Published in J Dent Res on February 01, 1997
Partial rescue of the amelogenin null dental enamel phenotype. J Biol Chem (2008) 1.19
The amelogenin C-terminus is required for enamel development. J Dent Res (2009) 1.13
A mutation in the mouse Amelx tri-tyrosyl domain results in impaired secretion of amelogenin and phenocopies human X-linked amelogenesis imperfecta. Hum Mol Genet (2010) 1.07
Enamel proteins and proteases in Mmp20 and Klk4 null and double-null mice. Eur J Oral Sci (2011) 1.02
The leucine-rich amelogenin peptide alters the amelogenin null enamel phenotype. Cells Tissues Organs (2008) 0.97
Origin, splicing, and expression of rodent amelogenin exon 8. J Dent Res (2006) 0.94
Identification of the functional activity of the [A-4] amelogenin gene splice product in newborn mouse ameloblasts. Bone (2008) 0.88
The Amelogenin Proteins and Enamel Development in Humans and Mice. J Oral Biosci (2011) 0.87
Leucine rich amelogenin peptide alters ameloblast differentiation in vivo. Matrix Biol (2013) 0.84
Amelogenins: Multi-Functional Enamel Matrix Proteins and Their Binding Partners. J Oral Biosci (2011) 0.80
Identification of a novel splicing form of amelogenin gene in a reptile, Ctenosaura similis. PLoS One (2012) 0.78
Exon4 amelogenin transcripts in enamel biomineralization. J Dent Res (2015) 0.75
Circadian Rhythm Regulates Development of Enamel in Mouse Mandibular First Molar. PLoS One (2016) 0.75
Alternative Splicing of the Amelogenin Gene in a Caudate Amphibian, Plethodoncinereus. PLoS One (2013) 0.75
Efficacy of systematic pelvic lymphadenectomy in endometrial cancer (MRC ASTEC trial): a randomised study. Lancet (2008) 8.12
Improvement of reading frame maintenance is a common function for several tRNA modifications. EMBO J (2001) 3.80
The structural biology of the developing dental enamel matrix. J Struct Biol (1999) 3.36
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
Characterization of recombinant pig enamelysin activity and cleavage of recombinant pig and mouse amelogenins. J Dent Res (1999) 2.50
Estimating a treatment effect under biased sampling. Proc Natl Acad Sci U S A (1988) 2.49
Proteinases in developing dental enamel. Crit Rev Oral Biol Med (1999) 2.37
Hereditary dentin defects. J Dent Res (2007) 2.33
Methicillin-resistant Staphylococcus aureus: comparison of susceptibility testing methods and analysis of mecA-positive susceptible strains. J Clin Microbiol (2001) 2.31
Delayed wound healing in CXCR2 knockout mice. J Invest Dermatol (2000) 2.20
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
Transfer RNA modification: influence on translational frameshifting and metabolism. FEBS Lett (1999) 1.73
Self-assembly of a recombinant amelogenin protein generates supramolecular structures. J Struct Biol (1994) 1.71
Mmp-20 and Klk4 cleavage site preferences for amelogenin sequences. J Dent Res (2009) 1.59
Human cytomegalovirus elevates levels of the cellular protein p53 in infected fibroblasts. J Virol (1994) 1.56
Serum beta-hydroxybutyrate measurement in patients with uncontrolled diabetes mellitus. Arch Intern Med (1999) 1.56
Molecular cloning and mRNA tissue distribution of a novel matrix metalloproteinase isolated from porcine enamel organ. Gene (1996) 1.56
The pck rat: a new model that resembles human autosomal dominant polycystic kidney and liver disease. Kidney Int (2001) 1.56
Estimating the superiority of a drug to a placebo when all and only those patients at risk are treated with the drug. Proc Natl Acad Sci U S A (1989) 1.52
Effective use of polymerase chain reaction for diagnosis of central nervous system infections. Clin Infect Dis (1999) 1.51
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
A novel splice acceptor mutation in the DSPP gene causing dentinogenesis imperfecta type II. Hum Genet (2004) 1.45
Comparative immunochemical analyses of the developmental expression and distribution of ameloblastin and amelogenin in rat incisors. J Histochem Cytochem (1998) 1.44
The onset of amelogenin nanosphere aggregation studied by small-angle X-ray scattering and dynamic light scattering. J Struct Biol (2005) 1.43
Phenotype of ENAM mutations is dosage-dependent. J Dent Res (2005) 1.42
Novel ENAM mutation responsible for autosomal recessive amelogenesis imperfecta and localised enamel defects. J Med Genet (2003) 1.40
Detection of monodisperse aggregates of a recombinant amelogenin by dynamic light scattering. Biopolymers (1994) 1.40
Identification and structural and functional characterization of human enamelysin (MMP-20). Biochemistry (1997) 1.35
Identification of a motif in the carboxyl terminus of CXCR2 that is involved in adaptin 2 binding and receptor internalization. Biochemistry (2001) 1.32
Near-cognate peptidyl-tRNAs promote +1 programmed translational frameshifting in yeast. Mol Cell (1999) 1.29
Sheathlin: cloning, cDNA/polypeptide sequences, and immunolocalization of porcine enamel sheath proteins. J Dent Res (1997) 1.28
