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

Clinical Applications of Electrical Conductivity Imaging Using MRI

磁共振成像技术在电导率成像中的临床应用

Mandija, Stefano; Tha, Khin Khin; Katoch, Nitish; Göksu, Cihan; Katscher, Ulrich; Sadleir, Rosalind; Jung, Kyu-Jin; Luo, Jierong; Giannakopoulos, Ilias I; Kim, Dong-Hyun; Shmueli, Karin; Lattanzi, Riccardo; Ider, Yusuf Ziya; Thielscher, Axel; van den Berg, Cornelis

Neuronal overexpression of Nrf2 reduces dystrophic neurites in 5XFAD Alzheimer's disease model mice.

神经元中 Nrf2 的过度表达可减少 5XFAD 阿尔茨海默病模型小鼠的营养不良性神经突。

Sadleir Katherine R, Gomez Karen P, Chandra Sidhanth, Ley Makenna L, Khatri Ammaarah W, Guo Joanna, Xue Yunlu, Cepko Constance L, Vassar Robert

The UNC5C T835M mutation associated with Alzheimer's disease leads to neurodegeneration involving oxidative stress and hippocampal atrophy in aged mice.

与阿尔茨海默病相关的 UNC5C T835M 突变会导致老年小鼠出现涉及氧化应激和海马萎缩的神经退行性变

Karunakaran Devi Krishna Priya, Ley Makenna, Guo Joanna, Khatri Ammaarah, Sadleir Katherine, Popovic Jelena, Upadhyay Arun Kumar, Savas Jeffrey, Procissi Daniele, Atwal Jasvinder, Vassar Robert

The gut microbiome controls reactive astrocytosis during Aβ amyloidosis via propionate-mediated regulation of IL-17.

肠道微生物群通过丙酸介导的IL-17调节来控制Aβ淀粉样变性期间的反应性星形胶质细胞增生

Chandra Sidhanth, Popovic Jelena, Singhal Naveen K, Watkins Elyse A, Dodiya Hemraj B, Weigle Ian Q, Salvo Miranda A, Ramakrishnan Abhirami, Chen Zhangying, Watson Thomas, Shetti Aashutosh, Piehl Natalie, Zhang Xiaoqiong, Cuddy Leah, Sadleir Katherine R, Schwulst Steven J, Prakriya Murali, Gate David, Sisodia Sangram S, Vassar Robert

SUDEP risk is influenced by longevity genomics: a polygenic risk score study

长寿基因组学影响 SUDEP 风险:一项多基因风险评分研究

Martins, Helena; Mills, James D; Pagni, Susanna; Gulcebi, Medine I; Vakrinou, Angeliki; Moloney, Patrick B; Clayton, Lisa M; Bellampalli, Ravishankara; Stamberger, Hannah; Weckhuysen, Sarah; Striano, Pasquale; Zara, Federico; Bagnall, Richard D; Harris, Rebekah V; Lawrence, Kate M; Sadleir, Lynette G; Crompton, Douglas E; Friedman, Daniel; Laze, Juliana; Li, Ling; Berkovic, Samuel F; Semsarian, Christopher; Scheffer, Ingrid E; Devinsky, Orrin; Kuchenbaecker, Karoline; Balestrini, Simona; Sisodiya, Sanjay M

Annexin A6 membrane repair protein protects against amyloid-induced dystrophic neurites and tau phosphorylation in Alzheimer's disease model mice

Annexin A6膜修复蛋白可保护阿尔茨海默病模型小鼠免受淀粉样蛋白诱导的营养不良性神经突和tau蛋白磷酸化的影响

Katherine R Sadleir ,Karen P Gomez ,Abigail E Edwards ,Armana J Patel ,Makenna L Ley ,Ammaarah W Khatri ,Joanna Guo ,Shreya Mahesh ,Elyse A Watkins ,Jelena Popovic ,Devi Krishna Priya Karunakaran ,Dmitry Prokopenko ,Rudolph E Tanzi ,Bernabe Bustos ,Steven J Lubbe ,Alexis R Demonbruen ,Elizabeth M McNally ,Robert Vassar

Development and Adaptive Function in Individuals With SCN2A-Related Disorders

SCN2A相关疾病患者的发育和适应功能

Goad, Beatrice Southby; Rodda, Jill; Allen, Meagan; Bamborschke, Daniel; Overmars, Isabella; Kerr, Rachel J; Bushlin, Ittai; Chopra, Saurabh; Coorg, Rohini; Dabscheck, Gabriel; Freeman, Jeremy L; Mackay, Mark T; Devinsky, Orrin; Guerrini, Renzo; Parrini, Elena; Bölsterli, Bigna; Hughes, Inna; Huh, Linda L; Kamate, Mahesh; Kunz, Abby B; Melikishvili, Gia; Miteff, Christina; Myers, Kenneth Alexis; Olson, Heather E; Poduri, Annapurna; Pillai, Sekhar; Riney, Catherine Kate; Sinclair, Adriane; Calvert, Sophie; Reynolds, Thomas Q; Martinez, Ana Roche; Russo, Angelo; Sadleir, Lynette Grant; Sanchez-Albisua, Iciar; Sartori, Stefano; Shea, Stephanie; Smith-Hicks, Constance L; Spooner, Claire G; Thomas, Rhys H; Ardern-Holmes, Simone L; Webster, Richard Ian; Valeriani, Massimiliano; Veggiotti, Pierangelo; Masnada, Silvia; Ware, Tyson L; Yoong, Michael; Berecki, Geza; De Dominicis, Angela; Specchio, Nicola; Trivisano, Marina; Møller, Rikke Steensbjerre; Wolff, Markus; Fazeli, Walid; Scheffer, Ingrid; Howell, Katherine B

SCN1A pathogenic variants do not have a distinctive blood-derived DNA methylation signature

SCN1A致病变异体不具有独特的血液来源DNA甲基化特征。

LaFlamme, Christy W; Karimi, Karim; Rastin, Cassandra; Almanza Fuerte, Edith P; Allan, Talia; Russ-Hall, Sophie J; Schneider, Amy L; Stobo, Daniel; Lesca, Gaetan; Symonds, Joseph D; Brunklaus, Andreas; Sadleir, Lynette G; Scheffer, Ingrid E; Sadikovic, Bekim; Mefford, Heather C

Identifying individuals with rare disease variants by inferring shared ancestral haplotypes from SNP array data

通过SNP芯片数据推断共享祖先单倍型来识别携带罕见疾病变异的个体

Robertson, Erandee; Grinton, Bronwyn E; Oliver, Karen L; Fearnley, Liam G; Hildebrand, Michael S; Sadleir, Lynette G; Scheffer, Ingrid E; Berkovic, Samuel F; Bennett, Mark F; Bahlo, Melanie

Comparison of modelled diffusion-derived electrical conductivities found using magnetic resonance imaging

利用磁共振成像技术对扩散衍生的模型电导率进行比较

Hakhu, Sasha; Hu, Leland S; Beeman, Scott; Sadleir, Rosalind J