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Mechanistic Insight into NMDA Receptor Dysregulation by Rare Variants in the GluN2A and GluN2B Agonist Binding Domains.
Swanger SA, Chen W, Wells G, Burger PB, Tankovic A, Bhattacharya S, Strong KL, Hu C, Kusumoto H, Zhang J, Adams DR, Millichap JJ, Petrovski S, Traynelis SF, Yuan H. Swanger SA, et al. Among authors: wells g. Am J Hum Genet. 2016 Dec 1;99(6):1261-1280. doi: 10.1016/j.ajhg.2016.10.002. Epub 2016 Nov 10. Am J Hum Genet. 2016. PMID: 27839871 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: wells ga. 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.
SENP3-FIS1 axis promotes mitophagy and cell survival under hypoxia.
Zhao A, Maple L, Jiang J, Myers KN, Jones CG, Gagg H, McGarrity-Cottrell C, Rominiyi O, Collis SJ, Wells G, Rahman M, Danson SJ, Robinson D, Smythe C, Guo C. Zhao A, et al. Among authors: wells g. Cell Death Dis. 2024 Dec 5;15(12):881. doi: 10.1038/s41419-024-07271-8. Cell Death Dis. 2024. PMID: 39638786 Free PMC article.
Diversity, community engagement and co-design in research: a rapid review.
Khan N, Keck L, Sykes C, Rowden C, Simister J, Fenlon S, Mccallum E, Bell M, Whiting D, Shelton C, Wells G, Giles R, Howard J, Peckham S. Khan N, et al. Among authors: wells g. BMJ Lead. 2024 Nov 27:leader-2024-001046. doi: 10.1136/leader-2024-001046. Online ahead of print. BMJ Lead. 2024. PMID: 39608816 Review.
2,033 results