review article | Q7318358 |
scholarly article | Q13442814 |
P50 | author | Ernst Peterhans | Q55187013 |
Matthias Schweizer | Q40556005 | ||
P2093 | author name string | Hanspeter Stalder | |
Claudia Bachofen | |||
P2860 | cites work | Epidemiology of bovine virus diarrhoea in cattle on communal alpine pastures in Switzerland. | Q44090869 |
Prevalence of cattle infected with bovine viral diarrhoea virus in Switzerland | Q45739793 | ||
Pathogenesis and epidemiology of bovine virus diarrhoea virus infection of cattle | Q45830386 | ||
Innate and adaptive immunity: specificities and signaling hierarchies revisited | Q57039670 | ||
[How the bovine viral diarrhea virus outwits the immune system] | Q57258289 | ||
Performance of acute flaccid paralysis (AFP) surveillance and incidence of poliomyelitis, 1998-1999 (as of 25 November 1999) | Q73379661 | ||
Not so fast: adaptive suppression of innate immunity | Q81400077 | ||
Do adaptive immune cells suppress or activate innate immunity? | Q82849384 | ||
Global trends in emerging infectious diseases | Q24575990 | ||
Pathogen recognition and inflammatory signaling in innate immune defenses | Q24643034 | ||
Loss of interferon regulatory factor 3 in cells infected with classical swine fever virus involves the N-terminal protease, Npro | Q27469610 | ||
Nonhomologous RNA recombination in bovine viral diarrhea virus: molecular characterization of a variety of subgenomic RNAs isolated during an outbreak of fatal mucosal disease | Q27469714 | ||
A Cellular J-Domain Protein Modulates Polyprotein Processing and Cytopathogenicity of a Pestivirus | Q27469858 | ||
Persistence of bovine viral diarrhea virus is determined by a cellular cofactor of a viral autoprotease | Q27470294 | ||
The amino-terminal domain of bovine viral diarrhea virus Npro protein is necessary for alpha/beta interferon antagonism | Q27472819 | ||
Dissection of a viral autoprotease elucidates a function of a cellular chaperone in proteolysis | Q27472857 | ||
Alpha/beta and gamma interferons are induced by infection with noncytopathic bovine viral diarrhea virus in vivo. | Q27472937 | ||
The NPro Product of Bovine Viral Diarrhea Virus Inhibits DNA Binding by Interferon Regulatory Factor 3 and Targets It for Proteasomal Degradation | Q27477650 | ||
Classical Swine Fever Virus Npro Interacts with Interferon Regulatory Factor 3 and Induces Its Proteasomal Degradation | Q27478373 | ||
Bovine viral diarrhea virus (BVDV) 1b: predominant BVDV subtype in calves with respiratory disease | Q27485583 | ||
Cell-Derived Sequences in the N-Terminal Region of the Polyprotein of a Cytopathogenic Pestivirus | Q27485664 | ||
Cytopathogenicity of Classical Swine Fever Virus Correlates with Attenuation in the Natural Host | Q27486926 | ||
Global epidemiology of hepatitis C virus infection | Q27860799 | ||
The challenge of emerging and re-emerging infectious diseases | Q29617354 | ||
Molecular characterization of pestiviruses | Q29620899 | ||
Emerging and reemerging diseases: a historical perspective | Q30228546 | ||
Identification of a novel virus in pigs--Bungowannah virus: a possible new species of pestivirus | Q33287302 | ||
Identification of a new group of bovine viral diarrhea virus strains associated with severe outbreaks and high mortalities | Q33491847 | ||
Hepatitis C kinetics: mathematical modeling of viral response to therapy | Q34006458 | ||
An apparently new transmissible disease of cattle. | Q34146324 | ||
Diversity among bovine pestiviruses | Q34177838 | ||
BVDV and innate immunity | Q35137993 | ||
The Pestiviruses | Q35227707 | ||
Aspects of the innate and adaptive immune responses to acute infections with BVDV | Q35576469 | ||
The immune response to bovine viral diarrhea virus: a constantly changing picture | Q35736396 | ||
HIV molecular epidemiology: transmission and adaptation to human populations | Q35955635 | ||
Interferons (IFNs) are key cytokines in both innate and adaptive antiviral immune responses--and viruses counteract IFN action | Q36080993 | ||
