402 related articles for article (PubMed ID: 17412506)
21. Molecular genetics of Alzheimer's disease: what have we learned?
Van Gassen G; Van Broeckhoven C
Acta Neurol Belg; 2000 Jun; 100(2):65-76. PubMed ID: 10934557
[TBL] [Abstract][Full Text] [Related]
22. Mutational analysis in early-onset familial Alzheimer's disease in Mainland China.
Jiao B; Tang B; Liu X; Xu J; Wang Y; Zhou L; Zhang F; Yan X; Zhou Y; Shen L
Neurobiol Aging; 2014 Aug; 35(8):1957.e1-6. PubMed ID: 24650794
[TBL] [Abstract][Full Text] [Related]
23. Atypical early-onset Alzheimer's disease caused by the Iranian APP mutation.
Lindquist SG; Nielsen JE; Stokholm J; Schwartz M; Batbayli M; Ballegaard M; Erdal J; Krabbe K; Waldemar G
J Neurol Sci; 2008 May; 268(1-2):124-30. PubMed ID: 18187157
[TBL] [Abstract][Full Text] [Related]
24. APP, PSEN1, and PSEN2 mutations in early-onset Alzheimer disease: A genetic screening study of familial and sporadic cases.
Lanoiselée HM; Nicolas G; Wallon D; Rovelet-Lecrux A; Lacour M; Rousseau S; Richard AC; Pasquier F; Rollin-Sillaire A; Martinaud O; Quillard-Muraine M; de la Sayette V; Boutoleau-Bretonniere C; Etcharry-Bouyx F; Chauviré V; Sarazin M; le Ber I; Epelbaum S; Jonveaux T; Rouaud O; Ceccaldi M; Félician O; Godefroy O; Formaglio M; Croisile B; Auriacombe S; Chamard L; Vincent JL; Sauvée M; Marelli-Tosi C; Gabelle A; Ozsancak C; Pariente J; Paquet C; Hannequin D; Campion D;
PLoS Med; 2017 Mar; 14(3):e1002270. PubMed ID: 28350801
[TBL] [Abstract][Full Text] [Related]
25. Molecular genetics of Alzheimer's disease: presenilin 1 gene analysis in a cohort of patients from the Poznań region.
Kowalska A; Wender M; Florczak J; Pruchnik-Wolinska D; Modestowicz R; Szczech J; Rossa G; Kozubski W
J Appl Genet; 2003; 44(2):231-4. PubMed ID: 12817569
[TBL] [Abstract][Full Text] [Related]
26. Molecular genetic analysis of the APP, PSEN1, and PSEN2 genes in Finnish patients with early-onset Alzheimer disease and frontotemporal lobar degeneration.
Krüger J; Moilanen V; Majamaa K; Remes AM
Alzheimer Dis Assoc Disord; 2012; 26(3):272-6. PubMed ID: 21959359
[TBL] [Abstract][Full Text] [Related]
27. Aberrant accentuation of neurofibrillary degeneration in the hippocampus of Alzheimer's disease with amyloid precursor protein 717 and presenilin-1 gene mutations.
Sudo S; Shiozawa M; Cairns NJ; Wada Y
J Neurol Sci; 2005 Jul; 234(1-2):55-65. PubMed ID: 15946688
[TBL] [Abstract][Full Text] [Related]
28. [Alzheimer disease: autosomal dominant forms].
Guyant-Maréchal L; Campion D; Hannequin D
Rev Neurol (Paris); 2009 Mar; 165(3):223-31. PubMed ID: 19081588
[TBL] [Abstract][Full Text] [Related]
29. [Genetics of Alzheimer's disease].
Setó-Salvia N; Clarimón J
Rev Neurol; 2010 Mar; 50(6):360-4. PubMed ID: 20309834
[TBL] [Abstract][Full Text] [Related]
30. 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]
31. [New mutation in the PSEN1 (E120G) gene associated with early onset Alzheimer's disease].
Lladó A; Sánchez-Valle R; Rey MJ; Mercadal P; Almenar C; López-Villegas D; Fortea J; Molinuevo JL
Neurologia; 2010; 25(1):13-6. PubMed ID: 20388456
[TBL] [Abstract][Full Text] [Related]
32. Interference with splicing of Presenilin transcripts has potent dominant negative effects on Presenilin activity.
Nornes S; Newman M; Verdile G; Wells S; Stoick-Cooper CL; Tucker B; Frederich-Sleptsova I; Martins R; Lardelli M
Hum Mol Genet; 2008 Feb; 17(3):402-12. PubMed ID: 17981814
[TBL] [Abstract][Full Text] [Related]
33. Screening Alzheimer's disease patients for mutations in the amyloid precursor protein gene.
Jones CT; Morris S; Moffoot A; St Clair D; Brock DJ
Mol Cell Probes; 1993 Apr; 7(2):161-5. PubMed ID: 8321254
[TBL] [Abstract][Full Text] [Related]
34. [Study on mutation of presenilin-1 gene in familial Alzheimer's disease].
Liu XY; Yin LD; Duan Y; Wang YM; Chen BW; Wang Y
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2004 Oct; 21(5):455-8. PubMed ID: 15476169
[TBL] [Abstract][Full Text] [Related]
35. A presenilin 1 mutation (Arg278Ser) associated with early onset Alzheimer's disease and spastic paraparesis.
Raman A; Lin X; Suri M; Hewitt M; Constantinescu CS; Phillips MF
J Neurol Sci; 2007 Sep; 260(1-2):78-82. PubMed ID: 17507029
[TBL] [Abstract][Full Text] [Related]
36. [A study on mutation of exon 5 of presenilin-1 in Alzheimer's disease].
Ma Q; Qian C; Liu Z; Lu X; Lin H
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 1999 Dec; 16(6):349-52. PubMed ID: 10581340
[TBL] [Abstract][Full Text] [Related]
37. Familial Alzheimer's disease: site of mutation influences clinical phenotype.
Lippa CF; Swearer JM; Kane KJ; Nochlin D; Bird TD; Ghetti B; Nee LE; St George-Hyslop P; Pollen DA; Drachman DA
Ann Neurol; 2000 Sep; 48(3):376-9. PubMed ID: 10976645
[TBL] [Abstract][Full Text] [Related]
38. Expression of APP pathway mRNAs and proteins in Alzheimer's disease.
Matsui T; Ingelsson M; Fukumoto H; Ramasamy K; Kowa H; Frosch MP; Irizarry MC; Hyman BT
Brain Res; 2007 Aug; 1161():116-23. PubMed ID: 17586478
[TBL] [Abstract][Full Text] [Related]
39. Novel presenilin mutations within Moroccan patients with Early-Onset Alzheimer's Disease.
El Kadmiri N; Zaid N; Zaid Y; Tadevosyan A; Hachem A; Dubé MP; Hamzi K; El Moutawakil B; Slassi I; Nadifi S
Neuroscience; 2014 Jun; 269():215-22. PubMed ID: 24704512
[TBL] [Abstract][Full Text] [Related]
40. The genetics of Alzheimer disease: back to the future.
Bertram L; Lill CM; Tanzi RE
Neuron; 2010 Oct; 68(2):270-81. PubMed ID: 20955934
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
