[Effects of oxidants and antioxidants on chromosome breaks in Fanconi's anemia]. 1983

B Porfirio, and B Dallapiccola, and V Mokini, and G Alimena, and G Isacchi, and F Mandelli, and E Gandini

UI MeSH Term Description Entries
D008623 Mercaptoethanol A water-soluble thiol derived from hydrogen sulfide and ethanol. It is used as a reducing agent for disulfide bonds and to protect sulfhydryl groups from oxidation. 2-ME,2-Mercaptoethanol,2 Mercaptoethanol
D009153 Mutagens Chemical agents that increase the rate of genetic mutation by interfering with the function of nucleic acids. A clastogen is a specific mutagen that causes breaks in chromosomes. Clastogen,Clastogens,Genotoxin,Genotoxins,Mutagen
D010101 Oxygen Consumption The rate at which oxygen is used by a tissue; microliters of oxygen STPD used per milligram of tissue per hour; the rate at which oxygen enters the blood from alveolar gas, equal in the steady state to the consumption of oxygen by tissue metabolism throughout the body. (Stedman, 25th ed, p346) Consumption, Oxygen,Consumptions, Oxygen,Oxygen Consumptions
D010545 Peroxides A group of compounds that contain a bivalent O-O group, i.e., the oxygen atoms are univalent. They can either be inorganic or organic in nature. Such compounds release atomic (nascent) oxygen readily. Thus they are strong oxidizing agents and fire hazards when in contact with combustible materials, especially under high-temperature conditions. The chief industrial uses of peroxides are as oxidizing agents, bleaching agents, and initiators of polymerization. (From Hawley's Condensed Chemical Dictionary, 11th ed) Peroxide
D002869 Chromosome Aberrations Abnormal number or structure of chromosomes. Chromosome aberrations may result in CHROMOSOME DISORDERS. Autosome Abnormalities,Cytogenetic Aberrations,Abnormalities, Autosome,Abnormalities, Chromosomal,Abnormalities, Chromosome,Chromosomal Aberrations,Chromosome Abnormalities,Cytogenetic Abnormalities,Aberration, Chromosomal,Aberration, Chromosome,Aberration, Cytogenetic,Aberrations, Chromosomal,Aberrations, Chromosome,Aberrations, Cytogenetic,Abnormalities, Cytogenetic,Abnormality, Autosome,Abnormality, Chromosomal,Abnormality, Chromosome,Abnormality, Cytogenetic,Autosome Abnormality,Chromosomal Aberration,Chromosomal Abnormalities,Chromosomal Abnormality,Chromosome Aberration,Chromosome Abnormality,Cytogenetic Aberration,Cytogenetic Abnormality
D003545 Cysteine A thiol-containing non-essential amino acid that is oxidized to form CYSTINE. Cysteine Hydrochloride,Half-Cystine,L-Cysteine,Zinc Cysteinate,Half Cystine,L Cysteine
D004852 Epoxy Compounds Organic compounds that include a cyclic ether with three ring atoms in their structure. They are commonly used as precursors for POLYMERS such as EPOXY RESINS. Epoxide,Epoxides,Epoxy Compound,Oxiranes,Compound, Epoxy,Compounds, Epoxy
D004988 Ethers, Cyclic Compounds of the general formula R-O-R arranged in a ring or crown formation. Cyclic Ether,Cyclic Ethers,Ether, Cyclic
D005199 Fanconi Anemia Congenital disorder affecting all bone marrow elements, resulting in ANEMIA; LEUKOPENIA; and THROMBOPENIA, and associated with cardiac, renal, and limb malformations as well as dermal pigmentary changes. Spontaneous CHROMOSOME BREAKAGE is a feature of this disease along with predisposition to LEUKEMIA. There are at least 7 complementation groups in Fanconi anemia: FANCA, FANCB, FANCC, FANCD1, FANCD2, FANCE, FANCF, FANCG, and FANCL. (from Online Mendelian Inheritance in Man, http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id Anemia, Fanconi,Fanconi Hypoplastic Anemia,Fanconi Pancytopenia,Fanconi Panmyelopathy,Fanconi's Anemia,Anemia, Fanconi's,Anemias, Fanconi,Fanconi Anemias
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man

Related Publications

B Porfirio, and B Dallapiccola, and V Mokini, and G Alimena, and G Isacchi, and F Mandelli, and E Gandini
January 1973, Cytogenetics and cell genetics,
B Porfirio, and B Dallapiccola, and V Mokini, and G Alimena, and G Isacchi, and F Mandelli, and E Gandini
January 1977, Hereditas,
B Porfirio, and B Dallapiccola, and V Mokini, and G Alimena, and G Isacchi, and F Mandelli, and E Gandini
January 1977, Hereditas,
B Porfirio, and B Dallapiccola, and V Mokini, and G Alimena, and G Isacchi, and F Mandelli, and E Gandini
December 1976, La semaine des hopitaux : organe fonde par l'Association d'enseignement medical des hopitaux de Paris,
B Porfirio, and B Dallapiccola, and V Mokini, and G Alimena, and G Isacchi, and F Mandelli, and E Gandini
January 1969, Folia medica,
B Porfirio, and B Dallapiccola, and V Mokini, and G Alimena, and G Isacchi, and F Mandelli, and E Gandini
March 1969, Orvosi hetilap,
B Porfirio, and B Dallapiccola, and V Mokini, and G Alimena, and G Isacchi, and F Mandelli, and E Gandini
January 1985, Pediatria polska,
B Porfirio, and B Dallapiccola, and V Mokini, and G Alimena, and G Isacchi, and F Mandelli, and E Gandini
June 1976, Clinical genetics,
B Porfirio, and B Dallapiccola, and V Mokini, and G Alimena, and G Isacchi, and F Mandelli, and E Gandini
June 1977, Human genetics,
B Porfirio, and B Dallapiccola, and V Mokini, and G Alimena, and G Isacchi, and F Mandelli, and E Gandini
December 1994, JAMA,
Copied contents to your clipboard!