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methoxsalen and Anemia, Aplastic

methoxsalen has been researched along with Anemia, Aplastic in 13 studies

Methoxsalen: A naturally occurring furocoumarin compound found in several species of plants, including Psoralea corylifolia. It is a photoactive substance that forms DNA ADDUCTS in the presence of ultraviolet A irradiation.
methoxsalen : A member of the class of psoralens that is 7H-furo[3,2-g]chromen-7-one in which the 9 position is substituted by a methoxy group. It is a constituent of the fruits of Ammi majus. Like other psoralens, trioxsalen causes photosensitization of the skin. It is administered topically or orally in conjunction with UV-A for phototherapy treatment of vitiligo and severe psoriasis.

Anemia, Aplastic: A form of anemia in which the bone marrow fails to produce adequate numbers of peripheral blood elements.

Research Excerpts

ExcerptRelevanceReference
"Five homozygous patients with Fanconi's anemia and nine heterozygous relatives were studied for mutagen sensitivity by a new method."1.27Response of lymphocytes from Fanconi's anemia patients and their heterozygous relatives to 8-methoxy-psoralene in a cloning survival test system. ( Fleischer-Reischmann, B; Wunder, E, 1983)

Research

Studies (13)

TimeframeStudies, this research(%)All Research%
pre-199011 (84.62)18.7374
1990's2 (15.38)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Wunder, E2
Fleischer-Reischmann, B1
Papadopoulo, D4
Porfirio, B1
Moustacchi, E7
Rousset, S1
Nocentini, S1
Revet, B1
Digweed, M2
Sperling, K2
Diatloff-Zito, C3
Averbeck, D2
Zakrzewski-Lüdcke, S1
Gök, MM1
Billardon, B1
Buchwald, M1
Gruenert, DC1
Kapp, LN1
Cleaver, JE1
Sasaki, MS1
Tonomura, A1

Other Studies

13 other studies available for methoxsalen and Anemia, Aplastic

ArticleYear
Response of lymphocytes from Fanconi's anemia patients and their heterozygous relatives to 8-methoxy-psoralene in a cloning survival test system.
    Human genetics, 1983, Volume: 64, Issue:2

    Topics: Adolescent; Adult; Anemia, Aplastic; Cell Survival; Clone Cells; Dose-Response Relationship, Drug; F

1983
Mutagenic response of Fanconi's anemia cells from a defined complementation group after treatment with photoactivated bifunctional psoralens.
    Cancer research, 1990, Jun-01, Volume: 50, Issue:11

    Topics: Anemia, Aplastic; Cell Survival; Fanconi Anemia; Furocoumarins; Humans; Hypoxanthine Phosphoribosylt

1990
Molecular analysis by electron microscopy of the removal of psoralen-photoinduced DNA cross-links in normal and Fanconi's anemia fibroblasts.
    Cancer research, 1990, Apr-15, Volume: 50, Issue:8

    Topics: Anemia, Aplastic; Cells, Cultured; DNA; Dose-Response Relationship, Radiation; Fanconi Anemia; Fibro

1990
Identification of a HeLa mRNA fraction which can correct the DNA-repair defect in Fanconi anaemia fibroblasts.
    Mutation research, 1989, Volume: 218, Issue:3

    Topics: Adenine; Anemia, Aplastic; Cell Line; Child, Preschool; Cross-Linking Reagents; DNA; DNA Repair; Fan

1989
Abnormal response to DNA crosslinking agents of Fanconi anemia fibroblasts can be corrected by transfection with normal human DNA.
    Proceedings of the National Academy of Sciences of the United States of America, 1986, Volume: 83, Issue:18

    Topics: Anemia, Aplastic; Base Sequence; Cell Line; Cross-Linking Reagents; DNA; Drug Resistance; Fanconi An

1986
Fanconi's anaemia: correlation of genetic complementation group with psoralen/UVA response.
    Human genetics, 1988, Volume: 78, Issue:1

    Topics: Anemia, Aplastic; Cell Line; DNA Repair; Fanconi Anemia; Genetic Complementation Test; Humans; Metho

1988
Microinjection of normal cell extracts into Fanconi anemia fibroblasts corrects defective scheduled DNA synthesis recovery after 8-methoxypsoralen plus UVa treatment.
    Human genetics, 1987, Volume: 75, Issue:4

    Topics: Anemia, Aplastic; Cells, Cultured; Child; DNA Damage; DNA Repair; Fanconi Anemia; Female; Humans; In

1987
The fate of 8-methoxypsoralen-photoinduced DNA interstrand crosslinks in Fanconi's anemia cells of defined genetic complementation groups.
    Mutation research, 1987, Volume: 184, Issue:3

    Topics: Anemia, Aplastic; Cell Line; Cell Survival; Cross-Linking Reagents; DNA Damage; DNA Repair; Fanconi

1987
Comparison of the sensitivity of Fanconi's anemia and normal fibroblasts to the induction of sister-chromatid exchanges by photoaddition of mono- and bi-functional psoralens.
    Mutation research, 1986, Volume: 174, Issue:3

    Topics: Anemia, Aplastic; Cells, Cultured; Cross-Linking Reagents; Fanconi Anemia; Fibroblasts; Furocoumarin

1986
Two complementation groups of Fanconi's anemia differ in their phenotypic response to a DNA-crosslinking treatment.
    Human genetics, 1987, Volume: 75, Issue:1

    Topics: Anemia, Aplastic; Cells, Cultured; Cross-Linking Reagents; DNA; Fanconi Anemia; Fibroblasts; Humans;

1987
Inhibition of DNA synthesis by psoralen-induced lesions in xeroderma pigmentosum and Fanconi's anemia fibroblasts.
    Photochemistry and photobiology, 1985, Volume: 41, Issue:5

    Topics: Anemia, Aplastic; Cell Line; DNA Replication; Fanconi Anemia; Humans; Methoxsalen; Ultraviolet Rays;

1985
DNA semi-conservative synthesis in normal and Fanconi anemia fibroblasts following treatment with 8-methoxypsoralen and near ultraviolet light or with X-rays.
    Human genetics, 1985, Volume: 70, Issue:3

    Topics: Adolescent; Adult; Anemia, Aplastic; Cell Line; Child; Child, Preschool; DNA; DNA Repair; Fanconi An

1985
A high susceptibility of Fanconi's anemia to chromosome breakage by DNA cross-linking agents.
    Cancer research, 1973, Volume: 33, Issue:8

    Topics: Alkanesulfonates; Alkylating Agents; Anemia, Aplastic; Antimetabolites; Caffeine; Cell Division; Cel

1973