Published in Int J Oncol on September 01, 1992
An upper limit on the stochastic gravitational-wave background of cosmological origin. Nature (2009) 1.42
Impact of chemotherapy-associated nausea and vomiting on patients' functional status and on costs: survey of five Canadian centres. CMAJ (1993) 1.03
Heterochromatin and ribosomal genes in Asellus aquaticus (Crust. Isop.). Chromosome Res (1996) 0.96
CD99 isoforms dictate opposite functions in tumour malignancy and metastases by activating or repressing c-Src kinase activity. Oncogene (2007) 0.96
Directional limits on persistent gravitational waves using LIGO S5 science data. Phys Rev Lett (2011) 0.93
Characterization of the human common fragile site FRA2G. Genomics (2003) 0.92
A novel mitochondrial tRNAPhe mutation causes MERRF syndrome. Neurology (2004) 0.92
Lack of association between mtDNA haplogroups and Alzheimer's disease in Tuscany. Neurol Sci (2007) 0.91
Replication timing of two human common fragile sites: FRA1H and FRA2G. Cytogenet Genome Res (2008) 0.88
Longitudinal differentiation of chromosomes of Asellus aquaticus (Crust. Isop.) by in situ nick translation using restriction enzymes and DNase I. Chromosome Res (1997) 0.86
Effect of DAPI on Chinese hamster chromosomes. Cytogenet Cell Genet (1980) 0.84
Autoradiographic identification of a 13-21 translocation. Cytogenetics (1970) 0.84
Secondary constrictions and nucleolus organizer regions in man. Exp Cell Res (1977) 0.82
Use of an interactive tool to assess patients' willingness-to-pay. J Biomed Inform (2001) 0.81
Coenzyme Q10, exercise lactate and CTG trinucleotide expansion in myotonic dystrophy. Brain Res Bull (2001) 0.81
Nucleolus organizer and N-band distribution in morphologic and fluorescence variants of human chromosomes. Hum Genet (1977) 0.81
Epidemiology of myotonic dystrophy in Italy: re-apprisal after genetic diagnosis. Clin Genet (2001) 0.81
Assignment of the human nebulin gene (NEB) to chromosome band 2q24.2 and the alpha 1 (III) collagen gene (COL3A1) to chromosome band 2q32.2 by in situ hybridization; the FRA2G common fragile site lies between the two genes in the 2q31 band. Cytogenet Cell Genet (1997) 0.81
Effects of distamycin A on human leukocytes in vitro. Cytogenet Cell Genet (1979) 0.80
A non-syndromic hearing loss caused by very low levels of the mtDNA A3243G mutation. Acta Neurol Scand (2004) 0.79
A marker chromosome number 14 with double satellite obseved in two generations: an unbalanced chromosome constitution associated with normal phenotype. Humangenetik (1972) 0.79
[Osteo-articular amyloidosis caused by dialysis. Clinical and radiologic aspects]. Minerva Med (1990) 0.79
No evidence for allelic association of serotonin 2A receptor and transporter gene polymorphisms with depression in Alzheimer disease. J Alzheimers Dis (2006) 0.79
Tetracycline treatment in patients with progressive external ophthalmoplegia. Acta Neurol Scand (2011) 0.79
Oxidative stress and APO E polymorphisms in Alzheimer's disease and in mild cognitive impairment. Free Radic Res (2013) 0.79
Factors affecting patients' and potential patients' choices among anaesthetics for periodontal recall visits. J Dent (2001) 0.79
In-vacuum optical isolation changes by heating in a Faraday isolator. Appl Opt (2008) 0.78
Clustering of two fragile sites and seven homeobox genes in human chromosome region 2q31-->q32.1. Cytogenet Cell Genet (2000) 0.78
Study of the relationships between common fragile sites, chromosome breakages and sister chromatid exchanges. Mutagenesis (1995) 0.78
In-vacuum Faraday isolation remote tuning. Appl Opt (2010) 0.78
Health-related quality of life in patients with major depression who are treated with moclobemide. J Clin Psychopharmacol (1995) 0.77
