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

A unified mechanism for mitochondrial damage sensing in PINK1-Parkin-mediated mitophagy.

PINK1-Parkin介导的线粒体自噬中线粒体损伤感知的统一机制。

Thayer Julia A, Petersen Jennifer D, Huang Xiaoping, Gruel Budet Luiza M, Hawrot James, Ramos Daniel M, Sekine Shiori, Li Yan, Ward Michael E, Narendra Derek P

A plasma proteomics-based candidate biomarker panel predictive of amyotrophic lateral sclerosis

基于血浆蛋白质组学的肌萎缩侧索硬化症预测候选生物标志物组合

Chia, Ruth; Moaddel, Ruin; Kwan, Justin Y; Rasheed, Memoona; Ruffo, Paola; Landeck, Natalie; Reho, Paolo; Vasta, Rosario; Calvo, Andrea; Moglia, Cristina; Canosa, Antonio; Manera, Umberto; Snyder, Allison; Saez-Atienzar, Sara; Grassano, Maurizio; Brunetti, Maura; Casale, Federico; Ray, Anindita; Arvind, Kumar; Comertpay, Betul; Zhu, Min; Gibbs, J Raphael; Alba, Camille; Dawson, Ted M; Rosenthal, Liana S; Hall, Anna J; Pantelyat, Alexander Y; Narendra, Derek P; Ehrlich, Debra J; Walker, Keenan A; Kosa, Peter; Bielekova, Bibiana; Egan, Josephine M; Candia, Julián; Tanaka, Toshiko; Ferrucci, Luigi; Dalgard, Clifton L; Scholz, Sonja W; Chiò, Adriano; Traynor, Bryan J

Dose-dependent CHCHD10 dysregulation dictates motor neuron disease severity and alters creatine metabolism.

剂量依赖性的 CHCHD10 失调决定运动神经元疾病的严重程度并改变肌酸代谢

Harjuhaahto Sandra, Jokela Manu, Rajendran Jayasimman, Rokka Minea, Hu Bowen, Kvist Jouni, Zhang Fuping, Zárybnický Tomáš, Haimilahti Kimmo, Euro Liliya, Pirinen Eija, Huber Nadine, Herukka Sanna-Kaisa, Haapasalo Annakaisa, Kuuluvainen Emilia, Gopalakrishnan Swetha, Katajisto Pekka, Hietakangas Ville, Burg Thibaut, Van Den Bosch Ludo, Huang Xiaoping, Narendra Derek P, Kuure Satu, Ylikallio Emil, Tyynismaa Henna

Clinical, neuropathological, and biochemical characterization of ALS in a large CHCHD10 R15L family.

对 CHCHD10 R15L 大家族中的 ALS 进行临床、神经病理学和生化特征分析。

Kwan Justin Y, Lantz Christian I, Korobeynikov Vlad A, Snyder Allison, Huang Xiaoping, Haselhuhn Taryn, Dore Katherine N, Madruga Angelo, Danielian Laura E, Schindler Alice B, Chia Ruth, Rasheed Memoona, Crook Jody, Szabo Marcell, Portley Makayla, Sherer Carolyn M, King Monique C, Huang Tzu-Hsiang, Kosa Peter, Bielekova Bibiana, Ward Michael E, Grunseich Chris, Shneider Neil A, Traynor Bryan J, Narendra Derek P

How to treat a "sweetheart" in mitochondrial cardiomyopathy

如何治疗线粒体心肌病中的“甜心”

Lin, Hsin-Pin; Narendra, Derek P

Heterozygous PRKN mutations are common but do not increase the risk of Parkinson's disease.

PRKN 杂合突变很常见,但不会增加患帕金森病的风险

Zhu William, Huang Xiaoping, Yoon Esther, Bandres-Ciga Sara, Blauwendraat Cornelis, Billingsley Kimberly J, Cade Joshua H, Wu Beverly P, Williams Victoria H, Schindler Alice B, Brooks Janet, Gibbs J Raphael, Hernandez Dena G, Ehrlich Debra, Singleton Andrew B, Narendra Derek P

Comment on "mt-Keima detects PINK1-PRKN mitophagy in vivo with greater sensitivity than mito-QC"

评论“mt-Keima 检测体内 PINK1-PRKN 线粒体自噬的灵敏度高于 mito-QC”

Liu, Yi-Ting; Sliter, Danielle A; Shammas, Mario K; Huang, Xiaoping; Wang, Chunxin; Calvelli, Hannah; Maric, Dragan S; Narendra, Derek P

α-Synuclein Deposition in Sympathetic Nerve Fibers in Genetic Forms of Parkinson's Disease

遗传性帕金森病中交感神经纤维的α-突触核蛋白沉积

Isonaka, Risa; Goldstein, David S; Zhu, William; Yoon, Esther; Ehrlich, Debra; Schindler, Alice B; Kokkinis, Angela D; Sabir, Marya S; Scholz, Sonja W; Bandres-Ciga, Sara; Blauwendraat, Cornelis; Gonzalez-Alegre, Pedro; Lopez, Grisel; Sidransky, Ellen; Narendra, Derek P

Managing risky assets - mitophagy in vivo

管理风险资产——体内线粒体自噬

Narendra, Derek P

Coupling APEX labeling to imaging mass spectrometry of single organelles reveals heterogeneity in lysosomal protein turnover.

将 APEX 标记与单个细胞器的成像质谱相结合,揭示了溶酶体蛋白质周转的异质性

Narendra Derek P, Guillermier Christelle, Gyngard Frank, Huang Xiaoping, Ward Michael E, Steinhauser Matthew L