BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

207 related articles for article (PubMed ID: 31020001)

  • 21. Amyloid-β
    Perrone F; Bjerke M; Hens E; Sieben A; Timmers M; De Roeck A; Vandenberghe R; Sleegers K; Martin JJ; De Deyn PP; Engelborghs S; van der Zee J; Van Broeckhoven C; Cacace R;
    Alzheimers Res Ther; 2020 Sep; 12(1):108. PubMed ID: 32917274
    [TBL] [Abstract][Full Text] [Related]  

  • 22. 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]  

  • 23. Early onset familial Alzheimer's disease: Mutation frequency in 31 families.
    Janssen JC; Beck JA; Campbell TA; Dickinson A; Fox NC; Harvey RJ; Houlden H; Rossor MN; Collinge J
    Neurology; 2003 Jan; 60(2):235-9. PubMed ID: 12552037
    [TBL] [Abstract][Full Text] [Related]  

  • 24. 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]  

  • 25. 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]  

  • 26. Systematic genetic study of Alzheimer disease in Latin America: mutation frequencies of the amyloid beta precursor protein and presenilin genes in Colombia.
    Arango D; Cruts M; Torres O; Backhovens H; Serrano ML; Villareal E; Montañes P; Matallana D; Cano C; Van Broeckhoven C; Jacquier M
    Am J Med Genet; 2001 Oct; 103(2):138-43. PubMed ID: 11568920
    [TBL] [Abstract][Full Text] [Related]  

  • 27. A New Presenilin-1 Missense Variant Associated With a Progressive Supranuclear Palsy-like Phenotype.
    Thomas Q; Nambot S; Béjot Y; Philippe C; Faivre L; Duffourd Y; Thauvin-Robinet C; Dupont G
    Alzheimer Dis Assoc Disord; 2023 Jan-Mar 01; 37(1):82-84. PubMed ID: 35383591
    [TBL] [Abstract][Full Text] [Related]  

  • 28. 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]  

  • 29. 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]  

  • 30. The associations of APP, PSEN1, and PSEN2 genes with Alzheimer's disease: A large case-control study in Chinese population.
    Xiao X; Liu H; Zhou L; Liu X; Xu T; Zhu Y; Yang Q; Hao X; Liu Y; Zhang W; Zhou Y; Wang J; Li J; Jiao B; Shen L; Liao X
    CNS Neurosci Ther; 2023 Jan; 29(1):122-128. PubMed ID: 36217304
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Genetic testing in familial and young-onset Alzheimer's disease: mutation spectrum in a Serbian cohort.
    Dobricic V; Stefanova E; Jankovic M; Gurunlian N; Novakovic I; Hardy J; Kostic V; Guerreiro R
    Neurobiol Aging; 2012 Jul; 33(7):1481.e7-12. PubMed ID: 22221884
    [TBL] [Abstract][Full Text] [Related]  

  • 32. PSEN2 (presenilin 2) mutants linked to familial Alzheimer disease impair autophagy by altering Ca
    Fedeli C; Filadi R; Rossi A; Mammucari C; Pizzo P
    Autophagy; 2019 Dec; 15(12):2044-2062. PubMed ID: 30892128
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Mutation screening in Chinese patients with familial Alzheimer's disease by whole-exome sequencing.
    Jiang B; Zhou J; Li HL; Chen YG; Cheng HR; Ye LQ; Liu DS; Chen DF; Tao QQ; Wu ZY
    Neurobiol Aging; 2019 Apr; 76():215.e15-215.e21. PubMed ID: 30598257
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Intracellular Calcium Dysregulation by the Alzheimer's Disease-Linked Protein Presenilin 2.
    Galla L; Redolfi N; Pozzan T; Pizzo P; Greotti E
    Int J Mol Sci; 2020 Jan; 21(3):. PubMed ID: 31991578
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Early-Onset Familial Alzheimer Disease Variant PSEN2 N141I Heterozygosity is Associated with Altered Microglia Phenotype.
    Fung S; Smith CL; Prater KE; Case A; Green K; Osnis L; Winston C; Kinoshita Y; Sopher B; Morrison RS; Garden GA; Jayadev S
    J Alzheimers Dis; 2020; 77(2):675-688. PubMed ID: 32741831
    [TBL] [Abstract][Full Text] [Related]  

  • 36. High striatal amyloid beta-peptide deposition across different autosomal Alzheimer disease mutation types.
    Villemagne VL; Ataka S; Mizuno T; Brooks WS; Wada Y; Kondo M; Jones G; Watanabe Y; Mulligan R; Nakagawa M; Miki T; Shimada H; O'Keefe GJ; Masters CL; Mori H; Rowe CC
    Arch Neurol; 2009 Dec; 66(12):1537-44. PubMed ID: 20008660
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Genomics of Alzheimer Disease: A Review.
    Rosenberg RN; Lambracht-Washington D; Yu G; Xia W
    JAMA Neurol; 2016 Jul; 73(7):867-74. PubMed ID: 27135718
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Screening of dementia genes by whole-exome sequencing in early-onset Alzheimer disease: input and lessons.
    Nicolas G; Wallon D; Charbonnier C; Quenez O; Rousseau S; Richard AC; Rovelet-Lecrux A; Coutant S; Le Guennec K; Bacq D; Garnier JG; Olaso R; Boland A; Meyer V; Deleuze JF; Munter HM; Bourque G; Auld D; Montpetit A; Lathrop M; Guyant-Maréchal L; Martinaud O; Pariente J; Rollin-Sillaire A; Pasquier F; Le Ber I; Sarazin M; Croisile B; Boutoleau-Bretonnière C; Thomas-Antérion C; Paquet C; Sauvée M; Moreaud O; Gabelle A; Sellal F; Ceccaldi M; Chamard L; Blanc F; Frebourg T; Campion D; Hannequin D
    Eur J Hum Genet; 2016 May; 24(5):710-6. PubMed ID: 26242991
    [TBL] [Abstract][Full Text] [Related]  

  • 39. 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]  

  • 40. Causative Mutations and Genetic Risk Factors in Sporadic Early Onset Alzheimer's Disease Before 51 Years.
    Lacour M; Quenez O; Rovelet-Lecrux A; Salomon B; Rousseau S; Richard AC; Quillard-Muraine M; Pasquier F; Rollin-Sillaire A; Martinaud O; Zarea A; 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; Godefroy O; Formaglio M; Croisile B; Auriacombe S; Magnin E; Sauvée M; Marelli C; Gabelle A; Pariente J; Paquet C; Boland A; Deleuze JF; Campion D; Hannequin D; Nicolas G; Wallon D;
    J Alzheimers Dis; 2019; 71(1):227-243. PubMed ID: 31381512
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 11.