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

Cellular Bioenergetics and AMPK and TORC1 Signalling in Blood Lymphoblasts Are Biomarkers of Clinical Status in FMR1 Premutation Carriers

血液淋巴母细胞中的细胞生物能量学和 AMPK 和 TORC1 信号传导是 FMR1 前突变携带者临床状态的生物标志物

Danuta Z Loesch, Bruce E Kemp, Minh Q Bui, Paul R Fisher, Claire Y Allan, Oana Sanislav, Kevin R W Ngoei, Anna Atkinson, Flora Tassone, Sarah J Annesley, Elsdon Storey

Relationships between Mitochondrial Function, AMPK, and TORC1 Signaling in Lymphoblasts with Premutation Alleles of the FMR1 Gene

具有 FMR1 基因前突变等位基因的淋巴母细胞中的线粒体功能、AMPK 和 TORC1 信号传导之间的关系

Paul R Fisher, Claire Y Allan, Oana Sanislav, Anna Atkinson, Kevin R W Ngoei, Bruce E Kemp, Elsdon Storey, Danuta Z Loesch, Sarah J Annesley

Baseline characteristics and age-related macular degeneration in participants of the "ASPirin in Reducing Events in the Elderly" (ASPREE)-AMD trial

“阿司匹林在减少老年人事件中的作用”(ASPREE)-AMD 试验参与者的基线特征和年龄相关性黄斑变性

Liubov D Robman, Le Thi Phuong Thao, Robyn H Guymer, Rory Wolfe, Robyn L Woods, Lauren Ab Hodgson, James Phung, Galina A Makeyeva, Y-Anh Le-Pham, Suzanne G Orchard, Jewhara Suleiman, Emily Maguire, Ruth E Trevaks, Stephanie A Ward, Moeen Riaz, Paul Lacaze, Elsdon Storey, Walter P Abhayaratna, Mark R

The Spectrum of Neurological and White Matter Changes and Premutation Status Categories of Older Male Carriers of the FMR1 Alleles Are Linked to Genetic (CGG and FMR1 mRNA) and Cellular Stress (AMPK) Markers

携带 FMR1 等位基因的老年男性的神经系统和白质变化谱以及前突变状态类别与遗传 (CGG 和 FMR1 mRNA) 和细胞应激 (AMPK) 标记物相关

Danuta Z Loesch, Nicholas Trost, Minh Q Bui, Eleanor Hammersley, Sui T Lay, Sarah J Annesley, Oana Sanislav, Claire Y Allan, Flora Tassone, Zhi-Ping Chen, Kevin R W Ngoei, Bruce E Kemp, David Francis, Paul R Fisher, Elsdon Storey

Immortalized Parkinson's disease lymphocytes have enhanced mitochondrial respiratory activity

永生化帕金森病淋巴细胞增强了线粒体呼吸活动

Sarah J Annesley, Sui T Lay, Shawn W De Piazza, Oana Sanislav, Eleanor Hammersley, Claire Y Allan, Lisa M Francione, Minh Q Bui, Zhi-Ping Chen, Kevin R W Ngoei, Flora Tassone, Bruce E Kemp, Elsdon Storey, Andrew Evans, Danuta Z Loesch, Paul R Fisher

Heterozygous mutations in HSD17B4 cause juvenile peroxisomal D-bifunctional protein deficiency

HSD17B4杂合突变导致青少年过氧化物酶体D-双功能蛋白缺乏

David J Amor, Ashley P L Marsh, Elsdon Storey, Rick Tankard, Greta Gillies, Martin B Delatycki, Kate Pope, Catherine Bromhead, Richard J Leventer, Melanie Bahlo, Paul J Lockhart