Increasing the bandwidth of resonant gravitational antennas: the case of explorer. Phys Rev Lett (2003) 0.77
Myopathic involvement and mitochondrial pathology in Kennedy disease and in other motor neuron diseases. Curr Mol Med (2014) 0.77
Nucleotide sequence and chromosomal mapping of the 5S rDNA repeat of the crustacean Proasellus coxalis. Genome (1998) 0.76
Evaluation of cytogenetic and DNA damage in mitochondrial disease patients: effects of coenzyme Q10 therapy. Mutagenesis (2004) 0.76
Sex chromosome differentiation revealed by genomic in-situ hybridization. Chromosome Res (2000) 0.75
GATA repeats in the genome of Asellus aquaticus (Crustacea, Isopoda). Chromosoma (1991) 0.75
Facioscapulohumeral muscular dystrophy type 1A in northwestern Tuscany: a molecular genetics-based epidemiological and genotype-phenotype study. Genet Test (2005) 0.75
Potential involvement of ubiquinone in myotonic dystrophy pathophysiology: new diagnostic approaches for new rationale therapeutics. Neurol Sci (2000) 0.75
Assignment of FRA1H common fragile site to human chromosome band 1q42.1 proximal to the nuclear NAD+ ADP-ribosyltransferase gene (ADPRT) and to the main 5S rRNA gene locus. Cytogenet Cell Genet (1998) 0.75
DAPI-inducible common fragile sites. Cytogenet Cell Genet (1986) 0.75
Labelling of human chromosomes with 3H-AMD. Humangenetik (1974) 0.75
Effect of distamycin A on Chinese hamster chromosomes. Exp Cell Res (1977) 0.75
Correction of the wrong name of a fragile site associated to the DMD gene. Cytogenet Genome Res (2012) 0.75
Frequency of satellite association in individuals with structural abnormalities of nucleolus organiser region. Humangenetik (1973) 0.75
Popliteal cysts in chronic hemodialysis patients. Nephron (1990) 0.75
The effect of caffeine on DAPI-inducible fragile sites. Mutat Res (1992) 0.75
Dissection and atherosclerosis of carotid arteries in the young: role of the apolipoprotein E polymorphism. Eur J Neurol (2002) 0.75
[Diagnostic imaging for the study of popliteal masses in dialyzed patients]. Radiol Med (1991) 0.75
A state observer for the Virgo inverted pendulum. Rev Sci Instrum (2011) 0.75
[Acquired cystic kidney disease among hemodialysis patients: echographic and clinical study]. Arch Ital Urol Nefrol Androl (1991) 0.75
[Calcification of peritoneal cysts in a patient on periodic hemodialysis]. Radiol Med (1989) 0.75
Effect of Hoechst 33258 on Chinese hamster chromosomes. Chromosoma (1976) 0.75
Double satellites: autoradiographic study of a chromosomal marker observed in two generations. Humangenetik (1971) 0.75
[Radiologic and clinical aspects of osteoarticular amyloidosis caused by dialysis]. Radiol Med (1991) 0.75
Inhibition of human chromosome condensation induced by DAPI as related to cell cycle. Exp Cell Res (1981) 0.75
Effects of DAPI on human leukocytes in vitro. Cytogenet Cell Genet (1979) 0.75
Nucleolus organizer and satellite association in a variant D-group chromosome. Hum Genet (1976) 0.75
[Cyst of the urethral meatus]. Rev Argent Urol Nefrol (1969) 0.75
Visualizing human 5S rDNA. Chromosome Res (1997) 0.75
Effects of Hoechst 33258 on human leukocytes in vitro. Cytogenet Cell Genet (1976) 0.75
N-banding and nucleolus organisers in Asellus aquaticus (Crust. Isop.). Heredity (Edinb) (1977) 0.75
Ag staining of the nucleolus organizer (NO) and its relationship to satellite association. Hum Genet (1978) 0.75
Localization of silver staining in interphase, prophase and metaphase lymphocytes. Exp Cell Res (1978) 0.75
Autoradiographic study of DNA synthesis in homologous chromosomes distinguishable by morphology. Cytogenetics (1971) 0.75