Conversion of the BASE prion strain into the BSE strain: the origin of BSE? - Wikidata - awgldk - TriplyDB

Conversion of the BASE prion strain into the BSE strain: the origin of BSE?

Conversion of the BASE prion strain into the BSE strain: the origin of BSE?

http://www.wikidata.org/entity/Q33277907

about

Whole Blood Gene Expression Profiling in Preclinical and Clinical Cattle Infected with Atypical Bovine Spongiform Encephalopathy Phenotype shift from atypical scrapie to CH1641 following experimental transmission in sheep Intraspecies transmission of BASE induces clinical dullness and amyotrophic changes Idiopathic Brainstem Neuronal Chromatolysis (IBNC): a novel prion protein related disorder of cattle?Atypical BSE (BASE) transmitted from asymptomatic aging cattle to a primate Molecular, biochemical and genetic characteristics of BSE in Canada Biochemical Characteristics and PrP(Sc) Distribution Pattern in the Brains of Cattle Experimentally Challenged with H-type and L-type Atypical BSE Is the prevalent human prion protein 129M/V mutation a living fossil from a Paleolithic panzootic superprion pandemic?Conformational switching within individual amyloid fibrils.Further characterisation of transmissible spongiform encephalopathy phenotypes after inoculation of cattle with two temporally separated sources of sheep scrapie from Great Britain Prevalence of the prion protein gene E211K variant in U.S. cattle.No major change in vCJD agent strain after secondary transmission via blood transfusion Identification of a heritable polymorphism in bovine PRNP associated with genetic transmissible spongiform encephalopathy: evidence of heritable BSE.A C-terminal protease-resistant prion fragment distinguishes ovine "CH1641-like" scrapie from bovine classical and L-Type BSE in ovine transgenic mice Time trends in exposure of cattle to bovine spongiform encephalopathy and cohort effect in France and Italy: value of the classical Age-Period-Cohort approach Prions of ruminants show distinct splenotropisms in an ovine transgenic mouse model.No H- and L-type cases in Belgium in cattle diagnosed with bovine spongiform encephalopathy (1999-2008) aging seven years and older.Transcriptional analysis implicates endoplasmic reticulum stress in bovine spongiform encephalopathy Mouse neuronal cells expressing exogenous bovine PRNP and simultaneous downregulation of endogenous mouse PRNP using siRNAs.Emergence of classical BSE strain properties during serial passages of H-BSE in wild-type mice.Phenotypic similarity of transmissible mink encephalopathy in cattle and L-type bovine spongiform encephalopathy in a mouse model Defining sporadic Creutzfeldt-Jakob disease strains and their transmission properties.Infectivity in skeletal muscle of cattle with atypical bovine spongiform encephalopathy.Experimental H-type and L-type bovine spongiform encephalopathy in cattle: observation of two clinical syndromes and diagnostic challenges.Experimental interspecies transmission studies of the transmissible spongiform encephalopathies to cattle: comparison to bovine spongiform encephalopathy in cattle.Individual factors associated with L- and H-type Bovine Spongiform encephalopathy in France.The pathological and molecular but not clinical phenotypes are maintained after second passage of experimental atypical bovine spongiform encephalopathy in cattle Clinical and pathologic features of H-type bovine spongiform encephalopathy associated with E211K prion protein polymorphism Molecular modeling of prion transmission to humans Evaluation of the zoonotic potential of transmissible mink encephalopathy.Experimental H-type bovine spongiform encephalopathy characterized by plaques and glial- and stellate-type prion protein deposits.Detection and discrimination of classical and atypical L-type bovine spongiform encephalopathy by real-time quaking-induced conversion Characterization of Syrian hamster adapted prions derived from L-type and C-type bovine spongiform encephalopathies An overview of animal prion diseases.Acquired transmissibility of sheep-passaged L-type bovine spongiform encephalopathy prion to wild-type mice Classical bovine spongiform encephalopathy by transmission of H-type prion in homologous prion protein context.Comparative analysis of Japanese and foreign L-type BSE prions.Detection and partial discrimination of atypical and classical bovine spongiform encephalopathies in cattle and primates using real-time quaking-induced conversion assay.Deer Prion Proteins Modulate the Emergence and Adaptation of Chronic Wasting Disease Strains.Atypical bovine spongiform encephalopathies, France, 2001-2007.

