Published in J Dent Res on January 01, 2010
Target gene analyses of 39 amelogenesis imperfecta kindreds. Eur J Oral Sci (2011) 1.97
Genetic variation in MMP20 contributes to higher caries experience. J Dent (2012) 1.16
Dental enamel development: proteinases and their enamel matrix substrates. ISRN Dent (2013) 1.10
Expression of kallikrein-related peptidase 4 in dental and non-dental tissues. Eur J Oral Sci (2011) 1.07
Why does enamel in Klk4-null mice break above the dentino-enamel junction? Cells Tissues Organs (2011) 0.99
Modulation of cell-cell junctional complexes by matrix metalloproteinases. J Dent Res (2012) 0.95
Assessment of dental fluorosis in Mmp20 +/- mice. J Dent Res (2011) 0.91
MMP20 cleaves E-cadherin and influences ameloblast development. Cells Tissues Organs (2011) 0.90
Matrix metalloproteinase 20 promotes a smooth enamel surface, a strong dentino-enamel junction, and a decussating enamel rod pattern. Eur J Oral Sci (2011) 0.89
Kallikrein-related peptidase-4 (KLK4): role in enamel formation and revelations from ablated mice. Front Physiol (2014) 0.86
Hypomaturation amelogenesis imperfecta due to WDR72 mutations: a novel mutation and ultrastructural analyses of deciduous teeth. Cells Tissues Organs (2010) 0.84
MMP20 modulates cadherin expression in ameloblasts as enamel develops. J Dent Res (2013) 0.84
Amelogenesis Imperfecta; Genes, Proteins, and Pathways. Front Physiol (2017) 0.82
Matrix metalloproteinase-20 over-expression is detrimental to enamel development: a Mus musculus model. PLoS One (2014) 0.82
Fluoride does not inhibit enamel protease activity. J Dent Res (2010) 0.81
Bmp2 deletion causes an amelogenesis imperfecta phenotype via regulating enamel gene expression. J Cell Physiol (2015) 0.81
Stress response pathways in ameloblasts: implications for amelogenesis and dental fluorosis. Cells (2012) 0.80
Transcription factor FoxO1 is essential for enamel biomineralization. PLoS One (2012) 0.78
Novel genetic linkage of rat Sp6 mutation to Amelogenesis imperfecta. Orphanet J Rare Dis (2012) 0.76
Shear bond strength of dentin and deproteinized enamel of amelogenesis imperfecta mouse incisors. Pediatr Dent (2014) 0.75
Analyses of MMP20 Missense Mutations in Two Families with Hypomaturation Amelogenesis Imperfecta. Front Physiol (2017) 0.75
Genetic variants in matrix metalloproteinase genes as disposition factors for ovarian cancer risk, survival, and clinical outcome. Mol Carcinog (2013) 0.75
Evolutionary Analysis Predicts Sensitive Positions of MMP20 and Validates Newly- and Previously-Identified MMP20 Mutations Causing Amelogenesis Imperfecta. Front Physiol (2017) 0.75
Amelogenesis imperfecta, dentinogenesis imperfecta and dentin dysplasia revisited: problems in classification. J Oral Pathol (1988) 3.52
MMP-20 mutation in autosomal recessive pigmented hypomaturation amelogenesis imperfecta. J Med Genet (2005) 2.99
Mutation in kallikrein 4 causes autosomal recessive hypomaturation amelogenesis imperfecta. J Med Genet (2004) 2.93
Endoplasmic reticulum-associated degradation. Annu Rev Cell Dev Biol (2005) 2.83
Enamelysin (matrix metalloproteinase 20)-deficient mice display an amelogenesis imperfecta phenotype. J Biol Chem (2002) 2.59
Characterization of recombinant pig enamelysin activity and cleavage of recombinant pig and mouse amelogenins. J Dent Res (1999) 2.50
FAM83H mutations in families with autosomal-dominant hypocalcified amelogenesis imperfecta. Am J Hum Genet (2008) 2.38
MMP20 active-site mutation in hypomaturation amelogenesis imperfecta. J Dent Res (2005) 2.12
ENAM mutations in autosomal-dominant amelogenesis imperfecta. J Dent Res (2005) 1.83
