A novel prion disease associated with diarrhea and autonomic neuropathy. - Wikidata - wikimedia - TriplyDB

A novel prion disease associated with diarrhea and autonomic neuropathy.

A novel prion disease associated with diarrhea and autonomic neuropathy.

http://www.wikidata.org/entity/Q37393739

about

Prions, prion-like prionoids, and neurodegenerative disorders Potential Interactions between the Autonomic Nervous System and Higher Level Functions in Neurological and Neuropsychiatric Conditions Prion Diseases Advanced tests for early and accurate diagnosis of Creutzfeldt-Jakob disease.Nonsense mutation in PRNP associated with clinical Alzheimer's disease Proteomics analysis of amyloid and nonamyloid prion disease phenotypes reveals both common and divergent mechanisms of neuropathogenesis The elusive role of the prion protein and the mechanism of toxicity in prion disease.Quantifying prion disease penetrance using large population control cohorts Genetic Prion Disease Caused by PRNP Q160X Mutation Presenting with an Orbitofrontal Syndrome, Cyclic Diarrhea, and Peripheral Neuropathy Distinct patterns of spread of prion infection in brains of mice expressing anchorless or anchored forms of prion protein The clinical approach to autonomic failure in neurological disorders.A new prion disease: relationship with central and peripheral amyloidoses.Hereditary Human Prion Diseases: an Update.Towards a functional pathology of hereditary neuropathies.Genetic prion disease: Experience of a rapidly progressive dementia center in the United States and a review of the literature.Preparation and Immunostaining of the Myenteric Plexus of Prion-Infected Mice.Ultrastructure and pathology of prion protein amyloid accumulation and cellular damage in extraneural tissues of scrapie-infected transgenic mice expressing anchorless prion protein.Transgenic mice recapitulate the phenotypic heterogeneity of genetic prion diseases without developing prion infectivity: Role of intracellular PrP retention in neurotoxicity Late onset hereditary sensory and autonomic neuropathy with cognitive impairment associated with Y163X prion mutation.Experimental transfusion of variant CJD-infected blood reveals previously uncharacterised prion disorder in mice and macaque.Amyloid fibril proteins and amyloidosis: chemical identification and clinical classification International Society of Amyloidosis 2016 Nomenclature Guidelines.A novel prion protein variant in a patient with semantic dementia.Prion protein inhibits fast axonal transport through a mechanism involving casein kinase 2.Methods for Molecular Diagnosis of Human Prion Disease.Different Complicated Brain Pathologies in Monozygotic Twins With Gerstmann-Sträussler-Scheinker Disease.C-Terminal-Deleted Prion Protein Fragment Is a Major Accumulated Component of Systemic PrP Deposits in Hereditary Prion Disease With a 2-Bp (CT) Deletion in PRNP Codon 178.Familial human prion diseases associated with prion protein mutations Y226X and G131V are transmissible to transgenic mice expressing human prion protein.Prion Proteins Without the Glycophosphatidylinositol Anchor: Potential Biomarkers in Neurodegenerative Diseases.Peripheral nervous system hyperexcitability in VV2 sporadic Creutzfeldt-Jakob disease.Q-Rich Yeast Prion [PSI+] Accelerates Aggregation of Transthyretin, a Non-Q-Rich Human Protein.Two novel PRNP truncating mutations broaden the spectrum of prion amyloidosis.Detection of tau in Gerstmann-Sträussler-Scheinker disease (PRNP F198S) by [F]Flortaucipir PET Evaluating the causality of novel sequence variants in the prion protein gene by example Characterization of mutations in (prion) gene and their possible roles in neurodegenerative diseases

