Published in Hereditas on January 01, 1977
Cytoprotective effect of honey against chromosomal breakage in fanconi anemia patients in vitro. Indian J Hum Genet (2011) 1.38
Fanconi anemia mutation causes cellular susceptibility to ambient oxygen. Am J Hum Genet (1988) 1.03
Superoxide-mediated clastogenesis and anticlastogenic effects of exogenous superoxide dismutase. Proc Natl Acad Sci U S A (1996) 0.95
DNA repair dependent NAD+ metabolism is impaired in cells from patients with Fanconi's anemia. EMBO J (1983) 0.89
Oxidative stress-related mechanisms are associated with xenobiotics exerting excess toxicity to Fanconi anemia cells. Environ Health Perspect (2003) 0.85
Improvement of genetic stability in lymphocytes from Fanconi anemia patients through the combined effect of α-lipoic acid and N-acetylcysteine. Orphanet J Rare Dis (2012) 0.83
Damaged mitochondria and overproduction of ROS in Fanconi anemia cells. Rare Dis (2013) 0.82
Fanconi anemia proteins and their interacting partners: a molecular puzzle. Anemia (2012) 0.82
Oxidative Stress in Cancer-Prone Genetic Diseases in Pediatric Age: The Role of Mitochondrial Dysfunction. Oxid Med Cell Longev (2016) 0.76
Oxidative stress-associated protein tyrosine kinases and phosphatases in Fanconi anemia. Antioxid Redox Signal (2014) 0.76
Increased red cell distribution width in Fanconi anemia: a novel marker of stress erythropoiesis. Orphanet J Rare Dis (2016) 0.75
Cancer risk in humans predicted by increased levels of chromosomal aberrations in lymphocytes: Nordic study group on the health risk of chromosome damage. Cancer Res (1994) 1.70
Occupational and environmental risks in and around a smelter in northern Sweden. III. Frequencies of spontaneous abortion. Hereditas (1978) 1.30
Occupational and environmental risks in and around a smelter in northern Sweden. V. Spontaneous abortion among female employees and decreased birth weight in their offspring. Hereditas (1979) 1.26
Fragile X syndrome in mildly mentally retarded children in a northern Swedish county. A prevalence study. Clin Genet (1983) 1.16
Familial X-linked mental retardation and fragile X chromosomes in two Swedish families. Clin Genet (1981) 1.11
The effect of superoxide dismutase and catalase on radiation-induced chromosome breaks. Hereditas (1976) 1.06
Homozygosity for the transthyretin-met30-gene in two Swedish sibs with familial amyloidotic polyneuropathy. Clin Genet (1988) 1.06
Individual differences with respect to the sneezing reflex: an inherited physiological trait in man? Hum Hered (1983) 1.01
Occupational and environmental risks in and around a smelter in northern Sweden. I. Variations in birth weight. Hereditas (1978) 1.00
An inter-Nordic prospective study on cytogenetic endpoints and cancer risk. Nordic Study Group on the Health Risk of Chromosome Damage. Cancer Genet Cytogenet (1990) 0.96
Occupational and environmental risks in and around a smelter in northern Sweden. IV. Chromosomal aberrations in workers exposed to lead. Hereditas (1978) 0.95
Fragile site X chromosomes and X-linked mental retardation in severely retarded boys in a northern Swedish county. A prevalence study. Clin Genet (1982) 0.94
Occupational and environmental risks in and around a smelter in northern Sweden. VI. Congenital malformations. Hereditas (1979) 0.92
Occupational and environmental risks in and around a smelter in northern Sweden. II. Chromosomal aberrations in workers exposed to arsenic. Hereditas (1978) 0.91
Incidence of Down's syndrome in Sweden during the years 1968-1977. Hum Genet Suppl (1981) 0.91
Chromosome aberrations in workers exposed to arsenic. Environ Health Perspect (1977) 0.90
Cancer predictive value of cytogenetic markers used in occupational health surveillance programs: a report from an ongoing study by the European Study Group on Cytogenetic Biomarkers and Health. Mutat Res (1998) 0.87
Prognostic impact of bone marrow karyotype in childhood acute lymphoblastic leukaemia: Swedish experiences 1986-91. Acta Paediatr (1997) 0.86
Characterization of two human ovarian carcinoma cell lines. Gynecol Oncol (1979) 0.86
Fragility of the centromeric region of chromosome 1 associated with combined immunodeficiency in siblings. A recessively inherited entity? Acta Paediatr Scand (1990) 0.86
Chromosomal abnormality in dementia of Alzheimer type. Lancet (1980) 0.85
Diagnosis of familial amyloidotic polyneuropathy in Sweden by RFLP analysis. Clin Genet (1988) 0.85
Cytogenetic abnormalities and leukemic transformation in hydroxyurea-treated patients with Philadelphia chromosome negative chronic myeloproliferative disease. Cancer Genet Cytogenet (1990) 0.83
Chromosomal aberrations and cancer risk. Hum Hered (1984) 0.81
Chromosome aberrations in psoriatic patients treated with arsenic. Hum Genet (1979) 0.81
