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1                                              BCV Drep RNA that lacked a poly(A) tail did not replicat
2                                              BCV is a prototype for the coronaviruses that express an
3                     MAb Z3A5 reacted with 90 BCV isolates from the United States and was an effective
4        This is the first identification of a BCV packaging signal.
5 y with Z3A5 and in situ hybridization with a BCV nucleoprotein cDNA probe.
6 (5) PFU of IHD-J-Luc VACV without additional BCV treatment.
7                                          All BCV-treated mice that survived challenge were also prote
8                                          All BCV-treated mice that survived infection were protected
9  the nucleoprotein gene sequences of ECV and BCV was observed.
10 chi Calossi Versaci front index (BCV(f)) and BCV back index (BCV(b)), root mean square of front and b
11      RNA transcripts were packaged into both BCV and MHV virions when the cloned region was appended
12 g superior vena cava (SVC), brachiocephalic (BCV), subclavian (SCV) and internal jugular vein (IJV).
13 s used to study the effect of brincidofovir (BCV) in normal and immune-deficient (nu/nu) mice infecte
14 stchallenge administration of brincidofovir (BCV, CMX001) was studied in normal and immune-deficient
15 rucella replication in the ER is followed by BCV conversion into a compartment with autophagic featur
16 or two group II viruses, bovine coronavirus (BCV) and mouse hepatitis coronavirus (MHV).
17 igenic relationship with bovine coronavirus (BCV) and porcine hemagglutinating encephalomyelitis viru
18         We have used the bovine coronavirus (BCV) as a model to study interactions between the viral
19          A region of the bovine coronavirus (BCV) genome that functions as a packaging signal has bee
20 spike protein subunit of bovine coronavirus (BCV) reacted with the virus in formalin-fixed intestines
21 nst the spike protein of bovine coronavirus (BCV), on an indirect fluorescent antibody test.
22 eplaced by the 3' UTR of bovine coronavirus (BCV), which diverges overall by 31% in nucleotide sequen
23                   Using previously described BCV primers, the N protein gene of isolate NC99 was ampl
24 ine (BCNU), cyclophosphamide, and etoposide (BCV) preparative regimen (27 patients) and an ABMT at 16
25  a published nucleoprotein gene sequence for BCV (Mebus isolate), we arbitrarily designed two primers
26         Replication of the defective genomes BCV Drep and MHV MIDI-C, along with several mutants, was
27 aci front index (BCV(f)) and BCV back index (BCV(b)), root mean square of front and back corneal surf
28 rface, Baiocchi Calossi Versaci front index (BCV(f)) and BCV back index (BCV(b)), root mean square of
29                                   Initiating BCV treatment earlier was more efficient in reducing vir
30             A three-dose regimen of 20 mg/kg BCV administered every 48 h starting either on day 1 or
31     Postchallenge administration of 20 mg/kg BCV rescued normal and immune-deficient mice partially r
32                    In immune-deficient mice, BCV extended survival.
33                    In immune-deficient mice, BCV protected animals from lethality and reduced viral l
34 as an effective reagent for the diagnosis of BCV.
35  sequence of NC99 and published sequences of BCV (Mebus and F15 strains) and human coronavirus (strai
36 of both ECV isolates were similar to that of BCV as determined by sodium dodecyl sulfate-polyacrylami
37                           The data show that BCV controls viral replication at the site of challenge
38            Together, these data suggest that BCV protects immunocompetent and partially T cell-recons
39 CUAAAC element which occurs only once in the BCV 5' untranslated region was either deleted or complet
40  substitution of a particular portion of the BCV 3' UTR for the corresponding region of the MHV 3' UT
41                The data demonstrate that the BCV genome contains a sequence that is conserved at both
42 nd redirecting Golgi-derived vesicles to the BCV.
43  Specific host protein interactions with the BCV 3' UTR [287 nt plus poly(A) tail] were identified us
44 ely related genetically and antigenically to BCV and will be a new member of antigenic group 2 of the
45  by forming the Brucella-containing vacuole (BCV), which traffics from the endocytic compartment to t
46 with 10(4) PFU of IHD-J-Luc and treated with BCV postchallenge survived the infection, cleared the vi

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