Decreased mineral content in MMP-20 null mouse enamel is prominent during the maturation stage. J Dent Res (2004) 1.52
Processing of ameloblastin by MMP-20. J Dent Res (2007) 1.46
Amelogenin p.M1T and p.W4S mutations underlying hypoplastic X-linked amelogenesis imperfecta. J Dent Res (2004) 1.45
Phenotype of ENAM mutations is dosage-dependent. J Dent Res (2005) 1.42
The hemopexin and O-glycosylated domains tune gelatinase B/MMP-9 bioavailability via inhibition and binding to cargo receptors. J Biol Chem (2006) 1.36
Mutational spectrum of FAM83H: the C-terminal portion is required for tooth enamel calcification. Hum Mutat (2008) 1.28
Premature stop codon in MMP20 causing amelogenesis imperfecta. J Dent Res (2008) 1.26
Enamelysin (matrix metalloproteinase-20): localization in the developing tooth and effects of pH and calcium on amelogenin hydrolysis. J Dent Res (1998) 1.17
Novel FAM83H mutations in Turkish families with autosomal dominant hypocalcified amelogenesis imperfecta. Clin Genet (2009) 1.11
Crystal structure of the haemopexin-like C-terminal domain of gelatinase A. Nat Struct Biol (1995) 0.96
A novel missense mutation (p.P52R) in amelogenin gene causing X-linked amelogenesis imperfecta. J Dent Res (2007) 0.88
Identification of the TIMP-2 binding site on the gelatinase A hemopexin C-domain by site-directed mutagenesis and the yeast two-hybrid system. Ann N Y Acad Sci (1999) 0.80
MMP-20 mutation in autosomal recessive pigmented hypomaturation amelogenesis imperfecta. J Med Genet (2005) 2.99
Association of a microRNA-323b polymorphism with the persistence of hepatitis B virus infection by the enhancement of viral replication. J Viral Hepat (2013) 1.98
ENAM mutations in autosomal-dominant amelogenesis imperfecta. J Dent Res (2005) 1.83
Enamel formation genes are associated with high caries experience in Turkish children. Caries Res (2008) 1.57
Clinical significance of mycobacterial genotyping in Mycobacterium avium lung disease in Korea. Int J Tuberc Lung Dis (2012) 1.44
Camellia japonica suppresses immunoglobulin E-mediated allergic response by the inhibition of Syk kinase activation in mast cells. Clin Exp Allergy (2008) 1.42
MicroRNA-193a represses c-kit expression and functions as a methylation-silenced tumor suppressor in acute myeloid leukemia. Oncogene (2011) 1.27
LAMB3 mutations causing autosomal-dominant amelogenesis imperfecta. J Dent Res (2013) 1.17
Damage maps for layered ceramics under simulated mastication. J Dent Res (2008) 1.16
Identification of 11 novel mutations in 49 Korean patients with mucopolysaccharidosis type II. Clin Genet (2011) 1.09
A novel mutation in the DSPP gene associated with dentinogenesis imperfecta type II. J Dent Res (2009) 1.08
Dopamine transporter density is decreased in parkinsonian patients with a history of manganese exposure: what does it mean? Mov Disord (2002) 1.06
Novel KLK4 and MMP20 mutations discovered by whole-exome sequencing. J Dent Res (2013) 1.04
Magnetically driven metal-insulator transition in NaOsO3. Phys Rev Lett (2012) 1.01
Enhanced ordering temperatures in antiferromagnetic manganite superlattices. Nat Mater (2009) 1.00
Identification of a novel TGFBR2 gene mutation in a Korean patient with Loeys-Dietz aortic aneurysm syndrome; no mutation in TGFBR2 gene in 30 patients with classic Marfan's syndrome. Clin Genet (2005) 0.98
Candidate gene strategy reveals ENAM mutations. J Dent Res (2009) 0.97
A novel locus for X-linked recessive CMT with deafness and optic neuropathy maps to Xq21.32-q24. Neurology (2005) 0.95
Phenotypic variation in dentinogenesis imperfecta/dentin dysplasia linked to 4q21. J Dent Res (2006) 0.95
