Page last updated: 2024-11-06

hydroxyproline and Mitochondrial Diseases

hydroxyproline has been researched along with Mitochondrial Diseases in 1 studies

Hydroxyproline: A hydroxylated form of the imino acid proline. A deficiency in ASCORBIC ACID can result in impaired hydroxyproline formation.
hydroxyproline : A proline derivative that is proline substituted by at least one hydroxy group.

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's0 (0.00)29.6817
2010's1 (100.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Koczor, CA1
Torres, RA1
Fields, E1
Qin, Q1
Park, J1
Ludaway, T1
Russ, R1
Lewis, W1

Other Studies

1 other study available for hydroxyproline and Mitochondrial Diseases

ArticleYear
Transgenic mouse model with deficient mitochondrial polymerase exhibits reduced state IV respiration and enhanced cardiac fibrosis.
    Laboratory investigation; a journal of technical methods and pathology, 2013, Volume: 93, Issue:2

    Topics: Analysis of Variance; Animals; Crosses, Genetic; Disease Models, Animal; DNA Polymerase gamma; DNA P

2013