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

FDXR variants cause adrenal insufficiency and atypical sexual development

FDXR 变异可导致肾上腺功能不全和异常性发育

Emanuele Pignatti, Jesse Slone, María Ángeles Gómez Cano, Teresa Margaret Campbell, Jimmy Vu, Kay-Sara Sauter, Amit V Pandey, Francisco Martínez-Azorín, Marina Alonso-Riaño, Derek E Neilson, Nicola Longo, Therina du Toit, Clarissa D Voegel, Taosheng Huang, Christa E Flück

Clinical study of ferredoxin-reductase-related mitochondriopathy: Genotype-phenotype correlation and proposal of ancestry-based carrier screening in the Mexican population

铁氧还蛋白还原酶相关线粒体病的临床研究:墨西哥人群的基因型-表型相关性和基于血统的携带者筛查建议

Teresa Campbell, Jesse Slone, Hallie Metzger, Wensheng Liu, Stephanie Sacharow, Amy Yang, Mariya Moosajee, Chiara La Morgia, Valerio Carelli, Flavia Palombo, Matthew A Lines, A Micheil Innes, Rebecca J Levy, Derek Neilson, Nicola Longo, Taosheng Huang

PINK1-mediated Drp1S616 phosphorylation modulates synaptic development and plasticity via promoting mitochondrial fission

PINK1 介导的 Drp1S616 磷酸化通过促进线粒体裂变来调节突触发育和可塑性

Qingtao Gao #, Runyi Tian #, Hailong Han, Jesse Slone, Caifang Wang, Xiao Ke, Tongmei Zhang, Xiangyu Li, Yuhong He, Panlin Liao, Fang Wang, Ye Chen, Shiqing Fu, Kexuan Zhang, Fangfang Zeng, Yingxuan Yang, Zhuo Li, Jieqiong Tan, Jiada Li, Youming Lu, Taosheng Huang, Zhonghua Hu, Zhuohua Zhang

Premature aging is associated with higher levels of 8-oxoguanine and increased DNA damage in the Polg mutator mouse

在Polg突变小鼠中,过早衰老与8-氧鸟嘌呤水平较高和DNA损伤增加有关

Tenghui Yu, Jesse Slone, Wensheng Liu, Ryan Barnes, Patricia L Opresko, Landon Wark, Sabine Mai, Steve Horvath, Taosheng Huang

Nanoscopic quantification of sub-mitochondrial morphology, mitophagy and mitochondrial dynamics in living cells derived from patients with mitochondrial diseases

线粒体疾病患者活细胞中亚线粒体形态、线粒体自噬和线粒体动力学的纳米级量化

Weiwei Zou #, Qixin Chen #, Jesse Slone, Li Yang, Xiaoting Lou, Jiajie Diao, Taosheng Huang

Validation of low-coverage whole-genome sequencing for mitochondrial DNA variants suggests mitochondrial DNA as a genetic cause of preterm birth

低覆盖度全基因组测序对线粒体DNA变异的验证表明,线粒体DNA可能是早产的遗传原因。

Zeyu Yang,Jesse Slone,Xinjian Wang,Jack Zhan,Yongbo Huang,Bahram Namjou,Kenneth M Kaufman,Michael Pauciulo,John B Harley,Louis J Muglia,Iouri Chepelev,Taosheng Huang

Systemic Delivery of AAV- Fdxr Mitigates the Phenotypes of Mitochondrial Disorders in Fdxr Mutant Mice

系统性递送 AAV-Fdxr 可减轻 Fdxr 突变小鼠的线粒体疾病表型

Li Yang, Jesse Slone, Weiwei Zou, Luis F Queme, Michael P Jankowski, Fei Yin, Taosheng Huang

Identification of a Drosophila glucose receptor using Ca2+ imaging of single chemosensory neurons

使用单个化学感应神经元的 Ca2+ 成像来识别果蝇葡萄糖受体

Tetsuya Miyamoto, Yan Chen, Jesse Slone, Hubert Amrein