ライフサイエンスコーパス: bovine coronavirus

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

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

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

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

8 5'-terminal untranslated regions (UTRs) of a bovine coronavirus (BCoV) defective interfering (DI) RNA

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

38 2.2-kb defective interfering (DI) RNA of the bovine coronavirus, structurally a simple fusion of the

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

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

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