactions in general.
findings suggest that expression of wild-type CSF1R in some cells, whether achieved by mosaicism or chimerism, may confer benefit in hereditary diffuse leukoencephalopathy with axonal spheroids.
This review showed that CSF1R mutation is related to Hereditary diffuse leukoencephalopathy with axonal spheroids.
High CSF-1R expression is associated with Clear Cell Renal Cell Carcinoma.
The aim of this study was to compare the expression of CSF-1R in nasopharyngeal carcinoma to nasopharyngitis.
CSF1R mutations account for 10% of idiopathic adult onset leukodystrophies.
The frequencies of the rare alleles of CCR2 (show CCR2 ELISA Kits), ITGB3 (show ITGB3 ELISA Kits), and 3'UTR (show UTS2R ELISA Kits) of c-fms in the Old Believers are lower than in the sample of Novosibirsk Russians, and the rare allele of DBH (show DBH ELISA Kits) is more frequent
Data show crystal structures of CSF1-CSF1R ternary complexes, and propose a mechanism for their cooperative action that relies on the adoption by dimeric CSF-1 (show CSF1 ELISA Kits) of an active conformational state and homotypic receptor interactions.
peripheral nerve injury induced de novo expression of colony-stimulating factor 1 (CSF1 (show CSF1 ELISA Kits)) in injured sensory neurons. CSF1 (show CSF1 ELISA Kits) was transported to the spinal cord, where it targeted the microglial CSF1 receptor (CSF1R).
NMB or NMBR (show NMBR ELISA Kits) silencing inhibited M-CSF/c-Fms-mediated downstream signaling pathways like activation of ERK (show EPHB2 ELISA Kits) and Akt (show AKT1 ELISA Kits) and induction of D-type cyclins, cyclin D1 (show CCND1 ELISA Kits) and D2.
CSF-1R role in the development of erythro-myeloid progenitor cells in the developing fetal liver
analysis of CSF1R-deficient mice establishes a distinct role of CSF1R in fetal B-lymphopoiesis.
study, therefore, provided insights into the sequence-structure-function relationships of the M-CSF/c-FMS interaction and of ligand/receptor tyrosine kinase (show ERBB3 ELISA Kits) interactions in general.
this study shows that the iRhom2 (show RHBDF2 ELISA Kits)/ADAM17 (show ADAM17 ELISA Kits) pathway plays an important role in regulating CSF1R expression in the myeloid cell compartment at steady state, and in modulating development of monocytes/macrophages during their repopulation
this study shows that macrophage maturation is accompanied by colony-stimulating factor (show CSF2 ELISA Kits) 1hypomethylation, and illustrates for the first time the ability of protein kinase A to increase Csf1r DNA methylation (show HELLS ELISA Kits)
Targeting of macrophages by either CSF1R signaling blockade or clodronate liposome-mediated cell killing has marked inhibitory effects on established leukemia.
Cav-1 (show CAV1 ELISA Kits)-dependent c-Fms stabilization contributes to efficient osteoclastogenesis.
these data indicate that CSF-1R signalling is critical for maintaining cardiac tissue resident M2-polarized macrophage population
Macropinosomes might be a central mechanism coupling CSF-1R signaling and macrophage growth.
Data suggest that fms is not required for establishing a population of precursor cells during embryogenesis but is required for recruiting pigment cell precursors to xanthophore fates, with concomitant effects on melanophore organization.
The protein encoded by this gene is the receptor for colony stimulating factor 1, a cytokine which controls the production, differentiation, and function of macrophages. This receptor mediates most if not all of the biological effects of this cytokine. Ligand binding activates the receptor kinase through a process of oligomerization and transphosphorylation. The encoded protein is a tyrosine kinase transmembrane receptor and member of the CSF1/PDGF receptor family of tyrosine-protein kinases. Mutations in this gene have been associated with a predisposition to myeloid malignancy. The first intron of this gene contains a transcriptionally inactive ribosomal protein L7 processed pseudogene oriented in the opposite direction.
colony stimulating factor 1 receptor, formerly McDonough feline sarcoma viral (v-fms) oncogene homolog
, macrophage colony stimulating factor I receptor
, macrophage colony-stimulating factor 1 receptor
, colony stimulating factor 1 receptor
, csf1r protein
, macrophage colony-stimulating factor 1 receptor-like
, macrophage colony-stimulating factor receptor
, CD115 antigen
, CSF-1 receptor
, FMS proto-oncogene
, McDonough feline sarcoma viral (v-fms) oncogene homolog
, proto-oncogene c-Fms
, proto-oncogene fms
, fms proto-oncogene
, fms proto-oncogene homolog
, proto-oncogene c-Fms homolog
, proto-oncogene fms homolog