223 related articles for article (PubMed ID: 35328387)
1. A Possible Pathogenic PSEN2 Gly56Ser Mutation in a Korean Patient with Early-Onset Alzheimer's Disease.
Shim KH; Kang MJ; Bae H; Kim D; Park J; An SA; Jeong DE
Int J Mol Sci; 2022 Mar; 23(6):. PubMed ID: 35328387
[TBL] [Abstract][Full Text] [Related]
2. Double Mutations in a Patient with Early-Onset Alzheimer's Disease in Korea: An
Bae H; Shim KH; Yoo J; Yang YS; An SSA; Kang MJ
Int J Mol Sci; 2023 Apr; 24(8):. PubMed ID: 37108607
[TBL] [Abstract][Full Text] [Related]
3.
Giau VV; Bagyinszky E; Youn YC; An SSA; Kim S
Int J Mol Sci; 2019 Sep; 20(19):. PubMed ID: 31557888
[TBL] [Abstract][Full Text] [Related]
4. Novel presenilin 1 and 2 double knock-out cell line for in vitro validation of PSEN1 and PSEN2 mutations.
Pimenova AA; Goate AM
Neurobiol Dis; 2020 May; 138():104785. PubMed ID: 32032730
[TBL] [Abstract][Full Text] [Related]
5. A genetic screen of the mutations in the Korean patients with early-onset Alzheimer's disease.
An SS; Park SA; Bagyinszky E; Bae SO; Kim YJ; Im JY; Park KW; Park KH; Kim EJ; Jeong JH; Kim JH; Han HJ; Choi SH; Kim S
Clin Interv Aging; 2016; 11():1817-1822. PubMed ID: 28008242
[TBL] [Abstract][Full Text] [Related]
6. Genetic screening in early-onset Alzheimer's disease identified three novel presenilin mutations.
Wong TH; Seelaar H; Melhem S; Rozemuller AJM; van Swieten JC
Neurobiol Aging; 2020 Feb; 86():201.e9-201.e14. PubMed ID: 30797548
[TBL] [Abstract][Full Text] [Related]
7. PSEN2 Thr421Met Mutation in a Patient with Early Onset Alzheimer's Disease.
Yang Y; Bagyinszky E; An SSA; Kim S
Int J Mol Sci; 2022 Nov; 23(21):. PubMed ID: 36362122
[TBL] [Abstract][Full Text] [Related]
8. Identification of the Third Case of PSEN1 Tyr389His Variant in Early-Onset Alzheimer's Disease in Korea.
Shim KH; Kang S; An SSA; Kang MJ
Int J Mol Sci; 2022 Dec; 23(24):. PubMed ID: 36555832
[TBL] [Abstract][Full Text] [Related]
9. A pathogenic
Giau VV; Pyun JM; Bagyinszky E; An SSA; Kim S
Clin Interv Aging; 2018; 13():1321-1329. PubMed ID: 30104866
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. Gene mutations in a Han Chinese Alzheimer's disease cohort.
Ma L; Zhang J; Shi Y; Wang W; Ren Z; Xia M; Zhang Y; Yang M
Brain Behav; 2019 Jan; 9(1):e01180. PubMed ID: 30549411
[TBL] [Abstract][Full Text] [Related]
12. Probable Novel APP Met671Leu Mutation in a Chinese Han Family with Early-Onset Alzheimer's Disease.
Ma L; Wang F; Chen S; Wang S; Wang Z; Xia M; Li Y; Ma H; Shang J; Zhang J
Neuromolecular Med; 2024 Mar; 26(1):6. PubMed ID: 38504005
[TBL] [Abstract][Full Text] [Related]
13. Clinical and neuroimaging characterization of Chinese dementia patients with PSEN1 and PSEN2 mutations.
Shi Z; Wang Y; Liu S; Liu M; Liu S; Zhou Y; Wang J; Cai L; Huo YR; Gao S; Ji Y
Dement Geriatr Cogn Disord; 2015; 39(1-2):32-40. PubMed ID: 25323700
[TBL] [Abstract][Full Text] [Related]
14. Discovery and validation of autosomal dominant Alzheimer's disease mutations.
Hsu S; Gordon BA; Hornbeck R; Norton JB; Levitch D; Louden A; Ziegemeier E; Laforce R; Chhatwal J; Day GS; McDade E; Morris JC; Fagan AM; Benzinger TLS; Goate AM; Cruchaga C; Bateman RJ; ; Karch CM
Alzheimers Res Ther; 2018 Jul; 10(1):67. PubMed ID: 30021643
[TBL] [Abstract][Full Text] [Related]
15. Mutation profile of APP, PSEN1, and PSEN2 in Chinese familial Alzheimer's disease.
Gao Y; Ren RJ; Zhong ZL; Dammer E; Zhao QH; Shan S; Zhou Z; Li X; Zhang YQ; Cui HL; Hu YB; Chen SD; Chen JJ; Guo QH; Wang G
Neurobiol Aging; 2019 May; 77():154-157. PubMed ID: 30822634
[TBL] [Abstract][Full Text] [Related]
16. Three-year follow-up of a patient with early-onset Alzheimer's disease with presenilin-2 N141I mutation - case report and review of the literature.
Nikisch G; Hertel A; Kiessling B; Wagner T; Krasz D; Hofmann E; Wiedemann G
Eur J Med Res; 2008 Dec; 13(12):579-84. PubMed ID: 19073399
[TBL] [Abstract][Full Text] [Related]
17. Systematic validation of variants of unknown significance in APP, PSEN1 and PSEN2.
Hsu S; Pimenova AA; Hayes K; Villa JA; Rosene MJ; Jere M; Goate AM; Karch CM
Neurobiol Dis; 2020 Jun; 139():104817. PubMed ID: 32087291
[TBL] [Abstract][Full Text] [Related]
18. Alternative splicing in a presenilin 2 variant associated with Alzheimer disease.
Braggin JE; Bucks SA; Course MM; Smith CL; Sopher B; Osnis L; Shuey KD; Domoto-Reilly K; Caso C; Kinoshita C; Scherpelz KP; Cross C; Grabowski T; Nik SHM; Newman M; Garden GA; Leverenz JB; Tsuang D; Latimer C; Gonzalez-Cuyar LF; Keene CD; Morrison RS; Rhoads K; Wijsman EM; Dorschner MO; Lardelli M; Young JE; Valdmanis PN; Bird TD; Jayadev S
Ann Clin Transl Neurol; 2019 Apr; 6(4):762-777. PubMed ID: 31020001
[TBL] [Abstract][Full Text] [Related]
19. Exome sequencing identifies 2 novel presenilin 1 mutations (p.L166V and p.S230R) in British early-onset Alzheimer's disease.
Sassi C; Guerreiro R; Gibbs R; Ding J; Lupton MK; Troakes C; Lunnon K; Al-Sarraj S; Brown KS; Medway C; Lord J; Turton J; Mann D; Snowden J; Neary D; Harris J; Bras J; ; Morgan K; Powell JF; Singleton A; Hardy J
Neurobiol Aging; 2014 Oct; 35(10):2422.e13-6. PubMed ID: 24880964
[TBL] [Abstract][Full Text] [Related]
20. A novel PSEN2 p.Ser175Phe variant in a family with Alzheimer's disease.
Guven G; Samanci B; Gulec C; Hanagasi H; Gurvit H; Gokalp EE; Tepgec F; Guler S; Uyguner O; Bilgic B
Neurol Sci; 2021 Jun; 42(6):2497-2504. PubMed ID: 33855622
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]