Published in Int J Legal Med on December 04, 2008
Brief communication: DNA from early Holocene American dog. Am J Phys Anthropol (2011) 0.84
Developing equine mtDNA profiling for forensic application. Int J Legal Med (2010) 0.81
Identification of species by multiplex analysis of variable-length sequences. Nucleic Acids Res (2010) 0.80
Gapped BLAST and PSI-BLAST: a new generation of protein database search programs. Nucleic Acids Res (1997) 665.31
Multiple and ancient origins of the domestic dog. Science (1997) 27.18
Dynamics of mitochondrial DNA evolution in animals: amplification and sequencing with conserved primers. Proc Natl Acad Sci U S A (1989) 12.95
Length heteroplasmy of sturgeon mitochondrial DNA: an illegitimate elongation model. Genetics (1990) 1.65
Length and sequence variation in evening bat D-loop mtDNA. Genetics (1991) 1.58
Species identification by means of the cytochrome b gene. Int J Legal Med (2000) 1.58
Complete nucleotide sequences of the domestic cat (Felis catus) mitochondrial genome and a transposed mtDNA tandem repeat (Numt) in the nuclear genome. Genomics (1996) 1.46
Two universal primer sets for species identification among vertebrates. Int J Legal Med (2006) 1.35
Forensic informativity of domestic dog mtDNA control region sequences. Forensic Sci Int (2004) 1.29
Improved MtDNA sequence analysis of forensic remains using a "mini-primer set" amplification strategy. J Forensic Sci (2001) 1.11
Routine forensic use of the mitochondrial 12S ribosomal RNA gene for species identification. J Forensic Sci (2007) 1.10
Phylogenetic analysis of forensically important Lucilia flies based on cytochrome oxidase I sequence: a cautionary tale for forensic species determination. Int J Legal Med (2007) 1.04
Mitochondrial DNA sequencing of shed hairs and saliva on robbery caps: sensitivity and matching probabilities. J Forensic Sci (1998) 1.01
Validation of cytochrome b sequence analysis as a method of species identification. J Forensic Sci (2003) 0.98
Species determination: the role and use of the cytochrome b gene. Methods Mol Biol (2005) 0.96
An extremely sensitive species-specific ARMS PCR test for the presence of tiger bone DNA. Forensic Sci Int (2002) 0.96
Multiplex amplification of mitochondrial DNA for human and species identification in forensic evaluation. Forensic Sci Int (1999) 0.95
Molecular characterization of the canine mitochondrial DNA control region for forensic applications. Int J Legal Med (2007) 0.93
Standardisation of nomenclature for dog mtDNA D-loop: a prerequisite for launching a Canis familiaris database. Forensic Sci Int (2004) 0.93
A multiplex assay to identify 18 European mammal species from mixtures using the mitochondrial cytochrome b gene. Electrophoresis (2008) 0.89
Forensic mtDNA hair analysis excludes a dog from having caused a traffic accident. Int J Legal Med (1999) 0.87
A molecular genetic approach for forensic animal species identification. Forensic Sci Int (2003) 0.87
A molecular genetic approach for species identification of mammals and sex determination of birds in a forensic case of poaching from South Korea. Forensic Sci Int (2006) 0.84
Species identification by means of pyrosequencing the mitochondrial 12S rRNA gene. Int J Legal Med (2005) 0.83
Forensic mitochondrial DNA analysis of 116 casework skeletal samples. J Forensic Sci (2007) 0.82
Sequence analysis of domestic dog mitochondrial DNA for forensic use. J Forensic Sci (1997) 0.81
A simple and inexpensive molecular method for sexing and identification of the forensic samples of elephant origin. J Forensic Sci (2006) 0.81
Ivory identification by DNA profiling of cytochrome b gene. Int J Legal Med (2008) 0.80
Forensic identification of ungulate species using restriction digests of PCR-amplified mitochondrial DNA. J Forensic Sci (1995) 0.80
Development of species identification tests targeting the 16S ribosomal RNA coding region in mitochondrial DNA. Int J Legal Med (2006) 0.79
Application of mitochondrial DNA sequence analysis in the forensic identification of Chinese sika deer subspecies. Forensic Sci Int (2005) 0.79
A simple method for domestic animal identification in Argentina using PCR-RFLP analysis of cytochrome b gene. Leg Med (Tokyo) (2004) 0.79
Multiple nuclear pseudogenes of mitochondrial DNA exist in the canine genome. Mamm Genome (2002) 0.76
Ribosomal ribonucleic acid (rRNA) gene typing for species identification. J Forensic Sci (1992) 0.76
Heteroplasmies detected in an amplified mitochondrial DNA control region from a small amount of template. J Forensic Sci (2008) 0.75
Extreme mtDNA homogeneity in continental Asian populations. Am J Phys Anthropol (2002) 1.47
Multiplex amplified product-length polymorphism analysis of 36 mitochondrial single-nucleotide polymorphisms for haplogrouping of East Asian populations. Electrophoresis (2005) 1.06
De novo mutations in SLC35A2 encoding a UDP-galactose transporter cause early-onset epileptic encephalopathy. Hum Mutat (2013) 0.98
Caucasian-specific allele in non-synonymous single nucleotide polymorphisms of the gene encoding deoxyribonuclease I-like 3, potentially relevant to autoimmunity, produces an inactive enzyme. Clin Chim Acta (2009) 0.96
Association of functional gene polymorphisms of matrix metalloproteinase (MMP)-1, MMP-3 and MMP-9 with the progression of chronic liver disease. J Gastroenterol Hepatol (2005) 0.94
