316) xposure, in order to understand how these cells may transition from their normal dev |
317) cedures for further enrichment of myeloid cells using CD11b+ magnetic beads, followe |
318) has limited function in the innate-like T cells using ROSA26floxed-Stop-tdTomato rep |
319) tively inhibit the growth of CALR mutated cells using high-throughput drug screening |
320) Human bronchial epithelial cells (HBECs) and mouse tracheal epithelia |
321) Primary human bronchial epithelial cells (HBECs) from nonsmokers and smokers |
322) Two major cell types, Hepatic Stellate Cells (HSCs) and Portal Fibroblasts (PFs) |
323) sition through activated hepatic stellate cells (HSCs) and the expansion of closely |
324) to be expressed exclusively in outer hair cells (OHCs) of the inner ear. |
325) sumptive postsynaptic sites on outer hair cells (OHCs) were labeled, but absent from |
326) human donor peripheral blood mononuclear cells (PBMCs) exposed to BpOmpW for 7 day |
327) d IgG-ASC in peripheral blood mononuclear cells (PBMCs). |
328) Selection acting on germ cells at any stage from the diploid germ c |
329) ation indicate that microcolonies move by cells at the base of the structure, attach |
330) inflamed gingiva-derived mesenchymal stem cells could be effective in terms of osteo |
331) d ex vivo expansion of tumor-primed CD4+T cells could induce effective tumor specifi |
332) Invariant natural killer T (iNKT) cells differentiate in the thymus into NKT |
333) Innate-like T cells differentiate into mature functional |
334) rotocol for immature naïve mouse CD4+ T cells, including details for splenocyte is |
335) Innate-like T cells, including invariant NKT cells, muco |
336) ent of fluid, ions, molecules, and immune cells into and out of the brain parenchyma |
337) cytes and effective infiltration of the T cells into tumor tissue. |
338) Loss of GPR171 in T cells leads to hyperactivity to antigen st |
339) differentiation program of skeletal stem cells leads to indecorous skeletogenesis. |
340) the chemosensitivity of colorectal cancer cells regardless of the microsatellite sta |
341) d enhance the chemosensitivity of tumoral cells regardless of the microsatellite sta |
342) lucose and glutamine by immune and cancer cells, respectively. |
343) or the upper route, subpolar, and abyssal cells, respectively. |
344) g 3D/2D Rb+-incorporated perovskite solar cells show a peak PCE of >20%, which is |
345) isease is transplantable and mutCALR stem cells show proliferative advantage when co |
346) dual allelic mutants in CRACR2A-deleted T cells showed that the CRACR2AE278D mutant |
347) By contrast, cancer cells showed the highest uptake of glutami |
348) nd basal mitochondrial oxidation of CD4+T cells, suggesting a role of high salt in e |
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