Published in Acta Biochim Pol on January 01, 1976
Genome fingerprinting by simple sequence repeat (SSR)-anchored polymerase chain reaction amplification. Genomics (1994) 6.40
Risk of childhood leukemia associated with exposure to pesticides and with gene polymorphisms. Epidemiology (1999) 2.85
Alu sequences in the coding regions of mRNA: a source of protein variability. Trends Genet (1994) 2.49
Standardized nomenclature for Alu repeats. J Mol Evol (1996) 2.00
Ethiopia: between Sub-Saharan Africa and western Eurasia. Ann Hum Genet (2005) 1.98
Relationship between 2'-hydroxyls and magnesium binding in the hammerhead RNA domain: a model for ribozyme catalysis. Biochemistry (1991) 1.75
Genetic structure of the ancestral population of modern humans. J Mol Evol (1998) 1.70
Linkage disequilibrium analysis in young populations: pseudo-vitamin D-deficiency rickets and the founder effect in French Canadians. Am J Hum Genet (1996) 1.68
Reverse transcriptase activity from human embryonal carcinoma cells NTera2D1. EMBO J (1990) 1.68
Alu RNA secondary structure consists of two independent 7 SL RNA-like folding units. J Biol Chem (1991) 1.60
Phylogenetic and familial estimates of mitochondrial substitution rates: study of control region mutations in deep-rooting pedigrees. Am J Hum Genet (2001) 1.59
Splice-mediated insertion of an Alu sequence inactivates ornithine delta-aminotransferase: a role for Alu elements in human mutation. Proc Natl Acad Sci U S A (1991) 1.56
The gene for incontinentia pigmenti is assigned to Xq28. Genomics (1989) 1.52
CORE-SINEs: eukaryotic short interspersed retroposing elements with common sequence motifs. Proc Natl Acad Sci U S A (1999) 1.50
Susceptibility to childhood acute lymphoblastic leukemia: influence of CYP1A1, CYP2D6, GSTM1, and GSTT1 genetic polymorphisms. Blood (1999) 1.45
Prostate cancer susceptibility genes: lessons learned and challenges posed. Endocr Relat Cancer (2003) 1.44
Phylogenetic analysis of a reported complementary DNA sequence. Science (1994) 1.43
Is selection responsible for the low level of variation in the last intron of the ZFY locus? Mol Biol Evol (1999) 1.42
Alu RNA transcripts in human embryonal carcinoma cells. Model of post-transcriptional selection of master sequences. J Mol Biol (1992) 1.40
Mixed DNA/RNA polymers are cleaved by the hammerhead ribozyme. Biochemistry (1990) 1.35
The genetic clock and the age of the founder effect in growing populations: a lesson from French Canadians and Ashkenazim. Am J Hum Genet (1997) 1.32
Ubiquitous mammalian-wide interspersed repeats (MIRs) are molecular fossils from the mesozoic era. Nucleic Acids Res (1995) 1.29
Nuclear DNA diversity in worldwide distributed human populations. Gene (1997) 1.22
Spatial and temporal distribution of the neutral polymorphisms in the last ZFX intron: analysis of the haplotype structure and genealogy. Genetics (1999) 1.21
Alumorphs--human DNA polymorphisms detected by polymerase chain reaction using Alu-specific primers. Genomics (1990) 1.14
mtDNA and Y chromosome-specific polymorphisms in modern Ojibwa: implications about the origin of their gene pool. Am J Hum Genet (1997) 1.09
Use of gamma irradiation to eliminate DNA contamination for PCR. Nucleic Acids Res (1990) 1.09
Evolutionary inventions and continuity of CORE-SINEs in mammals. J Mol Biol (2000) 1.07
Genetic susceptibility to childhood acute lymphoblastic leukemia. Leuk Lymphoma (2000) 1.07
High resolution deletion mapping reveals frequent allelic losses at the DNA mismatch repair loci hMLH1 and hMSH3 in non-small cell lung cancer. Int J Cancer (1998) 1.03
Linkage study of chronic childhood-onset spinal muscular atrophy (SMA): confirmation of close linkage to D5S39 in French Canadian families. Genomics (1992) 1.01
A young Alu subfamily amplified independently in human and African great apes lineages. Nucleic Acids Res (1994) 1.01
