BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

208 related articles for article (PubMed ID: 10349860)

  • 1. A novel presenilin-2 splice variant in human Alzheimer's disease brain tissue.
    Sato N; Hori O; Yamaguchi A; Lambert JC; Chartier-Harlin MC; Robinson PA; Delacourte A; Schmidt AM; Furuyama T; Imaizumi K; Tohyama M; Takagi T
    J Neurochem; 1999 Jun; 72(6):2498-505. PubMed ID: 10349860
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Molecular analysis of the presenilin 1 (S182) gene in "sporadic" cases of Alzheimer's disease: identification and characterisation of unusual splice variants.
    Anwar R; Moynihan TP; Ardley H; Brindle N; Coletta PL; Cairns N; Markham AF; Robinson PA
    J Neurochem; 1996 Apr; 66(4):1774-7. PubMed ID: 8627338
    [TBL] [Abstract][Full Text] [Related]  

  • 3. The Glu318Gly mutation of the presenilin-1 gene does not necessarily cause Alzheimer's disease.
    Mattila KM; Forsell C; Pirttilä T; Rinne JO; Lehtimäki T; Röyttä M; Lilius L; Eerola A; St George-Hyslop PH; Frey H; Lannfelt L
    Ann Neurol; 1998 Dec; 44(6):965-7. PubMed ID: 9851443
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Expression of truncated presenilin 2 splice variant in Alzheimer's disease, bipolar disorder, and schizophrenia brain cortex.
    Smith MJ; Sharples RA; Evin G; McLean CA; Dean B; Pavey G; Fantino E; Cotton RG; Imaizumi K; Masters CL; Cappai R; Culvenor JG
    Brain Res Mol Brain Res; 2004 Aug; 127(1-2):128-35. PubMed ID: 15306129
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Structure and alternative splicing of the presenilin-2 gene.
    Prihar G; Fuldner RA; Perez-Tur J; Lincoln S; Duff K; Crook R; Hardy J; Philips CA; Venter C; Talbot C; Clark RF; Goate A; Li J; Potter H; Karran E; Roberts GW; Hutton M; Adams MD
    Neuroreport; 1996 Jul; 7(10):1680-4. PubMed ID: 8904781
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Alteration in brain presenilin-1 mRNA expression in sporadic Alzheimer's disease.
    Isoe-Wada K; Urakami K; Wakutani Y; Adachi Y; Arai H; Sasaki H; Nakashima K
    Eur J Neurol; 1999 Mar; 6(2):163-7. PubMed ID: 10053228
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Induced HMGA1a expression causes aberrant splicing of Presenilin-2 pre-mRNA in sporadic Alzheimer's disease.
    Manabe T; Katayama T; Sato N; Gomi F; Hitomi J; Yanagita T; Kudo T; Honda A; Mori Y; Matsuzaki S; Imaizumi K; Mayeda A; Tohyama M
    Cell Death Differ; 2003 Jun; 10(6):698-708. PubMed ID: 12761578
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Prominent expression of presenilin-1 in senile plaques and reactive astrocytes in Alzheimer's disease brain.
    Weggen S; Diehlmann A; Buslei R; Beyreuther K; Bayer TA
    Neuroreport; 1998 Oct; 9(14):3279-83. PubMed ID: 9831464
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A mutation in Alzheimer's disease destroying a splice acceptor site in the presenilin-1 gene.
    Perez-Tur J; Froelich S; Prihar G; Crook R; Baker M; Duff K; Wragg M; Busfield F; Lendon C; Clark RF
    Neuroreport; 1995 Dec; 7(1):297-301. PubMed ID: 8742474
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Molecular genetics of Alzheimer's disease.
    Goate AM
    Geriatrics; 1997 Sep; 52 Suppl 2():S9-12. PubMed ID: 9307578
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. Familial Alzheimer's disease genes in Japanese.
    Kamimura K; Tanahashi H; Yamanaka H; Takahashi K; Asada T; Tabira T
    J Neurol Sci; 1998 Sep; 160(1):76-81. PubMed ID: 9804121
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Somatic mutation analysis of the APP and Presenilin 1 and 2 genes in Alzheimer's disease brains.
    Reznik-Wolf H; Machado J; Haroutunian V; DeMarco L; Walter GF; Goldman B; Davidson M; Johnston JA; Lannfelt L; Dani SU; Friedman E
    J Neurogenet; 1998 Jan; 12(1):55-65. PubMed ID: 9666901
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A novel mutation in the predicted TM2 domain of the presenilin 2 gene in a Spanish patient with late-onset Alzheimer's disease.
    Lao JI; Beyer K; Fernández-Novoa L; Cacabelos R
    Neurogenetics; 1998 Aug; 1(4):293-6. PubMed ID: 10732806
    [TBL] [Abstract][Full Text] [Related]  

  • 15. ApoE genotype is a risk factor in nonpresenilin early-onset Alzheimer's disease families.
    Houlden H; Crook R; Backhovens H; Prihar G; Baker M; Hutton M; Rossor M; Martin JJ; Van Broeckhoven C; Hardy J
    Am J Med Genet; 1998 Feb; 81(1):117-21. PubMed ID: 9514597
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Identification of regulatory cis-acting elements for alternative splicing of presenilin 2 exon 5 under hypoxic stress conditions.
    Higashide S; Morikawa K; Okumura M; Kondo S; Ogata M; Murakami T; Yamashita A; Kanemoto S; Manabe T; Imaizumi K
    J Neurochem; 2004 Dec; 91(5):1191-8. PubMed ID: 15569262
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Presenilin-1 polymorphism in Alzheimer's disease and vascular dementia.
    Matsushita S; Arai H; Muramatsu T; Makimoto K; Nakagawa T; Sasaki H; Higuchi S
    Exp Neurol; 1997 Aug; 146(2):567-9. PubMed ID: 9270069
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Presenilin-1 mutation L271V results in altered exon 8 splicing and Alzheimer's disease with non-cored plaques and no neuritic dystrophy.
    Kwok JB; Halliday GM; Brooks WS; Dolios G; Laudon H; Murayama O; Hallupp M; Badenhop RF; Vickers J; Wang R; Naslund J; Takashima A; Gandy SE; Schofield PR
    J Biol Chem; 2003 Feb; 278(9):6748-54. PubMed ID: 12493737
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Genetic factors and a polygenic model of Alzheimer's disease].
    Rogaev EI
    Genetika; 1999 Nov; 35(11):1558-71. PubMed ID: 10624576
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Alzheimer's disease associated with mutations in presenilin 2 is rare and variably penetrant.
    Sherrington R; Froelich S; Sorbi S; Campion D; Chi H; Rogaeva EA; Levesque G; Rogaev EI; Lin C; Liang Y; Ikeda M; Mar L; Brice A; Agid Y; Percy ME; Clerget-Darpoux F; Piacentini S; Marcon G; Nacmias B; Amaducci L; Frebourg T; Lannfelt L; Rommens JM; St George-Hyslop PH
    Hum Mol Genet; 1996 Jul; 5(7):985-8. PubMed ID: 8817335
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.