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 respiratorychain 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 respiratorychain 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 ... Cached
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