P2860

Q26747002-D87F5605-1776-41ED-8834-0742A1370F76 Q26782934-BFAC752E-76D3-47CC-A811-B5028327FF8E Q28080751-5EE39F73-5A28-4098-B187-A2C02D6C91E0 Q31095751-F520AA98-E23A-4FDC-968E-BD372D8FFACF Q34244138-D30D74EA-E5D2-47F6-8B7D-F16E2ABB40AA Q34488612-50C00588-A904-48A3-8088-4E76C2C24EC6 Q35624321-045D3C45-3DF2-4EC4-BC77-07153A26CC5B Q36639581-C3FBD2CC-8CEF-417F-BECD-17F174184E94 Q37491711-8EF2FE43-96B6-4BE4-9911-497098DFDFAB Q37522591-0163FAE4-35E6-45F7-B121-4E96C688926D Q38215382-4590379E-E86F-4B28-A6FF-E6E7DF5EE0A0 Q38333529-CF280589-8D30-430B-983A-6E9458520966 Q38871224-80AD4923-AEE6-4A96-AE26-FB913C5A53CF Q39023144-21481672-FA4B-441A-A630-58DB4BC4F5E3 Q39036368-D6CD9063-92E1-4B81-8E34-34675DA6D8AB Q40071072-47CE47D5-C92E-4E2B-8081-3FB78135E369 Q40101379-09F907A6-19CB-4752-9E67-1C03F3BBE16A Q40796560-74969600-214C-4CFE-AF8B-65202E850B07 Q42976956-6C2569C1-C2E1-44DD-8D72-3ED89D131EA1 Q43028951-8108E50F-CA34-4EDC-A12C-500EDA53E2DB Q46502103-86C7CB68-5F08-4619-B569-D5BB18901D05 Q47096801-C65177B2-1DA5-4786-9713-0F7608BE0D11 Q47271332-6E4ABD50-CD88-4CFB-B7FD-415B70AF2D47 Q47690532-4AA651CA-574A-4911-8280-7F84F7A978AF Q47784219-52604EF9-395A-4159-9DB0-0FA390375B04 Q48000756-31A62D10-C508-4AD3-BAB7-2B8014796A02 Q49843002-4CB28D0C-B518-4515-8B8C-934A9F2EB0AB Q49957320-037427CE-4A4F-477F-AFA9-C3F2B7CE308A Q50007931-5689CF3A-0D94-4CF3-A538-664E5BB42555 Q55080630-B221092B-8A5D-43A0-8BE4-7C4F016B21B8 Q55285207-DC9BC011-4C9B-4EE0-B2AA-0B8416B561C3 Q58099840-27A13A13-22FD-43A3-B9F0-E022462852BA Q58702787-8EC28597-F0B7-4253-B13A-6159018EE0AA Q58781975-25266B5E-43FE-497F-A608-F91C4FB89DD0

P2860

A novel prion disease associated with diarrhea and autonomic neuropathy.

http://www.wikidata.org/entity/Q37393739

description

2013 nî lūn-bûn

@nan

2013年の論文

@ja

2013年学术文章

@wuu

2013年学术文章

@zh-cn

2013年学术文章

@zh-hans

2013年学术文章

@zh-my

2013年学术文章

@zh-sg

2013年學術文章

@yue

2013年學術文章

@zh

2013年學術文章

@zh-hant

name

A novel prion disease associated with diarrhea and autonomic neuropathy.

@en

A novel prion disease associated with diarrhea and autonomic neuropathy.

@nl

type

label

A novel prion disease associated with diarrhea and autonomic neuropathy.

@en

A novel prion disease associated with diarrhea and autonomic neuropathy.

@nl

prefLabel

A novel prion disease associated with diarrhea and autonomic neuropathy.

@en

A novel prion disease associated with diarrhea and autonomic neuropathy.

