Published in BMC Med Genet on August 08, 2007
Hereditary dentine disorders: dentinogenesis imperfecta and dentine dysplasia. Orphanet J Rare Dis (2008) 1.66
Porcine dentin sialophosphoprotein: length polymorphisms, glycosylation, phosphorylation, and stability. J Biol Chem (2008) 1.10
A dentin sialophosphoprotein mutation that partially disrupts a splice acceptor site causes type II dentin dysplasia. J Endod (2008) 1.03
A novel DSPP mutation causes dentinogenesis imperfecta type II in a large Mongolian family. BMC Med Genet (2010) 0.94
Isolated dentinogenesis imperfecta and dentin dysplasia: revision of the classification. Eur J Hum Genet (2014) 0.92
Enamel malformations associated with a defined dentin sialophosphoprotein mutation in two families. Eur J Oral Sci (2011) 0.90
Porcine dentin sialoprotein glycosylation and glycosaminoglycan attachments. BMC Biochem (2011) 0.84
A novel splicing mutation alters DSPP transcription and leads to dentinogenesis imperfecta type II. PLoS One (2011) 0.81
Phenotype characterization and DSPP mutational analysis of three Brazilian dentinogenesis imperfecta type II families. Cells Tissues Organs (2008) 0.80
A DSPP mutation causing dentinogenesis imperfecta and characterization of the mutational effect. Biomed Res Int (2012) 0.78
Detection of a Novel DSPP Mutation by NGS in a Population Isolate in Madagascar. Front Physiol (2016) 0.75
The dentin phosphoprotein repeat region and inherited defects of dentin. Mol Genet Genomic Med (2015) 0.75
Dentin sialophosphoprotein knockout mouse teeth display widened predentin zone and develop defective dentin mineralization similar to human dentinogenesis imperfecta type III. J Biol Chem (2003) 3.03
Dentinogenesis imperfecta 1 with or without progressive hearing loss is associated with distinct mutations in DSPP. Nat Genet (2001) 2.75
Dentin phosphoprotein and dentin sialoprotein are cleavage products expressed from a single transcript coded by a gene on human chromosome 4. Dentin phosphoprotein DNA sequence determination. J Biol Chem (1997) 2.69
DSPP mutation in dentinogenesis imperfecta Shields type II. Nat Genet (2001) 2.39
A proposed classification for heritable human dentine defects with a description of a new entity. Arch Oral Biol (1973) 2.16
Hereditary defects in enamel and dentin. Acta Genet Stat Med (1957) 2.06
Mutation of the signal peptide region of the bicistronic gene DSPP affects translocation to the endoplasmic reticulum and results in defective dentine biomineralization. Hum Mol Genet (2002) 1.64
Cloning and sequence determination of rat dentin sialoprotein, a novel dentin protein. J Biol Chem (1994) 1.48
A novel splice acceptor mutation in the DSPP gene causing dentinogenesis imperfecta type II. Hum Genet (2004) 1.45
Splicing site mutations in dentin sialophosphoprotein causing dentinogenesis imperfecta type II. Eur J Oral Sci (2006) 1.42
Manifestations of genetic diseases in the human pulp. Oral Surg Oral Med Oral Pathol (1971) 1.40
Dentin glycoprotein: the protein in the middle of the dentin sialophosphoprotein chimera. J Biol Chem (2005) 1.38
Porcine dentin sialoprotein is a proteoglycan with glycosaminoglycan chains containing chondroitin 6-sulfate. J Biol Chem (2004) 1.33
Clinical, histopathologic, and genetic investigation in two large families with dentinogenesis imperfecta type II. Hum Genet (2004) 1.30
Mutational hot spot in the DSPP gene causing dentinogenesis imperfecta type II. Hum Genet (2004) 1.26
Dentin sialoprotein and dentin phosphoprotein overexpression during amelogenesis. J Biol Chem (2005) 1.24
Phenotypes and genotypes in 2 DGI families with different DSPP mutations. Oral Surg Oral Med Oral Pathol Oral Radiol Endod (2006) 1.15
Dentin phosphoprotein compound mutation in dentin sialophosphoprotein causes dentinogenesis imperfecta type III. Am J Med Genet A (2005) 1.15
