| P50 | author | Eric J Snijder | Q55186759 |
| P2093 | author name string | W J Spaan | |
| | E D Chirnside | |
| | M C Horzinek | |
| | J A den Boon | |
| | A A de Vries | |
| P2860 | cites work | A new principle of RNA folding based on pseudoknotting | Q24624606 |
| | Viral cysteine proteases are homologous to the trypsin-like family of serine proteases: structural and functional implications | Q24647040 |
| | Improved tools for biological sequence comparison | Q24652199 |
| | A comprehensive set of sequence analysis programs for the VAX | Q26778432 |
| | Processing the nonstructural polyproteins of sindbis virus: nonstructural proteinase is in the C-terminal half of nsP2 and functions both in cis and in trans | Q27486629 |
| | Eukaryotic transient-expression system based on recombinant vaccinia virus that synthesizes bacteriophage T7 RNA polymerase | Q27860943 |
| | Thiol proteases. Comparative studies based on the high-resolution structures of papain and actinidin, and on amino acid sequence information for cathepsins B and H, and stem bromelain | Q28306293 |
| | Identification of four conserved motifs among the RNA-dependent polymerase encoding elements | Q29617964 |
| | N-terminal domains of putative helicases of flavi- and pestiviruses may be serine proteases | Q29620797 |
| | Detection of a trypsin-like serine protease domain in flaviviruses and pestiviruses | Q29620969 |
| | Cysteine proteases of positive strand RNA viruses and chymotrypsin-like serine proteases. A distinct protein superfamily with a common structural fold | Q30196037 |
| | An efficient ribosomal frame-shifting signal in the polymerase-encoding region of the coronavirus IBV. | Q33929986 |
| | Isolation of a filterable agent causing arteritis of horses and abortion by mares; its differentiation from the equine abortion (influenza) virus. | Q34240651 |
| | Purification and partial characterization of a new enveloped RNA virus (Berne virus). | Q34272717 |
| | Coronavirus subgenomic minus-strand RNAs and the potential for mRNA replicons | Q34292813 |
| | Evolutionary relationship between luteoviruses and other RNA plant viruses based on sequence motifs in their putative RNA polymerases and nucleic acid helicases | Q35540954 |
| | The primary structure and expression of the second open reading frame of the polymerase gene of the coronavirus MHV-A59; a highly conserved polymerase is expressed by an efficient ribosomal frameshifting mechanism | Q35835343 |
| | The current status and portability of our sequence handling software | Q36087229 |
| | Coronavirus transcription: subgenomic mouse hepatitis virus replicative intermediates function in RNA synthesis. | Q36801938 |
| | Viral proteins containing the purine NTP-binding sequence pattern | Q38306984 |
| | Togaviridae | Q39497769 |
| | Evolution of plus-strand RNA viruses | Q39545382 |
| | Coronaviruses: structure and genome expression | Q39545838 |
| | The genome of equine arteritis virus | Q39965580 |
| | The structural proteins of equine arteritis virus | Q40011368 |
| | A 3'-coterminal nested set of independently transcribed mRNAs is generated during Berne virus replication | Q40107528 |
| | The structure and replication of coronaviruses. | Q40334048 |
| | Coronavirus genome: prediction of putative functional domains in the non-structural polyprotein by comparative amino acid sequence analysis. | Q40450738 |
| | All subgenomic mRNAs of equine arteritis virus contain a common leader sequence | Q40517176 |
| | The carboxyl-terminal part of the putative Berne virus polymerase is expressed by ribosomal frameshifting and contains sequence motifs which indicate that toro- and coronaviruses are evolutionarily related | Q40519022 |
| | RNA helicase: a novel activity associated with a protein encoded by a positive strand RNA virus | Q40526962 |
| | The complete sequence (22 kilobases) of murine coronavirus gene 1 encoding the putative proteases and RNA polymerase | Q41697955 |
| | Primary structure and post-translational processing of the Berne virus peplomer protein. | Q42633991 |
| | Map location of lactate dehydrogenase-elevating virus (LDV) capsid protein (Vp1) gene | Q42637188 |
| | Characterization of an efficient coronavirus ribosomal frameshifting signal: requirement for an RNA pseudoknot | Q42646008 |
| | Intracellular equine arteritis virus (EAV)-specific RNAs contain common sequences | Q43513718 |
| | Characterization of Berne Virus Genomic and Messenger RNAs | Q44977383 |
| | An outbreak of abortion caused by the equine arteritis virus. | Q45719960 |
| | Equine arteritis virus-infected cells contain six polyadenylated virus-specific RNAs | Q45800234 |
| | Structural proteins of equine arteritis virus. | Q45815930 |
| | The peplomers of Berne virus | Q45829380 |
| | Completion of the sequence of the genome of the coronavirus avian infectious bronchitis virus | Q45835443 |
| | Demonstration of the carrier state in naturally acquired equine arteritis virus infection in the stallion | Q45835867 |
| | Signals for ribosomal frameshifting in the Rous sarcoma virus gag-pol region | Q45840877 |
| | Identification and antigenic comparison of equine arteritis virus isolated from an outbreak of epidemic abortion of mares | Q45848169 |
| | Equine arteritis virus-induced polypeptide synthesis | Q45848288 |
| | A new superfamily of replicative proteins | Q59069349 |
| | Togaviridae | Q67243600 |
| | RNA pseudoknots: translational frameshifting and readthrough on viral RNAs | Q68924260 |
| | Studies on the substructure of togaviruses. II. Analysis of equine arteritis, rubella, bovine viral diarrhea, and hog cholera viruses | Q93710786 |
| P433 | issue | 6 | |
| P921 | main subject | virus | Q808 |
| P304 | page(s) | 2910-20 | |
| P577 | publication date | 1991-06-01 | |
| P1433 | published in | Journal of Virology | Q1251128 |
| P1476 | title | Equine arteritis virus is not a togavirus but belongs to the coronaviruslike superfamily | |
| P478 | volume | 65 | |