Compounds > nad
Page last updated: 2024-08-17

nad and Cockayne Syndrome

nad has been researched along with Cockayne Syndrome in 9 studies

Research

Studies (9)

TimeframeStudies, this research(%)All Research%
pre-19905 (55.56)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's4 (44.44)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Babbar, M; Bohr, VA; Croteau, DL; De, S; Demarest, TG; Kim, EW; Lee, JH; Okur, MN1
Guarente, L1
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, MA1
Scheibye-Knudsen, M1
Broughton, BC; Lehmann, AR; Mayne, LV1
Fujiwara, Y; Goto, K; Ichihashi, M; Yamamoto, K1
Fujiwara, Y; Goto, K; Kano, Y1
Auer, B; Burtscher, HJ; Hirsch-Kauffmann, M; Klocker, H; Schneider, R; Schweiger, M1
Kukita, A; Otsuka, F1

Reviews

1 review(s) available for nad and Cockayne Syndrome

ArticleYear
Neurodegeneration in accelerated aging.
    Danish medical journal, 2016, Volume: 63, Issue:11

    Topics: Aging, Premature; Animals; Ataxia Telangiectasia; Bloom Syndrome; Cockayne Syndrome; DNA Repair; Dyskeratosis Congenita; Fanconi Anemia; Humans; Mitochondria; Mitophagy; NAD; Neurodegenerative Diseases; Poly(ADP-ribose) Polymerases; Progeria; Rothmund-Thomson Syndrome; Sirtuin 1; Telomere Shortening; Werner Syndrome; Xeroderma Pigmentosum

2016

Other Studies

8 other study(ies) available for nad and Cockayne Syndrome

ArticleYear
Cockayne syndrome group B deficiency reduces H3K9me3 chromatin remodeler SETDB1 and exacerbates cellular aging.
    Nucleic acids research, 2019, 09-19, Volume: 47, Issue:16

    Topics: Cell Line, Transformed; Cellular Senescence; Chromatin; Cockayne Syndrome; DNA; DNA Damage; DNA Helicases; DNA Repair Enzymes; Fibroblasts; Gene Expression Regulation; Histone-Lysine N-Methyltransferase; Histones; Humans; Methyltransferases; Mitochondria; Mutation; NAD; Poly Adenosine Diphosphate Ribose; Poly-ADP-Ribose Binding Proteins; Poly(ADP-ribose) Polymerases; Protein Methyltransferases; Repressor Proteins; Signal Transduction; Transcription Factors; Transcription Initiation Site; Transcription, Genetic

2019
Linking DNA damage, NAD(+)/SIRT1, and aging.
    Cell metabolism, 2014, Nov-04, Volume: 20, Issue:5

    Topics: Aging, Premature; Animals; Cockayne Syndrome; Diet, High-Fat; Humans; NAD; Sirtuin 1

2014
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; Enzyme Activation; Humans; Mice; Mice, Inbred C57BL; Mitochondria; NAD; Poly (ADP-Ribose) Polymerase-1; Poly(ADP-ribose) Polymerases; Sirtuin 1

2014
The ultraviolet sensitivity of Cockayne syndrome cells is not a consequence of reduced cellular NAD content.
    American journal of human genetics, 1984, Volume: 36, Issue:2

    Topics: Cell Survival; Cells, Cultured; Cockayne Syndrome; DNA; Dwarfism; Fibroblasts; Humans; Male; NAD; Photosensitivity Disorders; RNA; Skin; Ultraviolet Rays

1984
Roles of poly(ADP-ribose) synthesis in repair and replication in normal human, Cockayne syndrome, and xeroderma pigmentosum fibroblasts after UV irradiation.
    Princess Takamatsu symposia, 1983, Volume: 13

    Topics: Benzamides; Cockayne Syndrome; DNA Repair; DNA Replication; Dwarfism; Fibroblasts; Humans; In Vitro Techniques; Methyl Methanesulfonate; NAD; Nucleoside Diphosphate Sugars; Poly Adenosine Diphosphate Ribose; Poly(ADP-ribose) Polymerase Inhibitors; Ultraviolet Rays; Xeroderma Pigmentosum

1983
Ultraviolet hypersensitivity of Cockayne's syndrome fibroblasts. Effects of nicotinamide adenine dinucleotide and poly(ADP-ribose) synthesis.
    Experimental cell research, 1982, Volume: 139, Issue:1

    Topics: Cells, Cultured; Cockayne Syndrome; DNA Repair; Dwarfism; Fibroblasts; Humans; Kinetics; NAD; Poly(ADP-ribose) Polymerases; Sister Chromatid Exchange; Ultraviolet Rays; Xeroderma Pigmentosum

1982
The Fritz-Lipmann lecture. DNA repair in human cells. Biochemistry of the hereditary diseases Fanconi's anaemia and Cockayne syndrome.
    European journal of biochemistry, 1987, Jun-01, Volume: 165, Issue:2

    Topics: Acetyltransferases; Anemia, Aplastic; Chloramphenicol O-Acetyltransferase; Cockayne Syndrome; DNA; DNA Repair; Dwarfism; Fanconi Anemia; Fibroblasts; Humans; NAD; Poly(ADP-ribose) Polymerases; Pyrimidine Dimers; Transcription, Genetic; Ultraviolet Rays; Xeroderma Pigmentosum

1987
Ultraviolet hypersensitivity of Cockayne syndrome lymphoblastoid lines--the effects of exogenous beta-nicotinamide adenine dinucleotide.
    Photochemistry and photobiology, 1986, Volume: 44, Issue:6

    Topics: Cell Line; Cockayne Syndrome; Dwarfism; Humans; Lymphocytes; NAD; Ultraviolet Rays; Xeroderma Pigmentosum

1986