Fluoroscopically guided percutaneous jejunostomy: outcomes in 25 consecutive patients. Clin Radiol (2007) 0.95
MicroRNA signatures associated with immortalization of EBV-transformed lymphoblastoid cell lines and their clinical traits. Cell Prolif (2011) 0.95
Fam83h is associated with intracellular vesicles and ADHCAI. J Dent Res (2009) 0.94
Limb lengthening with a submuscular locking plate. J Bone Joint Surg Br (2009) 0.93
A Clinico-pathological study on the effect of vincristine on transmissible venereal tumour in dogs. J Vet Med A Physiol Pathol Clin Med (2005) 0.93
Coexistence of IgM antihepatitis A virus and IgM antihepatitis E virus in acute viral hepatitis: a prospective, multicentre study in Korea. J Viral Hepat (2011) 0.93
Clevudine for chronic hepatitis B: antiviral response, predictors of response, and development of myopathy. J Viral Hepat (2011) 0.92
Damage and reliability of Y-TZP after cementation surface treatment. J Dent Res (2010) 0.92
Axis inhibition protein 2 (AXIN2) polymorphisms and tooth agenesis. Arch Oral Biol (2008) 0.92
Nucleolar protein GLTSCR2 stabilizes p53 in response to ribosomal stresses. Cell Death Differ (2012) 0.92
Does angiogenesis predict recurrence in superficial transitional cell carcinoma of the bladder? Urology (2001) 0.92
Validation of limited lymphadenectomy for lower-third gastric cancer based on depth of tumour invasion. Br J Surg (2010) 0.91
Novel WDR72 mutation and cytoplasmic localization. J Dent Res (2010) 0.91
Clinical and genetic analysis of the CHD7 gene in Korean patients with CHARGE syndrome. Clin Genet (2009) 0.91
Early hardness and shear bond strength of dual-cure resin cement light cured through resin overlays with different dentin-layer thicknesses. Oper Dent (2013) 0.91
Mutation analysis of BRCA1 and BRCA2 from 793 Korean patients with sporadic breast cancer. Clin Genet (2006) 0.91
Charge order, dynamics, and magnetostructural transition in multiferroic LuFe2O4. Phys Rev Lett (2008) 0.90
DNA probes for unambiguous identification of Listeria monocytogenes epidemic clone II strains. Appl Environ Microbiol (2010) 0.90
Clinical and genetic analysis of Korean patients with Marfan syndrome: possible ethnic differences in clinical manifestation. Clin Genet (2009) 0.90
A fully validated HPLC method for the simultaneous determination of acitretin and etretinate in plasma and its application to a pharmacokinetic study in healthy Korean subjects. Int J Clin Pharmacol Ther (2009) 0.89
The mechanisms and managements of hormone-therapy resistance in breast and prostate cancers. Endocr Relat Cancer (2005) 0.88
Fine-mapping of 5q12.1-13.3 unveils new genetic contributors to caries. Caries Res (2013) 0.88
Mutation analysis of the PMP22, MPZ, EGR2, LITAF, and GJB1 genes in Korean patients with Charcot-Marie-Tooth neuropathy type 1. Clin Genet (2006) 0.87
Identification of a novel FAM83H mutation and microhardness of an affected molar in autosomal dominant hypocalcified amelogenesis imperfecta. Int Endod J (2009) 0.87
Clinical analysis of the characterization of magnetic resonance imaging in 102 cases of refractory haematospermia. Andrology (2013) 0.86
Charge order in LuFe2O4: antiferroelectric ground state and coupling to magnetism. Phys Rev Lett (2008) 0.86
RUNX2 mutations in cleidocranial dysplasia. Genet Mol Res (2013) 0.85
[Prostatic calculi: silent stones]. Actas Urol Esp (2010) 0.84
Novel dentin phosphoprotein frameshift mutations in dentinogenesis imperfecta type II. Clin Genet (2011) 0.84
Interleukin-10 haplotype associated with total serum IgE in atopic dermatitis patients. Allergy (2005) 0.84
