Inherited Creutzfeldt-Jakob disease in a British family associated with a novel 144 base pair insertion of the prion protein gene.
about
Context dependent neuroprotective properties of prion protein (PrP).Creutzfeldt-Jakob disease and the eye. I. Background and patient management.Creutzfeldt-Jakob disease and the eye. II. Ophthalmic and neuro-ophthalmic features.Clinical characterization of a kindred with a novel 12-octapeptide repeat insertion in the prion protein gene.Familial prion disease in a Hungarian family with a novel 144-base pair insertion in the prion protein geneProtease-sensitive prions with 144-bp insertion mutationsTwo mutant prion proteins expressed in cultured cells acquire biochemical properties reminiscent of the scrapie isoform.A mutant prion protein displays an aberrant membrane association when expressed in cultured cells.Hereditary Human Prion Diseases: an Update.Familial Creutzfeldt-Jakob disease with a novel 120-bp insertion in the prion protein gene[Creutzfeldt-Jakob disease: case report with spinal cord involvement]Prion encephalopathy with insertion of octapeptide repeats: the number of repeats determines the type of cerebellar deposits.Sequence variation in intron of prion protein gene, crucial for complete diagnostic strategies.The prion diseases: Creutzfeldt-Jakob, Gerstmann-Sträussler-Scheinker, and related disorders.
P2860
Q33595425-64C5F8A1-04E0-48C7-8024-24CAE88B27ACQ34057654-8F7034E7-1796-48BC-B6FD-9E019880BF94Q34057658-86483DBE-AB8A-4D84-A710-DFA9F93B06EAQ35889725-9BC812FC-C25D-4AD7-9933-ADA7E14267F0Q36226900-1BC03EB6-CD60-4780-A124-EDC2D8E2F5C2Q36774861-4A5E150A-532F-4C1F-BAB4-4B35DA7E47C8Q37593764-F315A7F7-3AAF-4691-A554-FC482A4386D0Q38290309-9951689D-5398-4BF1-922E-09F350F51F9CQ38871224-0C1447DE-3E88-4436-A584-ABCC040F7EAFQ41604182-617728D8-00D3-481C-8B62-66E2F66EA5CCQ43815986-4E99E557-2665-4E2D-AA8E-C873B0859859Q47950242-AAF82FDF-E412-4A49-93FD-511A982284F7Q48067405-E3F432EA-D2E5-458A-B675-63C4B5A25EB2Q48313878-228CF1BF-8EB4-4A46-B697-5BB9E12CB0AF
P2860
Inherited Creutzfeldt-Jakob disease in a British family associated with a novel 144 base pair insertion of the prion protein gene.
description
1995 nî lūn-bûn
@nan
1995 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
1995 թվականի հունվարին հրատարակված գիտական հոդված
@hy
1995年の論文
@ja
1995年論文
@yue
1995年論文
@zh-hant
1995年論文
@zh-hk
1995年論文
@zh-mo
1995年論文
@zh-tw
1995年论文
@wuu
name
Inherited Creutzfeldt-Jakob di ...... ion of the prion protein gene.
@ast
Inherited Creutzfeldt-Jakob di ...... ion of the prion protein gene.
@en
type
label
Inherited Creutzfeldt-Jakob di ...... ion of the prion protein gene.
@ast
Inherited Creutzfeldt-Jakob di ...... ion of the prion protein gene.
@en
prefLabel
Inherited Creutzfeldt-Jakob di ...... ion of the prion protein gene.
@ast
Inherited Creutzfeldt-Jakob di ...... ion of the prion protein gene.
@en
P2093
P2860
P356
P1476
Inherited Creutzfeldt-Jakob di ...... ion of the prion protein gene.
@en
P2093
Dempster M
Estibeiro JP
Ironside JW
de Silva R
P2860
P356
10.1136/JNNP.58.1.65
P407
P577
1995-01-01T00:00:00Z