These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
350 related articles for article (PubMed ID: 8461023)
1. Novel missense variants of prion protein in Creutzfeldt-Jakob disease or Gerstmann-Sträussler syndrome. Kitamoto T; Ohta M; Doh-ura K; Hitoshi S; Terao Y; Tateishi J Biochem Biophys Res Commun; 1993 Mar; 191(2):709-14. PubMed ID: 8461023 [TBL] [Abstract][Full Text] [Related]
2. [Molecular genetics in Creutzfeldt-Jakob disease]. Kitamoto T Rinsho Shinkeigaku; 1994 Dec; 34(12):1222-3. PubMed ID: 7774117 [TBL] [Abstract][Full Text] [Related]
3. A case of sporadic Creutzfeldt-Jakob disease with a Gerstmann-Sträussler-Scheinker phenotype but no alterations in the PRNP gene. Liberski PP; Barcikowska M; Cervenakova L; Bratosiewicz J; Marczewska M; Brown P; Gajdusek DC Acta Neuropathol; 1998 Oct; 96(4):425-30. PubMed ID: 9797009 [TBL] [Abstract][Full Text] [Related]
4. New variant prion protein in a Japanese family with Gerstmann-Sträussler syndrome. Furukawa H; Kitamoto T; Tanaka Y; Tateishi J Brain Res Mol Brain Res; 1995 Jun; 30(2):385-8. PubMed ID: 7637591 [TBL] [Abstract][Full Text] [Related]
5. Creutzfeldt-Jakob disease with codon 129 polymorphism (valine): a comparative study of patients with codon 102 point mutation or without mutations. Miyazono M; Kitamoto T; Doh-ura K; Iwaki T; Tateishi J Acta Neuropathol; 1992; 84(4):349-54. PubMed ID: 1359725 [TBL] [Abstract][Full Text] [Related]
6. Insertions in the prion protein gene in atypical dementias. Owen F; Poulter M; Collinge J; Leach M; Shah T; Lofthouse R; Chen YF; Crow TJ; Harding AE; Hardy J Exp Neurol; 1991 May; 112(2):240-2. PubMed ID: 1674696 [TBL] [Abstract][Full Text] [Related]
7. [Genetic background of human prion diseases]. Kovács GG Ideggyogy Sz; 2007 Nov; 60(11-12):438-46. PubMed ID: 18198790 [TBL] [Abstract][Full Text] [Related]
9. An amber mutation of prion protein in Gerstmann-Sträussler syndrome with mutant PrP plaques. Kitamoto T; Iizuka R; Tateishi J Biochem Biophys Res Commun; 1993 Apr; 192(2):525-31. PubMed ID: 8097911 [TBL] [Abstract][Full Text] [Related]
10. Creutzfeldt-Jakob disease patients with congophilic kuru plaques have the missense variant prion protein common to Gerstmann-Sträussler syndrome. Doh-ura K; Tateishi J; Kitamoto T; Sasaki H; Sakaki Y Ann Neurol; 1990 Feb; 27(2):121-6. PubMed ID: 2180366 [TBL] [Abstract][Full Text] [Related]
11. The primary structure of the prion protein influences the distribution of abnormal prion protein in the central nervous system. Kitamoto T; Doh-ura K; Muramoto T; Miyazono M; Tateishi J Am J Pathol; 1992 Aug; 141(2):271-7. PubMed ID: 1353945 [TBL] [Abstract][Full Text] [Related]
12. [Recent advances in the research of Creutzfeldt-Jakob disease (CJD) and Gerstmann-Strüssler syndrome (GSS)]. Tateishi J Rinsho Shinkeigaku; 1991 Dec; 31(12):1306-8. PubMed ID: 1687809 [TBL] [Abstract][Full Text] [Related]
13. [A trend of molecular genetics on prion diseases and prion protein]. Muramatsu Y; Shinagawa M Nihon Rinsho; 1993 Sep; 51(9):2494-502. PubMed ID: 8411733 [TBL] [Abstract][Full Text] [Related]
14. Presymptomatic detection or exclusion of prion protein gene defects in families with inherited prion diseases. Collinge J; Poulter M; Davis MB; Baraitser M; Owen F; Crow TJ; Harding AE Am J Hum Genet; 1991 Dec; 49(6):1351-4. PubMed ID: 1684089 [TBL] [Abstract][Full Text] [Related]
15. A New Transgenic Mouse Model of Gerstmann-Straussler-Scheinker Syndrome Caused by the A117V Mutation of PRNP. Yang W; Cook J; Rassbach B; Lemus A; DeArmond SJ; Mastrianni JA J Neurosci; 2009 Aug; 29(32):10072-80. PubMed ID: 19675240 [TBL] [Abstract][Full Text] [Related]
16. An Israeli family with Gerstmann-Sträussler-Scheinker disease manifesting the codon 102 mutation in the prion protein gene. Goldhammer Y; Gabizon R; Meiner Z; Sadeh M Neurology; 1993 Dec; 43(12):2718-9. PubMed ID: 7902971 [TBL] [Abstract][Full Text] [Related]
17. A missense mutation at codon 105 with codon 129 polymorphism of the prion protein gene in a new variant of Gerstmann-Sträussler-Scheinker disease. Yamada M; Itoh Y; Fujigasaki H; Naruse S; Kaneko K; Kitamoto T; Tateishi J; Otomo E; Hayakawa M; Tanaka J Neurology; 1993 Dec; 43(12):2723-4. PubMed ID: 7902972 [No Abstract] [Full Text] [Related]
18. Codon 129 polymorphism and the E200K mutation do not affect the cellular prion protein isoform composition in the cerebrospinal fluid from patients with Creutzfeldt-Jakob disease. Schmitz M; Schlomm M; Hasan B; Beekes M; Mitrova E; Korth C; Breil A; Carimalo J; Gawinecka J; Varges D; Zerr I Eur J Neurosci; 2010 Jun; 31(11):2024-31. PubMed ID: 20529115 [TBL] [Abstract][Full Text] [Related]
19. Mutation in codon 200 and polymorphism in codon 129 of the prion protein gene in Libyan Jews with Creutzfeldt-Jakob disease. Gabizon R; Rosenman H; Meiner Z; Kahana I; Kahana E; Shugart Y; Ott J; Prusiner SB Philos Trans R Soc Lond B Biol Sci; 1994 Mar; 343(1306):385-90. PubMed ID: 7913755 [TBL] [Abstract][Full Text] [Related]
20. Different patterns of truncated prion protein fragments correlate with distinct phenotypes in P102L Gerstmann-Sträussler-Scheinker disease. Parchi P; Chen SG; Brown P; Zou W; Capellari S; Budka H; Hainfellner J; Reyes PF; Golden GT; Hauw JJ; Gajdusek DC; Gambetti P Proc Natl Acad Sci U S A; 1998 Jul; 95(14):8322-7. PubMed ID: 9653185 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]