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For: Kat R, Arroyo-Araujo M, de Vries RBM, Koopmans MA, de Boer SF, Kas MJH. Translational validity and methodological underreporting in animal research: A systematic review and meta-analysis of the Fragile X syndrome (Fmr1 KO) rodent model. Neurosci Biobehav Rev 2022;139:104722. [PMID: 35690123 DOI: 10.1016/j.neubiorev.2022.104722] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 2.0] [Reference Citation Analysis]
Number Citing Articles
1 Louros SR, Seo SS, Maio B, Martinez-gonzalez C, Gonzalez-lozano MA, Muscas M, Verity NC, Wills JC, Li KW, Nolan MF, Osterweil EK. Excessive proteostasis contributes to pathology in fragile X syndrome. Neuron 2022. [DOI: 10.1016/j.neuron.2022.11.012] [Reference Citation Analysis]
2 Cogram P, Fernández-beltrán LC, Casarejos MJ, Sánchez-yepes S, Rodríguez-martín E, García-rubia A, Sánchez-barrena MJ, Gil C, Martínez A, Mansilla A. The inhibition of NCS-1 binding to Ric8a rescues fragile X syndrome mice model phenotypes. Front Neurosci 2022;16. [DOI: 10.3389/fnins.2022.1007531] [Reference Citation Analysis]
3 Petroni V, Subashi E, Premoli M, Memo M, Lemaire V, Pietropaolo S. Long-term behavioral effects of prenatal stress in the Fmr1-knock-out mouse model for fragile X syndrome. Front Cell Neurosci 2022;16. [DOI: 10.3389/fncel.2022.917183] [Reference Citation Analysis]
4 Kat R, Kas MJH. Largely unaffected auditory and visual sensory processing phenotypes in the evoked potentials of Fmr1 KO2 mice. Eur J Neurosci 2022;56:5260-73. [PMID: 36017614 DOI: 10.1111/ejn.15808] [Reference Citation Analysis]
5 Morrill NK, Joly-Amado A, Li Q, Prabhudeva S, Weeber EJ, Nash KR. Reelin central fragment supplementation improves cognitive deficits in a mouse model of Fragile X Syndrome. Exp Neurol 2022;357:114170. [PMID: 35863501 DOI: 10.1016/j.expneurol.2022.114170] [Reference Citation Analysis]