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- T淋巴细胞活化抗原T lymphocyte activation antigen
- 一种新的恒河猴T淋巴细胞活化抗原PTA1A Novel Antigen PTA1 Expressed on Rhesus Monkey Activated T Lymphocytes
- 结论：粘附状态抗CD3单抗比游离状态抗CD3单抗具有更强的诱导人T淋巴细胞活化增殖能力。Immobile CD 3McAb was more potent on activating T lymphocytes than soluble CD 3McAb.
- 进一步用小鼠T淋巴细胞活化体系的研究发现，未经ConA激活的T淋巴细胞中，BAF复合物和转录因子NF1/CTF不表达或低水平表达。Further, in the mouse spleen T lymphocytes activation system, it was found that, without activation by ConA, there were no or extremely low level of expression of BAF complex and NF1/CTF in the spleen T lymphocytes.
- 极晚期活化抗原1-5very late activation antigen 1-5(VLA 1-5)
- 淋巴细胞活化lymphocyte activation
- 淋巴细胞活化因子lymphocyte activating factor (LAF)
- 血小板/T细胞活化抗原1融合蛋白的表达、纯化及其配体的初步鉴定Research on a Novel Platelet and T Cell Activation Antigen 1 (PTA1) Ligand by PTA1/Ig Fusion Protein
- B淋巴细胞活化因子B cell activating factor belonging to the TNF family(BAFF)
- 结肠癌细胞系Colo205细胞膜表面表达血小板和T细胞活化抗原1的配体Ligand of platelet and T cell activation antigen 1 (PTA1) expressed on Colo205 cell surface
- 妊高征患者胎盘床蜕膜T淋巴细胞亚群的表达与临床意义。The expression of T-lymphocyte subpopulations of decidual-placental bed in pregnancy with pre-eclampsia and clinical significance.
- 淋巴细胞活化决定簇LAD; Lads; lymphocyte activating determinants; lymphocyte-activating determinant
- 人血小板/T细胞活化抗原PTA1/Ig融合蛋白表达载体的构建、表达及鉴定Construction and expression of a novel human platelet/T cell activation antigen 1 (PTA1) fusion protein in COS 7 cells
- T淋巴细胞群T-lymphocytes
- 脾T淋巴细胞spleen T lymphocytes
- 类风湿关节炎患者关节滑膜液淋巴细胞活化标志的表达及意义Expression of Activation Markers on Lymphocytes in Synovial Fluid From Patients with Rheumatoid Arthritis
- 目的：探讨单纯疱疹病毒胸苷激酶基因（HSV－tk）、B细胞活化抗原（B7）联合基因治疗乳腺癌的协同性。Objective: To explore the therapeutic value of HSV tk expression in the presence of B7 in treatment of breast cancer. Methods: We genetically modified Line SHZ 88, a mammary cancer line.
- T淋巴细胞转化T -lymphocyte transformation
- T淋巴细胞计数T lymphocyte count
- 将纯化的PTD BCR/ABL融合蛋白与CML患者外周血单个核细胞 (PBMC)体外共孵育 ,用流式细胞仪分别检测CD4 + 、CD8+ T细胞上活化抗原CD2 5的表达。coli . The PBMCs from CML patients were stimulated in vitro with purified PTD BCR/ABL antigen and then expression of the activation antigen CD25 on CD8 + and CD4 + T cells after stimulation was detected by flow cytometry (FCM).
