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mechlorethamine and Anemia, Fanconi

mechlorethamine has been researched along with Anemia, Fanconi in 16 studies

nitrogen mustard : Compounds having two beta-haloalkyl groups bound to a nitrogen atom, as in (X-CH2-CH2)2NR.

Research Excerpts

ExcerptRelevanceReference
" A total of 271 patients underwent nitrogen mustard (NTM) and diepoxybutane (DEB) tests in our laboratory; baseline chromosomal breakage was studied for all of them."7.72Differential diagnosis of Fanconi anemia by nitrogen mustard and diepoxybutane. ( Deviren, A; Hacihanefioglu, S; Yalman, N, 2003)
" A total of 271 patients underwent nitrogen mustard (NTM) and diepoxybutane (DEB) tests in our laboratory; baseline chromosomal breakage was studied for all of them."3.72Differential diagnosis of Fanconi anemia by nitrogen mustard and diepoxybutane. ( Deviren, A; Hacihanefioglu, S; Yalman, N, 2003)
"Fanconi anemia (FA) is a human autosomal disorder characterized by cancer susceptibility and cellular sensitivity to DNA crosslinking agents such as mitomycin C and diepoxybutane."3.71The Chinese hamster FANCG/XRCC9 mutant NM3 fails to express the monoubiquitinated form of the FANCD2 protein, is hypersensitive to a range of DNA damaging agents and exhibits a normal level of spontaneous sister chromatid exchange. ( Bryant, PE; D'Andrea, AD; Johnson, MA; Jones, NJ; May, S; Meyn, RE; Stuckert, AP; Trueman, KL; Wilson, JB, 2001)
"Fanconi anemia (FA) cells are hypersensitive to cytotoxicity, cell cycle arrest, and chromosomal aberrations induced by DNA cross-linking agents, such as mitomycin C (MMC) and nitrogen mustard (HN2)."3.69The Fanconi anemia complementation group C protein corrects DNA interstrand cross-link-specific apoptosis in HSC536N cells. ( Ashmun, RA; Brent, TP; Howell, SR; Marathi, UK, 1996)
"Fanconi anemia is a cancer-prone disease characterized by progressive loss of blood cells, skeletal defects and stunted growth."1.28Alteration of a nuclease in Fanconi anemia. ( Boyd, JB; Buchwald, M; Harris, PV; Ryan, C; Sakaguchi, K, 1991)

Research

Studies (16)

TimeframeStudies, this research(%)All Research%
pre-19905 (31.25)18.7374
1990's8 (50.00)18.2507
2000's2 (12.50)29.6817
2010's1 (6.25)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Voter, AF1
Manthei, KA1
Keck, JL1
Deviren, A1
Yalman, N1
Hacihanefioglu, S1
Cohen, MM1
Fruchtman, CE1
Simpson, SJ1
Martin, AO1
Dean, SW2
Fox, M1
Berger, R4
Bernheim, A1
Le Coniat, M4
Vecchione, D1
Schaison, G1
Sognier, MA1
Hittelman, WN1
Gendron, MC1
Marathi, UK1
Howell, SR1
Ashmun, RA1
Brent, TP1
Stringer, JA1
Kirk, SH1
Ahmad, SI1
Wilson, JB1
Johnson, MA1
Stuckert, AP1
Trueman, KL1
May, S1
Bryant, PE1
Meyn, RE1
D'Andrea, AD1
Jones, NJ1
Sakaguchi, K1
Harris, PV1
Ryan, C1
Buchwald, M1
Boyd, JB1
Howell, RT1
Desangles, F1
Miglierina, R2
Gendron, M1
Sykes, HR1
Lehmann, AR1

Other Studies

16 other studies available for mechlorethamine and Anemia, Fanconi

ArticleYear
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; Fanc

2016
Differential diagnosis of Fanconi anemia by nitrogen mustard and diepoxybutane.
    Annals of hematology, 2003, Volume: 82, Issue:4

    Topics: Alkylating Agents; Chromosome Breakage; Diagnosis, Differential; Epoxy Compounds; Fanconi Anemia; Hu

2003
The cytogenetic response of Fanconi's anemia lymphoblastoid cell lines to various clastogens.
    Cytogenetics and cell genetics, 1982, Volume: 34, Issue:3

    Topics: Adult; Anemia, Aplastic; Ataxia Telangiectasia; Bleomycin; Cell Line; Child; Child, Preschool; Epoxy

