169 related articles for article (PubMed ID: 10732806)
1. A novel mutation in the predicted TM2 domain of the presenilin 2 gene in a Spanish patient with late-onset Alzheimer's disease.
Lao JI; Beyer K; Fernández-Novoa L; Cacabelos R
Neurogenetics; 1998 Aug; 1(4):293-6. PubMed ID: 10732806
[TBL] [Abstract][Full Text] [Related]
2. Familial Alzheimer's disease genes in Japanese.
Kamimura K; Tanahashi H; Yamanaka H; Takahashi K; Asada T; Tabira T
J Neurol Sci; 1998 Sep; 160(1):76-81. PubMed ID: 9804121
[TBL] [Abstract][Full Text] [Related]
3. Frequency of mutations in the presenilin and amyloid precursor protein genes in early-onset Alzheimer disease in Spain.
Lleó A; Blesa R; Queralt R; Ezquerra M; Molinuevo JL; Peña-Casanova J; Rojo A; Oliva R
Arch Neurol; 2002 Nov; 59(11):1759-63. PubMed ID: 12433263
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. Systematic genetic study of Alzheimer disease in Latin America: mutation frequencies of the amyloid beta precursor protein and presenilin genes in Colombia.
Arango D; Cruts M; Torres O; Backhovens H; Serrano ML; Villareal E; Montañes P; Matallana D; Cano C; Van Broeckhoven C; Jacquier M
Am J Med Genet; 2001 Oct; 103(2):138-43. PubMed ID: 11568920
[TBL] [Abstract][Full Text] [Related]
6. Early onset familial Alzheimer's disease: Mutation frequency in 31 families.
Janssen JC; Beck JA; Campbell TA; Dickinson A; Fox NC; Harvey RJ; Houlden H; Rossor MN; Collinge J
Neurology; 2003 Jan; 60(2):235-9. PubMed ID: 12552037
[TBL] [Abstract][Full Text] [Related]
7. Two novel (M233T and R278T) presenilin-1 mutations in early-onset Alzheimer's disease pedigrees and preliminary evidence for association of presenilin-1 mutations with a novel phenotype.
Kwok JB; Taddei K; Hallupp M; Fisher C; Brooks WS; Broe GA; Hardy J; Fulham MJ; Nicholson GA; Stell R; St George Hyslop PH; Fraser PE; Kakulas B; Clarnette R; Relkin N; Gandy SE; Schofield PR; Martins RN
Neuroreport; 1997 Apr; 8(6):1537-42. PubMed ID: 9172170
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. ApoE genotype is a risk factor in nonpresenilin early-onset Alzheimer's disease families.
Houlden H; Crook R; Backhovens H; Prihar G; Baker M; Hutton M; Rossor M; Martin JJ; Van Broeckhoven C; Hardy J
Am J Med Genet; 1998 Feb; 81(1):117-21. PubMed ID: 9514597
[TBL] [Abstract][Full Text] [Related]
10. A founder mutation in presenilin 1 causing early-onset Alzheimer disease in unrelated Caribbean Hispanic families.
Athan ES; Williamson J; Ciappa A; Santana V; Romas SN; Lee JH; Rondon H; Lantigua RA; Medrano M; Torres M; Arawaka S; Rogaeva E; Song YQ; Sato C; Kawarai T; Fafel KC; Boss MA; Seltzer WK; Stern Y; St George-Hyslop P; Tycko B; Mayeux R
JAMA; 2001 Nov; 286(18):2257-63. PubMed ID: 11710891
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. F175S change and a novel polymorphism in presenilin-1 gene in late-onset familial Alzheimer's disease.
Colacicco AM; Panza F; Basile AM; Solfrizzi V; Capurso C; D'Introno A; Torres F; Capurso S; Cozza S; Flora R; Capurso A
Eur Neurol; 2002; 47(4):209-13. PubMed ID: 12037434
[TBL] [Abstract][Full Text] [Related]
13. Two novel presenilin-1 mutations (Y256S and Q222H) are associated with early-onset Alzheimer's disease.
Miklossy J; Taddei K; Suva D; Verdile G; Fonte J; Fisher C; Gnjec A; Ghika J; Suard F; Mehta PD; McLean CA; Masters CL; Brooks WS; Martins RN
Neurobiol Aging; 2003 Sep; 24(5):655-62. PubMed ID: 12885573
[TBL] [Abstract][Full Text] [Related]
14. Molecular genetics of Alzheimer's disease.
Goate AM
Geriatrics; 1997 Sep; 52 Suppl 2():S9-12. PubMed ID: 9307578
[TBL] [Abstract][Full Text] [Related]
15. Alzheimer's disease associated with mutations in presenilin 2 is rare and variably penetrant.
Sherrington R; Froelich S; Sorbi S; Campion D; Chi H; Rogaeva EA; Levesque G; Rogaev EI; Lin C; Liang Y; Ikeda M; Mar L; Brice A; Agid Y; Percy ME; Clerget-Darpoux F; Piacentini S; Marcon G; Nacmias B; Amaducci L; Frebourg T; Lannfelt L; Rommens JM; St George-Hyslop PH
Hum Mol Genet; 1996 Jul; 5(7):985-8. PubMed ID: 8817335
[TBL] [Abstract][Full Text] [Related]
16. Alzheimer's disease phenotypes and genotypes associated with mutations in presenilin 2.
Jayadev S; Leverenz JB; Steinbart E; Stahl J; Klunk W; Yu CE; Bird TD
Brain; 2010 Apr; 133(Pt 4):1143-54. PubMed ID: 20375137
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. Founder effect for the Ala431Glu mutation of the presenilin 1 gene causing early-onset Alzheimer's disease in Mexican families.
Yescas P; Huertas-Vazquez A; Villarreal-Molina MT; Rasmussen A; Tusié-Luna MT; López M; Canizales-Quinteros S; Alonso ME
Neurogenetics; 2006 Jul; 7(3):195-200. PubMed ID: 16628450
[TBL] [Abstract][Full Text] [Related]
19. E280A PS-1 mutation causes Alzheimer's disease but age of onset is not modified by ApoE alleles.
Lendon CL; Martinez A; Behrens IM; Kosik KS; Madrigal L; Norton J; Neuman R; Myers A; Busfield F; Wragg M; Arcos M; Arango Viana JC; Ossa J; Ruiz A; Goate AM; Lopera F
Hum Mutat; 1997; 10(3):186-95. PubMed ID: 9298817
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]