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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

60 related articles for article (PubMed ID: 10705652)

  • 1. Molecular analysis of PRNP gene in Polish population and in Creutzfeldt-Jakob disease.
    Bratosiewicz J; Kordek R; Kulczycki J; Botts G; Liberski PP
    Folia Neuropathol; 1999; 37(4):277-80. PubMed ID: 10705652
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Codon 129 polymorphism of the PRNP gene in normal Polish population and in Creutzfeldt-Jakob disease, and the search for new mutations in PRNP gene.
    Bratosiewicz J; Liberski PP; Kulczycki J; Kordek R
    Acta Neurobiol Exp (Wars); 2001; 61(3):151-6. PubMed ID: 11584448
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Genetic basis of Creutzfeldt-Jakob disease in the United Kingdom: a systematic analysis of predisposing mutations and allelic variation in the PRNP gene.
    Windl O; Dempster M; Estibeiro JP; Lathe R; de Silva R; Esmonde T; Will R; Springbett A; Campbell TA; Sidle KC; Palmer MS; Collinge J
    Hum Genet; 1996 Sep; 98(3):259-64. PubMed ID: 8707291
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Creutzfeldt-Jakob disease with E200K mutation in Slovakia: characterization and development.
    Mitrová E; Belay G
    Acta Virol; 2002; 46(1):31-9. PubMed ID: 12197632
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Codon 219 in Creutzfeldt-Jakob disease in Poland.
    Bratosiewicz-Wasik J; Wasik TJ; Liberski PP
    Acta Neurobiol Exp (Wars); 2002; 62(3):149-51. PubMed ID: 12416392
    [TBL] [Abstract][Full Text] [Related]  

  • 6. PRNP variation in UK sporadic and variant Creutzfeldt Jakob disease highlights genetic risk factors and a novel non-synonymous polymorphism.
    Bishop MT; Pennington C; Heath CA; Will RG; Knight RS
    BMC Med Genet; 2009 Dec; 10():146. PubMed ID: 20035629
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Polymorphisms of the prion protein gene in Italian patients with Creutzfeldt-Jakob disease.
    Salvatore M; Genuardi M; Petraroli R; Masullo C; D'Alessandro M; Pocchiari M
    Hum Genet; 1994 Oct; 94(4):375-9. PubMed ID: 7927332
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. Codon 219 Lys allele of PRNP is not found in sporadic Creutzfeldt-Jakob disease.
    Shibuya S; Higuchi J; Shin RW; Tateishi J; Kitamoto T
    Ann Neurol; 1998 Jun; 43(6):826-8. PubMed ID: 9629853
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Distribution of the M129V polymorphism of the prion protein gene in a Turkish population suggests a high risk for Creutzfeldt-Jakob disease.
    Erginel-Unaltuna N; Peoc'h K; Komurcu E; Acuner TT; Issever H; Laplanche JL
    Eur J Hum Genet; 2001 Dec; 9(12):965-8. PubMed ID: 11840201
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. The M129V polymorphism of codon 129 in the prion gene (PRNP) in the Danish population.
    Dyrbye H; Broholm H; Dziegiel MH; Laursen H
    Eur J Epidemiol; 2008; 23(1):23-7. PubMed ID: 17987393
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Analysis of PRNP gene codon 129 polymorphism in the Greek population.
    Saetta AA; Michalopoulos NV; Malamis G; Papanastasiou PI; Mazmanian N; Karlou M; Kouzoupis A; Korkolopoulou P; Patsouris E
    Eur J Epidemiol; 2006; 21(3):211-5. PubMed ID: 16547836
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Association of sporadic Creutzfeldt-Jakob disease with homozygous genotypes at PRNP codons 129 and 219 in the Korean population.
    Jeong BH; Lee KH; Kim NH; Jin JK; Kim JI; Carp RI; Kim YS
    Neurogenetics; 2005 Dec; 6(4):229-32. PubMed ID: 16217673
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Genetic markers in four Chilean families with familial Creutzfeldt-Jakob disease].
    Cartier R L; Fernández O J; Ramírez V E
    Rev Med Chil; 2006 Sep; 134(9):1116-22. PubMed ID: 17171212
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Polymorphisms of the prion protein gene (PRNP) in a Korean population.
    Jeong BH; Nam JH; Lee YJ; Lee KH; Jang MK; Carp RI; Lee HD; Ju YR; Ahn Jo S; Park KY; Kim YS
    J Hum Genet; 2004; 49(6):319-324. PubMed ID: 15148589
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A new point mutation in the prion protein gene at codon 210 in Creutzfeldt-Jakob disease.
    Ripoll L; Laplanche JL; Salzmann M; Jouvet A; Planques B; Dussaucy M; Chatelain J; Beaudry P; Launay JM
    Neurology; 1993 Oct; 43(10):1934-8. PubMed ID: 8105421
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Polymorphisms in the prion protein gene and in the doppel gene increase susceptibility for Creutzfeldt-Jakob disease.
    Croes EA; Alizadeh BZ; Bertoli-Avella AM; Rademaker T; Vergeer-Drop J; Dermaut B; Houwing-Duistermaat JJ; Wientjens DP; Hofman A; Van Broeckhoven C; van Duijn CM
    Eur J Hum Genet; 2004 May; 12(5):389-94. PubMed ID: 14970845
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Creutzfeldt-Jakob disease associated with a V203I homozygous mutation in the prion protein gene.
    Komatsu J; Sakai K; Hamaguchi T; Sugiyama Y; Iwasa K; Yamada M
    Prion; 2014; 8(5):336-8. PubMed ID: 25495585
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Clinicopathological characteristics of Creutzfeldt-Jakob disease with a PrP V180I mutation and M129V polymorphism on different alleles].
    Iwaski Y; Sone M; Kato T; Yoshida E; Indo T; Yoshida M; Hashizume Y; Yamada M
    Rinsho Shinkeigaku; 1999 Aug; 39(8):800-6. PubMed ID: 10586622
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 3.