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1 rom the presence of a vascular smooth muscle cell coat.
2 erular capillary development, arterial mural cell coating, and lymphatic vessel development, required
4 2 (P2), outer hair cell bundles have a dense cell coat, but have lost many of the lateral links seen
8 encodes rhabduscin's aglycone, and bacterial cell-coated immunosuppressants could be a general strate
10 r maturation, mediating formation of a mural cell coat investing infarct neovessels and protecting fr
11 thered aggrecan drops significantly when the cell coat is enriched with bottlebrush proteoglycans.
15 fore, this work has demonstrated a promising cell coating method for the display of aptamers for enha
16 our study, we developed an in vitro model of cell-coated microsized hydrogel spheres (MHSs) which all
21 ure scar, infarct neovessels acquire a mural cell coat that contributes to the stabilization of the m
22 cultured on human umbilical vein endothelial cell-coated transwells in the presence or absence of buc
23 1 and immobilized IgG or human breast cancer cells coated with a therapeutic mAb (trastuzumab) secret
24 ukin (IL)-2 or IL-12 and human breast cancer cells coated with an antitumor antibody (trastuzumab).
25 d in antiphospholipid syndrome, or red blood cells coated with anti-(alpha)-Rh(D) antibodies that med
27 HNE-induced apoptosis was compared in HLE-B3 cells coated with anti-RLIP76 IgG or preimmune IgG, by c
29 endent cellular cytotoxicity against stromal cells coated with donor-specific antibodies in vitro.
30 eads that are specifically bound to cultured cells coated with extracellular matrix proteins or integ
32 the intravascular survival of autologous red cells coated with human recombinant IgG antibody contain
34 thereby enhancing leukocyte killing of tumor cells coated with iC3b via naturally occurring antitumor
36 ponsive to LCMV NP 118-126 recognized target cells coated with NP 118-126 peptides derived from LCMV,
39 alveolar macrophage cell line and parasitic cells coated with SOWgp showed that the addition of anti
41 ls had increased activation against lymphoma cells coated with the clinically relevant anti-CD20 Abs
42 ct ex vivo cytotoxic activity against target cells coated with the epitope peptide, demonstrating tha
43 l killer (NK) cell-mediated killing of tumor cells coated with the Fc-optimized CD33 antibody DLE-HuM
44 molar levels of pE4R but did not lyse target cells coated with the self peptide at micromolar levels.
45 ed whether DCs phagocytosing killed lymphoma cells coated with tumor-specific antibody could elicit a
46 ice induced antiviral CTLs that lysed target cells coated with two of the three immunodominant epitop
48 report the development of biomimetic cancer cell coated zeolitic imidazolate frameworks (ZIFs) for t