日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Intracerebroventricular SPAST-AAV9 gene therapy prevents manifestation of symptoms in a mouse model of SPG4 hereditary spastic paraplegia.

脑室内 SPAST-AAV9 基因治疗可预防 SPG4 遗传性痉挛性截瘫小鼠模型出现症状。

Piermarini Emanuela, Guha Shrobona, Qiang Liang, Gray-Edwards Heather, Sena-Esteves Miguel, Baas Peter W

Modeling spastic paraplegia 4 with corticospinal motor neuron-enriched cortical organoids reveals genotype-phenotype and HDAC6-targetable pathology.

利用富含皮质脊髓运动神经元的皮质类器官对痉挛性截瘫 4 进行建模,揭示了基因型-表型和 HDAC6 可靶向的病理。

Mohan Neha, Ramakrishnan Skandha, Sun Xiaohuan, Sun Ying, Connors Theresa, Chai Victor, Piermarini Emanuela, Baas Peter W, Cai James, Liu Mei, Qiang Liang

Genotype-Phenotype Distinctions in Spastic Paraplegia 4 Reveal HDAC6 as a Therapeutic Target

痉挛性截瘫4的基因型-表型差异揭示HDAC6作为治疗靶点

Mohan, Neha; Ramakrishnan, Skandha; Sun, Xiaohuan; Sun, Ying; Connors, Theresa; Chai, Victor; Piermarini, Emanuela; Baas, Peter W; Cai, James; Liu, Mei; Qiang, Liang

Human mini brains and spinal cords in a dish: Modeling strategies, current challenges, and prospective advances

体外培养的人类迷你大脑和脊髓:建模策略、当前挑战和未来进展

Kofman, Simeon; Mohan, Neha; Sun, Xiaohuan; Ibric, Larisa; Piermarini, Emanuela; Qiang, Liang

TBCE Mutations Cause Early-Onset Progressive Encephalopathy with Distal Spinal Muscular Atrophy

TBCE基因突变导致早发性进行性脑病伴远端脊髓性肌萎缩

Sferra, Antonella; Baillat, Gilbert; Rizza, Teresa; Barresi, Sabina; Flex, Elisabetta; Tasca, Giorgio; D'Amico, Adele; Bellacchio, Emanuele; Ciolfi, Andrea; Caputo, Viviana; Cecchetti, Serena; Torella, Annalaura; Zanni, Ginevra; Diodato, Daria; Piermarini, Emanuela; Niceta, Marcello; Coppola, Antonietta; Tedeschi, Enrico; Martinelli, Diego; Dionisi-Vici, Carlo; Nigro, Vincenzo; Dallapiccola, Bruno; Compagnucci, Claudia; Tartaglia, Marco; Haase, Georg; Bertini, Enrico

Biallelic Mutations in TBCD, Encoding the Tubulin Folding Cofactor D, Perturb Microtubule Dynamics and Cause Early-Onset Encephalopathy.

TBCD 基因的双等位基因突变编码微管折叠辅因子 D,扰乱微管动力学并导致早发性脑病

Flex Elisabetta, Niceta Marcello, Cecchetti Serena, Thiffault Isabelle, Au Margaret G, Capuano Alessandro, Piermarini Emanuela, Ivanova Anna A, Francis Joshua W, Chillemi Giovanni, Chandramouli Balasubramanian, Carpentieri Giovanna, Haaxma Charlotte A, Ciolfi Andrea, Pizzi Simone, Douglas Ganka V, Levine Kara, Sferra Antonella, Dentici Maria Lisa, Pfundt Rolph R, Le Pichon Jean-Baptiste, Farrow Emily, Baas Frank, Piemonte Fiorella, Dallapiccola Bruno, Graham John M Jr, Saunders Carol J, Bertini Enrico, Kahn Richard A, Koolen David A, Tartaglia Marco

Frataxin deficiency leads to reduced expression and impaired translocation of NF-E2-related factor (Nrf2) in cultured motor neurons.

Frataxin 缺乏会导致培养的运动神经元中 NF-E2 相关因子 (Nrf2) 的表达减少和转位受损

D'Oria Valentina, Petrini Stefania, Travaglini Lorena, Priori Chiara, Piermarini Emanuela, Petrillo Sara, Carletti Barbara, Bertini Enrico, Piemonte Fiorella