BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

176 related articles for article (PubMed ID: 1679288)

  • 1. APP717, APP693, and PRIP gene mutations are rare in Alzheimer disease.
    Schellenberg GD; Anderson L; O'dahl S; Wisjman EM; Sadovnick AD; Ball MJ; Larson EB; Kukull WA; Martin GM; Roses AD
    Am J Hum Genet; 1991 Sep; 49(3):511-7. PubMed ID: 1679288
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Linkage and mutational analysis of familial Alzheimer disease kindreds for the APP gene region.
    Kamino K; Orr HT; Payami H; Wijsman EM; Alonso ME; Pulst SM; Anderson L; O'dahl S; Nemens E; White JA
    Am J Hum Genet; 1992 Nov; 51(5):998-1014. PubMed ID: 1415269
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Assessment of amyloid beta-protein precursor gene mutations in a large set of familial and sporadic Alzheimer disease cases.
    Tanzi RE; Vaula G; Romano DM; Mortilla M; Huang TL; Tupler RG; Wasco W; Hyman BT; Haines JL; Jenkins BJ
    Am J Hum Genet; 1992 Aug; 51(2):273-82. PubMed ID: 1642228
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Affected siblings with Alzheimer's disease had missense mutation of codon 717 in amyloid precursor protein gene].
    Katsuya T; Miki T; Tanabe H; Takeda M; Hosokawa K; Hayashi H; Hashimoto S; Nishimura T; Ogihara T
    Nihon Ronen Igakkai Zasshi; 1992 Feb; 29(2):129-34. PubMed ID: 1349930
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Gene mutations in inherited amyloidopathies of the nervous system.
    Tanzi RE
    Am J Hum Genet; 1991 Sep; 49(3):507-10. PubMed ID: 1831958
    [No Abstract]   [Full Text] [Related]  

  • 6. Beta A4 protein deposition in familial Alzheimer's disease with the mutation in codon 717 of the beta A4 amyloid precursor protein gene and sporadic Alzheimer's disease.
    Cairns NJ; Chadwick A; Lantos PL; Levy R; Rossor MN
    Neurosci Lett; 1993 Jan; 149(2):137-40. PubMed ID: 8474686
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Regulation of Alzheimer beta-amyloid precursor trafficking and metabolism.
    Gandy S; Petanceska S
    Biochim Biophys Acta; 2000 Jul; 1502(1):44-52. PubMed ID: 10899430
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Mutations of amyloid precursor protein in early-onset familial Alzheimer's disease].
    Naruse S; Tsuji S; Miyatake T
    Nihon Rinsho; 1992 Sep; 50(9):2270-7. PubMed ID: 1434023
    [TBL] [Abstract][Full Text] [Related]  

  • 9. DNA diagnosis for hereditary cerebral hemorrhage with amyloidosis (Dutch type).
    Bakker E; van Broeckhoven C; Haan J; Voorhoeve E; van Hul W; Levy E; Lieberburg I; Carman MD; van Ommen GJ; Frangione B
    Am J Hum Genet; 1991 Sep; 49(3):518-21. PubMed ID: 1679289
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Clinical comparison of Alzheimer's disease in pedigrees with the codon 717 Val-->Ile mutation in the amyloid precursor protein gene.
    Mullan M; Tsuji S; Miki T; Katsuya T; Naruse S; Kaneko K; Shimizu T; Kojima T; Nakano I; Ogihara T
    Neurobiol Aging; 1993; 14(5):407-19. PubMed ID: 8247223
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Mutations in amyloid precursor protein gene and disease.
    Brown J
    Lancet; 1991 Apr; 337(8746):923-4. PubMed ID: 1673006
    [No Abstract]   [Full Text] [Related]  

  • 12. Presenile Alzheimer dementia characterized by amyloid angiopathy and large amyloid core type senile plaques in the APP 692Ala-->Gly mutation.
    Cras P; van Harskamp F; Hendriks L; Ceuterick C; van Duijn CM; Stefanko SZ; Hofman A; Kros JM; Van Broeckhoven C; Martin JJ
    Acta Neuropathol; 1998 Sep; 96(3):253-60. PubMed ID: 9754958
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Segregation of a missense mutation in the amyloid precursor protein gene with familial Alzheimer's disease.
    Goate A; Chartier-Harlin MC; Mullan M; Brown J; Crawford F; Fidani L; Giuffra L; Haynes A; Irving N; James L
    Nature; 1991 Feb; 349(6311):704-6. PubMed ID: 1671712
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Abundance of the longer A beta 42 in neocortical and cerebrovascular amyloid beta deposits in Swedish familial Alzheimer's disease and Down's syndrome.
    Kalaria RN; Cohen DL; Greenberg BD; Savage MJ; Bogdanovic NE; Winblad B; Lannfelt L; Adem A
    Neuroreport; 1996 May; 7(8):1377-81. PubMed ID: 8856679
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Molecular and prospective phenotypic characterization of a pedigree with familial Alzheimer's disease and a missense mutation in codon 717 of the beta-amyloid precursor protein gene.
    Karlinsky H; Vaula G; Haines JL; Ridgley J; Bergeron C; Mortilla M; Tupler RG; Percy ME; Robitaille Y; Noldy NE
    Neurology; 1992 Aug; 42(8):1445-53. PubMed ID: 1520398
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Two kindreds with familial Alzheimer's disease--analysis of the APP717 mutation and the mutated genes for the prion protein].
    Nagano K; Miki T; Yoshioka K; Katsumi D; Katsuya T; Takeda M; Ikeda M; Tanabe H; Nishimura T; Sakai Y
    Nihon Ronen Igakkai Zasshi; 1992 Jun; 29(6):509-14. PubMed ID: 1356166
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Predominant deposition of amyloid-beta 42(43) in plaques in cases of Alzheimer's disease and hereditary cerebral hemorrhage associated with mutations in the amyloid precursor protein gene.
    Mann DM; Iwatsubo T; Ihara Y; Cairns NJ; Lantos PL; Bogdanovic N; Lannfelt L; Winblad B; Maat-Schieman ML; Rossor MN
    Am J Pathol; 1996 Apr; 148(4):1257-66. PubMed ID: 8644866
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Distinguishable effects of presenilin-1 and APP717 mutations on amyloid plaque deposition.
    Ishii K; Lippa C; Tomiyama T; Miyatake F; Ozawa K; Tamaoka A; Hasegawa T; Fraser PE; Shoji S; Nee LE; Pollen DA; St George-Hyslop PH; Ii K; Ohtake T; Kalaria RN; Rossor MN; Lantos PL; Cairns NJ; Farrer LA; Mori H
    Neurobiol Aging; 2001; 22(3):367-76. PubMed ID: 11378241
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Screening of amyloid precursor protein gene mutation (APP 717 Val-->Ile) in Swedish families with Alzheimer's disease.
    Almqvist E; Lake S; Axelman K; Johansson K; Winblad B
    J Neural Transm Park Dis Dement Sect; 1993; 6(2):151-6. PubMed ID: 8117412
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Screening for mutations in the open reading frame and promoter of the beta-amyloid precursor protein gene in familial Alzheimer's disease: identification of a further family with APP717 Val-->Ile.
    Fidani L; Rooke K; Chartier-Harlin MC; Hughes D; Tanzi R; Mullan M; Roques P; Rossor M; Hardy J; Goate A
    Hum Mol Genet; 1992 Jun; 1(3):165-8. PubMed ID: 1303172
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.