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608 related items for PubMed ID: 18396294

  • 1. Genetic analysis of tumor necrosis factor-alpha (TNF-alpha) G-308A and Saitohin Q7R polymorphisms with Alzheimer's disease.
    Wang B, Zhou S, Yang Z, Xie YC, Wang J, Zhang P, Lv Z, Zheng C, Ma X.
    J Neurol Sci; 2008 Jul 15; 270(1-2):148-51. PubMed ID: 18396294
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  • 2. Association between somatostatin gene polymorphisms and sporadic Alzheimer's disease in Chinese population.
    Xue S, Jia L, Jia J.
    Neurosci Lett; 2009 Nov 13; 465(2):181-3. PubMed ID: 19733630
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  • 3. Association between apolipoprotein E polymorphism and Alzheimer disease in Tehran, Iran.
    Raygani AV, Zahrai M, Raygani AV, Doosti M, Javadi E, Rezaei M, Pourmotabbed T.
    Neurosci Lett; 2005 Feb 25; 375(1):1-6. PubMed ID: 15664112
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  • 4. The CDC2 I-G-T haplotype associated with the APOE epsilon4 allele increases the risk of sporadic Alzheimer's disease in Sicily.
    Bosco P, Caraci F, Copani A, Spada RS, Sortino MA, Salluzzo R, Salemi M, Nicoletti F, Ferri R.
    Neurosci Lett; 2007 Jun 04; 419(3):195-8. PubMed ID: 17498878
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  • 8. Association between presenilin 1 intronic polymorphism and late onset Alzheimer's disease in the North Chinese population.
    Jia L, Zhou C, Lv H, Wang W, Ye J, Zhang X, Zhou W, Xu J, Wang L, Jia J.
    Brain Res; 2006 Oct 20; 1116(1):201-5. PubMed ID: 16938285
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  • 9. Apolipoprotein E epsilon4 allele frequency in elderly depressed patients with and without cerebrovascular disease.
    Traykov L, Bayle AC, Latour F, Lenoir H, Seux ML, Hanon O, Péquignot R, Bert P, Moulin F, Cantegreil I, Wenisch E, Batouche F, Mehrabian S, Rotrou Jd, Rigaud AS.
    J Neurol Sci; 2007 Jun 15; 257(1-2):280-3. PubMed ID: 17337010
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  • 10. Molecular evolution and genetics of the Saitohin gene and tau haplotype in Alzheimer's disease and argyrophilic grain disease.
    Conrad C, Vianna C, Schultz C, Thal DR, Ghebremedhin E, Lenz J, Braak H, Davies P.
    J Neurochem; 2004 Apr 15; 89(1):179-88. PubMed ID: 15030402
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  • 11. Association study of the GAB2 gene with the risk of developing Alzheimer's disease.
    Chapuis J, Hannequin D, Pasquier F, Bentham P, Brice A, Leber I, Frebourg T, Deleuze JF, Cousin E, Thaker U, Amouyel P, Mann D, Lendon C, Campion D, Lambert JC.
    Neurobiol Dis; 2008 Apr 15; 30(1):103-6. PubMed ID: 18272374
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  • 12. TAU haplotype and the Saitohin Q7R gene polymorphism do not influence CSF Tau in Alzheimer's disease and are not associated with frontotemporal dementia or Parkinson's disease.
    Johansson A, Zetterberg H, Håkansson A, Nissbrandt H, Blennow K.
    Neurodegener Dis; 2005 Apr 15; 2(1):28-35. PubMed ID: 16909000
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  • 13. Interleukin 6-174 G/C promoter and variable number of tandem repeats (VNTR) gene polymorphisms in sporadic Alzheimer's disease.
    Capurso C, Solfrizzi V, Colacicco AM, D'Introno A, Frisardi V, Imbimbo BP, Lorusso M, Vendemiale G, Denitto M, Santamato A, Seripa D, Pilotto A, Fiore P, Capurso A, Panza F.
    Prog Neuropsychopharmacol Biol Psychiatry; 2010 Feb 01; 34(1):177-82. PubMed ID: 19897004
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  • 14. Association between the TNFalpha-308 A/G polymorphism and the onset-age of Alzheimer disease.
    Alvarez V, Mata IF, González P, Lahoz CH, Martínez C, Peña J, Guisasola LM, Coto E.
    Am J Med Genet; 2002 Jul 08; 114(5):574-7. PubMed ID: 12116197
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  • 15. Association analysis of the paraoxonase-1 gene with Alzheimer's disease.
    Cellini E, Tedde A, Bagnoli S, Nacmias B, Piacentini S, Bessi V, Bracco L, Sorbi S.
    Neurosci Lett; 2006 Nov 20; 408(3):199-202. PubMed ID: 16996683
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  • 16. The APOC3 SstI polymorphism is weakly associated with sporadic Alzheimer's disease in a Chinese population.
    Sun Y, Shi J, Zhang S, Tang M, Han H, Guo Y, Ma C, Liu X, Li T.
    Neurosci Lett; 2005 Jun 03; 380(3):219-22. PubMed ID: 15862889
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  • 19. TNF polymorphisms in Alzheimer disease and functional implications on CSF beta-amyloid levels.
    Laws SM, Perneczky R, Wagenpfeil S, Müller U, Förstl H, Martins RN, Kurz A, Riemenschneider M.
    Hum Mutat; 2005 Jul 03; 26(1):29-35. PubMed ID: 15895461
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  • 20. Association between tumor necrosis factor (TNF)-alpha G-308A gene polymorphism and preeclampsia complicated by severe fetal growth restriction.
    Molvarec A, Jermendy A, Nagy B, Kovács M, Várkonyi T, Hupuczi P, Prohászka Z, Rigó J.
    Clin Chim Acta; 2008 Jun 03; 392(1-2):52-7. PubMed ID: 18396154
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