about
Molecular and biological characterization of deformed wing virus of honeybees (Apis mellifera L.)Intraspecies transmission of BASE induces clinical dullness and amyotrophic changesEmergence of a new lagovirus related to Rabbit Haemorrhagic Disease VirusA pandemic strain of calicivirus threatens rabbit industries in the Americas.Field and experimental data indicate that the eastern cottontail (Sylvilagus floridanus) is susceptible to infection with European brown hare syndrome (EBHS) virus and not with rabbit haemorrhagic disease (RHD) virus.An in vivo system for directed experimental evolution of rabbit haemorrhagic disease virus.Immunochemical characterization of human liver and heart ferritins with monoclonal antibodies.Diagnosis of viral haemorrhagic disease of rabbits and the European brown hare syndrome.Identification of a second bovine amyloidotic spongiform encephalopathy: molecular similarities with sporadic Creutzfeldt-Jakob disease.The new French 2010 Rabbit Hemorrhagic Disease Virus causes an RHD-like disease in the Sardinian Cape hare (Lepus capensis mediterraneus).Arrival of rabbit haemorrhagic disease virus 2 to northern Europe: Emergence and outbreaks in wild and domestic rabbits (Oryctolagus cuniculus) in Sweden.Single dose adenovirus vectored vaccine induces a potent and long-lasting immune response against rabbit hemorrhagic disease virus after parenteral or mucosal administration.Two independent pathways of expression lead to self-assembly of the rabbit hemorrhagic disease virus capsid proteinIncreased pathogenicity in rabbit haemorrhagic disease virus type 2 (RHDV2).RHDV2 overcoming RHDV immunity in wild rabbits (Oryctolagus cuniculus) in Australia.Spillover Events of Infection of Brown Hares (Lepus europaeus) with Rabbit Haemorrhagic Disease Type 2 Virus (RHDV2) Caused Sporadic Cases of an European Brown Hare Syndrome-Like Disease in Italy and Spain.Detection of the new emerging rabbit haemorrhagic disease type 2 virus (RHDV2) in Sicily from rabbit (Oryctolagus cuniculus) and Italian hare (Lepus corsicanus).Molecular evolution and antigenic variation of European brown hare syndrome virus (EBHSV).A serological survey of antibodies to rabbit haemorrhagic disease virus (rabbit calicivirus disease) in two rural Central Otago communities.A further step in the evolution of rabbit hemorrhagic disease virus: the appearance of the first consistent antigenic variant.Preliminary characterization of a non-haemagglutinating strain of rabbit haemorrhagic disease virus from the United Kingdom.Immune protection against foot-and-mouth disease virus studied using virus-neutralizing and non-neutralizing concentrations of monoclonal antibodies.Characterization of a parvovirus isolated from a pig fetus.DNA synthesis catalyzed in vitro by yeast extracts using A 2 μm DNA containing plasmid as template for enzymatic DNA synthesis.Development and validation of a monoclonal antibody-based competitive ELISA for detection of antibodies against porcine epidemic diarrhoea virus (PEDV)Analysis of Gene Expression in White Blood Cells of Cattle Orally Challenged with Bovine Amyloidotic Spongiform EncephalopathyThe non-pathogenic Australian lagovirus RCV-A1 causes a prolonged infection and elicits partial cross-protection to rabbit haemorrhagic disease virusEvaluation of Three Rapid Diagnostic Tests Used in Bovine Spongiform Encephalopathy Monitoring in ItalyUse of ELISAs in field studies of rabbit haemorrhagic disease (RHD) in AustraliaProduction and characterization of monoclonal antibodies differentiating subpopulations of porcine B lymphocytes in blood and lymphoid tissuesPolypeptide structure of DNA polymerase I from Saccharomyces cerevisiaePolypeptide structure of human terminal transferaseCharacterization of the IgA response to PRRS virus in pig oral fluids
P50
Q24545875-FE3B5640-CF09-496A-9FBA-45DEC411594EQ27318658-C4AECBD3-5A24-494F-B043-FA68CBD3EA49Q28297981-D394C525-60AE-4A77-9BD4-1C63C882CA04Q30364933-2859FB4D-6C73-4054-A427-F46D33DF2848Q30920520-84598285-AA0C-4C69-A62F-23A7C876D07AQ36306331-0BA09956-964F-4FD8-9F88-360EE247E757Q36430612-EB712E31-F850-413D-959B-CB8F46CEC000Q36452054-AF89B300-7460-4914-B360-41CD0F23764EQ36853707-A1961427-89F8-4407-858B-AB84E5379B2FQ37368070-D46A5F19-37ED-434D-AC65-3C4A6DEF3828Q38375027-D830CBEB-1F19-4BF9-8D42-5A8689357967Q39534390-417265B6-7244-46D0-99DE-890009F1053EQ39871753-3DB0B79A-B531-47F2-8A1B-AA713F0F32DEQ40274322-6BD23878-235D-4169-8747-31CE981C7003Q40382832-324C0555-B5DB-424B-AD05-35C3EF6BB8E9Q40544255-E467FC0C-C9D6-45DE-869D-6266365AD57FQ41627996-B8825DE0-FFFE-4CE8-A35A-85D501F0C341Q42198075-F362CE2E-B77E-4E19-B98C-ED16B1AB2C64Q45737957-8754CCBE-AB8D-4075-9C8E-52735A3BD743Q45751945-8A6686A4-F014-4311-B0A7-8CF73D536FAFQ45768825-733CB433-5A6C-48CE-A0C3-35DA0C98F9A8Q45836423-02CBC2F9-D0AA-4A2D-A1BE-40A941983E97Q46674235-C1C5F92D-111C-4282-8328-7944B3617995Q47730919-98C9F37B-7451-4281-84B3-1809C29F6F95Q59231143-ED1F7371-8BA2-4F86-B4BA-89C69D8D1822Q59231190-1B648BA2-732B-45A4-BA6C-74C2605BDFD5Q59231204-7EF8D76A-3E25-44A5-B236-C50818EB9DB9Q59231209-852622F3-7A63-41B1-ACE2-AB73CC2A929CQ59231228-C577245F-C814-4256-948A-16E6CBD9804CQ59231280-CDF7CDD2-5702-4BF3-AA76-985940CE3AC5Q59231318-B048338C-3841-4EBF-8AA0-0397BB564FBBQ59231328-095A906D-DFC9-4B2F-8524-B41D353854C7Q89997862-787EF69A-92B5-49D2-A456-68EC4E351832
P50
description
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Lorenzo Capucci
@ast
Lorenzo Capucci
@en
Lorenzo Capucci
@es
Lorenzo Capucci
@nl
type
label
Lorenzo Capucci
@ast
Lorenzo Capucci
@en
Lorenzo Capucci
@es
Lorenzo Capucci
@nl
prefLabel
Lorenzo Capucci
@ast
Lorenzo Capucci
@en
Lorenzo Capucci
@es
Lorenzo Capucci
@nl
P106
P21
P31
P496
0000-0002-1830-3929