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Journal Abstract Search

66 related items for PubMed ID: 7485229

  • 1. SSCP analysis and sequencing of the human prion protein gene (PRNP) detects two different 24 bp deletions in an atypical Alzheimer's disease family.
    Perry RT, Go RC, Harrell LE, Acton RT.
    Am J Med Genet; 1995 Feb 27; 60(1):12-8. PubMed ID: 7485229
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  • 2. Molecular genetics of familial Alzheimer's disease.
    Schellenberg GD.
    Arzneimittelforschung; 1995 Mar 27; 45(3A):418-24. PubMed ID: 7763337
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  • 3. 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 27; 109(3):319-25. PubMed ID: 11702213
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  • 4. [Mutation site of presenilin-1 gene in familial Alzheimer's disease].
    Xu E, Jia J, Sun W.
    Zhonghua Yi Xue Za Zhi; 2002 Nov 25; 82(22):1518-20. PubMed ID: 12609057
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  • 11. Prion protein codon 129 genotype prevalence is altered in primary progressive aphasia.
    Li X, Rowland LP, Mitsumoto H, Przedborski S, Bird TD, Schellenberg GD, Peskind E, Johnson N, Siddique T, Mesulam MM, Weintraub S, Mastrianni JA.
    Ann Neurol; 2005 Dec 25; 58(6):858-64. PubMed ID: 16315279
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  • 13. Novel PKD1 deletions and missense variants in a cohort of Hellenic polycystic kidney disease families.
    Bouba I, Koptides M, Mean R, Costi CE, Demetriou K, Georgiou I, Pierides A, Siamopoulos K, Deltas CC.
    Eur J Hum Genet; 2001 Sep 25; 9(9):677-84. PubMed ID: 11571556
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  • 14. Germline mutational analysis of presenilin 1 and APP genes in Jewish-Israeli individuals with familial or early-onset Alzheimer disease using denaturing gradient gel electrophoresis (DGGE).
    Reznik-Wolf H, Treves TA, Shabtai H, Aharon-Peretz J, Chapman J, Davidson M, Barkai G, Hyslop PH, Goldman B, Korczyn AD, Friedman E.
    Eur J Hum Genet; 1998 Sep 25; 6(2):176-80. PubMed ID: 9781063
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  • 15. Novel presenilin 1 mutation (S170F) causing Alzheimer disease with Lewy bodies in the third decade of life.
    Snider BJ, Norton J, Coats MA, Chakraverty S, Hou CE, Jervis R, Lendon CL, Goate AM, McKeel DW, Morris JC.
    Arch Neurol; 2005 Dec 25; 62(12):1821-30. PubMed ID: 16344340
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  • 16. Oncogenic pathway of sporadic colorectal cancer with novel germline missense mutations in the hMSH2 gene.
    Yamada K, Zhong X, Kanazawa S, Koike J, Tsujita K, Hemmi H.
    Oncol Rep; 2003 Dec 25; 10(4):859-66. PubMed ID: 12792735
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  • 17. Presence of a major WFS1 mutation in Spanish Wolfram syndrome pedigrees.
    Gómez-Zaera M, Strom TM, Rodríguez B, Estivill X, Meitinger T, Nunes V.
    Mol Genet Metab; 2001 Jan 25; 72(1):72-81. PubMed ID: 11161832
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  • 18. Association study and meta-analysis of low-density lipoprotein receptor related protein in Alzheimer's disease.
    Pritchard A, Harris J, Pritchard CW, St Clair D, Lemmon H, Lambert JC, Chartier-Harlin MC, Hayes A, Thaker U, Iwatsubo T, Mann DM, Lendon C.
    Neurosci Lett; 2005 Jul 15; 382(3):221-6. PubMed ID: 15925094
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  • 19. The familial aggregation of Alzheimer's disease: an epidemiological review.
    Rocca WA, Amaducci L.
    Psychiatr Dev; 1988 Jul 15; 6(1):23-36. PubMed ID: 3050982
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  • 20. Polymorphisms at codons 129 and 219 of the prion protein gene (PRNP) are not associated with sporadic Alzheimer's disease in the Korean population.
    Jeong BH, Lee KH, Jeong YE, Hwang KA, Lee YJ, Carp RI, Ju YR, Kim YS.
    Eur J Neurol; 2007 Jun 15; 14(6):621-6. PubMed ID: 17539938
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