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Items: 1 to 50 of 72

1.

Dependence of coronavirus RNA replication on an NH2-terminal partial nonstructural protein 1 in cis.

Su YP, Fan YH, Brian DA.

J Virol. 2014 Aug;88(16):8868-82. doi: 10.1128/JVI.00738-14. Epub 2014 May 28.

2.

Reselection of a genomic upstream open reading frame in mouse hepatitis coronavirus 5'-untranslated-region mutants.

Wu HY, Guan BJ, Su YP, Fan YH, Brian DA.

J Virol. 2014 Jan;88(2):846-58. doi: 10.1128/JVI.02831-13. Epub 2013 Oct 30.

3.
4.
5.

Subgenomic messenger RNA amplification in coronaviruses.

Wu HY, Brian DA.

Proc Natl Acad Sci U S A. 2010 Jul 6;107(27):12257-62. doi: 10.1073/pnas.1000378107. Epub 2010 Jun 18.

6.

Bovine coronavirus nonstructural protein 1 (p28) is an RNA binding protein that binds terminal genomic cis-replication elements.

Gustin KM, Guan BJ, Dziduszko A, Brian DA.

J Virol. 2009 Jun;83(12):6087-97. doi: 10.1128/JVI.00160-09. Epub 2009 Apr 8.

7.

An RNA stem-loop within the bovine coronavirus nsp1 coding region is a cis-acting element in defective interfering RNA replication.

Brown CG, Nixon KS, Senanayake SD, Brian DA.

J Virol. 2007 Jul;81(14):7716-24. Epub 2007 May 2.

9.
11.

Coronavirus genome structure and replication.

Brian DA, Baric RS.

Curr Top Microbiol Immunol. 2005;287:1-30. Review.

PMID:
15609507
12.
13.
14.

Nidovirus genome replication and subgenomic mRNA synthesis. Pathways followed and cis-acting elements required.

Brian DA.

Adv Exp Med Biol. 2001;494:415-28. Review. No abstract available.

PMID:
11774502
16.

Downstream ribosomal entry for translation of coronavirus TGEV gene 3b.

O'Connor JB, Brian DA.

Virology. 2000 Mar 30;269(1):172-82.

17.
21.
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25.

Precise large deletions by the PCR-based overlap extension method.

Senanayake SD, Brian DA.

Mol Biotechnol. 1995 Aug;4(1):13-5.

PMID:
8521036
26.

Evidence for a pseudoknot in the 3' untranslated region of the bovine coronavirus genome.

Williams GD, Chang RY, Brian DA.

Adv Exp Med Biol. 1995;380:511-4.

PMID:
8830533
27.

A cis-acting function for the coronavirus leader in defective interfering RNA replication.

Chang RY, Hofmann MA, Sethna PB, Brian DA.

J Virol. 1994 Dec;68(12):8223-31.

28.

Role of subgenomic minus-strand RNA in coronavirus replication.

Brian DA, Chang RY, Hofmann MA, Sethna PB.

Arch Virol Suppl. 1994;9:173-80.

PMID:
8032248
29.

A translation-attenuating intraleader open reading frame is selected on coronavirus mRNAs during persistent infection.

Hofmann MA, Senanayake SD, Brian DA.

Proc Natl Acad Sci U S A. 1993 Dec 15;90(24):11733-7.

31.

Sequencing DNA amplified directly from a bacterial colony.

Hofmann MA, Brian DA.

Methods Mol Biol. 1993;15:205-10. doi: 10.1385/0-89603-244-2:205.

PMID:
21400278
32.

The Coronaviridae now comprises two genera, coronavirus and torovirus: report of the Coronaviridae Study Group.

Cavanagh D, Brian DA, Brinton MA, Enjuanes L, Holmes KV, Horzinek MC, Lai MM, Laude H, Plagemann PG, Siddell SG, et al.

Adv Exp Med Biol. 1993;342:255-7.

PMID:
8209739
33.

An intraleader open reading frame is selected from a hypervariable 5' terminus during persistent infection by the bovine coronavirus.

Hofmann MA, Senanayake SD, Brian DA.

Adv Exp Med Biol. 1993;342:105-9. No abstract available.

PMID:
8209714
34.

The nucleocapsid protein gene of bovine coronavirus is bicistronic.

Senanayake SD, Hofmann MA, Maki JL, Brian DA.

J Virol. 1992 Sep;66(9):5277-83.

35.

The 9-kDa hydrophobic protein encoded at the 3' end of the porcine transmissible gastroenteritis coronavirus genome is membrane-associated.

Tung FY, Abraham S, Sethna M, Hung SL, Sethna P, Hogue BG, Brian DA.

Virology. 1992 Feb;186(2):676-83.

PMID:
1310191
36.
37.

A PCR-enhanced method for determining the 5' end sequence of mRNAs.

Hofmann MA, Brian DA.

PCR Methods Appl. 1991 Aug;1(1):43-5.

38.

Sequencing PCR DNA amplified directly from a bacterial colony.

Hofmann MA, Brian DA.

Biotechniques. 1991 Jul;11(1):30-1.

PMID:
1954013
39.

Minus-strand copies of replicating coronavirus mRNAs contain antileaders.

Sethna PB, Hofmann MA, Brian DA.

J Virol. 1991 Jan;65(1):320-5.

40.
42.

Recommendations of the Coronavirus Study Group for the nomenclature of the structural proteins, mRNAs, and genes of coronaviruses.

Cavanagh D, Brian DA, Enjuanes L, Holmes KV, Lai MM, Laude H, Siddell SG, Spaan W, Taguchi F, Talbot PJ.

Virology. 1990 May;176(1):306-7. No abstract available.

PMID:
2184577
43.

Deduced sequence of the bovine coronavirus spike protein and identification of the internal proteolytic cleavage site.

Abraham S, Kienzle TE, Lapps W, Brian DA.

Virology. 1990 May;176(1):296-301.

PMID:
2184576
44.

Structure and orientation of expressed bovine coronavirus hemagglutinin-esterase protein.

Kienzle TE, Abraham S, Hogue BG, Brian DA.

J Virol. 1990 Apr;64(4):1834-8.

45.

Structure and expression of the bovine coronavirus hemagglutinin protein.

Kienzle TE, Abraham S, Hogue BG, Brian DA.

Adv Exp Med Biol. 1990;276:95-102. No abstract available.

PMID:
2103108
46.

Coronavirus subgenomic replicons as a mechanism for mRNA amplification.

Sethna PB, Hung SL, Brian DA.

Adv Exp Med Biol. 1990;276:335-40. No abstract available.

PMID:
1966420
47.

Coronavirus subgenomic minus-strand RNAs and the potential for mRNA replicons.

Sethna PB, Hung SL, Brian DA.

Proc Natl Acad Sci U S A. 1989 Jul;86(14):5626-30.

48.
49.

Synthesis and processing of the bovine enteric coronavirus haemagglutinin protein.

Hogue BG, Kienzle TE, Brian DA.

J Gen Virol. 1989 Feb;70 ( Pt 2):345-52.

PMID:
2732694
50.

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