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X Chen, DR Thorburn, LJ Wong… - Genetics in …, 2011 - journals.lww.com
Purpose: The diagnosis of a mitochondrial disorder relies heavily on the enzymatic analysis
of mitochondrial respiratory chain complexes in muscle or other tissues. However, considerable
differences exist between clinical laboratories in the protocols or particular tests used for ...
All 3 versions
JW Taanman, S Rahman, P Clayton, JV Leonard… - 2011 - discovery.ucl.ac.uk
... Mitochondrial respiratory chain enzyme deficiency expressed during muscle development.
Taanman, JW and Rahman, S and Clayton, P and Leonard, JV and King, R and Orth, M (2011)
Mitochondrial respiratory chain enzyme deficiency expressed during muscle development. ...
Cached - All 2 versions
T Meyer, J Gross, C Blanck, M Schmutz… - The Journal of …, 2011 - ACS Publications
The electrochemical behavior of three proteins fragments from the respiratory chain of the extremophilic
bacterium Thermus thermophilus, namely, cytochrome c 1 (Cyt-c 1 ), cytochrome c 552 (Cyt-c
552 ), and Cu A , immobilized on three-dimensional gold nanoparticles electrodes was ...
Related articles - All 2 versions
JP Kemp, PM Smith, A Pyle, V Neeve, HAL Tuppen… - Brain, 2011 - Oxford Univ Press
Mutations in several mitochondrial DNA and nuclear genes involved in mitochondrial protein
synthesis have recently been reported in combined respiratory chain deficiency, indicating a
generalized defect in mitochondrial translation. However, the number of patients with ...
Cited by 2 - Related articles - All 5 versions
[HTML] from plos.orgA Mourier… - PLoS Biology, 2011 - dx.plos.org
Mitochondria are the structures that produce the bulk part of the cellular energy currency
ATP, which drives numerous energy requiring processes in the cell. This process involves a
series of large enzyme complexes—the respiratory chain—that couples the transfer of ...
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