Chromosomal aberrations and male infertility. J Urol (1982) 0.81
Cancer predictive value of cytogenetic markers used in occupational health surveillance programs. Recent Results Cancer Res (1998) 0.80
Is exposure to sulphur dioxide clastogenic? Hereditas (1980) 0.80
Chromosome breaks in Werner's syndrome and their prevention in vitro by radical-scavenging enzymes. Hereditas (1977) 0.80
Cytogenetic and flow cytometric DNA analysis in renal cell carcinoma. Eur Urol (1991) 0.80
Increased frequencies of chromosomal abnormalities in families with a history of fetal wastage. Clin Genet (1981) 0.79
Interaction between some common genotoxic agents. Hum Hered (1986) 0.79
Alpha 1-antitrypsin phenotypes in Northern Sweden. Hum Hered (1980) 0.79
A study of chromosomal aberrations in miners exposed to diesel exhausts. Scand J Work Environ Health (1981) 0.79
Somatic chromosomal aberrations and male infertility. Hum Hered (1984) 0.78
A pair of siblings with diastrophic dysplasia and E trisomy mosaicism. Hum Hered (1984) 0.78
Occupational and environmental risks in and around a smelter in northern Sweden. VII. Reanalysis and follow-up of chromosomal aberrations in workers exposed to arsenic. Hereditas (1982) 0.78
Chromosomal changes in rheumatoid arthritis patients treated with CPH82. Clin Rheumatol (1996) 0.78
Comparison between five Nordic laboratories on scoring of human lymphocyte chromosome aberrations. Hereditas (1984) 0.77
Effects of superoxide dismutase and catalase on radiation-induced chromosome aberrations: dose and cell cycle dependence. Hereditas (1978) 0.77
Patient with acute B-cell leukemia of Burkitt's type (L3) and marker chromosomes including an (8;14) translocation. Leuk Res (1982) 0.76
Establishment and characterization of a human EBV-negative B cell line (MN 60). Leuk Res (1982) 0.76
Chromosome aberrations in cultured human lymphocytes exposed to trivalent and pentavalent arsenic. Scand J Work Environ Health (1981) 0.76
Microcephaly, mental retardation and chromosomal aberrations in a girl following radiation therapy during late fetal life. Acta Radiol Oncol (1981) 0.76
Transferrin C2 and radiation-induced chromosomal damage. Hum Hered (1988) 0.76
Clastogenic effects in human lymphocytes of power frequency electric fields: in vivo and in vitro studies. Radiat Environ Biophys (1984) 0.75
Population studies in northern Sweden. IX. Incidence of Down's syndrome by time, region and maternal age. Hereditas (1979) 0.75
Multiple DNA rearrangements in the BCL2 region in a patient with follicular lymphoma. Genes Chromosomes Cancer (1991) 0.75
Chromosomal aberrations in children exposed to diagnostic X-rays. Hereditas (1980) 0.75
Myelodysplastic syndromes--a population-based study on transformation and survival. Acta Oncol (1995) 0.75
Simultaneous immunoglobulin/T-cell receptor gene rearrangements and multiclonality in childhood acute lymphoblastic leukemia. Acta Paediatr (1994) 0.75
[Inherited mental retardation in the male caused by a structural X chromosomal defect]. Lakartidningen (1981) 0.75
Ig-gene and T-cell receptor gene rearrangements in a secondary, mono-histiocytic malignancy. Acta Oncol (1993) 0.75
Chromosomal aberrations in lymphocytes of workers exposed to low levels of styrene. Hum Hered (1984) 0.75
Different composition of the eosinophilic bone marrow pool in reactive eosinophilia and eosinophilic leukaemia. Acta Med Scand (1977) 0.75
Occupational and environmental risks in and around a smelter in northern Sweden. VIII. Three-year follow-up of chromosomal aberrations in workers exposed to lead. Hereditas (1982) 0.75
Prevention of chromosomal breakage in Fanconi's anemia by cocultivation with normal cells. Hum Genet (1980) 0.75
Chromosomal aberrations in lead-exposed workers. Hereditas (1982) 0.75
Population studies in northern Sweden. VII. Serum transferrin variants as markers of Finnish admixture. Hereditas (1975) 0.75
Patient with B-cell neoplasia (immunoblastic sarcoma) and the Philadelphia chromosome. Cancer Genet Cytogenet (1983) 0.75
Population studies in northern Sweden. XI. The Duffy blood group polymorphism. Hum Hered (1983) 0.75
Chronic monocytic leukemia terminating in blastic transformation. Blut (1986) 0.75
Philadelphia chromosome negative acute lymphoblastic leukemia preceding Philadelphia positive chronic myelogenous leukemia. Cancer Genet Cytogenet (1989) 0.75
Cluster formation in PHA-stimulated mononuclear cells from peripheral blood: effects of colcemid and taxol. Lymphology (1988) 0.75
The effect of CPH 82 on the growth of human lymphocytes in vitro. Definition of cytobiological action. Br J Rheumatol (1989) 0.75
Population studies in northern Sweden. X. The MN blood groups. Hum Hered (1981) 0.75