INT69029
From wiki-pain
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Sentences Mentioned In
Key: | Protein | Mutation | Event | Anatomy | Negation | Speculation | Pain term | Disease term |
In this gate, CECs were identified as positive for the specific marker CD146 (melanoma cell adhesion molecule (MCAM), a cell-adhesion molecule used as a marker for endothelial cell lineage) and negative for the hematopoietic marker CD45 (PTPRC, present on all differentiated hematopoietic cells; Figure 1). | |||||||||||||||
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The identity of gated cells was further confirmed to be microglial, as opposed to intravascular neutrophils or monocytes, by their lower levels of CD45 expression (Sedgwick et al., 1991) in control and injured rats (data not shown). | |||||||||||||||
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In this gate, CECs were identified as positive for the specific marker CD146 (melanoma cell adhesion molecule (MCAM), a cell-adhesion molecule used as a marker for endothelial cell lineage) and negative for the hematopoietic marker CD45 (PTPRC, present on all differentiated hematopoietic cells; Figure 1). | |||||||||||||||
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Immunoreactivity with vs38c, CD79a, kappa light chain, and IgG was readily identified in tumor cells; while only focal cells expressed CD20 and LCA (CD45RB). | |||||||||||||||
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By gating intact leukocytes on forward scatter (FSC) and side scatter (SSC) properties as well as by their CD16 and CD45 signals (Figure 1), leukocytes were separated into neutrophils (R4 in Figure 1D), eosinophils (R8 in Figure 1C), basophils (R5 in Figure 1B), monocytes (R6 in Figure 1B) and lymphocytes (R7 in Figure 1B) [24,25]. | |||||||||||||||
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All samples were labeled with CD16-Pcy5 (IM2642, Immunotech, Marseille, France) and CD45-ECD (IM2710, Immunotech) for 15 minutes at RT. | |||||||||||||||
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Blast cells were positive for leukocyte common antigen (CD 45). | |||||||||||||||
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Immunohistochemically the lesion was diffuse strong positive with CD99 and NSE, negative with LCA, pancytokeratin, vimentin, desmin, smooth muscle actin, chromogranine A and S-100. | |||||||||||||||
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Consistent with other studies using a similar approach [49], preliminary experiments using the same conditioning regimen and transplanting CD45.1+ bone marrow into irradiated CD45.1? | |||||||||||||||
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Consistent with other studies using a similar approach [49], preliminary experiments using the same conditioning regimen and transplanting CD45.1+ bone marrow into irradiated CD45.1? | |||||||||||||||
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T cell receptor and for CD45 contains predominantly ?? | |||||||||||||||
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Tumor cells were negative for cytokeratin, CD45, CD20, CD3, CD30, CD68, CD35 and CD1a; Ki-67 was positive in about 15% of the cells. | |||||||||||||||
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Stratification with respect to the expression of CD45 indicates that specifically the CD45dimCD34+KDR+ cell population correlates with cardiovascular disease and is significantly regulated by statin treatment, suggesting that the CD45dim fraction contains the prognostic relevant EPC populations. | |||||||||||||||
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The Ki-67 index (MIB-1) was >50%, but other markers such as cytokeratin AE1/AE3, smooth muscle actin, S-100 protein, CD34, and CD45 were negative. | |||||||||||||||
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As expected, CD34, CD45 and TERT could not be detected on any examined time point [see Additional file 2].
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Since recent studies suggest that particularly the fraction of CD45? | |||||||||||||||
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This will exclude CD45? | |||||||||||||||
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Quantification was performed strictly following the sequential gating strategy [13] and CD34+ cells were additionally subdivided in CD45? | |||||||||||||||
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The lower limit of CD45 expression is adapted from a CD34 vs. | |||||||||||||||
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The Ki-67 index (MIB-1) was >50%, but other markers such as cytokeratin AE1/AE3, smooth muscle actin, S-100 protein, CD34, and CD45 were negative. | |||||||||||||||
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General Comments
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