Comment on “mt-Keima detects PINK1-PRKN mitophagy in vivo with greater sensitivity than mito-QC”-Reference-Cited by-同舟云学术

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

Published:2021-04-23 Issue:12 Volume:17 Page:4484-4485
ISSN:1554-8627
Container-title:Autophagy
language:en
Short-container-title:Autophagy

Author:

Liu Yi-Ting¹,Sliter Danielle A.²,Shammas Mario K¹,Huang Xiaoping¹,Wang Chunxin²,Calvelli Hannah¹,Maric Dragan S.³,Narendra Derek P.¹

Affiliation:

1. Inherited Movement Disorders Unit, Neurogenetics Branch, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD, USA

2. Surgical Neurology Branch, National Institute of Neurological Disorders and Stroke, NIH, Bethesda, MD, USA

3. Flow and Imaging Cytometry Core Facility, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD, USA

Funder

NINDS

Publisher

Informa UK Limited

Subject

Cell Biology,Molecular Biology

Link

https://www.tandfonline.com/doi/pdf/10.1080/15548627.2021.1909999

Reference7 articles.

1. Deficiency of parkin and PINK1 impairs age-dependent mitophagy in Drosophila

2. Basal mitophagy is widespread in Drosophila but minimally affected by loss of Pink1 or parkin

3. The PINK1-Parkin pathway promotes both mitophagy and selective respiratory chain turnover in vivo

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1. Alterations of PINK1-PRKN signaling in mice during normal aging;2024-05-01

2. The interplay between sex, time of day, fasting status, and their impact on cardiac mitochondrial structure, function, and dynamics;Scientific Reports;2023-12-07

3. Mitochondrial degradation: Mitophagy and beyond;Molecular Cell;2023-10