P2860

Q27314189-4C9EC454-5C4F-4B54-BDB5-2E210158B0B2 Q27316697-3A33C781-8CC6-4D07-B5F3-3CE89D1A1B2E Q27318658-A44484E4-4BB1-4242-9147-06B97CF495AA Q27498926-EB4D2518-F63C-4138-82C9-A2D19D3462AA Q28473442-E024E274-6035-47C6-9984-6445B78F6523 Q28473930-EE7C006F-3325-49A1-8711-7CA29A61B6A2 Q28534150-BD0CBC16-C29F-4767-BF35-EF0D1171D4FA Q30357614-17A10EBF-EC49-4599-8763-561A55DDEF6C Q30481423-B690D7C1-8E73-43ED-BA7A-E386EF62A582 Q30670498-5FE21E3A-39E7-4018-A1ED-89CCF6C072BB Q33351519-8E4C4D22-D11A-4BAE-91B8-3674F0397A46 Q33358045-8C1010E0-910D-4774-938C-25AB5D759DEB Q33359531-6884C110-B1B4-47AC-9A9D-F90EDF2A3E75 Q33366536-DDC14875-EE1E-4CF2-B074-A6E48C031FDA Q33504444-9FC16000-74C4-456B-9CCE-0BDF41664BAA Q33570442-9BBEA351-9FFC-4C18-9CCD-360EBD942E6B Q33584245-E31C0F87-66F3-4671-BD85-5392DB7BBAA7 Q33769602-0BA819BB-B7E4-4A61-9DE8-2DFAEA533465 Q33772925-08405669-75CF-4917-B15A-0967679DE1CF Q33802746-3EF543C1-DECE-400D-B698-C95E140A2964 Q33877843-E30BAB3B-4229-4667-9288-B720B8927171 Q33977675-53D0464E-1920-431B-B0AF-3740F9CC9010 Q34170964-4F1B018C-FE0A-41B2-B498-ED97C2E7CB9A Q34188414-D850DE95-2F90-4DB7-BF17-A4F61903AFD7 Q34215267-FB376A59-DB73-454D-BF89-45DA1675513E Q34286785-D62BE2E7-88B3-49C1-842D-775258FD8409 Q34309351-A2C2B048-AACA-49F8-85FD-421116967163 Q34310346-11D291FA-1C61-4D22-A9D1-2CB1170C49DE Q34423397-DB904046-01B5-455D-91E8-1F716ECDF6C6 Q34533468-7D426ACA-DDC6-4102-B059-F5271A367AAC Q35094833-55EA2A68-D32D-4AA2-B768-B99507368C2D Q35193339-37943152-DCA3-4CC4-BB71-EB8D417DF12A Q35194921-578F89FA-D56D-4D1B-A2F7-BD4360734D11 Q35586642-CEA959B2-52D4-46DE-B7A4-6C8CCCC36DAD Q35844725-1A9FDA94-7B8A-4E12-81C6-F4E4A18024E3 Q35877485-64AB62D8-9F9C-496A-BD8D-C51BBD493541 Q35918953-0FAAB20A-C656-4DC4-8B94-56F71F8B1244 Q36288523-05CB65EB-F846-4648-9DF8-BEDE4B17B479 Q36334348-F54822FD-3A71-4C94-A1D1-071B6AAA564D Q37009050-191C7E50-B16F-4E39-A5F3-AA7A88E5745E

P2860

Conversion of the BASE prion strain into the BSE strain: the origin of BSE?

http://www.wikidata.org/entity/Q33277907

description

2007 nî lūn-bûn

@nan

2007 թուականի Մարտին հրատարակուած գիտական յօդուած

@hyw

2007 թվականի մարտին հրատարակված գիտական հոդված

@hy

2007年の論文

@ja

2007年論文

@yue

2007年論文

@zh-hant

2007年論文

@zh-hk

2007年論文

@zh-mo

2007年論文

@zh-tw

2007年论文

@wuu

name

Conversion of the BASE prion strain into the BSE strain: the origin of BSE?

@ast

Conversion of the BASE prion strain into the BSE strain: the origin of BSE?

@en

Conversion of the BASE prion strain into the BSE strain: the origin of BSE?

@nl

type

label

Conversion of the BASE prion strain into the BSE strain: the origin of BSE?

@ast

Conversion of the BASE prion strain into the BSE strain: the origin of BSE?

@en

Conversion of the BASE prion strain into the BSE strain: the origin of BSE?

@nl

prefLabel

Conversion of the BASE prion strain into the BSE strain: the origin of BSE?

@ast

Conversion of the BASE prion strain into the BSE strain: the origin of BSE?

@en

Conversion of the BASE prion strain into the BSE strain: the origin of BSE?

