ライフサイエンスコーパス: bovine coronavirus

1 report that HECV-4408 is likely a variant of bovine coronavirus.

2 quence, is entirely conserved in the related bovine coronavirus.

3 Although structure probing of the bovine coronavirus 5' untranslated region indicated that

4 human seasonal coronaviruses HKU1 and OC43, bovine coronavirus and porcine haemagglutinating encepha

5 for each of the nine species of mRNA in the bovine coronavirus and ranging in length from 70 nucleot

6 S-CoV-2 RNA as well as coronavirus recovery (bovine coronavirus) and fecal strength (pepper mild mott

7 translated region (UTR) in the genome of the bovine coronavirus (BCoV) and 339-nt 3' UTR in the sever

8 al protein 1 (nsp1), a 28-kDa protein in the bovine coronavirus (BCoV) and closely related mouse hepa

9 e spike protein N-terminal domains (NTDs) of bovine coronavirus (BCoV) and mouse hepatitis coronaviru

10 mic respiratory CoV infections of livestock: bovine coronavirus (BCoV) and porcine respiratory corona

11 5'-terminal untranslated regions (UTRs) of a bovine coronavirus (BCoV) defective interfering (DI) RNA

12 anslated region (UTR) in the positive-strand bovine coronavirus (BCoV) genome is predicted to contain

13 the 210-nucleotide (nt) 5' UTR of the 32-kb bovine coronavirus (BCoV) genome.

14 OC43 apparently emerged from a bovine coronavirus (BCoV) spillover.

15 ally and genetically more closely related to bovine coronavirus (BCoV) than to human coronavirus OC43

16 r in a defective interfering (DI) RNA of the bovine coronavirus (BCoV) that map within a 322-nucleoti

17 es for three different airborne viruses: (1) bovine coronavirus (BCoV), (2) influenza A virus (IAV),

18 of the mouse hepatitis coronavirus (MHV) and bovine coronavirus (BCoV), separate species in the betac

19 tacoronavirus-1, and more closely related to bovine coronavirus (BCoV)-its presumptive ancestor-and p

20 ith its counterpart from the closely related bovine coronavirus (BCoV).

21 udoknot in the 3' UTR of the closely related bovine coronavirus (BCoV).

22 as replaced with that of its close relative, bovine coronavirus (BCoV).

23 rs in this process for two group II viruses, bovine coronavirus (BCV) and mouse hepatitis coronavirus

24 nstrated a close antigenic relationship with bovine coronavirus (BCV) and porcine hemagglutinating en

25 We have used the bovine coronavirus (BCV) as a model to study interaction

26 A region of the bovine coronavirus (BCV) genome that functions as a pack

27 MAb) (Z3A5) against spike protein subunit of bovine coronavirus (BCV) reacted with the virus in forma

28 clonal antibody against the spike protein of bovine coronavirus (BCV), on an indirect fluorescent ant

29 TR of MHV could be replaced by the 3' UTR of bovine coronavirus (BCV), which diverges overall by 31%

30 naviruses such as human coronavirus OC43 and bovine coronavirus bind sugars.

31 virus, bovine adenovirus, bovine rhinovirus, bovine coronavirus, bovine reovirus, bovine enterovirus

32 lves and complete cross-protection against a bovine coronavirus (DB2 strain) showing 98.2% amino acid

33 donor sequence engineered into a packageable bovine coronavirus defective interfering (DI) RNA and ma

34 y placed 22-nt-long donor sequences within a bovine coronavirus defective interfering (DI) RNA we hav

35 The 65-nucleotide leader on the cloned bovine coronavirus defective interfering (DI) RNA, when

36 rotein in cis for optimal replication of the bovine coronavirus DI RNA and suggest that a similar req

37 e pseudoknot within the 288-nt 3' UTR of the bovine coronavirus genome and show by mutational analysi

38 tch an acceptor core (UCUAAAC in the case of bovine coronavirus) near the 3' end of the 5'-terminal g

39 After challenge with bovine coronavirus, no diarrhea or virus shedding was de

40 oup B rotaviruses (in a mixed infection with bovine coronavirus or singly in fecal contents) in adult

41 Respiratory bovine coronaviruses (RBCV) were isolated from nasal sec

42 has recently been shown to be necessary for bovine coronavirus replication.

43 A substitution of the corresponding bovine coronavirus sequence for the MHV sequence within

44 2.2-kb defective interfering (DI) RNA of the bovine coronavirus, structurally a simple fusion of the

45 In the bovine coronavirus, the major fusion site for synthesis

46 oductive and respiratory syndrome (PRRS) and bovine coronavirus viruses.

47 Three bovine nasal samples infected with bovine coronavirus were used to infect human and bovine