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

Evidence of synergism among three genetic variants in a patient with LMNA-related lipodystrophy and amyotrophic lateral sclerosis leading to a remarkable nuclear phenotype

有证据表明,在患有 LMNA 相关脂肪营养不良和肌萎缩侧索硬化症的患者中,三种基因变异之间存在协同作用,从而导致显著的核表型

Kathryn Volkening, Sali M K Farhan, Jessica Kao, Cheryl Leystra-Lantz, Lee Cyn Ang, Adam McIntyre, Jian Wang, Robert A Hegele, Michael J Strong

Concentration, distribution, and influence of aging on the 18 kDa translocator protein in human brain: Implications for brain imaging studies

人类大脑中 18 kDa 转运蛋白的浓度、分布及衰老影响:对脑成像研究的意义

Junchao Tong, Belinda Williams, Pablo M Rusjan, Romina Mizrahi, Jean-Jacques Lacapère, Tina McCluskey, Yoshiaki Furukawa, Mark Guttman, Lee-Cyn Ang, Isabelle Boileau, Jeffrey H Meyer, Stephen J Kish

Serotonin transporter protein in autopsied brain of chronic users of cocaine

可卡因长期使用者尸检脑中的血清素转运蛋白

Junchao Tong, Jeffrey H Meyer, Isabelle Boileau, Lee-Cyn Ang, Paul J Fletcher, Yoshiaki Furukawa, Stephen J Kish

MECP2 Mutation Interrupts Nucleolin-mTOR-P70S6K Signaling in Rett Syndrome Patients

MECP2 突变阻断雷特综合征患者的核仁素-mTOR-P70S6K 信号传导

Carl O Olson, Shervin Pejhan, Daniel Kroft, Kimia Sheikholeslami, David Fuss, Marjorie Buist, Annan Ali Sher, Marc R Del Bigio, Yehezkel Sztainberg, Victoria Mok Siu, Lee Cyn Ang, Marianne Sabourin-Felix, Tom Moss, Mojgan Rastegar

Brain monoamine oxidase B and A in human parkinsonian dopamine deficiency disorders

人类帕金森病多巴胺缺乏症中的脑单胺氧化酶 B 和 A

Junchao Tong, Gausiha Rathitharan, Jeffrey H Meyer, Yoshiaki Furukawa, Lee-Cyn Ang, Isabelle Boileau, Mark Guttman, Oleh Hornykiewicz, Stephen J Kish

Low levels of astroglial markers in Parkinson's disease: relationship to α-synuclein accumulation

帕金森病中星形胶质细胞标志物水平低:与 α-突触核蛋白积累的关系

Junchao Tong, Lee-Cyn Ang, Belinda Williams, Yoshiaki Furukawa, Paul Fitzmaurice, Mark Guttman, Isabelle Boileau, Oleh Hornykiewicz, Stephen J Kish

Transportin 1 accumulates specifically with FET proteins but no other transportin cargos in FTLD-FUS and is absent in FUS inclusions in ALS with FUS mutations

运输蛋白 1 特异性地与 FET 蛋白一起积累,但在 FTLD-FUS 中没有其他运输蛋白货物,并且在发生 FUS 突变的 ALS 的 FUS 内含物中不存在

Manuela Neumann, Chiara F Valori, Olaf Ansorge, Hans A Kretzschmar, David G Munoz, Hirofumi Kusaka, Osamu Yokota, Kenji Ishihara, Lee-Cyn Ang, Juan M Bilbao, Ian R A Mackenzie

FET proteins TAF15 and EWS are selective markers that distinguish FTLD with FUS pathology from amyotrophic lateral sclerosis with FUS mutations

FET 蛋白 TAF15 和 EWS 是区分伴有 FUS 病理的 FTLD 与伴有 FUS 突变的肌萎缩侧索硬化症的选择性标记物

Manuela Neumann, Eva Bentmann, Dorothee Dormann, Ali Jawaid, Mariely DeJesus-Hernandez, Olaf Ansorge, Sigrun Roeber, Hans A Kretzschmar, David G Munoz, Hirofumi Kusaka, Osamu Yokota, Lee-Cyn Ang, Juan Bilbao, Rosa Rademakers, Christian Haass, Ian R A Mackenzie

Pathological heterogeneity in amyotrophic lateral sclerosis with FUS mutations: two distinct patterns correlating with disease severity and mutation

伴有 FUS 突变的肌萎缩侧索硬化症的病理异质性:与疾病严重程度和突变相关的两种不同模式

Ian R A Mackenzie, Olaf Ansorge, Michael Strong, Juan Bilbao, Lorne Zinman, Lee-Cyn Ang, Matt Baker, Heather Stewart, Andrew Eisen, Rosa Rademakers, Manuela Neumann