Utilization of MO6-G3 immortalized odontoblast cells in studies regarding dentinogenesis. Adv Dent Res (2001) 0.80
HTRA1 promoter polymorphism in wet age-related macular degeneration. Science (2006) 7.12
A review of group ICA for fMRI data and ICA for joint inference of imaging, genetic, and ERP data. Neuroimage (2008) 3.91
Dissecting the unique role of the retinoblastoma tumor suppressor during cellular senescence. Cancer Cell (2010) 3.81
Suppression of tumorigenesis by the p53 target PUMA. Proc Natl Acad Sci U S A (2004) 3.42
Mutations in SLC20A2 link familial idiopathic basal ganglia calcification with phosphate homeostasis. Nat Genet (2012) 3.34
Calcium-sensitive potassium channelopathy in human epilepsy and paroxysmal movement disorder. Nat Genet (2005) 3.32
Moxifloxacin versus ethambutol in the first 2 months of treatment for pulmonary tuberculosis. Am J Respir Crit Care Med (2006) 3.20
Identification of an angiogenic factor that when mutated causes susceptibility to Klippel-Trenaunay syndrome. Nature (2004) 2.90
Genetic susceptibility to myocardial infarction and coronary artery disease. Hum Mol Genet (2006) 2.76
Mouse models of human AML accurately predict chemotherapy response. Genes Dev (2009) 2.75
Non-cell-autonomous tumor suppression by p53. Cell (2013) 2.40
Pharmacokinetics of rifapentine at 600, 900, and 1,200 mg during once-weekly tuberculosis therapy. Am J Respir Crit Care Med (2004) 2.40
Four SNPs on chromosome 9p21 in a South Korean population implicate a genetic locus that confers high cross-race risk for development of coronary artery disease. Arterioscler Thromb Vasc Biol (2007) 2.38
Association between acquired rifamycin resistance and the pharmacokinetics of rifabutin and isoniazid among patients with HIV and tuberculosis. Clin Infect Dis (2005) 2.34
Genome-wide association identifies a susceptibility locus for coronary artery disease in the Chinese Han population. Nat Genet (2011) 2.32
Genome-wide association study in Han Chinese identifies four new susceptibility loci for coronary artery disease. Nat Genet (2012) 2.17
Parental delay or refusal of vaccine doses, childhood vaccination coverage at 24 months of age, and the Health Belief Model. Public Health Rep (2011) 1.89
Association between four SNPs on chromosome 9p21 and myocardial infarction is replicated in an Italian population. J Hum Genet (2007) 1.87
Genetic rescue of nonclassical ERα signaling normalizes energy balance in obese Erα-null mutant mice. J Clin Invest (2011) 1.81
In vitro sensitivity of Plasmodium falciparum from China-Myanmar border area to major ACT drugs and polymorphisms in potential target genes. PLoS One (2012) 1.74
Prevalence of breastfeeding in the United States: the 2001 National Immunization Survey. Pediatrics (2003) 1.68
Novel CACNA1S mutation causes autosomal dominant hypokalemic periodic paralysis in a Chinese family. J Mol Med (Berl) (2005) 1.63
Determinants of sensitivity and resistance to rapamycin-chemotherapy drug combinations in vivo. Cancer Res (2006) 1.60
An LRP8 variant is associated with familial and premature coronary artery disease and myocardial infarction. Am J Hum Genet (2007) 1.48
[{Cu(phen)2}(mu-malato){Cu(phen)(NO3)}](NO3).4H2O: malate acting as a tetradentate and dibridging ligand in a dinuclear copper complex. Acta Crystallogr C (2005) 1.47
Functional analysis of TBX5 missense mutations associated with Holt-Oram syndrome. J Biol Chem (2002) 1.45
The transduction channel TRPM5 is gated by intracellular calcium in taste cells. J Neurosci (2007) 1.45
Candidate pathway-based genome-wide association studies identify novel associations of genomic variants in the complement system associated with coronary artery disease. Circ Cardiovasc Genet (2014) 1.45
