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 *

99 related articles for article (PubMed ID: 9544835)

  • 21. Presenilin function in APP processing.
    Annaert W; Cupers P; Saftig P; De Strooper B
    Ann N Y Acad Sci; 2000; 920():158-64. PubMed ID: 11193144
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Uncommon polymorphism in the presenilin genes in human familial Alzheimer's disease: not to be mistaken with a pathogenic mutation.
    Lleó A; Castellví M; Blesa R; Oliva R
    Neurosci Lett; 2002 Feb; 318(3):166-8. PubMed ID: 11803125
    [TBL] [Abstract][Full Text] [Related]  

  • 23. The genetics and pathophysiology of Alzheimer's disease.
    Lannfelt L
    J Intern Med; 1997 Oct; 242(4):281-4. PubMed ID: 9366805
    [No Abstract]   [Full Text] [Related]  

  • 24. Incomplete penetrance of familial Alzheimer's disease in a pedigree with a novel presenilin-1 gene mutation.
    Rossor MN; Fox NC; Beck J; Campbell TC; Collinge J
    Lancet; 1996 Jun; 347(9014):1560. PubMed ID: 8684135
    [No Abstract]   [Full Text] [Related]  

  • 25. [Autosomal dominant Alzheimer's disease. Study of a Moroccan family].
    Asri F; Moussaoui D; Kadri N
    Encephale; 2003; 29(3 Pt 1):254-8. PubMed ID: 12876550
    [TBL] [Abstract][Full Text] [Related]  

  • 26. [Presenilins: detection and characterization of Alzheimer's disease genes].
    Rogaev EI
    Mol Biol (Mosk); 1998; 32(1):71-83. PubMed ID: 9566253
    [No Abstract]   [Full Text] [Related]  

  • 27. [Neuroradiological findings in Alzheimer dementia with the presenile mutation].
    Hentschel F; Zerfass R; Becker G; Beyreuther K; Förstl H
    Rofo; 1998 Jan; 168(1):97-100. PubMed ID: 9501942
    [No Abstract]   [Full Text] [Related]  

  • 28. [New variant of Alzheimer's disease].
    Verkkoniemi A; Somer M; Haltia M
    Duodecim; 1998; 114(24):2509-11. PubMed ID: 11757118
    [No Abstract]   [Full Text] [Related]  

  • 29. Two novel presenilin-1 mutations (Ser169Leu and Pro436Gln) associated with very early onset Alzheimer's disease.
    Taddei K; Kwok JB; Kril JJ; Halliday GM; Creasey H; Hallupp M; Fisher C; Brooks WS; Chung C; Andrews C; Masters CL; Schofield PR; Martins RN
    Neuroreport; 1998 Oct; 9(14):3335-9. PubMed ID: 9831473
    [TBL] [Abstract][Full Text] [Related]  

  • 30. NACP/alpha-synuclein, NAC, and beta-amyloid pathology of familial Alzheimer's disease with the E184D presenilin-1 mutation: a clinicopathological study of two autopsy cases.
    Yokota O; Terada S; Ishizu H; Ujike H; Ishihara T; Nakashima H; Yasuda M; Kitamura Y; Uéda K; Checler F; Kuroda S
    Acta Neuropathol; 2002 Dec; 104(6):637-48. PubMed ID: 12410385
    [TBL] [Abstract][Full Text] [Related]  

  • 31. The structure of the presenilin 1 (S182) gene and identification of six novel mutations in early onset AD families.
    Alzheimer's Disease Collaborative Group
    Nat Genet; 1995 Oct; 11(2):219-22. PubMed ID: 7550356
    [TBL] [Abstract][Full Text] [Related]  

  • 32. The R269H mutation in presenilin-1 presenting as late-onset autosomal dominant Alzheimer's disease.
    Larner AJ; Ray PS; Doran M
    J Neurol Sci; 2007 Jan; 252(2):173-6. PubMed ID: 17188713
    [TBL] [Abstract][Full Text] [Related]  

  • 33. [Mutation of presenilin ++ genes and their role in pathogenesis of Alzheimer's disease].
    Kowalska A; Wender M
    Neurol Neurochir Pol; 1998; 32(5):1207-17. PubMed ID: 10463234
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Identification of a novel mutation (Leu282Arg) of the human presenilin 1 gene in Alzheimer's disease.
    Aldudo J; Bullido MJ; Arbizu T; Oliva R; Valdivieso F
    Neurosci Lett; 1998 Jan; 240(3):174-6. PubMed ID: 9502232
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Novel presenilin 1 mutation with profound neurofibrillary pathology in an indigenous Southern African family with early-onset Alzheimer's disease.
    Heckmann JM; Low WC; de Villiers C; Rutherfoord S; Vorster A; Rao H; Morris CM; Ramesar RS; Kalaria RN
    Brain; 2004 Jan; 127(Pt 1):133-42. PubMed ID: 14570818
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Amyloid angiopathy and variability in amyloid beta deposition is determined by mutation position in presenilin-1-linked Alzheimer's disease.
    Mann DM; Pickering-Brown SM; Takeuchi A; Iwatsubo T;
    Am J Pathol; 2001 Jun; 158(6):2165-75. PubMed ID: 11395394
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Novel presenilin mutations within Moroccan patients with Early-Onset Alzheimer's Disease.
    El Kadmiri N; Zaid N; Zaid Y; Tadevosyan A; Hachem A; Dubé MP; Hamzi K; El Moutawakil B; Slassi I; Nadifi S
    Neuroscience; 2014 Jun; 269():215-22. PubMed ID: 24704512
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Alzheimer's disease due to an intronic presenilin-1 (PSEN1 intron 4) mutation: A clinicopathological study.
    Janssen JC; Hall M; Fox NC; Harvey RJ; Beck J; Dickinson A; Campbell T; Collinge J; Lantos PL; Cipolotti L; Stevens JM; Rossor MN
    Brain; 2000 May; 123 ( Pt 5)():894-907. PubMed ID: 10775535
    [TBL] [Abstract][Full Text] [Related]  

  • 39. [Presenilin-1 (S182) causative gene of early-onset familial Alzheimer's disease].
    Ikeda M
    Tanpakushitsu Kakusan Koso; 1996 Aug; 41(10):1441-7. PubMed ID: 8741394
    [No Abstract]   [Full Text] [Related]  

  • 40. A novel mutation in the PSEN2 gene (T430M) associated with variable expression in a family with early-onset Alzheimer disease.
    Ezquerra M; Lleó A; Castellví M; Queralt R; Santacruz P; Pastor P; Molinuevo JL; Blesa R; Oliva R
    Arch Neurol; 2003 Aug; 60(8):1149-51. PubMed ID: 12925374
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 5.