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1 in the plant-parasitic nematode Pratylenchus penetrans.
2 hemolytic and hemoxidative activities in M. penetrans.
3 ce to the root-lesion nematode (Pratylenchus penetrans), a migratory endoparasite of many crops, have
6 logical differences were observed between M. penetrans and M. iowae by scanning electron microscopy (
7 The Triton X-100-insoluble fractions of M. penetrans and M. iowae consisted of similar structures t
11 cluster formation were inhibited by anti-M. penetrans antibodies, suggesting the involvement of spec
14 ent during cell division was observed for M. penetrans by microcinematography, and this suggests a ro
15 Here, we describe a 78-kDa protein from M. penetrans, designated MYPE9110, that exhibits sequence s
17 pse microcinematography of two strains of M. penetrans, GTU-54-6A1 and HF-2, and two serovars of M. i
20 comparison, live Mycoplasma fermentans or M. penetrans infection for 4 to 5 weeks induced malignant t
24 ively, these findings strongly imply that P. penetrans is an ancient member of the Bacillus group.
25 Additionally, all analyses revealed that P. penetrans is surprisingly more closely related to the sa
29 pression of TNF-alpha in cells induced by M. penetrans lipid extract of PK-digested LAMPs is associat
31 peritoneal (TEP) macrophages treated with M. penetrans lipid extract of proteinase K (PK)-digested LA
33 ated membrane proteins (LAMPs) of Mycoplasma penetrans rapidly induced macrophages to produce proinfl
35 alyses of 33 bacterial species (including P. penetrans) using concatenation of 40 housekeeping genes,
36 ca. 65-kDa fibronectin-binding protein of M. penetrans was eluted following Sepharose-fibronectin aff
37 esian methods to the resulting data sets, P. penetrans was found to cluster tightly, with a high leve
38 copy demonstrated that the interaction of M. penetrans with target cells triggers a signal that cause
39 udies, we incubated different isolates of M. penetrans with various RBC species and observed hemolyti
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