Published in Genomics on February 01, 1991
The human enamel protein gene amelogenin is expressed from both the X and the Y chromosomes. Am J Hum Genet (1992) 2.02
Possible association of amelogenin to high caries experience in a Guatemalan-Mayan population. Caries Res (2007) 1.67
The amelogenin loci span an ancient pseudoautosomal boundary in diverse mammalian species. Proc Natl Acad Sci U S A (2003) 1.64
Enamel formation genes are associated with high caries experience in Turkish children. Caries Res (2008) 1.57
Rare failures in the amelogenin sex test. Int J Legal Med (2002) 1.57
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Sex determination in highly fragmented human DNA by high-resolution melting (HRM) analysis. PLoS One (2014) 1.48
Identification and characterization of amelogenin genes in monotremes, reptiles, and amphibians. Proc Natl Acad Sci U S A (1998) 1.43
Partial rescue of the amelogenin null dental enamel phenotype. J Biol Chem (2008) 1.19
A large interstitial deletion encompassing the amelogenin gene on the short arm of the Y chromosome. Hum Genet (2005) 1.13
Deletions in the Y-derived amelogenin gene fragment in the Indian population. BMC Med Genet (2006) 1.07
Human beta-globin gene polymorphisms characterized in DNA extracted from ancient bones 12,000 years old. Am J Hum Genet (1995) 1.01
A model for the molecular underpinnings of tooth defects in Axenfeld-Rieger syndrome. Hum Mol Genet (2013) 1.00
Quantifying the relative amount of mouse and human DNA in cancer xenografts using species-specific variation in gene length. Biotechniques (2010) 0.94
Binding of amelogenin to MMP-9 and their co-expression in developing mouse teeth. J Mol Histol (2012) 0.92
Attachment of benzaldehyde-modified oligodeoxynucleotide probes to semicarbazide-coated glass. Nucleic Acids Res (2001) 0.90
The Human Y Chromosome: The Biological Role of a "Functional Wasteland" J Biomed Biotechnol (2001) 0.88
Y chromosome interstitial deletion induced Y-STR allele dropout in AMELY-negative individuals. Int J Legal Med (2012) 0.86
Constitutional duplication of a region of chromosome Yp encoding AMELY, PRKY, and TBL1Y: implications for sex chromosome analysis and bone marrow engraftment analysis. J Mol Diagn (2007) 0.86
Analysis of radiocarbon, stable isotopes and DNA in teeth to facilitate identification of unknown decedents. PLoS One (2013) 0.85
TBX1 protein interactions and microRNA-96-5p regulation controls cell proliferation during craniofacial and dental development: implications for 22q11.2 deletion syndrome. Hum Mol Genet (2015) 0.84
"GenderPlex" a PCR multiplex for reliable gender determination of degraded human DNA samples and complex gender constellations. Int J Legal Med (2008) 0.83
Prenatal detection of fetal aneuploidies using transcervical cell samples. J Med Genet (1997) 0.81
Dental Evidence in Forensic Identification - An Overview, Methodology and Present Status. Open Dent J (2015) 0.81
An accurate and rapid gender determination assay in single cells by the capillary polymerase chain reaction method. J Assist Reprod Genet (1999) 0.80
Porcine Amelogenin : Alternative Splicing, Proteolytic Processing, Protein - Protein Interactions, and Possible Functions. J Oral Biosci (2011) 0.80
Molecular characterization of a polymorphic 3-Mb deletion at chromosome Yp11.2 containing the AMELY locus in Singapore and Malaysia populations. Hum Genet (2007) 0.79
Graft-versus-host disease after kidney transplantation. J Korean Surg Soc (2011) 0.79
Null alleles of the X and Y chromosomal amelogenin gene in a Chinese population. Int J Legal Med (2011) 0.78
Uniparental ancestry markers in Chilean populations. Genet Mol Biol (2016) 0.77
A pituitary homeobox 2 (Pitx2):microRNA-200a-3p:β-catenin pathway converts mesenchymal cells to amelogenin-expressing dental epithelial cells. J Biol Chem (2014) 0.76
Species and sex identification of western lowland gorillas (Gorilla gorilla gorilla), eastern lowland gorillas (Gorilla beringei graueri) and humans. Primates (2005) 0.76
