BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

156 related articles for article (PubMed ID: 10889050)

  • 1. 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]  

  • 2. 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]  

  • 3. Preimplantation exclusion of embryos at risk for prion diseases.
    Meiner V; Weinberg N; Safran A; Israela L; Sagi M; Rosenmann H; Aizenman E; Abeliovich D; Laufer N; Simon A
    Neurology; 2006 Feb; 66(4):607-8. PubMed ID: 16505327
    [No Abstract]   [Full Text] [Related]  

  • 4. Transmission of spongiform encephalopathy from a familial Creutzfeldt-Jakob disease patient of Jewish Libyan origin carrying the PRNP codon 200 mutation.
    Chapman J; Brown P; Rabey JM; Goldfarb LG; Inzelberg R; Gibbs CJ; Gajdusek DC; Korczyn AD
    Neurology; 1992 Jun; 42(6):1249-50. PubMed ID: 1351274
    [No Abstract]   [Full Text] [Related]  

  • 5. Mutation of the prion protein in Libyan Jews with Creutzfeldt-Jakob disease.
    Hsiao K; Meiner Z; Kahana E; Cass C; Kahana I; Avrahami D; Scarlato G; Abramsky O; Prusiner SB; Gabizon R
    N Engl J Med; 1991 Apr; 324(16):1091-7. PubMed ID: 2008182
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Familial Creutzfeldt-Jakob disease with D178N-129M mutation of PRNP presenting as cerebellar ataxia without insomnia.
    Taniwaki Y; Hara H; Doh-Ura K; Murakami I; Tashiro H; Yamasaki T; Shigeto H; Arakawa K; Araki E; Yamada T; Iwaki T; Kira J
    J Neurol Neurosurg Psychiatry; 2000 Mar; 68(3):388. PubMed ID: 10787305
    [No Abstract]   [Full Text] [Related]  

  • 7. 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]  

  • 8. 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]  

  • 9. Presymptomatic signs in healthy CJD mutation carriers.
    Gigi A; Vakil E; Kahana E; Hadar U
    Dement Geriatr Cogn Disord; 2005; 19(5-6):246-55. PubMed ID: 15775715
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Complete penetrance of Creutzfeldt-Jakob disease in Libyan Jews carrying the E200K mutation in the prion protein gene.
    Spudich S; Mastrianni JA; Wrensch M; Gabizon R; Meiner Z; Kahana I; Rosenmann H; Kahana E; Prusiner SB
    Mol Med; 1995 Sep; 1(6):607-13. PubMed ID: 8529127
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. 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]  

  • 13. 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]  

  • 14. Identification of three novel mutations (E196K, V203I, E211Q) in the prion protein gene (PRNP) in inherited prion diseases with Creutzfeldt-Jakob disease phenotype.
    Peoc'h K; Manivet P; Beaudry P; Attane F; Besson G; Hannequin D; Delasnerie-Lauprêtre N; Laplanche JL
    Hum Mutat; 2000 May; 15(5):482. PubMed ID: 10790216
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A novel three extra-repeat insertion in the prion protein gene (PRNP) in a patient with Creutzfeldt-Jakob disease.
    Grasbon-Frodl E; Schmalzbauer R; Weber P; Krebs B; Windl O; Zerr I; Kretzschmar HA
    Neurogenetics; 2004 Dec; 5(4):249-50. PubMed ID: 15480878
    [No Abstract]   [Full Text] [Related]  

  • 16. 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]  

  • 17. Prion protein with an E200K mutation displays properties similar to those of the cellular isoform PrP(C).
    Rosenmann H; Talmor G; Halimi M; Yanai A; Gabizon R; Meiner Z
    J Neurochem; 2001 Mar; 76(6):1654-62. PubMed ID: 11259483
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A case of sporadic Creutzfeldt-Jakob disease with a Gerstmann-Sträussler-Scheinker phenotype but no alterations in the PRNP gene.
    Liberski PP; Bratosiewicz J; Barcikowska M; Cervenakova L; Marczewska M; Brown P; Gajdusek DC
    Acta Neuropathol; 2000 Aug; 100(2):233-4. PubMed ID: 10963373
    [No Abstract]   [Full Text] [Related]  

  • 19. 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]  

  • 20. Genetic Creutzfeldt-Jakob disease in Turkish Jews-demographic and clinical features.
    Menendez L; Milo R; Cohen OS; Chapman J; Rosenmann H; Nitsan Z; Kahana E; Appel S
    Acta Neurol Scand; 2022 Nov; 146(5):586-589. PubMed ID: 35974683
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.