1982
Investigation of the cell cycle response of normal and Fanconi's anaemia fibroblasts to nitrogen mustard using flow cytometry.
    Journal of cell science, 1983, Volume: 64

    Topics: Anemia, Aplastic; Cell Cycle; Cell Survival; Cells, Cultured; DNA; Dose-Response Relationship, Drug;

1983
[Effect of chlormethin chlorhydrate on the chromosomes in Fanconi's anemia: application to diagnosis and detection of heterozygotes].
    Comptes rendus des seances de l'Academie des sciences. Serie D, Sciences naturelles, 1980, Feb-11, Volume: 290, Issue:6

    Topics: Anemia, Aplastic; Cells, Cultured; Chromosomes, Human; Fanconi Anemia; Genetic Carrier Screening; Hu

1980
Loss of repairability of DNA interstrand crosslinks in Fanconi's anemia cells with culture age.
    Mutation research, 1983, Volume: 108, Issue:1-3

    Topics: Anemia, Aplastic; Cell Survival; Cells, Cultured; Cross-Linking Reagents; DNA Repair; Fanconi Anemia

1983
Fanconi anemia. Chromosome breakage and cell cycle studies.
    Cancer genetics and cytogenetics, 1993, Volume: 69, Issue:1

    Topics: Cell Cycle; Cells, Cultured; Chromosome Aberrations; Cytogenetics; Fanconi Anemia; Flow Cytometry; H

1993
The Fanconi anemia complementation group C protein corrects DNA interstrand cross-link-specific apoptosis in HSC536N cells.
    Blood, 1996, Sep-15, Volume: 88, Issue:6

    Topics: Apoptosis; Cell Cycle; Cell Cycle Proteins; Cross-Linking Reagents; DNA Adducts; DNA Repair; DNA-Bin

1996
Studies on double strand DNA damage, repair and mutagenesis in E coli and the implications to Fanconi's anaemia.
    Biochemical Society transactions, 1997, Volume: 25, Issue:1

    Topics: Amino Acid Sequence; Bacterial Proteins; Cisplatin; DNA Damage; DNA Repair; Escherichia coli; Fancon

1997
The Chinese hamster FANCG/XRCC9 mutant NM3 fails to express the monoubiquitinated form of the FANCD2 protein, is hypersensitive to a range of DNA damaging agents and exhibits a normal level of spontaneous sister chromatid exchange.
    Carcinogenesis, 2001, Volume: 22, Issue:12

    Topics: Animals; Bleomycin; Cell Line; CHO Cells; Cricetinae; DNA Damage; DNA-Binding Proteins; Epoxy Compou

2001
Alteration of a nuclease in Fanconi anemia.
    Mutation research, 1991, Volume: 255, Issue:1

    Topics: Cell Fractionation; Cell Line, Transformed; Deoxyribonucleases; Fanconi Anemia; Fibroblasts; Humans;

1991
Sister chromatid exchange evaluation as an aid to the diagnosis and exclusion of Fanconi's anaemia by induced chromosome damage analysis.
    Journal of medical genetics, 1991, Volume: 28, Issue:7

    Topics: Cells, Cultured; Chromosome Aberrations; Chromosomes, Human; Cross-Linking Reagents; DNA; DNA Damage

1991
[Diagnosis of Fanconi's anemia by nitrogen mustard induction of chromosome breakage in fibroblasts].
    Pathologie-biologie, 1991, Volume: 39, Issue:2

    Topics: Chromosome Aberrations; Chromosome Disorders; Chromosomes; Dose-Response Relationship, Drug; Fanconi

1991
A simple diagnostic test for Fanconi anemia by flow cytometry.
    Analytical cellular pathology : the journal of the European Society for Analytical Cellular Pathology, 1991, Volume: 3, Issue:2

    Topics: Cell Cycle; Cells, Cultured; Chromosomes; Erythrocytes; Fanconi Anemia; Flow Cytometry; Humans; Mech

1991
Diagnosis of Fanconi's anemia by flow cytometry.
    Nouvelle revue francaise d'hematologie, 1990, Volume: 32, Issue:6

    Topics: Cell Cycle; Chromosome Aberrations; DNA; Fanconi Anemia; Flow Cytometry; Heterozygote; Humans; Lymph

1990
Inactivation by nitrogen mustard of plasmids introduced into normal and Fanconi's anaemia cells.
    Mutation research, 1988, Volume: 194, Issue:1

    Topics: Acetyltransferases; Anemia, Aplastic; Cell Line, Transformed; Cell Survival; Chloramphenicol O-Acety

1988