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 *

177 related articles for article (PubMed ID: 12112163)

  • 21. A presenilin 1 mutation (Arg278Ser) associated with early onset Alzheimer's disease and spastic paraparesis.
    Raman A; Lin X; Suri M; Hewitt M; Constantinescu CS; Phillips MF
    J Neurol Sci; 2007 Sep; 260(1-2):78-82. PubMed ID: 17507029
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Presenilin 1 mutations in Polish families with early-onset Alzheimer's disease.
    Kowalska A; Pruchnik-Wolińska D; Florczak J; Szczech J; Kozubski W; Rossa G; Wender M
    Folia Neuropathol; 2004; 42(1):9-14. PubMed ID: 15119739
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Novel presenilin 1 mutation (Ile408Thr) in an Italian family with late-onset Alzheimer's disease.
    Tedde A; Bartoli A; Piaceri I; Ferrara S; Bagnoli S; Serio A; Sorbi S; Nacmias B
    Neurosci Lett; 2016 Jan; 610():150-3. PubMed ID: 26549787
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Wide range of disease onset in a family with Alzheimer disease and a His163Tyr mutation in the presenilin-1 gene.
    Axelman K; Basun H; Lannfelt L
    Arch Neurol; 1998 May; 55(5):698-702. PubMed ID: 9605727
    [TBL] [Abstract][Full Text] [Related]  

  • 25. [Molecular genetics of Alzheimer's disease--presenilin and other genes].
    Tabira T
    Rinsho Shinkeigaku; 1997 Dec; 37(12):1095-6. PubMed ID: 9577654
    [TBL] [Abstract][Full Text] [Related]  

  • 26. 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]  

  • 27. [Clinical characteristics of a family with early-onset Alzheimer's disease associated with a presenilin 1 mutation (M139T)].
    Lleó A; Blesa R; Gendre J; Castellví M; Molinuevo JL; Oliva R
    Med Clin (Barc); 2002 May; 118(18):698-700. PubMed ID: 12042135
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Presenilin 2 familial Alzheimer's disease mutations result in partial loss of function and dramatic changes in Abeta 42/40 ratios.
    Walker ES; Martinez M; Brunkan AL; Goate A
    J Neurochem; 2005 Jan; 92(2):294-301. PubMed ID: 15663477
    [TBL] [Abstract][Full Text] [Related]  

  • 29. 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]  

  • 30. A novel PSEN1 mutation (K239N) associated with Alzheimer's disease with wide range age of onset and slow progression.
    Lladó A; Fortea J; Ojea T; Bosch B; Sanz P; Valls-Solé J; Clarimon J; Molinuevo JL; Sánchez-Valle R
    Eur J Neurol; 2010 Jul; 17(7):994-6. PubMed ID: 20158511
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Pathogenic presenilin 1 mutations (P436S & I143F) in early-onset Alzheimer's disease in the UK. Mutations in brief no. 223. Online.
    Palmer MS; Beck JA; Campbell TA; Humphries CB; Roques PK; Fox NC; Harvey R; Rossor MN; Collinge J
    Hum Mutat; 1999; 13(3):256. PubMed ID: 10090481
    [TBL] [Abstract][Full Text] [Related]  

  • 32. 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]  

  • 33. Presenilin-1 protein expression in familial and sporadic Alzheimer's disease.
    Levey AI; Heilman CJ; Lah JJ; Nash NR; Rees HD; Wakai M; Mirra SS; Rye DB; Nochlin D; Bird TD; Mufson EJ
    Ann Neurol; 1997 Jun; 41(6):742-53. PubMed ID: 9189035
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Presenilins and early-onset familial Alzheimer's disease.
    Rohan de Silva HA; Patel AJ
    Neuroreport; 1997 May; 8(8):i-xii. PubMed ID: 9223053
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Early-onset Alzheimer's disease caused by a novel mutation at codon 219 of the presenilin-1 gene.
    Smith MJ; Gardner RJ; Knight MA; Forrest SM; Beyreuther K; Storey E; McLean CA; Cotton RG; Cappal R; Masters CL
    Neuroreport; 1999 Feb; 10(3):503-7. PubMed ID: 10208579
    [TBL] [Abstract][Full Text] [Related]  

  • 36. 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]  

  • 37. A novel mutation of presenilin 1 in familial Alzheimer's disease in Israel detected by denaturing gradient gel electrophoresis.
    Reznik-Wolf H; Treves TA; Davidson M; Aharon-Peretz J; St George Hyslop PH; Chapman J; Korczyn AD; Goldman B; Friedman E
    Hum Genet; 1996 Dec; 98(6):700-2. PubMed ID: 8931704
    [TBL] [Abstract][Full Text] [Related]  

  • 38. A presenilin 1 mutation (Ser169Pro) associated with early-onset AD and myoclonic seizures.
    Ezquerra M; Carnero C; Blesa R; Gelpí JL; Ballesta F; Oliva R
    Neurology; 1999 Feb; 52(3):566-70. PubMed ID: 10025789
    [TBL] [Abstract][Full Text] [Related]  

  • 39. 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]  

  • 40. Phenotypic profile of early-onset familial Alzheimer's disease caused by presenilin-1 E280A mutation.
    Sepulveda-Falla D; Glatzel M; Lopera F
    J Alzheimers Dis; 2012; 32(1):1-12. PubMed ID: 22766738
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.