| scholarly article | Q13442814 |
| P356 | DOI | 10.1002/1531-8249(199911)46:5<693::AID-ANA3>3.0.CO;2-Z |
| P698 | PubMed publication ID | 10553985 |
| 10970246 |
| P2093 | author name string | Kretzschmar HA | |
| Poser S | |||
| Schulz-Schaeffer WJ | |||
| Zerr I | |||
| Giese A | |||
| Vieregge P | |||
| Windl O | |||
| Nagele A | |||
| Bergk J | |||
| Nägele A | |||
| Skworc KH | |||
| Zerr I I | |||
| P2860 | cites work | Molecular cloning of a human prion protein cDNA | Q24299790 |
| Detection of polymorphisms of human DNA by gel electrophoresis as single-strand conformation polymorphisms | Q28256462 | ||
| Novel proteinaceous infectious particles cause scrapie | Q29547678 | ||
| Inherited Creutzfeldt-Jakob disease in a British family associated with a novel 144 base pair insertion of the prion protein gene | Q33733564 | ||
| The cellular prion protein binds copper in vivo | Q34450742 | ||
| Molecular biology of prion diseases | Q34534878 | ||
| Transmissible familial Creutzfeldt-Jakob disease associated with five, seven, and eight extra octapeptide coding repeats in the PRNP gene | Q34569015 | ||
| Prion disease associated with a novel nine octapeptide repeat insertion in the PRNP gene. | Q34734259 | ||
| Familial Creutzfeldt-Jakob disease with a five-repeat octapeptide insert mutation | Q34734603 | ||
| Tissue handling in suspected Creutzfeldt-Jakob disease (CJD) and other human spongiform encephalopathies (prion diseases) | Q40922200 | ||
| Creutzfeldt-Jakob disease: Patterns of worldwide occurrence and the significance of familial and sporadic clustering | Q41015587 | ||
| A dementing illness associated with a novel insertion in the prion protein gene | Q42601361 | ||
| Molecular basis of phenotypic variability in sporadic Creutzfeldt-Jakob disease | Q42631333 | ||
| An in-frame insertion in the prion protein gene in familial Creutzfeldt-Jakob disease | Q42631640 | ||
| A simple and effective method for inactivating virus infectivity in formalin‐fixed tissue samples from patients with Creutzfeldt‐Jakob disease | Q45860273 | ||
| Two novel insertions in the prion protein gene in patients with lateonset dementia | Q48073209 | ||
| Prion disease with 144 base pair insertion in a Japanese family line | Q48076727 | ||
| Inherited prion disease with 144 base pair gene insertion. 2. Clinical and pathological features | Q48477322 | ||
| Inherited prion disease with 144 base pair gene insertion. 1. Genealogical and molecular studies | Q48477334 | ||
| Familial prion disease with a novel 144-bp insertion in the prion protein gene in a Basque family. | Q48672320 | ||
| Diagnostic criteria for sporadic Creutzfeldt-Jakob disease | Q48934056 | ||
| Genetic basis of Creutzfeldt-Jakob disease in the United Kingdom: a systematic analysis of predisposing mutations and allelic variation in the PRNP gene | Q48939051 | ||
| A prion disease with a novel 96-base pair insertional mutation in the prion protein gene | Q49103297 | ||
| Classification of sporadic Creutzfeldt-Jakob disease based on molecular and phenotypic analysis of 300 subjects | Q59690387 | ||
| Hypokinesia and presenile dementia in a Dutch family with a novel insertion in the prion protein gene | Q70987295 | ||
| Insert mutation in Creutzfeldt‐Jakob disease | Q72066613 | ||
| A new (two-repeat) octapeptide coding insert mutation in Creutzfeldt-Jakob disease | Q72586596 | ||
| Gene influences on Creutzfeldt-Jakob disease | Q72824505 | ||
| B lymphocytes and neuroinvasion | Q95802945 | ||
| P433 | issue | 5 | |
| P921 | main subject | prion protein family | Q24724413 |
| Creutzfeldt-Jakob disease | Q49989 | ||
| P304 | page(s) | 693-700 | |
| P577 | publication date | 1999-11-01 | |
| P1433 | published in | Annals of Neurology | Q564414 |
| P1476 | title | Familial Creutzfeldt-Jakob disease with a novel 120-bp insertion in the prion protein gene | |
| P478 | volume | 46 |
| Q35889725 | Clinical characterization of a kindred with a novel 12-octapeptide repeat insertion in the prion protein gene |
| Q28910222 | Early onset prion disease from octarepeat expansion correlates with copper binding properties |
| Q46560834 | Genetic PrP Prion Diseases |
| Q39036368 | Genetic prion disease: Experience of a rapidly progressive dementia center in the United States and a review of the literature. |
| Q35122319 | Hereditary Creutzfeldt-Jakob disease and fatal familial insomnia. |
| Q38871224 | Hereditary Human Prion Diseases: an Update |
| Q36359872 | Prion disease genetics |
| Q79564001 | The configuration of the Cu2+ binding region in full-length human prion protein |
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