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Artificial intelligence-derived neurofibrillary tangle burden is associated with antemortem cognitive impairment.
Marx GA, Koenigsberg DG, McKenzie AT, Kauffman J, Hanson RW, Whitney K, Signaevsky M, Prastawa M, Iida MA, White CL 3rd, Walker JM, Richardson TE, Koll J, Fernandez G, Zeineh J, Cordon-Cardo C, Crary JF, Farrell K; PART working group. Marx GA, et al. Among authors: hanson rw. Acta Neuropathol Commun. 2022 Oct 31;10(1):157. doi: 10.1186/s40478-022-01457-x. Acta Neuropathol Commun. 2022. PMID: 36316708 Free PMC article.
SARS-CoV-2 detection with aptamer-functionalized gold nanoparticles.
Aithal S, Mishriki S, Gupta R, Sahu RP, Botos G, Tanvir S, Hanson RW, Puri IK. Aithal S, et al. Among authors: hanson rw. Talanta. 2022 Jan 1;236:122841. doi: 10.1016/j.talanta.2021.122841. Epub 2021 Sep 1. Talanta. 2022. PMID: 34635231 Free PMC article.
Low-level blast exposure disrupts gliovascular and neurovascular connections and induces a chronic vascular pathology in rat brain.
Gama Sosa MA, De Gasperi R, Perez Garcia GS, Perez GM, Searcy C, Vargas D, Spencer A, Janssen PL, Tschiffely AE, McCarron RM, Ache B, Manoharan R, Janssen WG, Tappan SJ, Hanson RW, Gandy S, Hof PR, Ahlers ST, Elder GA. Gama Sosa MA, et al. Among authors: hanson rw. Acta Neuropathol Commun. 2019 Jan 9;7(1):6. doi: 10.1186/s40478-018-0647-5. Acta Neuropathol Commun. 2019. PMID: 30626447 Free PMC article.
Reprogramming of energy metabolism as a driver of aging.
Feng Z, Hanson RW, Berger NA, Trubitsyn A. Feng Z, et al. Among authors: hanson rw. Oncotarget. 2016 Mar 29;7(13):15410-20. doi: 10.18632/oncotarget.7645. Oncotarget. 2016. PMID: 26919253 Free PMC article. Review.
Reciprocal Changes in Phosphoenolpyruvate Carboxykinase and Pyruvate Kinase with Age Are a Determinant of Aging in Caenorhabditis elegans.
Yuan Y, Hakimi P, Kao C, Kao A, Liu R, Janocha A, Boyd-Tressler A, Hang X, Alhoraibi H, Slater E, Xia K, Cao P, Shue Q, Ching TT, Hsu AL, Erzurum SC, Dubyak GR, Berger NA, Hanson RW, Feng Z. Yuan Y, et al. Among authors: hanson rw. J Biol Chem. 2016 Jan 15;291(3):1307-19. doi: 10.1074/jbc.M115.691766. Epub 2015 Dec 2. J Biol Chem. 2016. PMID: 26631730 Free PMC article.
Three rare diseases in one Sib pair: RAI1, PCK1, GRIN2B mutations associated with Smith-Magenis Syndrome, cytosolic PEPCK deficiency and NMDA receptor glutamate insensitivity.
Adams DR, Yuan H, Holyoak T, Arajs KH, Hakimi P, Markello TC, Wolfe LA, Vilboux T, Burton BK, Fajardo KF, Grahame G, Holloman C, Sincan M, Smith AC, Wells GA, Huang Y, Vega H, Snyder JP, Golas GA, Tifft CJ, Boerkoel CF, Hanson RW, Traynelis SF, Kerr DS, Gahl WA. Adams DR, et al. Among authors: hanson rw. Mol Genet Metab. 2014 Nov;113(3):161-70. doi: 10.1016/j.ymgme.2014.04.001. Epub 2014 Apr 13. Mol Genet Metab. 2014. PMID: 24863970 Free PMC article.
257 results