Page last updated: 2024-10-28

guanidine and Mitochondrial Diseases

guanidine has been researched along with Mitochondrial Diseases 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.

Mitochondrial Diseases: Diseases caused by abnormal function of the MITOCHONDRIA. They may be caused by mutations, acquired or inherited, in mitochondrial DNA or in nuclear genes that code for mitochondrial components. They may also be the result of acquired mitochondria dysfunction due to adverse effects of drugs, infections, or other environmental causes.

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 Mitochondrial Diseases

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