@nl

P1433

Q33277907-1C7F5AAB-7A91-454F-ACD3-9E18FBF69CEF

P1476

Q33277907-1E572A4B-108B-4169-83C2-52FBF6435266

P2093

Q33277907-0E493577-2F66-4377-951A-B85E53D124AD

Q33277907-2E11EDEE-1B10-4175-A805-BF31BFA84C4A

Q33277907-319CF276-B51C-4982-9D35-16FA3462B611

Q33277907-31CF53BF-3363-49AF-82D9-351A62F13F49

Q33277907-445322CA-912A-47B2-8081-BB84E6BE46B9

Q33277907-654E5C32-4878-4B92-ACDA-96B6CD350ECB

Q33277907-8456DA96-D8BC-483A-A079-7596B9A5488F

Q33277907-89096DDA-1DED-44E4-BECE-C5184DB0FB4E

Q33277907-AF319BE1-3E1E-4EE7-A587-ECBEB6410AC3

Q33277907-BC31B6E2-4395-4EB0-8A9E-EA2B767C4D2B

P2860

Q33277907-0AEF1DAA-CB58-482B-8FCA-D24311C307BD

Q33277907-15651FA4-05FC-4928-9A1F-608725DBC209

Q33277907-187A73BF-A306-44BB-9BCF-D74FD776F640

Q33277907-1E2C1E35-020A-4679-9A13-9D5346792351

Q33277907-2A5A5A24-8087-41CC-83BF-51EEB81328E6

Q33277907-2BF959DA-4AFC-49E8-997C-821C0F19B327

Q33277907-2DA4B224-A581-4D52-9D11-CE2AD2CB9D40

Q33277907-4851091F-58BD-4441-A610-F6006CC6D4E2

Q33277907-4EB6E294-34FA-46F3-913D-B42071BA8F09

Q33277907-4EC2EC93-49FA-44F2-A11C-B3CF8F3F028E

P304

Q33277907-E550ABDF-4B61-43D4-9AF4-ECDA392E33A2

P31

Q33277907-D0585158-7ACD-4B5F-9464-B3CC4AC61775

P356

Q33277907-B0524FA7-B8F3-4737-9480-4CEED7559036

P433

Q33277907-DA303593-46DE-428E-A940-F95BCA183BBD

P478

Q33277907-9E0661B3-80C2-4A2B-A9C3-67DFCE146290

P50

Q33277907-3C6DB9D0-DAE0-4691-8FE7-64187D4D6E7C

Q33277907-429234F7-94CC-46EB-A829-D30033EA77A0

Q33277907-59AD3768-A104-477A-A3A3-ECA42BE4853A

Q33277907-610FF36B-2C2C-45EA-A409-6898C6AC0BBE

Q33277907-92DE63FB-812A-4785-936F-CDF21254AC1D

Q33277907-C6A94201-3F46-4063-A07C-1E01145BFD4A

Q33277907-C955672B-EF3B-496C-B150-07C4123DD873

Q33277907-F698D42A-3D4A-46A6-BA3A-57846F504101

P577

Q33277907-5BB96218-883A-4822-9255-265B2E084331

P5875

Q33277907-A5AD6398-8898-47F6-998A-AB6AB8293A87

P698

Q33277907-855514A9-98B2-4CB0-B83D-BBB622AB2A89

P921

Q33277907-71536E76-E550-455A-9376-D800E29F5C41

P932

Q33277907-E3D6F95B-0509-4868-ADAF-0018A0A8B81E

P356

JOURNAL.PPAT.0030031

P1433

P1476

Conversion of the BASE prion strain into the BSE strain: the origin of BSE?

@en

P2093

Anne Buschmann

http://www.w3.org/2001/XMLSchema#string

Claudia Miccolo

http://www.w3.org/2001/XMLSchema#string

Cristiano Corona

http://www.w3.org/2001/XMLSchema#string

Daniela Gelmetti

http://www.w3.org/2001/XMLSchema#string

Giacomina Rossi

http://www.w3.org/2001/XMLSchema#string

Giorgio Giaccone

http://www.w3.org/2001/XMLSchema#string

Guerino Lombardi

http://www.w3.org/2001/XMLSchema#string

Lucia Limido

http://www.w3.org/2001/XMLSchema#string

Marcella Catania

http://www.w3.org/2001/XMLSchema#string

Maria Caramelli

http://www.w3.org/2001/XMLSchema#string

P2860

Novel proteinaceous infectious particles cause scrapie

Detection of cattle-derived BSE prions using transgenic mice overexpressing bovine PrP(C).

Distinct molecular phenotypes in bovine prion diseases

A new variant of Creutzfeldt-Jakob disease in the UK.

In vitro generation of infectious scrapie prions.

Abbreviated incubation times for human prions in mice expressing a chimeric mouse-human prion protein transgene

Adaptation of the bovine spongiform encephalopathy agent to primates and comparison with Creutzfeldt-- Jakob disease: implications for human health

Other animal prion diseases.

Transmission of new bovine prion to mice.

P304

e31

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.1371/JOURNAL.PPAT.0030031

http://www.w3.org/2001/XMLSchema#string

P433

3

http://www.w3.org/2001/XMLSchema#string

P478

3

http://www.w3.org/2001/XMLSchema#string

P50

Gianluigi Zanusso

Giuseppe Di Fede

Ludovico Minati

Salvatore Monaco

Pier Luigi Acutis

Maria Grazia Bruzzone

Fabrizio Tagliavini

P577

2007-03-01T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P5875

6453652

http://www.w3.org/2001/XMLSchema#string

P698

17352534

http://www.w3.org/2001/XMLSchema#string

P921

Prion protein family

P932

1817656

http://www.w3.org/2001/XMLSchema#string