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4. Incomplete penetrance of familial Alzheimer's disease in a pedigree with a novel presenilin-1 gene mutation. Rossor MN; Fox NC; Beck J; Campbell TC; Collinge J Lancet; 1996 Jun; 347(9014):1560. PubMed ID: 8684135 [No Abstract] [Full Text] [Related]
5. The structure of the presenilin 1 (S182) gene and identification of six novel mutations in early onset AD families. Alzheimer's Disease Collaborative Group Nat Genet; 1995 Oct; 11(2):219-22. PubMed ID: 7550356 [TBL] [Abstract][Full Text] [Related]
6. Molecular genetic analysis of familial early-onset Alzheimer's disease linked to chromosome 14q24.3. Cruts M; Backhovens H; Wang SY; Van Gassen G; Theuns J; De Jonghe CD; Wehnert A; De Voecht J; De Winter G; Cras P Hum Mol Genet; 1995 Dec; 4(12):2363-71. PubMed ID: 8634711 [TBL] [Abstract][Full Text] [Related]
7. [Mutation analysis of S182 (presenilin-I) in patients with familial Alzheimer's disease and its biological function]. Ikeda M Nihon Ronen Igakkai Zasshi; 1998 Apr; 35(4):285-9. PubMed ID: 9643011 [TBL] [Abstract][Full Text] [Related]
8. S182: from worm sperm to Alzheimer's disease. Harrison PJ Lancet; 1995 Aug; 346(8972):388. PubMed ID: 7623564 [No Abstract] [Full Text] [Related]
10. Cloning of a gene bearing missense mutations in early-onset familial Alzheimer's disease. Sherrington R; Rogaev EI; Liang Y; Rogaeva EA; Levesque G; Ikeda M; Chi H; Lin C; Li G; Holman K; Tsuda T; Mar L; Foncin JF; Bruni AC; Montesi MP; Sorbi S; Rainero I; Pinessi L; Nee L; Chumakov I; Pollen D; Brookes A; Sanseau P; Polinsky RJ; Wasco W; Da Silva HA; Haines JL; Perkicak-Vance MA; Tanzi RE; Roses AD; Fraser PE; Rommens JM; St George-Hyslop PH Nature; 1995 Jun; 375(6534):754-60. PubMed ID: 7596406 [TBL] [Abstract][Full Text] [Related]
11. Familial Alzheimer's disease in kindreds with missense mutations in a gene on chromosome 1 related to the Alzheimer's disease type 3 gene. Rogaev EI; Sherrington R; Rogaeva EA; Levesque G; Ikeda M; Liang Y; Chi H; Lin C; Holman K; Tsuda T Nature; 1995 Aug; 376(6543):775-8. PubMed ID: 7651536 [TBL] [Abstract][Full Text] [Related]
12. S182 and STM2 gene missense mutations in sporadic Alzheimer disease. Higuchi S; Matsushita S; Hasegawa Y; Muramatsu T; Itabashi S; Arai H Am J Med Genet; 1996 Jul; 67(4):429. PubMed ID: 8837717 [No Abstract] [Full Text] [Related]
13. Chromosome 14 familial Alzheimer's disease: the clinical and neuropathological characteristics of a family with a leucine-->serine (L250S) substitution at codon 250 of the presenilin 1 gene. Harvey RJ; Ellison D; Hardy J; Hutton M; Roques PK; Collinge J; Fox NC; Rossor MN J Neurol Neurosurg Psychiatry; 1998 Jan; 64(1):44-9. PubMed ID: 9436726 [TBL] [Abstract][Full Text] [Related]
14. Failure to detect missense mutations in the S182 gene in a series of late-onset Alzheimer's disease cases. Tsuda T; Chi H; Liang Y; Rogaeva EA; Sherrington R; Levesque G; Ikeda M; Rogaev EI; Pollen D; Freedman M Neurosci Lett; 1995 Dec; 201(2):188-90. PubMed ID: 8848249 [TBL] [Abstract][Full Text] [Related]
15. A novel missense mutation in the presenilin-1 gene in a familial Alzheimer's disease pedigree with abundant amyloid angiopathy. Yasuda M; Maeda K; Ikejiri Y; Kawamata T; Kuroda S; Tanaka C Neurosci Lett; 1997 Aug; 232(1):29-32. PubMed ID: 9292884 [TBL] [Abstract][Full Text] [Related]
16. 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]
17. Two homologous genes causing early-onset familial Alzheimer's disease. St George-Hyslop PH; Levesque G; Levesque L; Rommens J; Westaway D; Fraser PE Cold Spring Harb Symp Quant Biol; 1996; 61():559-64. PubMed ID: 9246482 [No Abstract] [Full Text] [Related]