MDM2 SNP309 polymorphism and colorectal cancer risk: a meta-analysis. DNA Cell Biol (2011) 1.45
Identification of a novel GPR143 mutation in a large Chinese family with congenital nystagmus as the most prominent and consistent manifestation. J Hum Genet (2007) 1.42
Discriminating schizophrenia and bipolar disorder by fusing fMRI and DTI in a multimodal CCA+ joint ICA model. Neuroimage (2011) 1.41
Regulation of Kiss1 and dynorphin gene expression in the murine brain by classical and nonclassical estrogen receptor pathways. J Neurosci (2009) 1.41
Investigation of relationships between fMRI brain networks in the spectral domain using ICA and Granger causality reveals distinct differences between schizophrenia patients and healthy controls. Neuroimage (2009) 1.37
The atypical E2F family member E2F7 couples the p53 and RB pathways during cellular senescence. Genes Dev (2012) 1.33
Assessment of association of rs2200733 on chromosome 4q25 with atrial fibrillation and ischemic stroke in a Chinese Han population. Hum Genet (2009) 1.25
Interleukin-6 is a potential biomarker for severe pandemic H1N1 influenza A infection. PLoS One (2012) 1.23
Mutations in ABCB6 cause dyschromatosis universalis hereditaria. J Invest Dermatol (2013) 1.21
System for infectious disease information sharing and analysis: design and evaluation. IEEE Trans Inf Technol Biomed (2007) 1.20
Identification of a novel genetic locus on chromosome 8p21.1-q11.23 for idiopathic basal ganglia calcification. Am J Med Genet B Neuropsychiatr Genet (2010) 1.20
Identification of a CRYAB mutation associated with autosomal dominant posterior polar cataract in a Chinese family. Invest Ophthalmol Vis Sci (2006) 1.19
Discovery of Time-Delayed Gene Regulatory Networks based on temporal gene expression profiling. BMC Bioinformatics (2006) 1.18
A Hybrid Machine Learning Method for Fusing fMRI and Genetic Data: Combining both Improves Classification of Schizophrenia. Front Hum Neurosci (2010) 1.18
Cassandra retrotransposons carry independently transcribed 5S RNA. Proc Natl Acad Sci U S A (2008) 1.18
Multifaceted genomic risk for brain function in schizophrenia. Neuroimage (2012) 1.16
A large scale multivariate parallel ICA method reveals novel imaging-genetic relationships for Alzheimer's disease in the ADNI cohort. Neuroimage (2012) 1.15
Blood-spinal cord barrier disruption contributes to early motor-neuron degeneration in ALS-model mice. Proc Natl Acad Sci U S A (2014) 1.14
TRPM5-expressing microvillous cells in the main olfactory epithelium. BMC Neurosci (2008) 1.14
Discovery of MK-8742: an HCV NS5A inhibitor with broad genotype activity. ChemMedChem (2013) 1.13
Repeated treatments with botulinum toxin type a produce sustained decreases in the limitations associated with focal upper-limb poststroke spasticity for caregivers and patients. Arch Phys Med Rehabil (2008) 1.12
Novel HSF4 mutation causes congenital total white cataract in a Chinese family. Am J Ophthalmol (2006) 1.11
Semiblind spatial ICA of fMRI using spatial constraints. Hum Brain Mapp (2010) 1.10
Genetic variants at newly identified lipid loci are associated with coronary heart disease in a Chinese Han population. PLoS One (2011) 1.09
Significant association of SNP rs2106261 in the ZFHX3 gene with atrial fibrillation in a Chinese Han GeneID population. Hum Genet (2010) 1.09
Identification of NPPA variants associated with atrial fibrillation in a Chinese GeneID population. Clin Chim Acta (2010) 1.09
Circulating levels of periostin may help identify patients with more aggressive colorectal cancer. Int J Oncol (2009) 1.08
Aerosol synthesis of cargo-filled graphene nanosacks. Nano Lett (2012) 1.06
Accelerated pericyte degeneration and blood-brain barrier breakdown in apolipoprotein E4 carriers with Alzheimer's disease. J Cereb Blood Flow Metab (2016) 1.05
