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3-hydroxybutyric acid and Cockayne Syndrome

3-hydroxybutyric acid has been researched along with Cockayne Syndrome in 1 studies

3-Hydroxybutyric Acid: BUTYRIC ACID substituted in the beta or 3 position. It is one of the ketone bodies produced in the liver.
3-hydroxybutyric acid : A straight-chain 3-hydroxy monocarboxylic acid comprising a butyric acid core with a single hydroxy substituent in the 3- position; a ketone body whose levels are raised during ketosis, used as an energy source by the brain during fasting in humans. Also used to synthesise biodegradable plastics.

Cockayne Syndrome: A syndrome characterized by multiple system abnormalities including DWARFISM; PHOTOSENSITIVITY DISORDERS; PREMATURE AGING; and HEARING LOSS. It is caused by mutations of a number of autosomal recessive genes encoding proteins that involve transcriptional-coupled DNA REPAIR processes. Cockayne syndrome is classified by the severity and age of onset. Type I (classical; CSA) is early childhood onset in the second year of life; type II (congenital; CSB) is early onset at birth with severe symptoms; type III (xeroderma pigmentosum; XP) is late childhood onset with mild symptoms.

Research Excerpts

ExcerptRelevanceReference
"Furthermore, premature aging in CS mice, nematodes, and human cells results from aberrant PARP activation due to deficient DNA repair leading to decreased SIRT1 activity and mitochondrial dysfunction."5.40A high-fat diet and NAD(+) activate Sirt1 to rescue premature aging in cockayne syndrome. ( Bergersen, LH; Bohr, VA; Cogger, VC; Croteau, DL; de Cabo, R; Dunn, CA; Fang, EF; Hasan-Olive, MM; Iyama, T; Le Couteur, DG; Mangerich, A; Mattson, MP; Mitchell, SJ; Moaddel, R; Scheibye-Knudsen, M; Singh, N; Veith, S; Wang, J; Ward, T; Warren, A; Wilson, DM; Wilson, MA, 2014)
"Furthermore, premature aging in CS mice, nematodes, and human cells results from aberrant PARP activation due to deficient DNA repair leading to decreased SIRT1 activity and mitochondrial dysfunction."1.40A high-fat diet and NAD(+) activate Sirt1 to rescue premature aging in cockayne syndrome. ( Bergersen, LH; Bohr, VA; Cogger, VC; Croteau, DL; de Cabo, R; Dunn, CA; Fang, EF; Hasan-Olive, MM; Iyama, T; Le Couteur, DG; Mangerich, A; Mattson, MP; Mitchell, SJ; Moaddel, R; Scheibye-Knudsen, M; Singh, N; Veith, S; Wang, J; Ward, T; Warren, A; Wilson, DM; Wilson, MA, 2014)

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
Scheibye-Knudsen, M1
Mitchell, SJ1
Fang, EF1
Iyama, T1
Ward, T1
Wang, J1
Dunn, CA1
Singh, N1
Veith, S1
Hasan-Olive, MM1
Mangerich, A1
Wilson, MA1
Mattson, MP1
Bergersen, LH1
Cogger, VC1
Warren, A1
Le Couteur, DG1
Moaddel, R1
Wilson, DM1
Croteau, DL1
de Cabo, R1
Bohr, VA1

Other Studies

1 other study available for 3-hydroxybutyric acid and Cockayne Syndrome

ArticleYear
A high-fat diet and NAD(+) activate Sirt1 to rescue premature aging in cockayne syndrome.
    Cell metabolism, 2014, Nov-04, Volume: 20, Issue:5

    Topics: 3-Hydroxybutyric Acid; Aging, Premature; Animals; Cell Line; Cockayne Syndrome; Diet, High-Fat; Enzy

2014