Investigation of variant Creutzfeldt-Jakob disease and other human prion diseases with tonsil biopsy samples.
about
Prevalent abnormal prion protein in human appendixes after bovine spongiform encephalopathy epizootic: large scale surveyA clinical study of kuru patients with long incubation periods at the end of the epidemic in Papua New GuineaKuru prions and sporadic Creutzfeldt-Jakob disease prions have equivalent transmission properties in transgenic and wild-type miceComparative evidence for a link between Peyer's patch development and susceptibility to transmissible spongiform encephalopathies.Multifaceted Role of Sialylation in Prion DiseasesBiomarkers for sporadic Creutzfeldt-Jakob diseasePrion DiseasesRe-assessment of PrP(Sc) distribution in sporadic and variant CJDImplications for Creutzfeldt-Jakob disease (CJD) in dentistry: a review of current knowledge.Is the prevalent human prion protein 129M/V mutation a living fossil from a Paleolithic panzootic superprion pandemic?Prominent and persistent extraneural infection in human PrP transgenic mice infected with variant CJD.Rationale for diagnosing human prion disease.Advanced tests for early and accurate diagnosis of Creutzfeldt-Jakob disease.Neuroradiology of human prion diseases, diagnosis and differential diagnosis.The release of prion protein from platelets during storage of apheresis platelets.Prevalence of disease related prion protein in anonymous tonsil specimens in Britain: cross sectional opportunistic survey.Prion protein expression and processing in human mononuclear cells: the impact of the codon 129 prion gene polymorphism.Repetitive immunization enhances the susceptibility of mice to peripherally administered prions.High-b-value diffusion MR imaging and basal nuclei apparent diffusion coefficient measurements in variant and sporadic Creutzfeldt-Jakob disease.The prepared tau exon-specific antibodies revealed distinct profiles of tau in CSF of the patients with Creutzfeldt-Jakob diseaseThe impact of new-variant Creutzfeldt-Jakob disease on blood transfusion practice.Prions and blood products.Variant Creutzfeldt-Jakob disease: immunocytochemical studies and image analysis.Detection of PrP in extraneural tissues.Variant Creutzfeldt-Jakob disease: a summary of current scientific knowledge in relation to public healthLaboratory diagnosis of variant Creutzfeldt-Jakob disease.Gene expression profiling: monitoring transcription and translation products using DNA microarrays and proteomics.Leucocyte depletion of the blood supply - how will patients benefit?Creutzfeldt-Jakob disease and the eye. I. Background and patient management.Creutzfeldt-Jakob disease and the eye. II. Ophthalmic and neuro-ophthalmic features.vCJD - predicting the future?Accumulation of prion protein in tonsil and appendix: review of tissue samplesPrPTSE distribution in a primate model of variant, sporadic, and iatrogenic Creutzfeldt-Jakob disease.Variant Creutzfeldt-Jakob disease with extremely low lymphoreticular deposition of prion protein.New-variant Creutzfeldt-Jacob disease.Clinical implications of bovine spongiform encephalopathy.Variant CJD. 18 years of research and surveillance.Molecular pathology of human prion disease.PrP polymorphisms tightly control sheep prion replication in cultured cellsThe transmissible spongiform encephalopathies (prion diseases): a review for dental surgeons.
