scholarly article | Q13442814 |
P356 | DOI | 10.1046/J.1365-2990.2003.00423.X |
P8608 | Fatcat ID | release_fgjfabq5drfadapyxof5fo7d54 |
P698 | PubMed publication ID | 12662318 |
P50 | author | Péter Lantos | Q1127948 |
P2093 | author name string | Rossor M | |
King A | |||
Collinge J | |||
Doey L | |||
Mead S | |||
P2860 | cites work | An inherited prion disease with a PrP P105L mutation: clinicopathologic and PrP heterogeneity | Q33688704 |
Fatal familial insomnia: clinical and pathologic heterogeneity in genetic half brothers | Q48327510 | ||
Familial prion disease with a novel 144-bp insertion in the prion protein gene in a Basque family. | Q48672320 | ||
P433 | issue | 2 | |
P921 | main subject | prion protein family | Q24724413 |
P304 | page(s) | 98-105 | |
P577 | publication date | 2003-04-01 | |
P1433 | published in | Neuropathology and Applied Neurobiology | Q7002494 |
P1476 | title | Phenotypic variability in the brains of a family with a prion disease characterized by a 144-base pair insertion in the prion protein gene | |
P478 | volume | 29 |
Q35103451 | A case of Gerstmann-Sträussler-Scheinker disease with a novel six octapeptide repeat insertion |
Q33966829 | Analysis of the [RNQ+] prion reveals stability of amyloid fibers as the key determinant of yeast prion variant propagation |
Q49076261 | Biology and neuropathology of prion diseases |
Q38924501 | Cerebellar compartmentation of prion pathogenesis |
Q28910222 | Early onset prion disease from octarepeat expansion correlates with copper binding properties |
Q36226900 | Familial prion disease in a Hungarian family with a novel 144-base pair insertion in the prion protein gene |
Q33716193 | Filamentous white matter prion protein deposition is a distinctive feature of multiple inherited prion diseases |
Q47577189 | Gerstmann-Sträussler-Scheinker disease with atypical presentation. |
Q37355539 | Insights into intragenic and extragenic effectors of prion propagation using chimeric prion proteins |
Q36310865 | Phenotypic variability in human prion diseases. |
Q36359872 | Prion disease genetics |
Q33325657 | Prion protein insertional mutations increase aggregation propensity but not fiber stability |
Q35950108 | Prion protein repeat expansion results in increased aggregation and reveals phenotypic variability. |
Q36774861 | Protease-sensitive prions with 144-bp insertion mutations |
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