402 related articles for article (PubMed ID: 17412506)
1. A mutation screening by DHPLC of PSEN1 and APP genes reveals no significant variation associated with the sporadic late-onset form of Alzheimer's disease.
Scacchi R; Gambina G; Moretto G; Corbo RM
Neurosci Lett; 2007 May; 418(3):282-5. PubMed ID: 17412506
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. Genetic study of Sardinian patients with Alzheimer's disease.
Piscopo P; Manfredi A; Malvezzi-Campeggi L; Crestini A; Spadoni O; Cherchi R; Deiana E; Piras MR; Confaloni A
Neurosci Lett; 2006 May; 398(1-2):124-8. PubMed ID: 16423463
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. Genetic risk and transcriptional variability of amyloid precursor protein in Alzheimer's disease.
Brouwers N; Sleegers K; Engelborghs S; Bogaerts V; Serneels S; Kamali K; Corsmit E; De Leenheir E; Martin JJ; De Deyn PP; Van Broeckhoven C; Theuns J
Brain; 2006 Nov; 129(Pt 11):2984-91. PubMed ID: 16931535
[TBL] [Abstract][Full Text] [Related]
6. [Genes in Alzheimer's disease].
Hoenicka J
Rev Neurol; 2006 Mar 1-15; 42(5):302-5. PubMed ID: 16538594
[TBL] [Abstract][Full Text] [Related]
7. Genetic study of familial cases of Alzheimer's disease.
Kowalska A; Pruchnik-Wolińska D; Florczak J; Modestowicz R; Szczech J; Kozubski W; Rossa G; Wender M
Acta Biochim Pol; 2004; 51(1):245-52. PubMed ID: 15094846
[TBL] [Abstract][Full Text] [Related]
8. PSEN1 polymorphisms alter the rate of cognitive decline in sporadic Alzheimer's disease patients.
Belbin O; Beaumont H; Warden D; Smith AD; Kalsheker N; Morgan K
Neurobiol Aging; 2009 Dec; 30(12):1992-9. PubMed ID: 18403054
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. Presenilin 1 polymorphism associated with Alzheimer's disease in apolipoprotein E4 carriers.
Martínez-García A; Aldudo J; Recuero M; Sastre I; Vilella-Cuadrada E; Rosich-Estragó M; Frank A; Valdivieso F; Bullido MJ
Dement Geriatr Cogn Disord; 2008; 26(5):440-4. PubMed ID: 18957849
[TBL] [Abstract][Full Text] [Related]
11. [Alzheimer's disease. Present and future role of genetics].
Roks G
Tijdschr Gerontol Geriatr; 2003 Feb; 34(1):13-20. PubMed ID: 12629906
[TBL] [Abstract][Full Text] [Related]
12. No association of spastic paraparesis genes in PSEN1 Alzheimer's disease with spastic paraparesis.
Karlstrom H; Kwok JB; Gregory GC; Hallupp M; Brooks WS; Schofield PR
Neuroreport; 2007 Aug; 18(12):1267-9. PubMed ID: 17632280
[TBL] [Abstract][Full Text] [Related]
13. The Glu318Gly mutation of the presenilin-1 gene does not necessarily cause Alzheimer's disease.
Mattila KM; Forsell C; Pirttilä T; Rinne JO; Lehtimäki T; Röyttä M; Lilius L; Eerola A; St George-Hyslop PH; Frey H; Lannfelt L
Ann Neurol; 1998 Dec; 44(6):965-7. PubMed ID: 9851443
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. A novel presenilin-1 mutation (Leu85Pro) in early-onset Alzheimer disease with spastic paraparesis.
Ataka S; Tomiyama T; Takuma H; Yamashita T; Shimada H; Tsutada T; Kawabata K; Mori H; Miki T
Arch Neurol; 2004 Nov; 61(11):1773-6. PubMed ID: 15534188
[TBL] [Abstract][Full Text] [Related]
16. Molecular genetics of Alzheimer's disease: an update.
Brouwers N; Sleegers K; Van Broeckhoven C
Ann Med; 2008; 40(8):562-83. PubMed ID: 18608129
[TBL] [Abstract][Full Text] [Related]
17. DGGE method for the mutational analysis of the coding and proximal promoter regions of the Alzheimer's disease presenilin-1 gene: two novel mutations.
Aldudo J; Bullido MJ; Valdivieso F
Hum Mutat; 1999; 14(5):433-9. PubMed ID: 10533070
[TBL] [Abstract][Full Text] [Related]
18. [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]
19. Novel amyloid precursor protein gene mutation (codon 665Asp) in a patient with late-onset Alzheimer's disease.
Peacock ML; Murman DL; Sima AA; Warren JT; Roses AD; Fink JK
Ann Neurol; 1994 Apr; 35(4):432-8. PubMed ID: 8154870
[TBL] [Abstract][Full Text] [Related]
20. [Genetic factors and a polygenic model of Alzheimer's disease].
Rogaev EI
Genetika; 1999 Nov; 35(11):1558-71. PubMed ID: 10624576
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