Influence of vitamin C on salivary absorbed dose of 131I in thyroid cancer patients: a prospective, randomized, single-blind, controlled trial. J Nucl Med (2010) 1.04
Rare copy number deletions predict individual variation in intelligence. PLoS One (2011) 1.04
Vulnerability analysis and passenger source prediction in urban rail transit networks. PLoS One (2013) 1.03
Functional dominant-negative mutation of sodium channel subunit gene SCN3B associated with atrial fibrillation in a Chinese GeneID population. Biochem Biophys Res Commun (2010) 1.03
Components of cross-frequency modulation in health and disease. Front Syst Neurosci (2011) 1.03
Minor allele C of chromosome 1p32 single nucleotide polymorphism rs11206510 confers risk of ischemic stroke in the Chinese Han population. Stroke (2010) 1.03
The same chromosome 9p21.3 locus is associated with type 2 diabetes and coronary artery disease in a Chinese Han population. Diabetes (2011) 1.02
Association between the chromosome 9p21 locus and angiographic coronary artery disease burden: a collaborative meta-analysis. J Am Coll Cardiol (2013) 1.02
Slit/Robo signaling modulates the proliferation of central nervous system progenitors. Neuron (2012) 1.01
Disrupted correlation between low frequency power and connectivity strength of resting state brain networks in schizophrenia. Schizophr Res (2012) 1.01
A cross-sectional survey of severe fever with thrombocytopenia syndrome virus infection of domestic animals in Laizhou City, Shandong Province, China. Jpn J Infect Dis (2014) 1.01
Characterization of the cardiac sodium channel SCN5A mutation, N1325S, in single murine ventricular myocytes. Biochem Biophys Res Commun (2006) 1.01
Cardiac-specific overexpression of SCN5A gene leads to shorter P wave duration and PR interval in transgenic mice. Biochem Biophys Res Commun (2007) 1.01
Acylation-stimulating protein (ASP)/complement C3adesArg deficiency results in increased energy expenditure in mice. J Biol Chem (2003) 1.01
An activated protein C analog stimulates neuronal production by human neural progenitor cells via a PAR1-PAR3-S1PR1-Akt pathway. J Neurosci (2013) 1.00
A pilot multivariate parallel ICA study to investigate differential linkage between neural networks and genetic profiles in schizophrenia. Neuroimage (2009) 1.00
Highly active catalysts of gold nanoparticles supported on three-dimensionally ordered macroporous LaFeO3 for soot oxidation. Angew Chem Int Ed Engl (2011) 0.99
Rectus abdominis muscle metastasis from papillary thyroid cancer identified by I-131 SPECT/CT. Clin Nucl Med (2010) 0.99
A novel mutation in GDF5 causes autosomal dominant symphalangism in two Chinese families. Am J Med Genet A (2006) 0.98
Formation of neutralizing antibodies in patients receiving botulinum toxin type A for treatment of poststroke spasticity: a pooled-data analysis of three clinical trials. Clin Ther (2007) 0.98
Guided exploration of genomic risk for gray matter abnormalities in schizophrenia using parallel independent component analysis with reference. Neuroimage (2013) 0.98
High intake of folate from food sources is associated with reduced risk of esophageal cancer in an Australian population. J Nutr (2010) 0.97
Effect of vaccine shortages on timeliness of pneumococcal conjugate vaccination: results from the 2001-2005 National Immunization Survey. Pediatrics (2007) 0.97
[Study on factors related to top 10 junk food consumption at 8 to 16 years of age, in Haidian District of Beijing]. Zhonghua Liu Xing Bing Xue Za Zhi (2008) 0.97
Genetic associations of brain structural networks in schizophrenia: a preliminary study. Biol Psychiatry (2010) 0.97
The IL-33-ST2L pathway is associated with coronary artery disease in a Chinese Han population. Am J Hum Genet (2013) 0.96