Prenatal sex determination in suspicious cases of X-linked recessive diseases by the amelogenin gene. Iran J Basic Med Sci (2014) 0.75
New nucleotide sequence data on the EMBL File Server. Nucleic Acids Res (1991) 0.75
Differential pattern of genetic variability at the DXYS156 locus on homologous regions of X and Y chromosomes in Indian population and its forensic implications. Int J Legal Med (2011) 0.75
Gestational Age and Sex Influence the Susceptibility of Human Neural Progenitor Cells to Low Levels of MeHg. Neurotox Res (2017) 0.75
Distinct breakpoints in two cases with deletion in the Yp11.2 region in Japanese population. Hum Genet (2010) 0.75
An ancient retrotransposal insertion causes Fukuyama-type congenital muscular dystrophy. Nature (1998) 3.86
L1 family of repetitive DNA sequences in primates may be derived from a sequence encoding a reverse transcriptase-related protein. Nature (1986) 2.66
A deletion in the amelogenin gene (AMG) causes X-linked amelogenesis imperfecta (AIH1). Genomics (1991) 1.99
Reactions of glyoxal with nucleic acids. Nucleotides and their component bases. Biochim Biophys Acta (1968) 1.83
Conflict among individual mitochondrial proteins in resolving the phylogeny of eutherian orders. J Mol Evol (1998) 1.74
Prenatal sex determination. Lancet (1990) 1.41
A human Y-chromosome specific repeated DNA family (DYZ1) consists of a tandem array of pentanucleotides. Nucleic Acids Res (1986) 1.34
Contrasting patterns of polymorphisms at the ABO-secretor gene (FUT2) and plasma alpha(1,3)fucosyltransferase gene (FUT6) in human populations. Genetics (2001) 1.30
Dichromatism in macaque monkeys. Nature (1999) 1.23
Restriction fragment length polymorphisms of the human N-myc gene: relationship to gene amplification. Oncogene (1987) 1.22
Sex identification by polymerase chain reaction using X-Y homologous primer. Am J Med Genet (1991) 1.14
Microsatellites in the bottlenose dolphin Tursiops truncatus. Mol Ecol (1997) 1.12
Mental retardation, malformation syndrome andpartial 7p monosomy [45, XX, tdic (7;15) (p21;p11)]. Clin Genet (1976) 1.10
Isolation and phylogeny of endogenous retrovirus sequences belonging to the HERV-W family in primates. J Gen Virol (1999) 1.07
A 6p trisomy detected in a family with a "giant satellite". Humangenetik (1975) 1.06
The LINE-1 family of primates may encode a reverse transcriptase-like protein. Cold Spring Harb Symp Quant Biol (1986) 1.06
LBA technique in the detection of chromosome variants. II. Chromosomes except for those with Q variants. Hum Genet (1977) 1.01
Diagnosis of twin zygosity by hypervariable RFLP markers. Am J Med Genet (1991) 1.01
A truncated immunoglobulin epsilon pseudogene is found in gorilla and man but not in chimpanzee. Proc Natl Acad Sci U S A (1985) 1.00
Points of exchange in a human no. 5 ring chromosome. Cytogenet Cell Genet (1973) 0.99
Serological survey and virus isolation of simian T-cell leukemia/T-lymphotropic virus type I (STLV-I) in non-human primates in their native countries. Int J Cancer (1987) 0.98
Evaluation of long-term results of Caroli's disease: 21 years' observation of a family with autosomal "dominant" inheritance, and review of the literature. Hepatogastroenterology (1995) 0.95
A minute deletion of the Y chromosome in men with azoospermia. J Urol (1993) 0.95
Partial tetrasomy 9(9pter to 9q2101) due to an extra iso-dicentric chromosome. Ann Genet (1977) 0.95
Two cases of 8p trisomy in one sibship. Clin Genet (1975) 0.95
Trisomy 10 with mosaicism. A clinical and cytogenetic entity. Jinrui Idengaku Zasshi (1973) 0.95
High-resolution banding by treating cells with acridine orange before fixation. Cytogenet Cell Genet (1983) 0.95
A case of (13q;18q) translocation with proximal 13q monosomy. Hum Genet (1977) 0.94
Hypervariable microsatellite loci in the Japanese macaque (Macaca fuscata) conserved in related species. Am J Primatol (1997) 0.93