Virus contaminations of cell cultures - A biotechnological view | Q36296676 | ||
Pestiviruses in wild animals | Q36535280 | ||
Dendritic cells: translating innate to adaptive immunity. | Q36627111 | ||
Innate control of adaptive immunity: dendritic cells and beyond | Q36727602 | ||
The control of bovine viral diarrhoea virus in Europe: today and in the future | Q36760223 | ||
The role of type I interferon production by dendritic cells in host defense | Q36838232 | ||
Overviews of pathogen emergence: which pathogens emerge, when and why? | Q36937221 | ||
Type I interferon as a stimulus for cross-priming | Q37027815 | ||
Field and laboratory evidence that Bungowannah virus, a recently recognised pestivirus, is the causative agent of the porcine myocarditis syndrome (PMC). | Q37373804 | ||
Pestiviruses: how to outmaneuver your hosts. | Q37619071 | ||
Pathogenesis of mucosal disease and molecular aspects of bovine virus diarrhoea virus | Q37893278 | ||
Genetic diversity of international bovine viral diarrhoea virus (BVDV) isolates: identification of a new BVDV-1 genetic group | Q39560898 | ||
The viral RNase E(rns) prevents IFN type-I triggering by pestiviral single- and double-stranded RNAs. | Q39911025 | ||
RNase-dependent inhibition of extracellular, but not intracellular, dsRNA-induced interferon synthesis by Erns of pestiviruses. | Q39939094 | ||
Maximum likelihood and Bayesian analyses of a combined nucleotide sequence dataset for genetic characterization of a novel pestivirus, SVA/cont-08. | Q39971048 | ||
Temporal modulation of an autoprotease is crucial for replication and pathogenicity of an RNA virus | Q39992086 | ||
Nonstructural proteins NS2-3 and NS4A of classical swine fever virus: essential features for infectious particle formation. | Q40136880 | ||
Role for bovine viral diarrhea virus Erns glycoprotein in the control of activation of beta interferon by double-stranded RNA | Q40376965 | ||
Phylogeny, classification and evolutionary insights into pestiviruses | Q40398935 | ||
Genetic and antigenic characterization of an atypical pestivirus isolate, a putative member of a novel pestivirus species | Q40520513 | ||
RNA recombination in vivo in the absence of viral replication | Q40551577 | ||
Genetic and antigenic characterization of novel pestivirus genotypes: implications for classification | Q40555908 | ||
Uncleaved NS2-3 is required for production of infectious bovine viral diarrhea virus | Q40589960 | ||
The genetic basis for cytopathogenicity of pestiviruses | Q40613213 | ||
Identification of pestiviruses contaminating cell lines and fetal calf sera. | Q40766871 | ||
Evaluation of vaccines, interferons and cell substrates for pestivirus contamination | Q40881999 | ||
Immunology of bovine viral diarrhea virus | Q40958816 | ||
Epidemiology of bovine viral diarrhea virus | Q40958824 | ||
The pathways for bovine virus diarrhoea virus biotypes in the pathogenesis of disease | Q41520954 | ||
Differential expression of the type I interferon pathway during persistent and transient bovine viral diarrhea virus infection | Q42445052 | ||
Sequencing and comparative analysis of a pig bovine viral diarrhea virus genome | Q42692016 | ||
Genetic heterogeneity of bovine viral diarrhoea virus (BVDV) isolates from Turkey: identification of a new subgroup in BVDV-1. | Q42977604 | ||
Co-existence of genetically and antigenically diverse bovine viral diarrhoea viruses in an endemic situation | Q42977893 | ||
Genetic diversity of pestivirus isolates in cattle from Western Austria | Q42983208 | ||
Border disease virus (BDV) infections of small ruminants in Turkey: a new BDV subgroup? | Q42983212 | ||
The development of early vs. late onset mucosal disease is a consequence of two different pathogenic mechanisms | Q42984412 | ||
Safety and efficacy of vaccination of seronegative bulls with modified-live, cytopathic bovine viral diarrhea viruses | Q42984466 | ||
