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

Modification of early behavioural, physiological and neuropathological endpoints by syntaxin-6 knockout in a humanised P301S transgenic model of tauopathy

在人源化P301S转基因tau蛋白病模型中,通过敲除突触蛋白-6来改变早期行为、生理和神经病理学终点。

Hill, Elizabeth; Linehan, Jacqueline; Farmer, Michael; Jakubcova, Tatiana; Hamdan, Shyma; Tomlinson, Andrew; Purro, Silvia; Argentina, Fabio; Jones, Emma; Kaye, Nicholas; Fitzhugh, Craig; de Silva, Rohan; Brandner, Sebastian; Collinge, John; Cunningham, Thomas J; Mead, Simon

Correction: Intracellular trafficking SNARE protein, syntaxin-6, modifies prion cellular phenotypes and risk of disease development in vivo

更正:细胞内转运SNARE蛋白syntaxin-6可改变朊病毒的细胞表型并影响体内疾病发生的风险。

Hill, Elizabeth; Patel, Mitali M; Ribes, Juan M; Linehan, Jacqueline; Zhang, Fuquan; Jakubcova, Tatiana; Hamdan, Shyma; Tomlinson, Andrew; Ercolani, Tiziana; Schmidt, Christian; Ahmed, Parvin; Thirlway, George; Argentina, Fabio; Marinho, Aline T; Jones, Emma; Kaye, Nicholas; Fitzhugh, Craig; Jackson, Graham S; Brandner, Sebastian; Klöhn, Peter-Christian; Collinge, John; Cunningham, Thomas J; Mead, Simon

Intracellular trafficking SNARE protein, syntaxin-6, modifies prion cellular phenotypes and risk of disease development in vivo

细胞内转运SNARE蛋白syntaxin-6可改变朊病毒的细胞表型,并影响体内疾病发生的风险。

Hill, Elizabeth; Patel, Mitali M; Ribes, Juan M; Linehan, Jacqueline; Zhang, Fuquan; Jakubcova, Tatiana; Hamdan, Shyma; Tomlinson, Andrew; Ercolani, Tiziana; Schmidt, Christian; Ahmed, Parvin; Thirlway, George; Argentina, Fabio; Marinho, Aline T; Jones, Emma; Kaye, Nicholas; Fitzhugh, Craig; Jackson, Graham S; Brandner, Sebastian; Klöhn, Peter-Christian; Collinge, John; Cunningham, Thomas J; Mead, Simon

TDP-43 dysregulation impairs cholesterol metabolism linked with myelination defects.

TDP-43失调会损害胆固醇代谢,从而导致髓鞘形成缺陷

García-Toledo Irene, Godoy-Corchuelo Juan M, Fernández-Beltrán Luis C, Ali Zeinab, Guindo-Arroyo Ariadna, Jiménez-Coca Irene, Jiménez-Rodríguez Jesús, Javaloyes-García Karen, Viñuela Marcos, Gómez-Pinedo Ulises, Saiz-Aúz Laura, Rábano Alberto, Área-Gómez Estela, Cunningham Thomas J, Corrochano Silvia

Isolation of a novel human prion strain from a PRNP codon 129 heterozygous vCJD patient

从一名PRNP基因129密码子杂合的vCJD患者中分离出一种新型人类朊病毒株

Zhang, Fuquan; Joiner, Susan; Linehan, Jacqueline M; Pintilii, Florin; Nazari, Tamsin; Argentina, Fabio; Preston, Connor; Taema, Maged; Cunningham, Thomas J; Asante, Emmanuel A; Mok, Tzehow; Mead, Simon; Brandner, Sebastian; Collinge, John; Wadsworth, Jonathan D F

Assigning Targetable Molecular Pathways to Transdiagnostic Subgroups Across Autism and Related Neurodevelopmental Disorders