Identification of translocated chromosomes by means of autoradiography. Paediatr Univ Tokyo (1967) 0.91
Chondrodysplasia punctata with X;Y translocation. Hum Genet (1988) 0.91
Chromosomal localisation of a Y specific growth gene(s). J Med Genet (1995) 0.91
Ancient origin of the null allele se(428) of the human ABO-secretor locus (FUT2). J Mol Evol (2000) 0.91
G-group chromosomes in satellite associations. Cytogenet Cell Genet (1973) 0.90
Molecular phylogeny of gibbons inferred from mitochondrial DNA sequences: preliminary report. J Mol Evol (1995) 0.90
GT dinucleotide repeat polymorphisms in a polygynous ant, Leptothorax spinosior and their use for measurement of relatedness. Naturwissenschaften (1993) 0.89
Sex determination of forensic samples by dual PCR amplification of an X-Y homologous gene. Forensic Sci Int (1992) 0.89
Two 47z [DXYS5] RFLPs on the X and the Y chromosome. Nucleic Acids Res (1989) 0.87
Genetic identity of Fukuyama-type congenital muscular dystrophy and Walker-Warburg syndrome. Ann Neurol (1995) 0.87
A malformed girl with duplication of chromosome 9q. J Med Genet (1984) 0.87
The L1 family (KpnI family) sequence near the 3' end of human beta-globin gene may have been derived from an active L1 sequence. Nucleic Acids Res (1987) 0.87
The "loss" of centromeres from chromosomes of aged women. Am J Hum Genet (1984) 0.87
Molecular cloning and mapping of 10 new probes on the human Y chromosome. Genomics (1991) 0.86
Primary structure of the inorganic pyrophosphatase from thermophilic bacterium PS-3. J Biochem (1990) 0.86
Trisomy 9 mosaicism with punctate mineralization in developing cartilages. Eur J Pediatr (1979) 0.86
Amplification of N-myc in a rhabdomyosarcoma. Jpn J Cancer Res (1986) 0.86
Dermatoglyphic study of Down's syndrome in Japan. Paediatr Univ Tokyo (1966) 0.85
Similar chromosomal patterns and lack of N-myc gene amplification in localized and IV-S stage neuroblastomas in infants. Med Pediatr Oncol (1989) 0.85
Lipoprotein(a) in nonhuman primates. Presence and characteristics of Lp(a) immunoreactive materials using anti-human Lp(a) serum. Atherosclerosis (1989) 0.85
Phylogenetic analysis of a retroposon family in african great apes. J Mol Evol (1999) 0.85
A comparison of TSPY genes from Y-chromosomal DNA of the great apes and humans: sequence, evolution, and phylogeny. Am J Phys Anthropol (1996) 0.84
Population differences in DNA sequence variation and linkage disequilibrium at the PON1 gene. Ann Hum Genet (2004) 0.84
Down's syndrome: chromosome analysis in 321 cases in Japan. J Med Genet (1969) 0.83
PCR detection of structurally abnormal Y chromosomes. Jpn J Hum Genet (1992) 0.83
Mitochondrial 16S rRNA sequence diversity of hominoids. J Hered (2002) 0.83
Genomic and spectral analyses of long to middle wavelength-sensitive visual pigments of common marmoset (Callithrix jacchus). Gene (2001) 0.83
A unique origin and multistep process for the generation of expanded DRPLA triplet repeats. Hum Mol Genet (1996) 0.83
Fluorescence of Barr body in human amniotic-fluid cells. Lancet (1973) 0.83
A novel nonsense mutation in the HMG box of the SRY gene in a patient with XY sex reversal. Hum Mol Genet (1994) 0.83
Mental retardation and congenital malformations associated with a ring chromosome 9. Hum Genet (1976) 0.83
The loss of centromeric heterochromatin from an inactivated centromere of a dicentric chromosome. Jinrui Idengaku Zasshi (1986) 0.82
Distribution of break points in human structural rearrangements. Am J Hum Genet (1983) 0.81
High-resolution studies in patients with aniridia-Wilms tumor association, Wilms tumor or related congenital abnormalities. Hum Genet (1984) 0.81
Nonrandom distribution of exchange points in patients with structural rearrangements. Am J Hum Genet (1976) 0.81
Effects of single and multiple injections of ketamine hydrochloride on serum hormone concentrations in male cynomolgus monkeys. Lab Anim Sci (1998) 0.81