P2860
Q24606150-A3D7C637-3D53-4763-95F2-861041DD9CABQ24642582-B1F5AEA6-4512-409D-80DD-2E5E86CD00ADQ24651920-41B0C889-4F93-4C4C-9D24-12A98B8FBA85Q25255274-CF6A205F-5F4B-47C0-B739-40A8318C9950Q26739884-8EBFB56C-D0C6-4AA9-BF8D-DC11BBD2342EQ26739995-4774546D-BF91-4B14-8AA1-7C62FE66448CQ28080751-891A043F-D51A-4C2F-9257-0540A5714BB0Q28534501-1AF9F66A-5AD8-4D59-B357-A349C2A8452DQ30228914-B66CFC5D-B170-4936-8BBB-A13F138E64D8Q30357614-CD6325C8-AC04-4FB3-ACED-931A395003BDQ30840051-B33DAFCA-D127-4254-9564-A1C4812FD10AQ30936688-FDAC2DD3-F13F-4061-9A0D-8FDE3B49732AQ31095751-4D07D83A-5FF3-4E45-809A-A41E0E59927DQ31155802-792C16AF-9867-4B0A-8522-FBFDA29B7EA4Q31846254-3FCA4A52-C2ED-4AC3-B521-A790A3A13167Q33450140-5A309E43-C7F2-4C53-A09F-AE7088773955Q33460414-03CBB2E5-EECF-4355-B3AF-2875DF6E8CBCQ33506629-6A7C7B49-0102-451C-9824-4F6F2E90A30FQ33518254-89D6DB73-2783-4A80-B7A1-7E6A555FA342Q33649832-C3E8D3EF-0DD3-40EA-A394-FFDD8DDD9A98Q33751238-1DBB7744-13CE-494D-A105-13AF54BC7EE7Q33925903-010A670F-DB2E-468E-8CE1-A7F5F16454C3Q33952844-F2B6D9FC-407A-45BB-B5FD-924C6710AEA2Q33952869-3533174E-76F6-4208-A803-D33692266230Q33956087-91B404FF-5960-4F5B-9009-EDACBC7C3B26Q33994500-DE356E83-D9C5-46DF-A507-8EE86E2F2672Q34020013-D09FA1E2-49E4-49CF-8CDB-49F9B83FD0A4Q34022474-E3C47557-95E2-448A-8B81-FB8636651ABDQ34057654-3BD4F104-8010-4154-9A49-64F88873D52CQ34057658-DF7D0D12-6A2A-4987-9A2D-B1D4C636B31EQ34071731-EC81A0F1-7556-4AD6-A909-AEF9F2E809EDQ34093841-AEDE1128-3AB5-4C7B-B56D-D792141D33A1Q34123943-0468E9B5-A3BD-4819-A2F5-133BAB6D918DQ34153667-BD8F6100-F24A-4813-BFD8-2239A9D9B92BQ34218851-8C23A1CF-36EA-4008-B52B-783570E5A4B0Q34255643-8DD4CF9A-EC78-42CC-934C-4DEF39CF7F8BQ34453109-1A77B5F7-D9C6-443E-A5B0-14BDE8A0EC7EQ34462913-F5770611-6021-4038-8CAF-664F3310A694Q34471219-7279E1BB-649B-4BFD-A6F4-ECED390F2873Q34492235-CC38D9C9-4ED7-478E-AFFE-7F620BA137D0
P2860
Investigation of variant Creutzfeldt-Jakob disease and other human prion diseases with tonsil biopsy samples.
description
1999 nî lūn-bûn
@nan
1999年の論文
@ja
1999年学术文章
@wuu
1999年学术文章
@zh-cn
1999年学术文章
@zh-hans
1999年学术文章
@zh-my
1999年学术文章
@zh-sg
1999年學術文章
@yue
1999年學術文章
@zh
1999年學術文章
@zh-hant
name
Investigation of variant Creut ...... es with tonsil biopsy samples.
@en
Investigation of variant Creut ...... es with tonsil biopsy samples.
@nl
type
label
Investigation of variant Creut ...... es with tonsil biopsy samples.
@en
Investigation of variant Creut ...... es with tonsil biopsy samples.
@nl
prefLabel
Investigation of variant Creut ...... es with tonsil biopsy samples.
@en
Investigation of variant Creut ...... es with tonsil biopsy samples.
@nl
P2093
P50
P1433
P1476
Investigation of variant Creut ...... ses with tonsil biopsy samples
@en
P2093
D J Thomas
J Collinge
P L Lantos
R J Butterworth
S Al-Sarraj
P304
P356
10.1016/S0140-6736(98)12075-5
P407
P577
1999-01-01T00:00:00Z