These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

128 related articles for article (PubMed ID: 37742650)

  • 21. In-Frame and Frameshift Mutations in Zebrafish
    Barthelson K; Pederson SM; Newman M; Jiang H; Lardelli M
    J Alzheimers Dis Rep; 2021 May; 5(1):395-404. PubMed ID: 34189411
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Contribution of homozygous and compound heterozygous missense mutations in VWA2 to Alzheimer's disease.
    Hoogmartens J; Hens E; Engelborghs S; Vandenberghe R; De Deyn PP; Cacace R; Van Broeckhoven C;
    Neurobiol Aging; 2021 Mar; 99():100.e17-100.e23. PubMed ID: 33023779
    [TBL] [Abstract][Full Text] [Related]  

  • 23. The Zebrafish Equivalent of Alzheimer's Disease-Associated PRESENILIN Isoform PS2V Regulates Inflammatory and Other Responses to Hypoxic Stress.
    Ebrahimie E; Moussavi Nik SH; Newman M; Van Der Hoek M; Lardelli M
    J Alzheimers Dis; 2016 Mar; 52(2):581-608. PubMed ID: 27031468
    [TBL] [Abstract][Full Text] [Related]  

  • 24. No observed effect on brain vasculature of Alzheimer's disease-related mutations in the zebrafish presenilin 1 gene.
    Barthelson K; Newman M; Nowell CJ; Lardelli M
    Mol Brain; 2021 Jan; 14(1):22. PubMed ID: 33494778
    [TBL] [Abstract][Full Text] [Related]  

  • 25. 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]  

  • 26. Presenilin 1 and APP Gene Mutations in Early-Onset AD Families from a Southeast Region of China.
    Zhou J; Chen Y; Meng F; Zhang K; Liu X; Peng G
    Curr Alzheimer Res; 2020; 17(6):540-546. PubMed ID: 32579498
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Epileptic seizures in autosomal dominant forms of Alzheimer's disease.
    Cortini F; Cantoni C; Villa C
    Seizure; 2018 Oct; 61():4-7. PubMed ID: 30041064
    [TBL] [Abstract][Full Text] [Related]  

  • 28. 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]  

  • 29. 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]  

  • 30. A Review of the Familial Alzheimer's Disease Locus PRESENILIN 2 and Its Relationship to PRESENILIN 1.
    Jiang H; Jayadev S; Lardelli M; Newman M
    J Alzheimers Dis; 2018; 66(4):1323-1339. PubMed ID: 30412492
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Genetic analyses of early-onset Alzheimer's disease using next generation sequencing.
    Giau VV; Bagyinszky E; Yang YS; Youn YC; An SSA; Kim SY
    Sci Rep; 2019 Jun; 9(1):8368. PubMed ID: 31182772
    [TBL] [Abstract][Full Text] [Related]  

  • 32. 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]  

  • 33. 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]  

  • 34.
    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]  

  • 35. 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]  

  • 36. Identification of PSEN2 mutation p.N141I in Argentine pedigrees with early-onset familial Alzheimer's disease.
    Muchnik C; Olivar N; Dalmasso MC; Azurmendi PJ; Liberczuk C; Morelli L; Brusco LI
    Neurobiol Aging; 2015 Oct; 36(10):2674-7.e1. PubMed ID: 26166204
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Investigating the role of rare coding variability in Mendelian dementia genes (APP, PSEN1, PSEN2, GRN, MAPT, and PRNP) in late-onset Alzheimer's disease.
    Sassi C; Guerreiro R; Gibbs R; Ding J; Lupton MK; Troakes C; Al-Sarraj S; Niblock M; Gallo JM; Adnan J; Killick R; Brown KS; Medway C; Lord J; Turton J; Bras J; ; Morgan K; Powell JF; Singleton A; Hardy J
    Neurobiol Aging; 2014 Dec; 35(12):2881.e1-2881.e6. PubMed ID: 25104557
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Presence of a mutation in PSEN1 or PSEN2 gene is associated with an impaired brain endothelial cell phenotype in vitro.
    Raut S; Patel R; Al-Ahmad AJ
    Fluids Barriers CNS; 2021 Jan; 18(1):3. PubMed ID: 33413468
    [TBL] [Abstract][Full Text] [Related]  

  • 39. A novel presenilin 1 mutation (Ser169del) in a Chinese family with early-onset Alzheimer's disease.
    Guo J; Wei J; Liao S; Wang L; Jiang H; Tang B
    Neurosci Lett; 2010 Jan; 468(1):34-7. PubMed ID: 19853643
    [TBL] [Abstract][Full Text] [Related]  

  • 40. A Unified Hypothesis of Early- and Late-Onset Alzheimer's Disease Pathogenesis.
    Atwood CS; Bowen RL
    J Alzheimers Dis; 2015; 47(1):33-47. PubMed ID: 26402752
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.