Compounds > camptothecin

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camptothecin and Anemia, Fanconi

camptothecin has been researched along with Anemia, Fanconi in 10 studies

Research

Studies (10)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	3 (30.00)	18.2507
2000's	2 (20.00)	29.6817
2010's	4 (40.00)	24.3611
2020's	1 (10.00)	2.80

Authors

Authors	Studies
Keck, JL; Manthei, KA; Voter, AF	1
Chen, J; Hu, Q; Kim, H; Klages-Mundt, N; Kuma Saha, L; Li, L; Lynn, E; Paull, T; Shen, X; Srivastava, M; Takeda, S; Tian, Y; Wang, R; Ye, Y; Zhang, H	1
Adelman, CA; Borel, V; Boulton, SJ; Matsuzaki, K; Schindler, D	1
Gautier, J; Hoatlin, ME; Stone, S; Wang, LC	1
Agarwal, S; Ali, AM; Andreassen, PR; Bakker, ST; de Winter, JP; Du, CH; Fan, Q; Godthelp, BC; Grassman, E; Jansen, M; Joenje, H; Meetei, AR; Rooimans, MA; Singh, TR; Steltenpool, J; Wahengbam, K; Williams, DA	1
Bettecken, T; de Winter, JP; Eirich, K; Hain, K; Hilhorst-Hofstee, Y; Jaspers, NG; Joenje, H; Korthof, ET; Nieuwint, AW; Oostra, AB; Rooimans, MA; Rouse, J; Schindler, D; Schuster, B; Steltenpool, J; Stoepker, C	1
Auerbach, AD; Kim, Y; Lach, FP; Smogorzewska, A; Spitz, GS; Veturi, U	1
Averbeck, D; Duchaud, E; Moustacchi, E; Rosselli, F	1
Grompe, M; Jakobs, PM; Moses, RE; Neeley, TL; Saito, H	1
Epe, B; Hoehn, H; Poot, M	1

