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 *

140 related articles for article (PubMed ID: 9109915)

  • 21. 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]  

  • 22. 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]  

  • 23. AMY plaques in familial AD: comparison with sporadic Alzheimer's disease.
    Lippa CF; Schmidt ML; Nee LE; Bird T; Nochlin D; Hulette C; Mori H; Lee VM; Trojanowski JQ
    Neurology; 2000 Jan; 54(1):100-4. PubMed ID: 10636133
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Presenilin-1 gene intronic polymorphism in sporadic and familial Alzheimer's disease.
    Sorbi S; Nacmias B; Tedde A; Forleo P; Piacentini S; Latorraca S; Amaducci L
    Neurosci Lett; 1997 Jan; 222(2):132-4. PubMed ID: 9111746
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Early-onset Alzheimer's disease due to mutations of the presenilin-1 gene on chromosome 14: a 7-year follow-up of a patient with a mutation at codon 139.
    Hüll M; Fiebich BL; Dykierek P; Schmidtke K; Nitzsche E; Orszagh M; Deuschl G; Moser E; Schumacher M; Lücking C; Berger M; Bauer J
    Eur Arch Psychiatry Clin Neurosci; 1998; 248(3):123-9. PubMed ID: 9728730
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Cerebral amyloid angiopathy is a pathogenic lesion in Alzheimer's disease due to a novel presenilin 1 mutation.
    Dermaut B; Kumar-Singh S; De Jonghe C; Cruts M; Löfgren A; Lübke U; Cras P; Dom R; De Deyn PP; Martin JJ; Van Broeckhoven C
    Brain; 2001 Dec; 124(Pt 12):2383-92. PubMed ID: 11701593
    [TBL] [Abstract][Full Text] [Related]  

  • 27. [Mutation site of presenilin-1 gene in familial Alzheimer's disease].
    Xu E; Jia J; Sun W
    Zhonghua Yi Xue Za Zhi; 2002 Nov; 82(22):1518-20. PubMed ID: 12609057
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Increased A beta 42(43)-plaque deposition in early-onset familial Alzheimer's disease brains with the deletion of exon 9 and the missense point mutation (H163R) in the PS-1 gene.
    Ishii K; Ii K; Hasegawa T; Shoji S; Doi A; Mori H
    Neurosci Lett; 1997 May; 228(1):17-20. PubMed ID: 9197277
    [TBL] [Abstract][Full Text] [Related]  

  • 29. 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]  

  • 30. The impact of different presenilin 1 andpresenilin 2 mutations on amyloid deposition, neurofibrillary changes and neuronal loss in the familial Alzheimer's disease brain: evidence for other phenotype-modifying factors.
    Gómez-Isla T; Growdon WB; McNamara MJ; Nochlin D; Bird TD; Arango JC; Lopera F; Kosik KS; Lantos PL; Cairns NJ; Hyman BT
    Brain; 1999 Sep; 122 ( Pt 9)():1709-19. PubMed ID: 10468510
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Alteration in brain presenilin 1 mRNA expression in early onset familial Alzheimer's disease.
    Barton AJ; Crook BW; Karran EH; Brown F; Dewar D; Mann DM; Pearson RC; Graham DI; Hardy J; Hutton M; Duff K; Goate AM; Clark RF; Roberts GW
    Neurodegeneration; 1996 Sep; 5(3):213-8. PubMed ID: 8910899
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Three different mutations of presenilin 1 gene in early-onset Alzheimer's disease families.
    Kamino K; Sato S; Sakaki Y; Yoshiiwa A; Nishiwaki Y; Takeda M; Tanabe H; Nishimura T; Ii K; St George-Hyslop PH; Miki T; Ogihara T
    Neurosci Lett; 1996 Apr; 208(3):195-8. PubMed ID: 8733303
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Cell-type-specific enhancement of amyloid-beta deposition in a novel presenilin-1 mutation (P117L).
    Wegiel J; Wisniewski HM; Kuchna I; Tarnawski M; Badmajew E; Popovitch E; Kulczycki J; Dowjat WK; Wisniewski T
    J Neuropathol Exp Neurol; 1998 Sep; 57(9):831-8. PubMed ID: 9737546
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Presenilin 1 mutation in an african american family presenting with atypical Alzheimer dementia.
    Rippon GA; Crook R; Baker M; Halvorsen E; Chin S; Hutton M; Houlden H; Hardy J; Lynch T
    Arch Neurol; 2003 Jun; 60(6):884-8. PubMed ID: 12810495
    [TBL] [Abstract][Full Text] [Related]  

  • 35. 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]  

  • 36. A novel pathogenic mutation (Leu262Phe) found in the presenilin 1 gene in early-onset Alzheimer's disease.
    Forsell C; Froelich S; Axelman K; Vestling M; Cowburn RF; Lilius L; Johnston JA; Engvall B; Johansson K; Dahlkild A; Ingelson M; St George-Hyslop PH; Lannfelt L
    Neurosci Lett; 1997 Sep; 234(1):3-6. PubMed ID: 9347932
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Presenilin 1 Met146Leu variant due to an A --> T transversion in an early-onset familial Alzheimer's disease pedigree from Argentina.
    Morelli L; Prat MI; Levy E; Mangone CA; Castaño EM
    Clin Genet; 1998 Jun; 53(6):469-73. PubMed ID: 9712537
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Clinical phenotype of G206D mutation in the presenilin 1 gene in pathologically confirmed familial Alzheimer's disease.
    Wu YY; Cheng IH; Lee CC; Chiu MJ; Lee MJ; Chen TF; Hsu JL
    J Alzheimers Dis; 2011; 25(1):145-50. PubMed ID: 21335660
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Ectopic white matter neurons, a developmental abnormality that may be caused by the PSEN1 S169L mutation in a case of familial AD with myoclonus and seizures.
    Takao M; Ghetti B; Murrell JR; Unverzagt FW; Giaccone G; Tagliavini F; Bugiani O; Piccardo P; Hulette CM; Crain BJ; Farlow MR; Heyman A
    J Neuropathol Exp Neurol; 2001 Dec; 60(12):1137-52. PubMed ID: 11764087
    [TBL] [Abstract][Full Text] [Related]  

  • 40. 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]  

    [Previous]   [Next]    [New Search]
    of 7.