Coldicott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

P74 Improving penicillin allergy risk-stratification through pharmacy-led education in a specialist elective orthopaedic hospital

P74 通过药学主导的教育改善专科择期骨科医院的青霉素过敏风险分层

期刊:British Journal of Anaesthesia

影响因子:9.2

doi:10.1016/j.bja.2025.06.038

Green, Sarah L; Krupowicz, Benedict A; Capon, Marc J; Li, Jamma; Coldicott, Hannah; Patel, Nickisha

发表日期：2025

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A bacterial artificial chromosome mouse model of amyotrophic lateral sclerosis manifests 'space cadet syndrome' on two FVB backgrounds

肌萎缩侧索硬化症的细菌人工染色体小鼠模型在两种 FVB 背景下表现出“太空学员综合征”

期刊:Disease Models & Mechanisms

doi:10.1242/dmm.052221

Sophie E Badger, Ian Coldicott, Ergita Kyrgiou-Balli, Adrian Higginbottom, Chloé Moutin, Kamallia Mohd Imran, John C Day, Johnathan Cooper-Knock, Richard J Mead, James J P Alix

发表日期：2025

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RuvBL1/2 reduce toxic dipeptide repeat protein burden in multiple models of C9orf72-ALS/FTD.

RuvBL1/2 可降低多种 C9orf72-ALS/FTD 模型中的毒性二肽重复蛋白负荷

期刊:Life Science Alliance

影响因子:2.9

doi:10.26508/lsa.202402757

Webster Christopher P, Hall Bradley, Crossley Olivia M, Dauletalina Dana, King Marianne, Lin Ya-Hui, Castelli Lydia M, Yang Zih-Liang, Coldicott Ian, Kyrgiou-Balli Ergita, Higginbottom Adrian, Ferraiuolo Laura, De Vos Kurt J, Hautbergue Guillaume M, Shaw Pamela J, West Ryan Jh, Azzouz Mimoun

免疫/内分泌

发表日期：2025

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Pre-clinical development of AP4B1 gene replacement therapy for hereditary spastic paraplegia type 47

遗传性痉挛性截瘫47型AP4B1基因替代疗法的临床前开发

期刊:EMBO Molecular Medicine

doi:10.1038/s44321-024-00148-5

Jessica P Wiseman, Joseph M Scarrott, João Alves-Cruzeiro, Afshin Saffari, Cedric Böger, Evangelia Karyka, Emily Dawes, Alexandra K Davies, Paolo M Marchi, Emily Graves, Fiona Fernandes, Zih-Liang Yang, Ian Coldicott, Jennifer Hirst, Christopher P Webster, J Robin Highley, Neil Hackett, Adrienn Angy

发表日期：2024

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Ap4b1-knockout mouse model of hereditary spastic paraplegia type 47 displays motor dysfunction, aberrant brain morphology and ATG9A mislocalization

遗传性痉挛性截瘫 47 型 Ap4b1 基因敲除小鼠模型表现出运动功能障碍、脑形态异常和 ATG9A 错误定位

期刊:Brain Communications

影响因子:4.1

doi:10.1093/braincomms/fcac335

Joseph M Scarrott, João Alves-Cruzeiro, Paolo M Marchi, Christopher P Webster, Zih-Liang Yang, Evangelia Karyka, Raffaele Marroccella, Ian Coldicott, Hannah Thomas, Mimoun Azzouz

发表日期：2023

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An interaction between synapsin and C9orf72 regulates excitatory synapses and is impaired in ALS/FTD

突触蛋白与 C9orf72 之间的相互作用可调节兴奋性突触，并且在 ALS/FTD 中受损

期刊:Acta Neuropathologica

影响因子:9.3

doi:10.1007/s00401-022-02470-z

Claudia S Bauer #, Rebecca N Cohen #, Francesca Sironi #, Matthew R Livesey, Thomas H Gillingwater, J Robin Highley, Daniel J Fillingham, Ian Coldicott, Emma F Smith, Yolanda B Gibson, Christopher P Webster, Andrew J Grierson, Caterina Bendotti, Kurt J De Vos

发表日期：2022

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Fiber optic Raman spectroscopy for the evaluation of disease state in Duchenne muscular dystrophy: An assessment using the mdx model and human muscle

光纤拉曼光谱法在杜氏肌营养不良症疾病状态评估中的应用：基于mdx模型和人肌肉的评估

期刊:Muscle & Nerve

影响因子:3.1

doi:10.1002/mus.27671

Alix, James J P; Plesia, Maria; Hool, Sarah A; Coldicott, Ian; Kendall, Catherine A; Shaw Dbe, Pamela J; Mead, Richard J; Day, John C

发表日期：2022

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SPG15 protein deficits are at the crossroads between lysosomal abnormalities, altered lipid metabolism and synaptic dysfunction

SPG15 蛋白缺陷是溶酶体异常、脂质代谢改变和突触功能障碍的交汇点

期刊:Human Molecular Genetics

影响因子:3.1

doi:10.1093/hmg/ddac063

Lara Marrone, Paolo M Marchi, Christopher P Webster, Raffaele Marroccella, Ian Coldicott, Steven Reynolds, João Alves-Cruzeiro, Zih-Liang Yang, Adrian Higginbottom, Mukhran Khundadze, Pamela J Shaw, Christian A Hübner, Matthew R Livesey, Mimoun Azzouz

发表日期：2022

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C9orf72 expansion within astrocytes reduces metabolic flexibility in amyotrophic lateral sclerosis

星形胶质细胞内的 C9orf72 扩增降低了肌萎缩侧索硬化症的代谢灵活性

影响因子:10.6

doi:10.1093/brain/awz302

Scott P Allen, Benjamin Hall, Ryan Woof, Laura Francis, Noemi Gatto, Allan C Shaw, Monika Myszczynska, Jordan Hemingway, Ian Coldicott, Amelia Willcock, Lucy Job, Rachel M Hughes, Camilla Boschian, Nadhim Bayatti, Paul R Heath, Oliver Bandmann, Heather Mortiboys, Laura Ferraiuolo, Pamela J Shaw

多发性硬化症

发表日期：2019

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Translating SOD1 Gene Silencing toward the Clinic: A Highly Efficacious, Off-Target-free, and Biomarker-Supported Strategy for fALS

将 SOD1 基因沉默转化为临床治疗：一种高效、无脱靶、生物标志物支持的 fALS 策略

期刊:Molecular Therapy-Nucleic Acids

影响因子:6.5

doi:10.1016/j.omtn.2018.04.015

Tommaso Iannitti, Joseph M Scarrott, Shibi Likhite, Ian R P Coldicott, Katherine E Lewis, Paul R Heath, Adrian Higginbottom, Monika A Myszczynska, Marta Milo, Guillaume M Hautbergue, Kathrin Meyer, Brian K Kaspar, Laura Ferraiuolo, Pamela J Shaw, Mimoun Azzouz

发表日期：2018

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