为自闭症及相关神经发育障碍的跨诊断亚组分配可靶向分子通路

Ellegood, Jacob; Beauchamp, Antoine; Yee, Yohan; Devenyi, Gabe; Ziolkowski, Justine; Qiu, Lily; Askalan, Rand; Ayub, Muhammad; Suetterlin, Philipp; Donovan, Alex; Basson, M Albert; Quesnel, Katherine M; Berube, Nathalie G; Woo, Taeseon; Beversdorf, David; Bjornsson, Hans; Blakely, Randy; Crawley, Jacqueline; Crosbie, Jennifer; Orr, Brian O; Davis, Graeme W; Genestine, Matthew; DiCicco-Bloom, Emanuel; Egan, Sean; Fink, Kyle D; Asbury, Sarah; Lai, Jonathan; Rilett, Kelly; Foster, Jane A; Vincent, John B; Frankland, Paul; Georgiades, Stelios; Penagarikano, Olga; Geschwind, Daniel; Giger, Roman J; Markx, Sander; Gogos, Joseph; Golzio, Christelle; Pagani, Marco; Gozzi, Alessandro; Pacey, Laura K; Hampson, David; Huang, Tzyy-Nan; Yen, Tzu-Li; Hsueh, Yi-Ping; Iaboni, Alana; Amar, Megha; Iakoucheva, Lilia M; Jones, Jessica K; Kelly, Elizabeth; Kieffer, Brigette; Bae, Mihyun; Jung, Hwajin; Kim, Hyosang; Park, Haram; Roh, Junye Daniel; Kim, Eunjoon; Konopka, Genevieve; Laliberte, Christine; Lefebvre, Julie L; Eagleson, Kathie; Levitt, Pat; Bach, Aurea Martins; Cunningham, Thomas J; Fisher, Elizabeth; Miller, Karla; Mills, Alea; Muotri, Alyson; Nicolson, Rob; Noakes, Leigh Spencer; Nieman, Brian J; Canales, Cesar P; Nord, Alex S; Nutter, Lauryl Mj; Tam, Elaine; Osborne, Lucy R; Clipperton-Allen, Amy; Page, Damon; Babineau, Brooke; Palmer, Theo D; Yan, Keqin; Picketts, David; Xia, Qiangqiang; Powell, Craig M; Raznahan, Armin; Robins, Diane M; Rumbaugh, Gavin; Sengar, Ameet S; Salter, Michael William; Schachar, Russell James; D'Abate, Lia; Bradley, Clarissa A; Scherer, Stephen W; Copping, Nycole W; Petkova, Stela P; Silverman, Jill L; Singh, Karun Kar; Kim, Nam-Shik; Yoon, Ki-Jun Kar; Ming, Guo-Li; Song, Hongjun; Spring, Shoshana; Nakatani, Jin; Nakai, Nobuhiro; Nomura, J; Takumi, Toru; Taylor, Margot; Tsai, Peter; Bruce, Matthew; Jones, Karen L; Van de Water, Judy; Van Eede, Matthijs C; Kerr, Travis M; Muller, Christopher L; VanderWeele, Jeremy Veenstra; Vandewouw, Marlee; Weksberg, Rosanna; Wevrick, Rachel; Belinson, Haim; Wynshaw-Boris, Anthony; Zarbalis, Konstantinos; Trost, Brett; Mars, Rogier B; Chakravarty, Mallar; Kushki, Azadek; Anagnostou, Evdokia; Lerch, Jason P

Generation of C9orf72 repeat knock-in iPSC lines for modelling ALS and FTD

构建C9orf72重复基因敲入的iPSC细胞系用于ALS和FTD模型研究

Coneys, Rachel; Cammack, Alexander J; Nair, Remya R; Thompson, David; Mechtersheimer, Jonas; Carcolé, Mireia; Gupta, Yashica; Rech, Gabriel E; Flower, Michael; O'Brien, Niamh; Ruepp, Marc-David; Mizielinska, Sarah; Ducotterd, Fiona; Tabrizi, Sarah J; Fisher, Elizabeth M C; Cunningham, Thomas J; Ward, Michael; Skarnes, William C; Isaacs, Adrian M

Corrigendum to "TDP-43-M323K causes abnormal brain development and progressive cognitive and motor deficits associated with mislocalised and increased levels of TDP-43" [Neurobiology of disease Volume 193, April 2024, 106437]

对“TDP-43-M323K 导致大脑发育异常以及与 TDP-43 定位错误和水平升高相关的进行性认知和运动缺陷”的更正[神经生物学疾病卷 193,2024 年 4 月,106437]

Godoy-Corchuelo, Juan M; Ali, Zeinab; Brito Armas, Jose M; Martins-Bach, Aurea B; García-Toledo, Irene; Fernandez-Beltrán, Luis C; Lopez-Carbonero, Juan I; Bascunana, Pablo; Spring, Shoshana; Jimenez-Coca, Irene; Muñozde Bustillo Alfaro, Ramón A; Sanchez-Barrena, Maria J; Nair, Remya R; Nieman, Brian J; Lerch, Jason P; Miller, Karla L; Ozdinler, Hande P; Fisher, Elizabeth M C; Cunningham, Thomas J; Acevedo-Arozena, Abraham; Corrochano, Silvia

TDP-43-M323K causes abnormal brain development and progressive cognitive and motor deficits associated with mislocalised and increased levels of TDP-43.

TDP-43-M323K 会导致大脑发育异常,并引起进行性认知和运动缺陷,这与 TDP-43 定位错误和水平升高有关

Godoy-Corchuelo Juan M, Ali Zeinab, Brito Armas Jose M, Martins-Bach Aurea B, García-Toledo Irene, Fernández-Beltrán Luis C, López-Carbonero Juan I, Bascuñana Pablo, Spring Shoshana, Jimenez-Coca Irene, Muñoz de Bustillo Alfaro Ramón A, Sánchez-Barrena Maria J, Nair Remya R, Nieman Brian J, Lerch Jason P, Miller Karla L, Ozdinler Hande P, Fisher Elizabeth M C, Cunningham Thomas J, Acevedo-Arozena Abraham, Corrochano Silvia

Modelling Alzheimer's disease in a dish: dissecting amyloid-β metabolism in human neurons

在体外模拟阿尔茨海默病:解析人类神经元中的β-淀粉样蛋白代谢

Hill, Elizabeth; Cunningham, Thomas J