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Expression of IL10R (show IL10RA ELISA Kits) subunits within the leukocyte population (CD45(+) cells) was significantly higher in primary brain tumors than in metastases.
As CD45 expression vs. SSc (show CYP11A1 ELISA Kits) is routinely measured in the diagnostics of acute leukemias.
A phosphosite within the SH2 Domain of Lck regulates its activation by CD45. A negative feedback loop that responds to signaling events tunes active Lck amounts and TCR sensitivity.
Our findings suggest that CD45 is a key regulator of BCR (show BCR ELISA Kits)-signaling thresholds mediated by T-cell help
we demonstrate for the first time the physiological existence of ct-CD45 in human plasma and show that it may be an extrinsic factor contributing to the maintenance of human T-cell quiescence.
Our findings suggest that if w/h ratio on SSC (show CYP11A1 ELISA Kits) versus CD45 plot is less than 1.6, AML (show RUNX1 ELISA Kits) may be considered, and if it is more than 1.6, ALL may be diagnosed. Using morphometric analysis of the blast cluster on SSC (show CYP11A1 ELISA Kits) versus CD45, it was possible to distinguish between ALL and AML (show RUNX1 ELISA Kits), and their subtypes.
Use of the common leukocyte marker CD45 increases the sensitivity of the diagnosis of lymphocytic myocarditis.
Review/Meta-analysis: Rheumatoid arthritis patients with PTPRC rs10919563 A allele show a poor response to anti-TNF (show TNF ELISA Kits) therapy.
Data suggest that CD41 and CD45 expression marked the onset of haemangioblastoma (HB) neovascularisation and the stepwise development of the angioformative period, and also the underlying therapeutic targets of anti-vascular treatment.
PTPRC has become the most replicated genetic biomarker of response to TNF (show TNF ELISA Kits) inhibitors
We identify differing roles for the phosphatase CD45 in innate and adaptive immune cells in intestinal inflammation. CD45 is required for optimal GM-CSF (show CSF2 ELISA Kits) and RA production in innate immune cells that affects alpha4beta7 expression and the homing of effector T cells to the intestine. Conversely, the absence of CD45 on adaptive immune cells leads to enhanced alpha4beta7 expression on T cells and homing to the intestine.
T cell receptor / TLR2 (show TLR2 ELISA Kits) co-stimulation expands CD25 (show IL2RA ELISA Kits)+CD45Rbhi T cells.
Both the number of lung CD31 (show PECAM1 ELISA Kits)-CD45-Sca-1 (show Ly6a ELISA Kits)+ cells and the expression levels of the Shh (show SHH ELISA Kits) signaling pathway were downregulated in the lung tissues of mice with pulmonary emphysema. These cells and Shh (show SHH ELISA Kits) signaling pathway are reactivated during acute adenovirus infection.
the transient upregulation of IL-1beta (show IL1B ELISA Kits) and PTPRC/CD45 during the early phase as well as the increased expression of collagen type I at later stages of repair and validate the differential expression of miR (show MLXIP ELISA Kits)-204, miR (show MLXIP ELISA Kits)-205, and miR (show MLXIP ELISA Kits)-31 in skin wounds.
Increased numbers of CD4 (show CD4 ELISA Kits)(+)CD45RA(-)FoxP3 (show FOXP3 ELISA Kits)(low) cells may cause an imbalance between Treg and Th17 cells that is mainly localized to the colon.
Aging induces loss of stemness with concomitant gain of myogenic properties of a pure population of CD34 (show CD34 ELISA Kits)+/CD45- muscle derived stem cells.
deletion of Pten in CD45-expressing cells induces development of T-cell acute lymphoblastic leukemia and lymphoma, but not other hematologic malignancies
A noncatalytic role for CD45 in regulating tonic, but not antigen-mediated, B-cell antigen receptor (BCR (show BCR ELISA Kits)) signaling through modulation of the function of the inhibitory coreceptor CD22 (show CD22 ELISA Kits), was identified.
The protein encoded by this gene is a member of the protein tyrosine phosphatase (PTP) family. PTPs are known to be signaling molecules that regulate a variety of cellular processes including cell growth, differentiation, mitosis, and oncogenic transformation. This PTP contains an extracellular domain, a single transmembrane segment and two tandem intracytoplasmic catalytic domains, and thus is classified as a receptor type PTP. This PTP has been shown to be an essential regulator of T- and B-cell antigen receptor signaling. It functions through either direct interaction with components of the antigen receptor complexes, or by activating various Src family kinases required for the antigen receptor signaling. This PTP also suppresses JAK kinases, and thus functions as a regulator of cytokine receptor signaling. Alternatively spliced transcripts variants of this gene, which encode distinct isoforms, have been reported.
receptor-type tyrosine-protein phosphatase C
, leukocyte common antigen, CD45
, protein tyrosine phosphatase, receptor type, C
, CD45 antigen
, leukocyte common antigen
, receptor-type tyrosine-protein phosphatase C-like
, T200 glycoprotein
, T200 leukocyte common antigen
, protein tyrosine phosphatase, receptor type, c polypeptide
, lymphocyte antigen 5
, lymphocyte common antigen
, Protein tyrosine phosphatase, receptor-type, c polypeptide
, leucocyte common antigen
, leukocyte common antigen A
, leukocyte common antigen B
, membrane tyrosine phosphatase