Virus recovery and full-length sequence analysis of atypical bovine pestivirus Th/04_KhonKaen | Q42986736 | ||
Persistently infected cattle stabilise bovine viral diarrhea virus leading to herd specific strains | Q42988583 | ||
Experimental induction of mucosal disease: consequences of superinfection of persistently infected cattle with different strains of cytopathogenic bovine viral diarrhea virus | Q42988654 | ||
A novel pestivirus associated with deaths in Pyrenean chamois (Rupicapra pyrenaica pyrenaica). | Q42988979 | ||
Retrospective genome analysis of a live vaccine strain of bovine viral diarrhea virus | Q42989587 | ||
Pathogenesis of mucosal disease, a deadly disease of cattle caused by a pestivirus | Q42990030 | ||
Viral sequence insertions and a novel cellular insertion in the NS2 gene of cytopathic isolates of bovine viral diarrhea virus as potential cytopathogenicity markers. | Q42991069 | ||
Clinical appearance and pathology of cattle persistently infected with bovine viral diarrhoea virus of different genetic subgroups | Q42991691 | ||
Effects of methodology and analysis strategy on robustness of pestivirus phylogeny. | Q42991931 | ||
Genetic clustering of bovine viral diarrhoea viruses in cattle farms: genetic identification and analysis of viruses directly from cattle sera. | Q42994338 | ||
Unscrambling hepatitis C virus-host interactions | Q42994469 | ||
Increased risk of BVDV infection of calves from pregnant dams on communal Alpine pastures in Switzerland | Q42995092 | ||
Genetic heterogeneity of pestiviruses of ruminants in Switzerland. | Q42995711 | ||
Genetic recombination at different points in the Npro-coding region of bovine viral diarrhea viruses and the potentials to change their antigenicities and pathogenicities | Q42995750 | ||
Genetic typing and prevalence of Border disease virus (BDV) in small ruminant flocks in Spain | Q43001434 | ||
Bovine viral diarrhoea virus genotype 1 can be separated into at least eleven genetic groups | Q43030530 | ||
The double-stranded RNA-induced apoptosis pathway is involved in the cytopathogenicity of cytopathogenic Bovine viral diarrhea virus | Q43031258 | ||
Establishment of persistent infection with non-cytopathic bovine viral diarrhoea virus in cattle is associated with a failure to induce type I interferon. | Q43032855 | ||
Transmission of a pestivirus infection in a population of Pyrenean chamois | Q43033348 | ||
Genetic and antigenic typing of border disease virus isolates in sheep from the Iberian Peninsula | Q43033976 | ||
Natural infection of cattle with an atypical 'HoBi'-like pestivirus--implications for BVD control and for the safety of biological products | Q43037795 | ||
Serological survey for antibodies against pestiviruses in sheep in Austria | Q43037996 | ||
The extended genetic diversity of BVDV-1: typing of BVDV isolates from France | Q43039564 | ||
Epidemiological study of border disease virus infection in Southern chamois (Rupicapra pyrenaica) after an outbreak of disease in the Pyrenees (NE Spain). | Q43040848 | ||
Genetic characterization of ovine pestiviruses isolated in France, between 1985 and 2006. | Q43046694 | ||
Identification of new genetic subtypes of bovine viral diarrhea virus genotype 1 isolated in Japan | Q43047796 | ||
Acute non-cytopathic bovine viral diarrhea virus infection induces pronounced type I interferon response in pregnant cows and fetuses | Q43048412 | ||
P275 | copyright license | Creative Commons Attribution-NonCommercial | Q6936496 |
P433 | issue | 6 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | extinction | Q123509 |
bovine viral diarrhea virus | Q895366 | ||
P5008 | on focus list of Wikimedia project | ScienceSource | Q55439927 |
P304 | page(s) | 44 | |
P577 | publication date | 2010-03-04 | |
P1433 | published in | Veterinary Research | Q15761008 |
P1476 | title | Cytopathic bovine viral diarrhea viruses (BVDV): emerging pestiviruses doomed to extinction | |
P478 | volume | 41 |