The genotypes of IL-1 beta and MMP-3 are associated with the prognosis of HCV-related hepatocellular carcinoma. Intern Med (2010) 0.90
Determination of ABO genotypes by real-time PCR using allele-specific primers. Leg Med (Tokyo) (2011) 0.87
Allele frequencies for 15 STR loci in Ovambo population using AmpFlSTR Identifiler Kit. Leg Med (Tokyo) (2008) 0.86
Global analysis of single nucleotide polymorphisms in the exons of human deoxyribonuclease I-like 1 and 2 genes. Electrophoresis (2010) 0.83
Genetic variants associated with arsenic metabolism within human arsenic (+3 oxidation state) methyltransferase show wide variation across multiple populations. Arch Toxicol (2010) 0.82
Genetic and expression analysis of all non-synonymous single nucleotide polymorphisms in the human deoxyribonuclease I-like 1 and 2 genes. Electrophoresis (2010) 0.82
The association of MMP-1, -3 and -9 genotypes with the prognosis of HCV-related hepatocellular carcinoma patients. Res Commun Mol Pathol Pharmacol (2005) 0.80
Three single nucleotide polymorphisms leading to non-synonymous amino acid substitution in the human ribonuclease 2 and angiogenin genes exhibit markedly less genetic heterogeneity in six populations. Cell Biochem Funct (2008) 0.80
A decreasing gradient of 374F allele frequencies in the skin pigmentation gene SLC45A2, from the north of West Europe to North Africa. Biochem Genet (2010) 0.79
Genetic and expression analysis of all 7 non-synonymous single nucleotide polymorphisms in the human deoxyribonuclease II gene, with potential relevance to autoimmunity. Clin Chim Acta (2009) 0.79
Complete mitochondrial DNA sequence of a tadpole shrimp (Triops cancriformis) and analysis of museum samples. Electrophoresis (2002) 0.78
Monozygotic twins discordant for Klippel-Feil syndrome. Pediatr Neurol (2006) 0.78
Transferrin mutations at the glycosylation site complicate diagnosis of congenital disorders of glycosylation type I. J Inherit Metab Dis (2011) 0.78
Simultaneous genotyping of 11 non-synonymous SNPs in the 4 glutathione peroxidase genes using the multiplex single base extension method. Clin Chim Acta (2008) 0.77
Near fixation of 374l allele frequencies of the skin pigmentation gene SLC45A2 in Africa. Biochem Genet (2013) 0.77
Variation of interleukin 8 -251 A>T polymorphism in worldwide populations and intra-ethnic differences in Japanese populations. Clin Chim Acta (2006) 0.77
Simultaneous determination of seven informative Y chromosome SNPs to differentiate East Asian, European, and African populations. Leg Med (Tokyo) (2011) 0.77
Novel nonsense mutation (R194X) in the PMM2 gene in a Japanese patient with congenital disorder of glycosylation type Ia. Brain Dev (2003) 0.76
Recent progress in mitochondrial DNA analysis. Leg Med (Tokyo) (2005) 0.76
Confirmation that SNPs in the high mobility group-A2 gene (HMGA2) are associated with adult height in the Japanese population; wide-ranging population survey of height-related SNPs in HMGA2. Electrophoresis (2011) 0.76
Allele frequencies of a SNP and a 27-bp deletion that are the determinant of earwax type in the ABCC11 gene. Leg Med (Tokyo) (2007) 0.75
Actin-inhibition and folding of vertebrate deoxyribonuclease I are affected by mutations at residues 67 and 114. Comp Biochem Physiol B Biochem Mol Biol (2005) 0.75
Global genetic analysis of all single nucleotide polymorphisms in exons of the human deoxyribonuclease I-like 3 gene and their effect on its catalytic activity. Electrophoresis (2011) 0.75
Parentally imprinted allele typing at a short tandem repeat locus in intron 1a of imprinted gene KCNQ1. Leg Med (Tokyo) (2006) 0.75
Replication study of the association of SNPs in the LHX3-QSOX2 and IGF1 loci with adult height in the Japanese population; wide-ranging comparison of each SNP genotype distribution. Leg Med (Tokyo) (2012) 0.75
Population genetics of 17 Y-chromosomal STR loci in Japanese. Forensic Sci Int Genet (2008) 0.75
Allele frequencies for nine STR loci in Ovambo population using AmpFlSTR Profiler Kit. Forensic Sci Int (2007) 0.75
Cutis laxa with frontoparietal cortical malformation: a novel type of congenital disorder of glycosylation. Eur J Paediatr Neurol (2008) 0.75
Origin and evolution of gene for prolactin-induced protein. Gene (2006) 0.75
Novel paternity testing by distinguishing parental alleles at a VNTR locus in the differentially methylated region upstream of the human H19 gene. J Forensic Sci (2003) 0.75
Nonsynonymous single-nucleotide polymorphisms of the human apoptosis-related endonuclease--DNA fragmentation factor beta polypeptide, endonuclease G, and Flap endonuclease-1--genes show a low degree of genetic heterogeneity. DNA Cell Biol (2011) 0.75
Development of genotyping methods for single nucleotide polymorphism in the human pancreatic ribonuclease gene (RNASE1) and their application to population studies. Biochem Genet (2008) 0.75
Analysis of genetic polymorphism of deoxyribonuclease I in Ovambo and Turk populations using a genotyping method. Biochem Genet (2005) 0.75
A novel 56-bp variable tandem repeat polymorphism in the human deoxyribonuclease I gene and its population data. Leg Med (Tokyo) (2004) 0.75
Allele frequencies and haplotypes for 28 Y-STRs in Ovambo population. Leg Med (Tokyo) (2009) 0.75