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 *

222 related articles for article (PubMed ID: 10090891)

  • 1. Ancestral origins and worldwide distribution of the PRNP 200K mutation causing familial Creutzfeldt-Jakob disease.
    Lee HS; Sambuughin N; Cervenakova L; Chapman J; Pocchiari M; Litvak S; Qi HY; Budka H; del Ser T; Furukawa H; Brown P; Gajdusek DC; Long JC; Korczyn AD; Goldfarb LG
    Am J Hum Genet; 1999 Apr; 64(4):1063-70. PubMed ID: 10090891
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Sporadic--but not variant--Creutzfeldt-Jakob disease is associated with polymorphisms upstream of PRNP exon 1.
    Mead S; Mahal SP; Beck J; Campbell T; Farrall M; Fisher E; Collinge J
    Am J Hum Genet; 2001 Dec; 69(6):1225-35. PubMed ID: 11704923
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Age and origin of the PRNP E200K mutation causing familial Creutzfeldt-Jacob disease in Libyan Jews.
    Colombo R
    Am J Hum Genet; 2000 Aug; 67(2):528-31. PubMed ID: 10889050
    [No Abstract]   [Full Text] [Related]  

  • 4. 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]  

  • 5. Familial Creutzfeldt-Jakob disease. Codon 200 prion disease in Libyan Jews.
    Meiner Z; Gabizon R; Prusiner SB
    Medicine (Baltimore); 1997 Jul; 76(4):227-37. PubMed ID: 9279329
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Ancestral origins of the prion protein gene D178N mutation in the Basque Country.
    Rodríguez-Martínez AB; Barreau C; Coupry I; Yagüe J; Sánchez-Valle R; Galdós-Alcelay L; Ibáñez A; Digón A; Fernández-Manchola I; Goizet C; Castro A; Cuevas N; Alvarez-Alvarez M; de Pancorbo MM; Arveiler B; Zarranz JJ
    Hum Genet; 2005 Jun; 117(1):61-9. PubMed ID: 15806397
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Mutation at codon 210 (V210I) of the prion protein gene in a North African patient with Creutzfeldt-Jakob disease.
    Mouillet-Richard S; Teil C; Lenne M; Hugon S; Taleb O; Laplanche JL
    J Neurol Sci; 1999 Oct; 168(2):141-4. PubMed ID: 10526198
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. 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]  

  • 10. Mutation of the PRNP gene at codon 211 in familial Creutzfeldt-Jakob disease.
    Ladogana A; Almonti S; Petraroli R; Giaccaglini E; Ciarmatori C; Liù QG; Bevivino S; Squitieri F; Pocchiari M
    Am J Med Genet; 2001 Oct; 103(2):133-7. PubMed ID: 11568919
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Polymorphism of PRNP codons in the normal Icelandic population.
    Georgsson G; Tryggvason T; Jonasdottir AD; Gudmundsson S; Thorgeirsdottir S
    Acta Neurol Scand; 2006 Jun; 113(6):419-25. PubMed ID: 16674609
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Familial Creutzfeldt-Jakob disease in Chile is associated with the codon 200 mutation of the PRNP amyloid precursor gene on chromosome 20.
    Brown P; Gálvez S; Goldfarb LG; Nieto A; Cartier L; Gibbs CJ; Gajdusek DC
    J Neurol Sci; 1992 Oct; 112(1-2):65-7. PubMed ID: 1469441
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A mutation in the prion protein gene in Creutzfeldt-Jakob disease in Jewish patients of Libyan, Greek, and Tunisian origin.
    Korczyn AD; Chapman J; Goldfarb LG; Brown P; Gajdusek DC
    Ann N Y Acad Sci; 1991; 640():171-6. PubMed ID: 1685643
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. Sporadic and familial CJD: classification and characterisation.
    Gambetti P; Kong Q; Zou W; Parchi P; Chen SG
    Br Med Bull; 2003; 66():213-39. PubMed ID: 14522861
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Significant association of a M129V independent polymorphism in the 5' UTR of the PRNP gene with sporadic Creutzfeldt-Jakob disease in a large German case-control study.
    Vollmert C; Windl O; Xiang W; Rosenberger A; Zerr I; Wichmann HE; Bickeböller H; Illig T; ; Kretzschmar HA
    J Med Genet; 2006 Oct; 43(10):e53. PubMed ID: 17047093
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Mutation and polymorphism of the prion protein gene in Libyan Jews with Creutzfeldt-Jakob disease (CJD).
    Gabizon R; Rosenmann H; Meiner Z; Kahana I; Kahana E; Shugart Y; Ott J; Prusiner SB
    Am J Hum Genet; 1993 Oct; 53(4):828-35. PubMed ID: 8105682
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Polymorphic microsatellite sites in the PRNP region point to excess of homozygotes in Creutzfeldt-Jakob disease patients.
    Geldermann H; Bartenschlager H; Preuss S; Melchinger-Wild E; Herzog K; Zerr I
    Gene; 2006 Nov; 382():66-70. PubMed ID: 16889908
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A patient with dementia with Lewy bodies and codon 232 mutation of PRNP.
    Koide T; Ohtake H; Nakajima T; Furukawa H; Sakai K; Kamei H; Makifuchi T; Fukuhara N
    Neurology; 2002 Nov; 59(10):1619-21. PubMed ID: 12451207
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Creutzfeldt-Jacob disease associated with the PRNP codon 200Lys mutation: an analysis of 45 families.
    Goldfarb LG; Brown P; Mitrovà E; Cervenáková L; Goldin L; Korczyn AD; Chapman J; Gálvez S; Cartier L; Rubenstein R
    Eur J Epidemiol; 1991 Sep; 7(5):477-86. PubMed ID: 1684755
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.