147 related articles for article (PubMed ID: 10404731)
1. Presenilin-2 mutation and polymorphism in Japanese Alzheimer disease patients.
Tanimukai H; Tsujio I; Hashimoto R; Kudo T; Kamino K; Shinozaki K; Takeda M
Clin Chim Acta; 1999 May; 283(1-2):57-61. PubMed ID: 10404731
[TBL] [Abstract][Full Text] [Related]
2. Polymorphism of the regulatory region of the presenilin-2 gene in sporadic Alzheimer's disease: a case-control study.
Quan W; Yasuda M; Hashimoto M; Yamamoto Y; Ishii K; Kazui H; Mori E; Kakigi T; Maeda K
J Neurol Sci; 2006 Jan; 240(1-2):71-5. PubMed ID: 16233903
[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. Case-control study of presenilin-1 intronic polymorphism in sporadic early and late onset Alzheimer's disease.
Yasuda M; Hirono N; Maeda K; Imamura T; Mori E; Tanaka C
J Neurol Neurosurg Psychiatry; 1999 Jun; 66(6):722-6. PubMed ID: 10329743
[TBL] [Abstract][Full Text] [Related]
5. A polymorphism in the presenilin 1 gene does not modify risk for Alzheimer's disease in a cohort with sporadic early onset.
Lendon CL; Myers A; Cumming A; Goate AM; St Clair D
Neurosci Lett; 1997 Jun; 228(3):212-4. PubMed ID: 9218645
[TBL] [Abstract][Full Text] [Related]
6. No association of the -48CT polymorphism of the presenilin 1 gene with Alzheimer disease in a late-onset sporadic population.
Araria-Goumidi L; Huguet JB; Lambert JC; Frigard B; Cottel D; Amouyel P; Chartier-Harlin MC
J Neural Transm (Vienna); 2002 Jul; 109(7-8):1023-7. PubMed ID: 12111439
[TBL] [Abstract][Full Text] [Related]
7. Presenilin-1 polymorphism in Alzheimer's disease and vascular dementia.
Matsushita S; Arai H; Muramatsu T; Makimoto K; Nakagawa T; Sasaki H; Higuchi S
Exp Neurol; 1997 Aug; 146(2):567-9. PubMed ID: 9270069
[TBL] [Abstract][Full Text] [Related]
8. Presenilin 1 intronic polymorphism is not associated with Alzheimer type neuropathological changes or sporadic Alzheimer's disease.
Sodeyama N; Itoh Y; Suematsu N; Matsushita M; Otomo E; Mizusawa H; Yamada M
J Neurol Neurosurg Psychiatry; 1998 Apr; 64(4):548-51. PubMed ID: 9576554
[TBL] [Abstract][Full Text] [Related]
9. T/G polymorphism at intron 9 of presenilin 1 gene is associated with, but not responsible for sporadic late-onset Alzheimer's disease in Japanese population.
Nishiwaki Y; Kamino K; Yoshiiwa A; Sato N; Tateishi K; Takeda M; Kobayashi T; Yamamoto H; Nonomura Y; Yoneda H; Sakai T; Imagawa M; Miki T; Ogihara T
Neurosci Lett; 1997 May; 227(2):123-6. PubMed ID: 9180219
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. No association of presenilin-1 intronic polymorphism and Alzheimer's disease in Australia.
Taddei K; Yang D; Fisher C; Clarnette R; Hallmayer J; Barnetson R; Maller R; Brooks WS; Whyte S; Nicholson GA; Masters CL; Broe GA; Gandy SE; Martins RN
Neurosci Lett; 1998 May; 246(3):178-80. PubMed ID: 9792621
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. No association or linkage between an intronic polymorphism of presenilin-1 and sporadic or late-onset familial Alzheimer disease.
Scott WK; Yamaoka LH; Locke PA; Rosi BL; Gaskell PC; Saunders AM; Conneally PM; Small GW; Farrer LA; Growdon JH; Roses AD; Pericak-Vance MA; Haines JL
Genet Epidemiol; 1997; 14(3):307-15. PubMed ID: 9181359
[TBL] [Abstract][Full Text] [Related]
14. Presenilin-1 polymorphism in patients with Alzheimer's disease, vascular dementia and alcohol-associated dementia in Japanese population.
Isoe K; Urakami K; Ji Y; Adachi Y; Nakashima K
Acta Neurol Scand; 1996 Nov; 94(5):326-8. PubMed ID: 8947284
[TBL] [Abstract][Full Text] [Related]
15. Evaluation of multiple presenilin 2 SNPs for association with early-onset sporadic Alzheimer disease.
Howell WM; Brookes AJ
Am J Med Genet; 2002 Aug; 111(2):157-63. PubMed ID: 12210343
[TBL] [Abstract][Full Text] [Related]
16. Is the presenilin-1 E318G missense mutation a risk factor for Alzheimer's disease?
Helisalmi S; Hiltunen M; Mannermaa A; Koivisto AM; Lehtovirta M; Alafuzoff I; Ryynänen M; Soininen H
Neurosci Lett; 2000 Jan; 278(1-2):65-8. PubMed ID: 10643802
[TBL] [Abstract][Full Text] [Related]
17. A pedigree with a novel presenilin 1 mutation at a residue that is not conserved in presenilin 2.
Yasuda M; Maeda K; Hashimoto M; Yamashita H; Ikejiri Y; Bird TD; Tanaka C; Schellenberg GD
Arch Neurol; 1999 Jan; 56(1):65-9. PubMed ID: 9923762
[TBL] [Abstract][Full Text] [Related]
18. Lack of association between an intronic polymorphism in the presenilin-1 gene and sporadic late-onset Alzheimer disease in Polish patients.
Kowalska A; Wender M; Lannfelt L
Dement Geriatr Cogn Disord; 1998; 9(3):137-9. PubMed ID: 9622000
[TBL] [Abstract][Full Text] [Related]
19. The 4,752 C/T polymorphism in the presenilin 1 gene increases the risk of Alzheimer's disease in apolipoprotein E4 carriers.
Matsubara-Tsutsui M; Yamagata H; Morishima A; Nakura J; Mitsuda N; Kamino K; Kondo I; Miki T
Intern Med; 2002 Oct; 41(10):823-8. PubMed ID: 12413003
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
