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hydroxyurea and Adult Premature Aging Syndrome

hydroxyurea has been researched along with Adult Premature Aging Syndrome in 8 studies

Research Excerpts

ExcerptRelevanceReference
" We show here that antisense suppression of WRN in two human glioma cell lines reproduces hallmarks of the drug cytotoxicity profile of WS cells, namely, hypersensitivity to 4-nitroquinoline 1-oxide, camptothecin and hydroxyurea."3.72The Werner syndrome protein confers resistance to the DNA lesions N3-methyladenine and O6-methylguanine: implications for WRN function. ( Blank, A; Bobola, MS; D Kolstoe, D; Gold, B; Loeb, LA; Meade, EH; Rabinovitch, PS; Silber, JR; Varadarajan, S, 2004)
"Werner syndrome is a genetic disorder characterized by genomic instability, elevated recombination and replication defects."1.32In vivo function of the conserved non-catalytic domain of Werner syndrome helicase in DNA replication. ( Brosh, RM; Sharma, S; Sommers, JA, 2004)
"Bloom's syndrome (BS) and Werner's syndrome (WS) are genetic disorders in which an increased rate of chromosomal aberration is detected."1.30Bloom's and Werner's syndrome genes suppress hyperrecombination in yeast sgs1 mutant: implication for genomic instability in human diseases. ( Furuichi, Y; Goto, M; Ikeda, H; Kato, J; Shimamoto, A; Yamagata, K, 1998)
"Hydroxyurea post-treatment potentiated the X-ray-induced aberration levels both in the normal and Werner's syndrome (KO375 and DJG) cell lines; in contrast caffeine was only effective in the normal cell line."1.30Lack of effect of caffeine post-treatment on X-ray-induced chromosomal aberrations in Werner's syndrome lymphoblastoid cell lines: a preliminary report. ( Franchitto, A; Mosesso, P; Palitti, F; Pichierri, P; Proietti De Santis, L, 1999)

Research

Studies (8)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's3 (37.50)18.2507
2000's5 (62.50)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Pichierri, P3
Rosselli, F1
Franchitto, A3
Blank, A1
Bobola, MS1
Gold, B1
Varadarajan, S1
D Kolstoe, D1
Meade, EH1
Rabinovitch, PS1
Loeb, LA1
Silber, JR1
Sharma, S1
Sommers, JA1
Brosh, RM1
Stewart, E1
Chapman, CR1
Al-Khodairy, F1
Carr, AM1
Enoch, T1
Yamagata, K1
Kato, J1
Shimamoto, A1
Goto, M1
Furuichi, Y1
Ikeda, H1
Proietti De Santis, L1
Mosesso, P2
Palitti, F2
Onoda, F1
Seki, M1
Miyajima, A1
Enomoto, T1

Other Studies

8 other studies available for hydroxyurea and Adult Premature Aging Syndrome

ArticleYear
Werner's syndrome protein is phosphorylated in an ATR/ATM-dependent manner following replication arrest and DNA damage induced during the S phase of the cell cycle.
    Oncogene, 2003, Mar-13, Volume: 22, Issue:10

    Topics: Ataxia Telangiectasia Mutated Proteins; Camptothecin; Cell Cycle Proteins; Cell Nucleus Structures;

2003
The Werner syndrome protein confers resistance to the DNA lesions N3-methyladenine and O6-methylguanine: implications for WRN function.
    DNA repair, 2004, Jun-03, Volume: 3, Issue:6

    Topics: 4-Nitroquinoline-1-oxide; Adenine; Alkylating Agents; Antineoplastic Agents; Apoptosis; Camptothecin

2004
In vivo function of the conserved non-catalytic domain of Werner syndrome helicase in DNA replication.
    Human molecular genetics, 2004, Oct-01, Volume: 13, Issue:19

    Topics: Adenosine Triphosphatases; Catalytic Domain; Cell Cycle; Cells, Cultured; Conserved Sequence; DNA He

2004
rqh1+, a fission yeast gene related to the Bloom's and Werner's syndrome genes, is required for reversible S phase arrest.
    The EMBO journal, 1997, May-15, Volume: 16, Issue:10

    Topics: Adenosine Triphosphatases; Amino Acid Sequence; Bloom Syndrome; DNA Helicases; DNA Replication; Exod

1997
Bloom's and Werner's syndrome genes suppress hyperrecombination in yeast sgs1 mutant: implication for genomic instability in human diseases.
    Proceedings of the National Academy of Sciences of the United States of America, 1998, Jul-21, Volume: 95, Issue:15

    Topics: Base Sequence; Bloom Syndrome; DNA; DNA Helicases; Humans; Hydroxyurea; Mutation; Recombination, Gen

1998
Lack of effect of caffeine post-treatment on X-ray-induced chromosomal aberrations in Werner's syndrome lymphoblastoid cell lines: a preliminary report.
    International journal of radiation biology, 1999, Volume: 75, Issue:11

    Topics: Caffeine; Cell Line, Transformed; Cell Transformation, Viral; Chromosome Aberrations; Chromosomes, H

1999
Elevation of sister chromatid exchange in Saccharomyces cerevisiae sgs1 disruptants and the relevance of the disruptants as a system to evaluate mutations in Bloom's syndrome gene.
    Mutation research, 2000, Apr-28, Volume: 459, Issue:3

    Topics: Alleles; Bloom Syndrome; DNA Helicases; Dose-Response Relationship, Drug; Genetic Complementation Te

2000
Werner's syndrome protein is required for correct recovery after replication arrest and DNA damage induced in S-phase of cell cycle.
    Molecular biology of the cell, 2001, Volume: 12, Issue:8

    Topics: Apoptosis; Camptothecin; Cells, Cultured; Comet Assay; DNA Damage; DNA Helicases; DNA Nucleotidyltra

2001