Page last updated: 2024-08-17

carbostyril and Adult Premature Aging Syndrome

carbostyril has been researched along with Adult Premature Aging Syndrome in 3 studies

Research

Studies (3)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's2 (66.67)29.6817
2010's1 (33.33)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Ishikawa, O; Motegi, S; Ogino, S; Perera, B; Takeuchi, Y; Uchiyama, A; Yamada, K; Yokoyama, Y1
Becker, KG; Bohr, VA; Kyng, KJ; Kølvrå, S; May, A; Stevnsner, T1
Ladiges, WC; Martin, GM; Ogburn, CE; Oshima, J; Wang, L; Ware, CB; Youssoufian, H1

Other Studies

3 other study(ies) available for carbostyril and Adult Premature Aging Syndrome

ArticleYear
Increased susceptibility to oxidative stress- and ultraviolet A-induced apoptosis in fibroblasts in atypical progeroid syndrome/atypical Werner syndrome with LMNA mutation.
    Experimental dermatology, 2016, Volume: 25 Suppl 3

    Topics: Amino Acid Substitution; Apoptosis; Cells, Cultured; Enzyme Inhibitors; Farnesyltranstransferase; Fibroblasts; Humans; Hydrogen Peroxide; Lamin Type A; Mutation, Missense; Necrosis; Oxidative Stress; Quinolones; Skin; Ultraviolet Rays; Werner Syndrome

2016
Gene expression responses to DNA damage are altered in human aging and in Werner Syndrome.
    Oncogene, 2005, Jul-28, Volume: 24, Issue:32

    Topics: 4-Nitroquinoline-1-oxide; Adult; Aged; Aging; Cell Line; DNA Damage; Fibroblasts; Gamma Rays; Gene Expression Regulation; Genes, Immediate-Early; Humans; Oligonucleotide Array Sequence Analysis; Quinolones; Skin; Stress, Physiological; Ultraviolet Rays; Werner Syndrome

2005
Cellular Werner phenotypes in mice expressing a putative dominant-negative human WRN gene.
    Genetics, 2000, Volume: 154, Issue:1

    Topics: 4-Nitroquinoline-1-oxide; Alleles; Animals; Cell Division; DNA Helicases; Down-Regulation; Exodeoxyribonucleases; Genes, Dominant; Humans; Mice; Mice, Transgenic; Phenotype; Quinolones; RecQ Helicases; Werner Syndrome; Werner Syndrome Helicase

2000