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4. Polymorphisms of the prion protein gene (PRNP) in a Serbian population. Dimitrijević R; Cadez I; Keckarević-Marković M; Keckarević D; Kecmanović M; Dobricić V; Savić-Pavićević D; Brajusković G; Romac S Int J Neurosci; 2010 Jul; 120(7):496-501. PubMed ID: 20583902 [TBL] [Abstract][Full Text] [Related]
5. Inherited prion disease with six octapeptide repeat insertional mutation--molecular analysis of phenotypic heterogeneity. Mead S; Poulter M; Beck J; Webb TE; Campbell TA; Linehan JM; Desbruslais M; Joiner S; Wadsworth JD; King A; Lantos P; Collinge J Brain; 2006 Sep; 129(Pt 9):2297-317. PubMed ID: 16923955 [TBL] [Abstract][Full Text] [Related]
6. Genotype-phenotype analysis in inherited prion disease with eight octapeptide repeat insertional mutation. Paucar M; Xiang F; Moore R; Walker R; Winnberg E; Svenningsson P Prion; 2013; 7(6):501-10. PubMed ID: 24275071 [TBL] [Abstract][Full Text] [Related]
7. Clinical characterization of a kindred with a novel 12-octapeptide repeat insertion in the prion protein gene. Kumar N; Boeve BF; Boot BP; Orr CF; Duffy J; Woodruff BK; Nair AK; Ellison J; Kuntz K; Kantarci K; Jack CR; Westmoreland BF; Fields JA; Baker M; Rademakers R; Parisi JE; Dickson DW Arch Neurol; 2011 Sep; 68(9):1165-70. PubMed ID: 21911696 [TBL] [Abstract][Full Text] [Related]
8. Prion protein with an octapeptide insertion has impaired neuroprotective activity in transgenic mice. Li A; Piccardo P; Barmada SJ; Ghetti B; Harris DA EMBO J; 2007 Jun; 26(11):2777-85. PubMed ID: 17510630 [TBL] [Abstract][Full Text] [Related]
9. Familial prion disease in a Hungarian family with a novel 144-base pair insertion in the prion protein gene. Kovács T; Beck JA; Papp MI; Lantos PL; Arányi Z; Szirmai IG; Farsang M; Stuke A; Csillik A; Collinge J J Neurol Neurosurg Psychiatry; 2007 Mar; 78(3):321-3. PubMed ID: 17308293 [TBL] [Abstract][Full Text] [Related]
10. Mutations and polymorphisms in the prion protein gene. Palmer MS; Collinge J Hum Mutat; 1993; 2(3):168-73. PubMed ID: 8364585 [TBL] [Abstract][Full Text] [Related]
11. Inherited prion disease with A117V mutation of the prion protein gene: a novel Hungarian family. Kovács GG; Ertsey C; Majtényi C; Jelencsik I; László L; Flicker H; Strain L; Szirmai I; Budka H J Neurol Neurosurg Psychiatry; 2001 Jun; 70(6):802-5. PubMed ID: 11385020 [TBL] [Abstract][Full Text] [Related]
12. A case with a 120 base pair insertional mutation in the prion protein gene: the first case in Japan. Beck G; Kawano T; Naba I; Nishimura T; Sawada J; Hazama T J Neurol Neurosurg Psychiatry; 2005 May; 76(5):756-7. PubMed ID: 15834045 [No Abstract] [Full Text] [Related]
14. [Prion protein coden 129 polymorphism (Val/Met) in a case of sporadic progressive multisystem degenerative disease]. Komai K; Masaharu T; Kitamoto T Rinsho Shinkeigaku; 1993 Jun; 33(6):666-7. PubMed ID: 8403690 [No Abstract] [Full Text] [Related]
15. Prion Protein Devoid of the Octapeptide Repeat Region Delays Bovine Spongiform Encephalopathy Pathogenesis in Mice. Hara H; Miyata H; Das NR; Chida J; Yoshimochi T; Uchiyama K; Watanabe H; Kondoh G; Yokoyama T; Sakaguchi S J Virol; 2018 Jan; 92(1):. PubMed ID: 29046443 [TBL] [Abstract][Full Text] [Related]
16. Is codon 129 of prion protein polymorphic in human beings but not in animals? Schätzl HM; Wopfner F; Gilch S; von Brunn A; Jäger G Lancet; 1997 May; 349(9065):1603-4. PubMed ID: 9174569 [No Abstract] [Full Text] [Related]
17. The influence of PRNP polymorphisms on human prion disease susceptibility: an update. Kobayashi A; Teruya K; Matsuura Y; Shirai T; Nakamura Y; Yamada M; Mizusawa H; Mohri S; Kitamoto T Acta Neuropathol; 2015 Aug; 130(2):159-70. PubMed ID: 26022925 [TBL] [Abstract][Full Text] [Related]
18. Distinct neuropsychological profiles correspond to distribution of cortical thinning in inherited prion disease caused by insertional mutation. Alner K; Hyare H; Mead S; Rudge P; Wroe S; Rohrer JD; Ridgway GR; Ourselin S; Clarkson M; Hunt H; Fox NC; Webb T; Collinge J; Cipolotti L J Neurol Neurosurg Psychiatry; 2012 Jan; 83(1):109-14. PubMed ID: 21849340 [TBL] [Abstract][Full Text] [Related]
19. [Prion disease: a new class of neurodegenerative disorders]. van Gool WA; Hoogerwaard EM; Kuiper MA; Portegies P; Bolhuis PA Ned Tijdschr Geneeskd; 1995 Mar; 139(12):606-13. PubMed ID: 7700403 [No Abstract] [Full Text] [Related]
20. Genetics of human prion disease. Ridley RM; Baker HF Dev Biol Stand; 1993; 80():15-23. PubMed ID: 7903647 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]