Finnie Peter S B相关文献与解析，生知库 | 链接生命科学的每一步

日期影响因子

A human electrophysiological signature of Fragile X pathophysiology is shared in V1 of Fmr1(-/y) mice

Fmr1(-/y)小鼠的V1区与人类脆性X染色体综合征的病理生理特征相似。

期刊:Nature Communications

影响因子:15.7

doi:10.1038/s41467-026-69243-0

Kornfeld-Sylla, Sara S; Gelegen, Cigdem; Norris, Jordan E; Chaloner, Francesca A; Lee, Maia; Khela, Michael; Heinrich, Maxwell J; Finnie, Peter S B; Ethridge, Lauren E; Erickson, Craig A; Schmitt, Lauren M; Cooke, Sam F; Wilkinson, Carol L; Bear, Mark F

发表日期：2026

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Alpha-methyl-para-tyrosine and amphetamine ameliorate hyperactivity in a novel mouse model of dopamine transporter deficiency syndrome

α-甲基-对-酪氨酸和苯丙胺可改善新型多巴胺转运体缺乏综合征小鼠模型中的多动症

期刊:EMBO Molecular Medicine

影响因子:8.3

doi:10.1038/s44321-026-00381-0

Russo, Emma E; Rezayof, Ameneh; Wallace, Conner; Williams, Erin Q; Beerepoot, Pieter; Milenkovic, Marija; Novalen, Maria; Blundell, Aled; Lipina, Tatiana V; Locke, Jason; Christian, Raveen; Finnie, Peter S B; Edgar, Landon J; Tyndale, Rachel F; Watkins-Chow, Dawn; Ramsey, Amy J; Jones, Sara R; Salahpour, Ali

发表日期：2026

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Neurodevelopmental disorder-causing GRIN1 Y647S variant alters red blood cell physiology in mice.

导致神经发育障碍的 GRIN1 Y647S 变异会改变小鼠的红细胞生理。

期刊:Physiological Reports

影响因子:1.9

doi:10.14814/phy2.70759

Okafor Sylvia C, Horsfall Wendy, Finnie Peter S B, Holicka Caroline, Wen Tao, Khatir Behrooz, Loriamini Melika, Salahpour Ali, Golovin Kevin, Branch Donald R, Scott Graham R, Edgar Landon J, Kalev-Zylinska Maggie L, Ramsey Amy J

细胞生物学

发表日期：2026

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Non-ionotropic signaling through the NMDA receptor GluN2B carboxy-terminal domain drives dendritic spine plasticity and reverses fragile X phenotypes.

通过 NMDA 受体 GluN2B 羧基末端结构域的非离子型信号传导驱动树突棘可塑性并逆转脆性 X 表型

期刊:Cell Reports

影响因子:6.9

doi:10.1016/j.celrep.2025.115311

Barnes Stephanie A, Thomazeau Aurore, Finnie Peter S B, Heinrich Maxwell J, Heynen Arnold J, Komiyama Noburu H, Grant Seth G N, Menniti Frank S, Osterweil Emily K, Bear Mark F

发表日期：2025

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A human electrophysiological biomarker of Fragile X Syndrome is shared in V1 of Fmr1 KO mice and caused by loss of FMRP in cortical excitatory neurons

脆性X综合征的一种人类电生理生物标志物在Fmr1基因敲除小鼠的V1区也存在，这是由于皮层兴奋性神经元中FMRP的缺失所致。

doi:10.1101/2025.03.19.644144

Kornfeld-Sylla, Sara S; Gelegen, Cigdem; Norris, Jordan E; Chaloner, Francesca A; Lee, Maia; Khela, Michael; Heinrich, Maxwell J; Finnie, Peter S B; Ethridge, Lauren E; Erickson, Craig A; Schmitt, Lauren M; Cooke, Sam F; Wilkinson, Carol L; Bear, Mark F

发表日期：2025

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Tricyclic and tetracyclic antidepressants upregulate VMAT2 activity and rescue disease-causing VMAT2 variants

三环类和四环类抗抑郁药可上调VMAT2活性并挽救致病性VMAT2变体。

期刊:Neuropsychopharmacology

影响因子:7.1

doi:10.1038/s41386-024-01914-2

Wang, Xunan; Marmouzi, Ilias; Finnie, Peter S B; Bucher, Meghan L; Yan, Yuanye; Williams, Erin Q; Støve, Svein I; Lipina, Tatiana V; Ramsey, Amy J; Miller, Gary W; Salahpour, Ali

发表日期：2024

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Grin1 (Y) (647) (S/+) Mice: A Preclinical Model of GRIN1 -Related Neurodevelopmental Disorder

Grin1 (Y) (647) (S/+) 小鼠：GRIN1 相关神经发育障碍的临床前模型

doi:10.1101/2024.08.21.608984

Sullivan, Megan T; Tidball, Patrick; Yan, Yuanye; Intson, Katheron; Chen, Wenjuan; Xu, Yuchen; Venkatesan, Sridevi; Horsfall, Wendy; Georgiou, John; Finnie, Peter S B; Lambe, Evelyn K; Traynelis, Stephen F; Salahpour, Ali; Yuan, Hongjie; Collingridge, Graham L; Ramsey, Amy J

发育与干细胞

发表日期：2024

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