DNA replication studies of human D-group chromosomes in satellite associations. Cytogenetics (1969) 0.81
High-resolution studies in patients with aniridia-Wilms tumor association. Hum Genet (1985) 0.81
Purification and characterization of goat pepsinogens and pepsins. Comp Biochem Physiol B Biochem Mol Biol (1999) 0.80
SINE-R.C2 (a Homo sapiens specific retroposon) is homologous to CDNA from postmortem brain in schizophrenia and to two loci in the Xq21.3/Yp block linked to handedness and psychosis. Am J Med Genet (1999) 0.80
Linkage-disequilibrium mapping narrows the Fukuyama-type congenital muscular dystrophy (FCMD) candidate region to <100 kb. Am J Hum Genet (1996) 0.80
Cloning and nucleotide sequence of retroposons specific to hominoid primates derived from an endogenous retrovirus (HERV-K). AIDS Res Hum Retroviruses (1999) 0.80
Nucleotide sequence analyses of human complement 6 (C6) gene suggest balancing selection. Ann Hum Genet (2005) 0.80
Species identification of blood and bloodstains by high-performance liquid chromatography. Int J Legal Med (1990) 0.80
Three translocations involving C- or G-group chromosomes. J Med Genet (1973) 0.79
Pitfalls in the use of chromosome variants for paternity dispute cases. Hum Genet (1977) 0.79
Restriction fragment length polymorphisms of the CYP11B1 gene in the Japanese population. Jpn J Hum Genet (1993) 0.79
Guidelines for genetic testing. The Japan Society of Human Genetics, Council Committee of Ethics. J Hum Genet (2001) 0.79
Experimental chemonucleolysis with chondroitinase ABC in monkeys. Spine (Phila Pa 1976) (1996) 0.79
Porcine muscle prolyl endopeptidase: limited proteolysis of tryptic peptides from hemoglobin beta-chains at prolyl and alanyl bonds. Biochim Biophys Acta (1988) 0.79
Effects of rabeprazole, a gastric proton pump inhibitor, on biliary and hepatic lysosomal enzymes in rats. Jpn J Pharmacol (1998) 0.79
Alterations in glutathione homeostasis in mutant Eisai hyperbilirubinemic rats. Hepatology (1996) 0.79
Sex identification of forensic specimens by polymerase chain reaction (PCR): two alternative methods. Forensic Sci Int (1991) 0.78
Detection of engraftment and chimerism after bone marrow transplantation by in situ hybridization using a Y-chromosome specific probe. Am J Hematol (1990) 0.78
Epitope expression on primate lymphocyte surface antigens. J Med Primatol (1986) 0.78
Novel hemoglobin components and their amino acid sequences from the crab-eating macaque (Macaca fascicularis). J Mol Evol (1989) 0.78
11q trisomy detected by fluorescence in situ hybridization. Clin Genet (1993) 0.78
Electroretinogram analysis of relative spectral sensitivity in genetically identified dichromatic macaques. Proc Natl Acad Sci U S A (2001) 0.78
YAC and cosmid contigs encompassing the Fukuyama-type congenital muscular dystrophy (FCMD) candidate region on 9q31. Genomics (1997) 0.78
The CpG island of the FMR-1 gene is methylated differently among embryonic tissues: implication for prenatal diagnosis. Hum Reprod (1994) 0.78
Molecular features of the TSPY gene of gibbons and Old World monkeys. Chromosome Res (1996) 0.78
[DNA PCR typing of non-human primates]. Anthropol Anz (2001) 0.78
Normal Y sequences in Smith-Lemli-Opitz syndrome with total failure of masculinization. Acta Paediatr (1992) 0.78
Sodium trichloroacetate-induced helical conformation of poly(L-lysine). Biochim Biophys Acta (1976) 0.78
Antibodies to an NH2-terminal myristoyl glycine moiety can detect NH2-terminal myristoylated proteins in the retrovirus-infected cells. Biochem Biophys Res Commun (1989) 0.78
Structural variations of the VWA locus in humans and comparison with non-human primates. Forensic Sci Int (2000) 0.78
Maternally transmitted extra ring (21) chromosome in a boy with Down's syndrome. Hum Genet (1982) 0.77
Familial cases of Down's syndrome a psu dic (21) (q22) and a rob (14q21q) in cousins. Jinrui Idengaku Zasshi (1981) 0.77