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1 oth hemolytic and hemoxidative activities in M. penetrans.
2 phological differences were observed between M. penetrans and M. iowae by scanning electron microscop
3      The Triton X-100-insoluble fractions of M. penetrans and M. iowae consisted of similar structure
4            Like other polarized mycoplasmas, M. penetrans and M. iowae have terminal organelles with
5                  SEM and light microscopy of M. penetrans and M. iowae showed the presence of membran
6 and cluster formation were inhibited by anti-M. penetrans antibodies, suggesting the involvement of s
7                                              M. penetrans bound selectively to immobilized fibronecti
8 lament during cell division was observed for M. penetrans by microcinematography, and this suggests a
9      Here, we describe a 78-kDa protein from M. penetrans, designated MYPE9110, that exhibits sequenc
10 -lapse microcinematography of two strains of M. penetrans, GTU-54-6A1 and HF-2, and two serovars of M
11 In comparison, live Mycoplasma fermentans or M. penetrans infection for 4 to 5 weeks induced malignan
12      Here we report the characteristics of 4 M. penetrans isolates from the urine of immunocompetent
13 mouse red blood cells (RBCs), indicated that M. penetrans lacked hemolytic activity.
14              Our study demonstrates that the M. penetrans lipid extract of PK-digested LAMP is a pote
15                                              M. penetrans lipid extract of PK-digested LAMPs activate
16  expression of TNF-alpha in cells induced by M. penetrans lipid extract of PK-digested LAMPs is assoc
17 f TNF-alpha in TEP macrophages stimulated by M. penetrans lipid extract of PK-digested LAMPs.
18 te peritoneal (TEP) macrophages treated with M. penetrans lipid extract of proteinase K (PK)-digested
19                                          All M. penetrans strains displayed hemolysis after 2 to 3 da
20    We conclude that subtle differences among M. penetrans strains may be critical for this organism t
21  A ca. 65-kDa fibronectin-binding protein of M. penetrans was eluted following Sepharose-fibronectin
22 roscopy demonstrated that the interaction of M. penetrans with target cells triggers a signal that ca
23  studies, we incubated different isolates of M. penetrans with various RBC species and observed hemol