A Drosophila model of mitochondrial disease caused by a complex I mutation that uncouples proton pumping from electron transfer
© 2014, Company of Biologists Ltd. All rights reserved. Mutations affecting mitochondrial complex I, a multi-subunit assembly that couples electron transfer to proton pumping, are the most frequent cause of heritable mitochondrial diseases. However, the mechanisms by which complex I dysfunction resu...
Saved in:
Main Authors: | Jonathon L. Burman, Leslie S. Itsara, Ernst Bernhard Kayser, Wichit Suthammarak, Adrienne M. Wang, Matt Kaeberlein, Margaret M. Sedensky, Philip G. Morgan, Leo J. Pallanck |
---|---|
Other Authors: | University of Washington, Seattle |
Format: | Article |
Published: |
2018
|
Subjects: | |
Online Access: | https://repository.li.mahidol.ac.th/handle/123456789/33459 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Institution: | Mahidol University |
Similar Items
-
Mutations in mitochondrial complex III uniquely affect complex I in Caenorhabditis elegans
by: Wichit Suthammarak, et al.
Published: (2018) -
Complex I function is defective in complex IV-deficient Caenorhabditis elegans
by: Wichit Suthammarak, et al.
Published: (2018) -
Studies of the effects of Vitamin E on mitochondrial Uncoupling Proteins
by: CHEONG YUH MENG, CLEMENT
Published: (2010) -
Proton pump inhibitors and risk of dementia
by: Karn Wijarnpreecha, et al.
Published: (2018) -
Proton pump inhibitors and risk of dementia
by: Wijarnpreecha K., et al.
Published: (2017)