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guanidine and Electron Transport Chain Deficiencies, Mitochondrial

guanidine has been researched along with Electron Transport Chain Deficiencies, Mitochondrial in 1 studies

Guanidine: A strong organic base existing primarily as guanidium ions at physiological pH. It is found in the urine as a normal product of protein metabolism. It is also used in laboratory research as a protein denaturant. (From Martindale, the Extra Pharmacopoeia, 30th ed and Merck Index, 12th ed) It is also used in the treatment of myasthenia and as a fluorescent probe in HPLC.
guanidine : An aminocarboxamidine, the parent compound of the guanidines.

Research

Studies (1)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's1 (100.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Blakely, EL1
Mitchell, AL1
Fisher, N1
Meunier, B1
Nijtmans, LG1
Schaefer, AM1
Jackson, MJ1
Turnbull, DM1
Taylor, RW1

Other Studies

1 other study available for guanidine and Electron Transport Chain Deficiencies, Mitochondrial

ArticleYear
A mitochondrial cytochrome b mutation causing severe respiratory chain enzyme deficiency in humans and yeast.
    The FEBS journal, 2005, Volume: 272, Issue:14

    Topics: Adult; Amino Acid Sequence; Animals; Arginine; Base Sequence; Biopsy; Cytochromes b; DNA, Mitochondr

2005