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 *

206 related articles for article (PubMed ID: 15337637)

  • 1. Genotype-phenotype analysis in early-onset Alzheimer's disease due to presenilin-1 mutations at codon 139.
    Hanisch F; Kölmel HW
    Eur J Med Res; 2004 Jul; 9(7):361-4. PubMed ID: 15337637
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A novel presenilin 1 L166H mutation in a pseudo-sporadic case of early-onset Alzheimer's disease.
    Pantieri R; Pardini M; Cecconi M; Dagna-Bricarelli F; Vitali A; Piccini A; Russo R; Borghi R; Tabaton M
    Neurol Sci; 2005 Dec; 26(5):349-50. PubMed ID: 16388371
    [TBL] [Abstract][Full Text] [Related]  

  • 3. The clinical phenotype of two missense mutations in the presenilin I gene in Japanese patients.
    Ikeda M; Sharma V; Sumi SM; Rogaeva EA; Poorkaj P; Sherrington R; Nee L; Tsuda T; Oda N; Watanabe M; Aoki M; Shoji M; Abe K; Itoyama Y; Hirai S; Schellenberg GD; Bird TD; St George-Hyslop PH
    Ann Neurol; 1996 Dec; 40(6):912-7. PubMed ID: 9007097
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Missense mutation in exon 11 (Codon 378) of the presenilin-1 gene in a French family with early-onset Alzheimer's disease and transmission study by mismatch enhanced allele specific amplification. Mutations in brief no. 141. Online. besancon@rockefeller1.univ.lyon1.fr.
    Besançon R; Lorenzi A; Cruts M; Radawiec S; Sturtz F; Broussolle E; Chazot G; van Broeckhoven C; Chamba G; Vandenberghe A
    Hum Mutat; 1998; 11(6):481. PubMed ID: 10200054
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Prominent behavioural and psychiatric symptoms in early-onset Alzheimer's disease in a sib pair with the presenilin-1 gene R269G mutation.
    Doran M; Larner AJ
    Eur Arch Psychiatry Clin Neurosci; 2004 Jun; 254(3):187-9. PubMed ID: 15205973
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Missense mutations in the chromosome 14 familial Alzheimer's disease presenilin 1 gene.
    Poorkaj P; Sharma V; Anderson L; Nemens E; Alonso ME; Orr H; White J; Heston L; Bird TD; Schellenberg GD
    Hum Mutat; 1998; 11(3):216-21. PubMed ID: 9521423
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A novel presenilin 1 mutation (Ser169del) in a Chinese family with early-onset Alzheimer's disease.
    Guo J; Wei J; Liao S; Wang L; Jiang H; Tang B
    Neurosci Lett; 2010 Jan; 468(1):34-7. PubMed ID: 19853643
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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; 6(2):176-80. PubMed ID: 9781063
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Identification of a novel 4.6-kb genomic deletion in presenilin-1 gene which results in exclusion of exon 9 in a Finnish early onset Alzheimer's disease family: an Alu core sequence-stimulated recombination?
    Hiltunen M; Helisalmi S; Mannermaa A; Alafuzoff I; Koivisto AM; Lehtovirta M; Pirskanen M; Sulkava R; Verkkoniemi A; Soininen H
    Eur J Hum Genet; 2000 Apr; 8(4):259-66. PubMed ID: 10854108
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Molecular genetics of Alzheimer's disease: presenilin 1 gene analysis in a cohort of patients from the Poznań region.
    Kowalska A; Wender M; Florczak J; Pruchnik-Wolinska D; Modestowicz R; Szczech J; Rossa G; Kozubski W
    J Appl Genet; 2003; 44(2):231-4. PubMed ID: 12817569
    [TBL] [Abstract][Full Text] [Related]  

  • 11. E280A PS-1 mutation causes Alzheimer's disease but age of onset is not modified by ApoE alleles.
    Lendon CL; Martinez A; Behrens IM; Kosik KS; Madrigal L; Norton J; Neuman R; Myers A; Busfield F; Wragg M; Arcos M; Arango Viana JC; Ossa J; Ruiz A; Goate AM; Lopera F
    Hum Mutat; 1997; 10(3):186-95. PubMed ID: 9298817
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Mutations in presenilin 1, presenilin 2 and amyloid precursor protein genes in patients with early-onset Alzheimer's disease in Poland.
    Zekanowski C; Styczyńska M; Pepłońska B; Gabryelewicz T; Religa D; Ilkowski J; Kijanowska-Haładyna B; Kotapka-Minc S; Mikkelsen S; Pfeffer A; Barczak A; Łuczywek E; Wasiak B; Chodakowska-Zebrowska M; Gustaw K; Łaczkowski J; Sobów T; Kuźnicki J; Barcikowska M
    Exp Neurol; 2003 Dec; 184(2):991-6. PubMed ID: 14769392
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A new presenilin Alzheimer's disease case confirms the helical alignment of pathogenic mutations in transmembrane domain 5.
    Coleman P; Kurlan R; Crook R; Werner J; Hardy J
    Neurosci Lett; 2004 Jul; 364(3):139-40. PubMed ID: 15196662
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. Molecular diagnosis of autosomal dominant early onset Alzheimer's disease: an update.
    Raux G; Guyant-Maréchal L; Martin C; Bou J; Penet C; Brice A; Hannequin D; Frebourg T; Campion D
    J Med Genet; 2005 Oct; 42(10):793-5. PubMed ID: 16033913
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Early-onset Alzheimer's disease with a presenilin-1 mutation at the site corresponding to the Volga German presenilin-2 mutation.
    Crook R; Ellis R; Shanks M; Thal LJ; Perez-Tur J; Baker M; Hutton M; Haltia T; Hardy J; Galasko D
    Ann Neurol; 1997 Jul; 42(1):124-8. PubMed ID: 9225696
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. Familial Alzheimer's disease co-segregates with a Met146I1e substitution in presenilin-1.
    Jørgensen P; Bus C; Pallisgaard N; Bryder M; Jørgensen AL
    Clin Genet; 1996 Nov; 50(5):281-6. PubMed ID: 9007311
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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; 62(12):1821-30. PubMed ID: 16344340
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Clinical-genetic correlations in familial Alzheimer's disease caused by presenilin 1 mutations.
    Gómez-Tortosa E; Barquero S; Barón M; Gil-Neciga E; Castellanos F; Zurdo M; Manzano S; Muñoz DG; Jiménez-Huete A; Rábano A; Sainz MJ; Guerrero R; Gobernado I; Pérez-Pérez J; Jiménez-Escrig A
    J Alzheimers Dis; 2010; 19(3):873-84. PubMed ID: 20157243
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.