BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

138 related articles for article (PubMed ID: 8411727)

  • 1. [Absence of linkage disequilibrium at amyloid precursor protein gene locus in Japanese familial Alzheimer's disease with 717Val-->Ile mutation].
    Tanaka H; Naruse S; Miyatake T; Tsuji S
    Nihon Rinsho; 1993 Sep; 51(9):2452-6. PubMed ID: 8411727
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Absence of linkage disequilibrium at amyloid precursor protein gene locus in Japanese familial Alzheimer's disease with 717Val-->Ile mutation.
    Tanaka H; Naruse S; Seki K; Onodera O; Kobayashi H; Miyatake T; Shibata A; Sakaki Y; Kamino K; Miki T
    Neurosci Lett; 1993 Nov; 162(1-2):63-6. PubMed ID: 8121639
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Japanese siblings with missense mutation (717Val --> Ile) in amyloid precursor protein of early-onset Alzheimer's disease.
    Matsumura Y; Kitamura E; Miyoshi K; Yamamoto Y; Furuyama J; Sugihara T
    Neurology; 1996 Jun; 46(6):1721-3. PubMed ID: 8649577
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Screening of the mis-sense mutation producing the 717Val-->Ile substitution in the amyloid precursor protein in Japanese familial and sporadic Alzheimer's disease.
    Yoshizawa T; Komatsuzaki Y; Iwamoto H; Mizusawa H; Kanazawa I
    J Neurol Sci; 1993 Jul; 117(1-2):12-5. PubMed ID: 8410047
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Progress of the molecular genetic analysis for Alzheimer's disease].
    Miki T
    Rinsho Byori; 1998 Oct; 46(10):1008-14. PubMed ID: 9816912
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Familial Alzheimer's disease in Japanese population].
    Nagano K; Katsuya T; Kamino K; Yoshiiwa A; Ikeda M; Tanabe H; Takeda M; Nishimura T; Yoshizawa T; Tanaka H
    Nihon Ronen Igakkai Zasshi; 1995 Feb; 32(2):111-22. PubMed ID: 7776534
    [TBL] [Abstract][Full Text] [Related]  

  • 7. The 717Val----Ile substitution in amyloid precursor protein is associated with familial Alzheimer's disease regardless of ethnic groups.
    Yoshioka K; Miki T; Katsuya T; Ogihara T; Sakaki Y
    Biochem Biophys Res Commun; 1991 Aug; 178(3):1141-6. PubMed ID: 1908231
    [TBL] [Abstract][Full Text] [Related]  

  • 8. ApoE genotype and familial Alzheimer's disease: a possible influence on age of onset in APP717 Val-->Ile mutated families.
    Nacmias B; Latorraca S; Piersanti P; Forleo P; Piacentini S; Bracco L; Amaducci L; Sorbi S
    Neurosci Lett; 1995 Jan; 183(1-2):1-3. PubMed ID: 7746463
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. [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]  

  • 11. Clinical characterization of an APP mutation (V717I) in five Han Chinese families with early-onset Alzheimer's disease.
    Zhang G; Xie Y; Wang W; Feng X; Jia J
    J Neurol Sci; 2017 Jan; 372():379-386. PubMed ID: 27838006
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Mutation analysis of amyloid precursor protein in early-onset familial Alzheimer's disease].
    Naruse S; Fujigasaki H; Miyatake T
    Nihon Rinsho; 1993 Sep; 51(9):2445-51. PubMed ID: 8411726
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Screening for mutations of the precursor of beta-amyloid protein in early forms of Alzheimer disease. French Study Group of Alzheimer Disease].
    Rev Neurol (Paris); 1993; 149(10):528-31. PubMed ID: 8023065
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A locus for familial early-onset Alzheimer's disease on the long arm of chromosome 14, proximal to the alpha 1-antichymotrypsin gene.
    Mullan M; Houlden H; Windelspecht M; Fidani L; Lombardi C; Diaz P; Rossor M; Crook R; Hardy J; Duff K
    Nat Genet; 1992 Dec; 2(4):340-2. PubMed ID: 1303291
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Age of onset in familial early onset Alzheimer's disease correlates with genetic aetiology.
    Mullan M; Houlden H; Crawford F; Kennedy A; Rogues P; Rossor M
    Am J Med Genet; 1993 Oct; 48(3):129-30. PubMed ID: 8291565
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Early-onset familial Alzheimer's disease (EOFAD).
    Wu L; Rosa-Neto P; Hsiung GY; Sadovnick AD; Masellis M; Black SE; Jia J; Gauthier S
    Can J Neurol Sci; 2012 Jul; 39(4):436-45. PubMed ID: 22728850
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Screening for the beta-amyloid precursor protein mutation (APP717: Val----Ile) in extended pedigrees with early onset Alzheimer's disease.
    Chartier-Harlin MC; Crawford F; Hamandi K; Mullan M; Goate A; Hardy J; Backhovens H; Martin JJ; Broeckhoven CV
    Neurosci Lett; 1991 Aug; 129(1):134-5. PubMed ID: 1922963
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Linkage and haplotype analysis of familial early-onset Alzheimer disease in Japanese population.
    Kamino K; Nagano K; Katsuya T; Nishiwaki Y; Takeda M; Tanabe H; Nishimura T; Ii K; Fujimoto K; Tsujimura R
    Jpn J Hum Genet; 1995 Sep; 40(3):229-41. PubMed ID: 8527797
    [TBL] [Abstract][Full Text] [Related]  

  • 19. No founder effect in three novel Alzheimer's disease families with APP 717 Val-->Ile mutation. Clerget-darpoux. French Alzheimer's Disease Study Group.
    Campion D; Brice A; Hannequin D; Charbonnier F; Dubois B; Martin C; Michon A; Penet C; Bellis M; Calenda A; Martinez M; Agid Y; Clerget-Darpoux F; Frebourg T
    J Med Genet; 1996 Aug; 33(8):661-4. PubMed ID: 8863158
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 7.