RUNX2 mutations in cleidocranial dysplasia patients. Oral Dis (2009) 0.84
Carrier frequency of the R778L, A874V, and N1270S mutations in the ATP7B gene in a Korean population. Clin Genet (2009) 0.83
DLX3 mutation in a new family and its phenotypic variations. J Dent Res (2008) 0.83
Defining predictors of cleft lip and palate risk. J Dent Res (2012) 0.83
Capecitabine monotherapy in patients with anthracycline- and taxane-pretreated metastatic breast cancer. Med Oncol (2004) 0.83
Functional splicing assay of DSPP mutations in hereditary dentin defects. Oral Dis (2011) 0.82
FAM83H mutations cause ADHCAI and alter intracellular protein localization. J Dent Res (2010) 0.82
Therapeutic potential of panduratin A, LKB1-dependent AMP-activated protein kinase stimulator, with activation of PPARα/δ for the treatment of obesity. Diabetes Obes Metab (2011) 0.82
Estimated daily intakes of butylated hydroxyanisole (BHA), butylated hydroxytoluene (BHT) and tert-butyl hydroquinone (TBHQ) antioxidants in Korea. Food Addit Contam (2005) 0.82
Exonal deletion of SLC24A4 causes hypomaturation amelogenesis imperfecta. J Dent Res (2014) 0.81
A novel ACAD8 mutation in asymptomatic patients with isobutyryl-CoA dehydrogenase deficiency and a review of the ACAD8 mutation spectrum. Clin Genet (2014) 0.81
Fulminant Type 1 diabetes mellitus associated with acute hepatitis A. Diabet Med (2010) 0.81
Novel LAMB3 mutations cause non-syndromic amelogenesis imperfecta with variable expressivity. Clin Genet (2014) 0.81
Expression of pS2 protein and its relation with the Ki-67 proliferative indices and tumor recurrence in superficial bladder carcinomas. Eur Urol (2001) 0.80
2-amino-N-(2,6-dichloropyridin-3-yl)acetamide derivatives as a novel class of HBV capsid assembly inhibitor. J Viral Hepat (2013) 0.80
Identification of the DSPP mutation in a new kindred and phenotype-genotype correlation. Oral Dis (2010) 0.80
Genotyping of Mycobacterium intracellulare isolates and clinical characteristics of lung disease. Int J Tuberc Lung Dis (2013) 0.80
Candidate gene studies in hypodontia suggest role for FGF3. Eur Arch Paediatr Dent (2013) 0.80
Genetic variation in Ameloblastin is associated with caries in asthmatic children. Eur Arch Paediatr Dent (2013) 0.80
Staphylococcal enterotoxin B upregulates fas-mediated apoptosis of peripheral blood mononuclear cells in childhood atopic dermatitis. Scand J Immunol (2003) 0.80
Reversible control of magnetic interactions by electric field in a single-phase material. Nat Commun (2013) 0.80
Technetium-99m hexamethylpropylene amine oxime lung scintigraphy findings in low-dose amiodarone therapy. Lung (2006) 0.80
Prognostic significance of angiogenesis and immunoreactivity of cathepsin D and type IV collagen in high-grade stage T1 primary bladder cancer. Urology (1999) 0.79
In vitro maturation, in vitro fertilization and embryonic development of canine oocytes. Zygote (2007) 0.79
Upregulation of Krüppel-like factor 6 in the mouse hippocampus after pilocarpine-induced status epilepticus. Neuroscience (2011) 0.79
Charge order in LuFe2O4: an unlikely route to ferroelectricity. Phys Rev Lett (2012) 0.79
In vivo evaluation of lumbrokinase, a fibrinolytic enzyme extracted from Lumbricus rubellus, in a prosthetic vascular graft. J Cardiovasc Surg (Torino) (2002) 0.78
Mutation spectrum of the glucose-6-phosphatase gene and its implication in molecular diagnosis of Korean patients with glycogen storage disease type Ia. Clin Genet (2004) 0.78
Incommensurate charge order phase in Fe2OBO3 due to geometrical frustration. Phys Rev Lett (2007) 0.78
Manganese does not alter the severe neurotoxicity of MPTP. Hum Exp Toxicol (2007) 0.78