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Journal Abstract Search
384 related items for PubMed ID: 14970845
1. 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 [Abstract] [Full Text] [Related]
2. Polymorphism at 3' UTR +28 of the prion-like protein gene is associated with sporadic Creutzfeldt-Jakob disease. Jeong BH, Kim NH, Choi EK, Lee C, Song YH, Kim JI, Carp RI, Kim YS. Eur J Hum Genet; 2005 Sep; 13(9):1094-7. PubMed ID: 15986038 [Abstract] [Full Text] [Related]
3. 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, KORA group, Kretzschmar HA. J Med Genet; 2006 Oct; 43(10):e53. PubMed ID: 17047093 [Abstract] [Full Text] [Related]
5. Polymorphisms within the prion-like protein gene (Prnd) and their implications in human prion diseases, Alzheimer's disease and other neurological disorders. Schröder B, Franz B, Hempfling P, Selbert M, Jürgens T, Kretzschmar HA, Bodemer M, Poser S, Zerr I. Hum Genet; 2001 Sep; 109(3):319-25. PubMed ID: 11702213 [Abstract] [Full Text] [Related]
7. Polymorphisms at codons 56 and 174 of the prion-like protein gene (PRND) are not associated with sporadic Creutzfeldt-Jakob disease. Jeong BH, Kim NH, Kim JI, Carp RI, Kim YS. J Hum Genet; 2005 Sep; 50(6):311-314. PubMed ID: 15933804 [Abstract] [Full Text] [Related]
8. 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 [Abstract] [Full Text] [Related]
9. Prion-like Doppel gene polymorphisms and scrapie susceptibility in Portuguese sheep breeds. Mesquita P, Batista M, Marques MR, Santos IC, Pimenta J, Silva Pereira M, Carolino I, Santos Silva F, Oliveira Sousa MC, Gama LT, Fontes CM, Horta AE, Prates JA, Pereira RM. Anim Genet; 2010 Jun; 41(3):311-4. PubMed ID: 19968641 [Abstract] [Full Text] [Related]
18. Cathepsin D (C224T) polymorphism in sporadic and genetic Creutzfeldt-Jakob disease. Kovacs GG, Sanchez-Juan P, Ströbel T, Schuur M, Poleggi A, Nocentini S, Giannattasio C, Belay G, Bishop M, Capellari S, Parchi P, Gelpi E, Gal A, Bakos A, Molnar MJ, Heinemann U, Zerr I, Knight RS, Mitrova E, van Duijn C, Budka H. Alzheimer Dis Assoc Disord; 2010 Nov 08; 24(1):104-7. PubMed ID: 19571726 [Abstract] [Full Text] [Related]
19. A polymorphism in the regulatory region of PRNP is associated with increased risk of sporadic Creutzfeldt-Jakob disease. Sanchez-Juan P, Bishop MT, Croes EA, Knight RS, Will RG, van Duijn CM, Manson JC. BMC Med Genet; 2011 May 22; 12():73. PubMed ID: 21600043 [Abstract] [Full Text] [Related]