Cleavage site specificity of MMP-20 for secretory-stage ameloblastin. J Dent Res (2010) 1.26
Premature stop codon in MMP20 causing amelogenesis imperfecta. J Dent Res (2008) 1.26
Cloning and characterization of porcine enamelin mRNAs. J Dent Res (1997) 1.25
The multivariate L1-median and associated data depth. Proc Natl Acad Sci U S A (2000) 1.25
Enamelysin mRNA displays a developmentally defined pattern of expression and encodes a protein which degrades amelogenin. Connect Tissue Res (1998) 1.19
A nomenclature for X-linked amelogenesis imperfecta. Arch Oral Biol (2002) 1.18
LAMB3 mutations causing autosomal-dominant amelogenesis imperfecta. J Dent Res (2013) 1.17
Enamelysin (matrix metalloproteinase-20): localization in the developing tooth and effects of pH and calcium on amelogenin hydrolysis. J Dent Res (1998) 1.17
Serum retinol-binding protein 4 levels are elevated in non-alcoholic fatty liver disease. Clin Endocrinol (Oxf) (2007) 1.13
Non-random distribution and sensory functions of primary cilia in vascular smooth muscle cells. Kidney Blood Press Res (2008) 1.13
Novel MSX1 frameshift causes autosomal-dominant oligodontia. J Dent Res (2006) 1.13
A comparison of enamelin and amelogenin expression in developing mouse molars. Eur J Oral Sci (2001) 1.12
Use of a real time continuous glucose monitoring system as a motivational device for poorly controlled type 2 diabetes. Diabetes Res Clin Pract (2008) 1.12
Localization of EMSP1 expression during tooth formation and cloning of mouse cDNA. J Dent Res (2000) 1.11
Alternative splicing of the mouse amelogenin primary RNA transcript contributes to amelogenin heterogeneity. Biochem Biophys Res Commun (1992) 1.10
Cloning, cDNA sequence, and alternative splicing of porcine amelogenin mRNAs. J Dent Res (1996) 1.10
Blood and brain concentrations of imipramine, clomipramine and their monomethylated metabolites after oral and intramuscular administration in rats. J Pharm Pharmacol (1977) 1.10
Cloning human enamelin cDNA, chromosomal localization, and analysis of expression during tooth development. J Dent Res (2000) 1.09
Effect of PPAR-alpha and -gamma agonist on the expression of visfatin, adiponectin, and TNF-alpha in visceral fat of OLETF rats. Biochem Biophys Res Commun (2005) 1.08
Characterization of a family with dominant hypophosphatasia. Eur J Oral Sci (2000) 1.08
Altered enamelin phosphorylation site causes amelogenesis imperfecta. J Dent Res (2010) 1.08
Oncolytic adenovirus-mediated shRNA against Apollon inhibits tumor cell growth and enhances antitumor effect of 5-fluorouracil. Gene Ther (2008) 1.08
A high-density single-nucleotide polymorphism screen of 23 candidate genes in attention deficit hyperactivity disorder: suggesting multiple susceptibility genes among Chinese Han population. Mol Psychiatry (2008) 1.07
Serum adiponectin, interleukin-10 levels and inflammatory markers in the metabolic syndrome. Diabetes Res Clin Pract (2006) 1.07
Serum osteoprotegerin levels are associated with inflammation and pulse wave velocity. Clin Endocrinol (Oxf) (2005) 1.07
Calcium binding of enamel proteins and their derivatives with emphasis on the calcium-binding domain of porcine sheathlin. Arch Oral Biol (2001) 1.07
Overlapping DSPP mutations cause dentin dysplasia and dentinogenesis imperfecta. J Dent Res (2008) 1.06
Novel KLK4 and MMP20 mutations discovered by whole-exome sequencing. J Dent Res (2013) 1.04
The antitumor activity of TRAIL and IL-24 with replicating oncolytic adenovirus in colorectal cancer. Cancer Gene Ther (2006) 1.04
Transgenic rescue of enamel phenotype in Ambn null mice. J Dent Res (2010) 1.03
Amelogenin is a cell adhesion protein. J Dent Res (2002) 1.01
A high resolution and large solid angle x-ray Raman spectroscopy end-station at the Stanford Synchrotron Radiation Lightsource. Rev Sci Instrum (2012) 0.99
Cloning and characterization of the mouse and human enamelin genes. J Dent Res (2001) 0.99
Amelogenin proteins of developing dental enamel. Ciba Found Symp (1997) 0.98
Odontoblasts enhance the maturation of enamel crystals by secreting EMSP1 at the enamel-dentin junction. J Dent Res (2002) 0.98
Splicing determines the glycosylation state of ameloblastin. J Dent Res (2007) 0.96
Phenotypic variation in dentinogenesis imperfecta/dentin dysplasia linked to 4q21. J Dent Res (2006) 0.95
Cloning, DNA sequence, and alternative splicing of opossum amelogenin mRNAs. J Dent Res (1996) 0.95
Leucine-rich amelogenin peptides regulate mineralization in vitro. J Dent Res (2011) 0.95
Effects of recombinant amelogenin on hydroxyapatite formation in vitro. Calcif Tissue Int (1999) 0.95
Fluid resuscitation attenuates early cytokine mRNA expression after peritonitis. J Trauma (1996) 0.94
Structural changes in amelogenin upon self-assembly and mineral interactions. J Dent Res (2012) 0.94
Origin, splicing, and expression of rodent amelogenin exon 8. J Dent Res (2006) 0.94
Fam83h is associated with intracellular vesicles and ADHCAI. J Dent Res (2009) 0.94