Unique origin and specific ethnic distribution of the Friedreich ataxia GAA expansion. Neurology (2000) 1.01
Monophyletic origin of Alu elements in primates. J Mol Evol (1998) 1.00
Analysis of nucleotide diversity of NAT2 coding region reveals homogeneity across Native American populations and high intra-population diversity. Pharmacogenomics J (2006) 1.00
Linkage mapping by simultaneous screening of multiple polymorphic loci using Alu oligonucleotide-directed PCR. Proc Natl Acad Sci U S A (1992) 0.99
Genetic susceptibility to breast cancer in French-Canadians: role of carcinogen-metabolizing enzymes and gene-environment interactions. Int J Cancer (2001) 0.99
Age and origin of major Smith-Lemli-Opitz syndrome (SLOS) mutations in European populations. J Med Genet (2007) 0.96
Mechanism of codon recognition by transfer RNA and codon-induced tRNA association. J Mol Biol (1984) 0.94
Deletions in the dystrophin gene: analysis of Duchenne and Becker muscular dystrophy patients in Quebec. Hum Genet (1992) 0.93
Phylogenetic affinities of tarsier in the context of primate Alu repeats. Mol Phylogenet Evol (1999) 0.92
Multistep mechanism of codon recognition by transfer ribonucleic acid. Biochemistry (1980) 0.92
Is Tb3+ fluorescence enhancement only due to binding to single stranded polynucleotides. Nucleic Acids Res (1981) 0.92
Magnesium ion inner sphere complex in the anticodon loop of phenylalanine transfer ribonucleic acid. Biochemistry (1982) 0.91
A nuclear tRNA(UGASer) gene from the wheat Triticum vulgare var. Aria. Gene (1989) 0.90
Parental smoking, CYP1A1 genetic polymorphisms and childhood leukemia (Québec, Canada). Cancer Causes Control (2000) 0.90
Codon-induced transfer RNA association. A property of transfer RNA involved in its adaptor function? J Mol Biol (1983) 0.90
Frequent loss of heterozygosity at the DNA mismatch-repair loci hMLH1 and hMSH3 in sporadic breast cancer. Br J Cancer (1999) 0.90
Human mitochondrial HMG CoA synthase: liver cDNA and partial genomic cloning, chromosome mapping to 1p12-p13, and possible role in vertebrate evolution. Genomics (1994) 0.89
Mosaic evolution of rodent B1 elements. J Mol Evol (1996) 0.87
Iodo-Gen-mediated radioiodination of nucleic acids. Anal Biochem (1988) 0.87
Single-strand conformational polymorphisms (SSCP): detection of useful polymorphisms at the dystrophin locus. Hum Genet (1992) 0.87
Genetic polymorphisms of N-acetyltransferases 1 and 2 and gene-gene interaction in the susceptibility to childhood acute lymphoblastic leukemia. Cancer Epidemiol Biomarkers Prev (2000) 0.87
Are CpG sites mutation hot spots in the dystrophin gene? Hum Mol Genet (1994) 0.84
Small cytoplasmic Ro RNA pseudogene and an Alu repeat in the human alpha-1 globin gene. Nucleic Acids Res (1988) 0.84
Detection of a mutator phenotype in cancer cells by inter-Alu polymerase chain reaction. Cancer Res (1996) 0.84
Mechanism of codon recognition by transfer RNA studied with oligonucleotides larger than triplets. Nucleic Acids Res (1985) 0.83
Genomic loci susceptible to replication errors in cancer cells. Br J Cancer (1998) 0.82
Codon-induced transfer ribonucleic acid association: quantitative analysis by sedimentation equilibrium. Biochemistry (1982) 0.82
The three conformations of the anticodon loop of yeast tRNA(Phe). J Biomol Struct Dyn (1989) 0.82
Overall informativity, OI, in DNA polymorphisms revealed by inter-Alu PCR: detection of genomic rearrangements. Genomics (1996) 0.81
Fraction of informative recombinations: a heuristic approach to analyze recombination rates. Genetics (2008) 0.81
Chromosomal assignment of loci susceptible to replication errors by radiation hybrid mapping. Mutat Res (1998) 0.80
Childhood acute lymphoblastic leukemia: genetic determinants of susceptibility and disease outcome. Rev Environ Health (2002) 0.80