@nl

P1433

Q37393739-EEC60134-5F0E-427D-84AC-57DC5CD9A9BF

P1476

Q37393739-BD552B69-5905-41A7-B67D-C1DFE28327E3

P2093

Q37393739-1859C5A7-E2FA-4A97-BB83-B4245EADC90A

Q37393739-228D4F7A-298D-4210-BB9F-099A620DF551

Q37393739-3ABAB133-72EB-4461-8255-8CEA6406BB75

Q37393739-4663AE3C-D641-48BD-82D6-688135BA51B9

Q37393739-53FC4C01-8FCC-44C9-BC26-7614ED6A2ADC

Q37393739-6AB36801-A427-40C0-B704-66355AEB5438

Q37393739-6C7D9958-6050-408A-9EB5-89AD34598FD2

Q37393739-73DE9D95-4033-49FB-A4A1-2BFF30AFCDD6

Q37393739-79B7751A-04B0-4AD0-89DD-520FE7DF5388

Q37393739-7E18EB5F-0FE9-49A2-9AC6-F09236A34486

P2860

Q37393739-0554ACE2-AC09-4DF0-8A21-3C0441F60887

Q37393739-08C97487-13D7-411D-81E1-D9C526B010E1

Q37393739-09F30293-2AAB-4197-8937-F42FE187E83B

Q37393739-0DFA811B-C847-4D94-BD26-4F4521663D1E

Q37393739-1E17DFED-F0D2-4725-9229-D20766174C0C

Q37393739-36543783-C6D3-45D0-B225-88157492C165

Q37393739-607FE094-4E9B-4703-AD52-FBDB14A82A8B

Q37393739-60E1F393-C05D-4A3B-B334-52810BBB035E

Q37393739-6963D9BD-F55F-425A-822E-1BAA32F942C8

Q37393739-766BAEBD-FF1E-496D-9B4B-6776616A5E8C

P304

Q37393739-C4B7B9D1-03FA-4FFD-AE9E-5F1B03B1D236

P31

Q37393739-667A2E97-48D3-4711-AA9A-17306C2F90BA

P356

Q37393739-1815C5AB-557D-493D-95D1-824A7ECD3D1C

P407

Q37393739-5379D3D1-6068-478A-AEE4-BF3BB7F7666C

P433

Q37393739-CE95F67A-E52C-4800-BD5D-9883165531A8

P478

Q37393739-A35DBFCD-16A5-41EE-B3EF-A183F1735962

P50

Q37393739-6CFFF60E-1DFC-4AE8-BE53-C3ABD9D516EC

Q37393739-92714E0D-DC3B-4910-973A-5E2876847C76

Q37393739-A3822237-BC62-4C02-83A1-32DC36650DA7

Q37393739-DD94A87F-2092-409F-A55B-DE73AC341DDF

P577

Q37393739-2394B27D-A611-4ADD-A2BC-5A52792BB975

P698

Q37393739-0A77F6C2-D857-44A0-BBFF-EFB4FEBBBB5E

P921

Q37393739-B855440F-C878-4506-B127-8A65AF9EE71C

Q37393739-CE5C1C65-8D1A-4D56-BF16-F371FF9807D9

P932

Q37393739-2B045505-A004-4B89-9D6B-53A2A708CCD2

P356

P1433

The New England Journal of Medicine

P1476

A novel prion disease associated with diarrhea and autonomic neuropathy.

@en

P2093

Bernadette Sharps

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

Christopher Carswell

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

Diana Caine

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

Dillip Gallujipali

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

Harpreet Hyare

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

Hilary Ayling

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

Huda Al-Doujaily

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

Jacqueline M Linehan

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

Jason D Warren

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

John Collinge

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

P2860

Kuru prions and sporadic Creutzfeldt-Jakob disease prions have equivalent transmission properties in transgenic and wild-type mice

Fatal familial insomnia, a prion disease with a mutation at codon 178 of the prion protein gene

Familial and sporadic fatal insomnia

Prion diseases of humans and animals: their causes and molecular basis

Mutations of the prion protein gene phenotypic spectrum

Anchorless prion protein results in infectious amyloid disease without clinical scrapie

A general model of prion strains and their pathogenicity

Prion protein amyloidosis with divergent phenotype associated with two novel nonsense mutations in PRNP.

Vascular variant of prion protein cerebral amyloidosis with tau-positive neurofibrillary tangles: the phenotype of the stop codon 145 mutation in PRNP.

Sporadic and familial CJD: classification and characterisation.

P304

1904-1914

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

P31

scholarly article

P356

10.1056/NEJMOA1214747

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

P407

P433

20

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

P478

369

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

P50

Jason D. Warren

Nicholas W. Wood

Alastair Forbes

P577

2013-11-01T00:00:00Z

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

P698

24224623

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

P921

Prion protein family

Afọ ọsịsa

P932

3863770

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