Detalhe da pesquisa
1.
A point mutation in GPI-attachment signal peptide accelerates the development of prion disease.
Acta Neuropathol
; 145(5): 637-650, 2023 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-36879070
2.
Potential for transmission of sporadic Creutzfeldt-Jakob disease through peripheral routes.
Lab Invest
; 101(10): 1327-1330, 2021 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-34253850
3.
Eliminating transmissibility of bovine spongiform encephalopathy by dry-heat treatment.
J Gen Virol
; 101(1): 136-142, 2020 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31718739
4.
Ganglioside Synthase Knockout Reduces Prion Disease Incubation Time in Mouse Models.
Am J Pathol
; 189(3): 677-686, 2019 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-30553837
5.
A Novel Combination of Prion Strain Co-Occurrence in Patients with Sporadic Creutzfeldt-Jakob Disease.
Am J Pathol
; 189(6): 1276-1283, 2019 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-30926338
6.
Transmission experiments verify sporadic V2 prion in a patient with E200K mutation.
Acta Neuropathol
; 147(1): 89, 2024 05 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-38767731
7.
Protective Effect of Val129-PrP against Bovine Spongiform Encephalopathy but not Variant Creutzfeldt-Jakob Disease.
Emerg Infect Dis
; 23(9): 1522-1530, 2017 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-28820136
8.
Multiple affinity purification of a baculovirus-derived recombinant prion protein with in vitro ability to convert to its pathogenic form.
Prep Biochem Biotechnol
; 47(1): 1-7, 2017 Jan 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-26918377
9.
Transmission properties of atypical Creutzfeldt-Jakob disease: a clue to disease etiology?
J Virol
; 89(7): 3939-46, 2015 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-25609817
10.
Neuropathological and biochemical criteria to identify acquired Creutzfeldt-Jakob disease among presumed sporadic cases.
Neuropathology
; 36(3): 305-10, 2016 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-26669818
11.
The influence of PRNP polymorphisms on human prion disease susceptibility: an update.
Acta Neuropathol
; 130(2): 159-70, 2015 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-26022925
12.
Characterization of variant Creutzfeldt-Jakob disease prions in prion protein-humanized mice carrying distinct codon 129 genotypes.
J Biol Chem
; 288(30): 21659-66, 2013 Jul 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-23792955
13.
Prion replication elicits cytopathic changes in differentiated neurosphere cultures.
J Virol
; 87(15): 8745-55, 2013 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-23740992
14.
Quantitative analysis of wet-heat inactivation in bovine spongiform encephalopathy.
Biochem Biophys Res Commun
; 432(1): 86-91, 2013 Mar 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-23376069
15.
Rapid assessment of bovine spongiform encephalopathy prion inactivation by heat treatment in yellow grease produced in the industrial manufacturing process of meat and bone meals.
BMC Vet Res
; 9: 134, 2013 Jul 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-23835086
16.
Glycosylphosphatidylinositol anchor-dependent stimulation pathway required for generation of baculovirus-derived recombinant scrapie prion protein.
J Virol
; 85(6): 2582-8, 2011 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-21228241
17.
Cytochalasin D enhances the accumulation of a protease-resistant form of prion protein in ScN2a cells: involvement of PI3 kinase/Akt signalling pathway.
Cell Biol Int
; 36(12): 1223-31, 2012.
Artigo
em Inglês
| MEDLINE | ID: mdl-22985412
18.
Ultrasensitive detection of scrapie prion protein derived from ARQ and AHQ homozygote sheep by interspecies in vitro amplification.
Microbiol Immunol
; 56(8): 541-7, 2012 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-22548476
19.
Experimental verification of a traceback phenomenon in prion infection.
J Virol
; 84(7): 3230-8, 2010 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-20089646
20.
Experimental H-type bovine spongiform encephalopathy characterized by plaques and glial- and stellate-type prion protein deposits.
Vet Res
; 42: 79, 2011 Jun 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-21699704