Other Studies

10 other study(ies) available for camptothecin and Anemia, Fanconi

Article	Year
A High-Throughput Screening Strategy to Identify Protein-Protein Interaction Inhibitors That Block the Fanconi Anemia DNA Repair Pathway. Journal of biomolecular screening, 2016, Volume: 21, Issue:6 Topics: Antineoplastic Agents; DNA Damage; DNA Helicases; DNA Repair; Drug Screening Assays, Antitumor; Fanconi Anemia; High-Throughput Screening Assays; Humans; Multiprotein Complexes; Protein Interaction Maps; RecQ Helicases	2016
The ARK Assay Is a Sensitive and Versatile Method for the Global Detection of DNA-Protein Crosslinks. Cell reports, 2020, 01-28, Volume: 30, Issue:4 Topics: Camptothecin; Cross-Linking Reagents; DNA; DNA Repair; DNA-Binding Proteins; Etoposide; Fanconi Anemia; Gene Knockout Techniques; Genetic Techniques; HeLa Cells; Humans; Topoisomerase I Inhibitors	2020
FANCJ suppresses microsatellite instability and lymphomagenesis independent of the Fanconi anemia pathway. Genes & development, 2015, Dec-15, Volume: 29, Issue:24 Topics: Animals; Antineoplastic Agents; Basic-Leucine Zipper Transcription Factors; Camptothecin; Cell Line; Cells, Cultured; DNA Damage; Fanconi Anemia; Fanconi Anemia Complementation Group D2 Protein; Fanconi Anemia Complementation Group Proteins; Female; Fibroblasts; Genetic Predisposition to Disease; Humans; Lymphoma; Male; Mice, Knockout; Microsatellite Instability; Mitomycin; Neoplasms, Glandular and Epithelial; RNA Helicases; Ultraviolet Rays	2015
Fanconi anemia proteins stabilize replication forks. DNA repair, 2008, Dec-01, Volume: 7, Issue:12 Topics: Animals; Antibiotics, Antineoplastic; Antineoplastic Agents, Phytogenic; Aphidicolin; Ataxia Telangiectasia Mutated Proteins; Camptothecin; Cell Cycle Proteins; Cell Nucleus; Cell-Free System; Chromatin; DNA Damage; DNA Repair; DNA Replication; Enzyme Inhibitors; Fanconi Anemia; Fanconi Anemia Complementation Group D2 Protein; Fanconi Anemia Complementation Group L Protein; Mitomycin; Phosphorylation; Protein Serine-Threonine Kinases; Xenopus laevis; Xenopus Proteins	2008
Impaired FANCD2 monoubiquitination and hypersensitivity to camptothecin uniquely characterize Fanconi anemia complementation group M. Blood, 2009, Jul-02, Volume: 114, Issue:1 Topics: Adenosine Triphosphatases; Camptothecin; Cell Line, Tumor; Cross-Linking Reagents; DNA Helicases; Drug Resistance; Fanconi Anemia; Fanconi Anemia Complementation Group A Protein; Fanconi Anemia Complementation Group D2 Protein; Gene Expression; Humans; Mutation; Radiation Tolerance; Recombinant Proteins; Transfection; Ubiquitination; Ultraviolet Rays	2009
SLX4, a coordinator of structure-specific endonucleases, is mutated in a new Fanconi anemia subtype. Nature genetics, 2011, Volume: 43, Issue:2 Topics: Alleles; Camptothecin; Child; Cross-Linking Reagents; DNA Repair; Dose-Response Relationship, Drug; Fanconi Anemia; Heat-Shock Proteins; HSC70 Heat-Shock Proteins; Humans; Immunoprecipitation; Male; Mitomycin; Mutation; Phenotype; Recombinases	2011
Regulation of multiple DNA repair pathways by the Fanconi anemia protein SLX4. Blood, 2013, Jan-03, Volume: 121, Issue:1 Topics: Camptothecin; Cell Line; Cross-Linking Reagents; DNA; DNA Mutational Analysis; DNA Repair; DNA Repair Enzymes; DNA-Binding Proteins; Endodeoxyribonucleases; Endonucleases; Fanconi Anemia; Humans; Mitomycin; Phthalazines; Piperazines; Poly(ADP-ribose) Polymerase Inhibitors; Protein Interaction Mapping; Protein Structure, Tertiary; Recombinant Fusion Proteins; Recombinases; Topoisomerase I Inhibitors	2013
Comparison of the effects of DNA topoisomerase inhibitors on lymphoblasts from normal and Fanconi anemia donors. Mutation research, 1994, Volume: 325, Issue:4 Topics: Camptothecin; Cell Division; Cells, Cultured; Chromosome Aberrations; DNA; DNA Damage; DNA Repair; Fanconi Anemia; Hematopoietic Stem Cells; Humans; Indoles; Isoquinolines; Lymphocytes; Methoxsalen; Nalidixic Acid; Novobiocin; Skin; Topoisomerase I Inhibitors	1994
Fanconi anemia cells have a normal gene structure for topoisomerase I. Human genetics, 1994, Volume: 93, Issue:5 Topics: Base Sequence; Camptothecin; Cell Line; Cell Survival; Cell Transformation, Viral; Cells, Cultured; DNA; DNA Mutational Analysis; DNA Primers; DNA Topoisomerases, Type I; Fanconi Anemia; Humans; Mitomycin; Molecular Sequence Data; Polymerase Chain Reaction	1994
Cell cycle effects of the DNA topoisomerase inhibitors camptothecin and m-AMSA in lymphoblastoid cell lines from patients with Fanconi anemia. Mutation research, 1992, Nov-16, Volume: 270, Issue:2 Topics: Amsacrine; Bromodeoxyuridine; Camptothecin; Cell Line; DNA Topoisomerases, Type I; DNA Topoisomerases, Type II; Fanconi Anemia; Flow Cytometry; G2 Phase; Humans; Lymphocytes; Topoisomerase I Inhibitors; Topoisomerase II Inhibitors	1992