Distribution of the mammalian-wide interspersed repeats (MIRs) in the isochores of the human genome. FEBS Lett (1998) 0.79
Allelic losses and DNA methylation at DNA mismatch repair loci in sporadic colorectal cancer. Carcinogenesis (1998) 0.79
Codon:anticodon and anticodon:anticodon interaction: evaluation of equilibrium and kinetic parameters of complexes involving a g:u wobble. Biochim Biophys Acta (1982) 0.79
Desalting of RPC-5 oligonucleotides on Dowex 50. Anal Biochem (1975) 0.79
Isolation and chromatographic behaviour of phenylalanine tRNA from barley embryos. Nucleic Acids Res (1974) 0.79
Aminoacids and the anticodon: anticodon interaction: a test of the stereochemical hypothesis? Biochimie (1981) 0.79
Dependence of tRNA structure in solution upon ionic condition of the solvent. Fluorescence studies of monovalent cation binding to tRNAPhe from barley embryos. Eur J Biochem (1977) 0.78
Direct analysis of amniotic fluid cells by multiplex PCR provides rapid prenatal diagnosis for Duchenne muscular dystrophy. Nucleic Acids Res (1991) 0.77
Anhydride-type basic artifacts of amino acids. Anal Biochem (1966) 0.77
Cooperativity in low-affinity Mg2+ binding to tRNA. J Biol Chem (1985) 0.77
Carrier status diagnosis in Duchenne muscular dystrophy with "conformational" DNA polymorphism. Lancet (1992) 0.77
Effect of nuclear matrix attachment regions on transgene expression in tobacco plants. Acta Biochim Pol (2001) 0.76
Lipid processing and lipoprotein synthesis by the developing human fetal colon. Am J Physiol (1996) 0.75
Conserved signals in the 5' flanking region of eukaryotic nuclear tRNA genes. DNA Seq (1992) 0.75
Leber's congenital amaurosis with Duchenne's muscular dystrophy. Can J Ophthalmol (1990) 0.75
Dependence of tRNA structure in solution upon ionic condition of the solvent. Fluorescence studies of Mg2+ binding to tRNAPhe from barley embryos. Eur J Biochem (1977) 0.75
Complementary DNA for 12-kilodalton B cell growth factor: misassigned. Science (1996) 0.75
An attempt at application of tRNA genes as promoters of protein-coding genes in transgenic plants. Acta Biochim Pol (1994) 0.75
Efficiency of biotin end-labeling of DNA fragments is rapidly tested by gel retardation with streptavidin analog. Biotechniques (1991) 0.75
A novel RNA digesting activity from commercial polynucleotide phosphorylase. FEBS Lett (1985) 0.75
Apparent cooperativity of cation binding to protonated transfer RNA measured by quantitation of released protons. Biochem Biophys Res Commun (1978) 0.75
Changes in thymocytes undergoing programmed death. Acta Biochim Pol (1992) 0.75
Effect of sodium ion concentration on transfer RNA conformation in solution studied by Rayleigh light scattering. Acta Biochim Pol (1981) 0.75
The nature of the basic compound formed from 2,5-diketopiperazine in acidic medium. Acta Biochim Pol (1965) 0.75
Nucleotide sequence of the coat protein gene of the Skierniewice isolate of plum pox virus (PPV). Acta Biochim Pol (1994) 0.75
Prenatal diagnosis using DNA probes in twins at risk for Duchenne muscular dystrophy. Lancet (1986) 0.75
Allelic instability of TBP gene in replication error positive tumors. Int J Cancer (1998) 0.75
Expression of the plum pox coat protein gene in transgenic Nicotiana tabacum plants. Acta Biochim Pol (1995) 0.75
G proteins in normal rat pituitaries and in prolactin-secreting rat pituitary tumors. Mol Cell Endocrinol (1991) 0.75
Salt induced deprotonation of initially salt-free transfer RNA. Biochem Biophys Res Commun (1976) 0.75
Lesch-Nyhan syndrome: molecular investigation of three French Canadian families using a hypoxanthine-guanine phosphoribosyltransferase cDNA probe. Hum Genet (1988) 0.75
Neutral polymorphisms in the deletion-prone regions of the dystrophin gene. Hum Hered (1995) 0.75
Complementary DNA for 12-kilodalton B cell growth factor: misassigned. Science (1996) 0.75