| scholarly article | Q13442814 |
| P50 | author | John D Bartlett | Q41850988 |
| P2093 | author name string | James P Simmer | |
| P2860 | cites work | Mutation in kallikrein 4 causes autosomal recessive hypomaturation amelogenesis imperfecta | Q24298594 |
| MMP20 hemopexin domain mutation in amelogenesis imperfecta | Q24606267 | ||
| Pseudogenization of the tooth gene enamelysin (MMP20) in the common ancestor of extant baleen whales | Q24609283 | ||
| MMP-20 mutation in autosomal recessive pigmented hypomaturation amelogenesis imperfecta | Q24673795 | ||
| A post-classical theory of enamel biomineralization… and why we need one | Q27014088 | ||
| Chymotrypsin C mutations in chronic pancreatitis | Q27693296 | ||
| Characterization of the mouse and human PRSS17 genes, their relationship to other serine proteases, and the expression of PRSS17 in developing mouse incisors | Q28138969 | ||
| Amelogenin-deficient mice display an amelogenesis imperfecta phenotype | Q28201910 | ||
| Purification, characterization, and cloning of enamel matrix serine proteinase 1 | Q28261781 | ||
| Enamel proteins and proteases in Mmp20 and Klk4 null and double-null mice | Q28505534 | ||
| Enamelin (Enam) is essential for amelogenesis: ENU-induced mouse mutants as models for different clinical subtypes of human amelogenesis imperfecta (AI) | Q28506893 | ||
| Hypomaturation enamel defects in Klk4 knockout/LacZ knockin mice | Q28509062 | ||
| Effect of kallikrein 4 loss on enamel mineralization: comparison with mice lacking matrix metalloproteinase 20 | Q28586715 | ||
| Enamel defects and ameloblast-specific expression in Enam knock-out/lacz knock-in mice | Q28591653 | ||
| Cellular and chemical events during enamel maturation | Q46291772 | ||
| Enamel matrix serine proteinase 1: stage-specific expression and molecular modeling | Q47816995 | ||
| Localization of EMSP1 expression during tooth formation and cloning of mouse cDNA. | Q47882331 | ||
| Homozygous and compound heterozygous MMP20 mutations in amelogenesis imperfecta. | Q51034242 | ||
| Enamelysin (matrix metalloproteinase 20)-deficient mice display an amelogenesis imperfecta phenotype. | Q52113450 | ||
| Mineral and protein concentrations in enamel of the developing permanent porcine dentition. | Q52253590 | ||
| Crystal structures of human tissue kallikrein 4: activity modulation by a specific zinc binding site. | Q54456467 | ||
| A Mutation in the Enamelin Gene in a Mouse Model | Q57315040 | ||
| Morphological evidence for the presence of contractile elements in secretory ameloblasts of the rat | Q69025944 | ||
| The pathway of enamel rods at the base of cusps of human teeth | Q71977511 | ||
| Characterization of recombinant pig enamelysin activity and cleavage of recombinant pig and mouse amelogenins | Q74650441 | ||
| An electron microscopic study of the amelogenesis in human teeth. I. The fine structure of the ameloblasts | Q79065083 | ||
| Dentin sialoprotein, dentin phosphoprotein, enamelysin and ameloblastin: tooth-specific molecules that are distinctively expressed during murine dental differentiation | Q28593089 | ||
| Dental enamel development: proteinases and their enamel matrix substrates | Q28677179 | ||
| Molecular decay of enamel matrix protein genes in turtles and other edentulous amniotes | Q28709278 | ||
| Molecular decay of the tooth gene Enamelin (ENAM) mirrors the loss of enamel in the fossil record of placental mammals | Q28751910 | ||
| Substrates of the prostate-specific serine protease prostase/KLK4 defined by positional-scanning peptide libraries | Q33207170 | ||
| The structural biology of the developing dental enamel matrix | Q33707684 | ||
| Proteinases in developing dental enamel | Q33817047 | ||
| Mutation of the gene encoding the enamel-specific protein, enamelin, causes autosomal-dominant amelogenesis imperfecta | Q34085947 | ||
| Amelogenesis imperfecta in two families with defined AMELX deletions in ARHGAP6. | Q34517566 | ||
| Chymotrypsin C (caldecrin) is associated with enamel development | Q35212921 | ||
| Why does enamel in Klk4-null mice break above the dentino-enamel junction? | Q35226541 | ||
| Expression of kallikrein-related peptidase 4 in dental and non-dental tissues | Q35727395 | ||
| MMP20 active-site mutation in hypomaturation amelogenesis imperfecta | Q35746047 | ||
| Kallikrein-related peptidase 4, matrix metalloproteinase 20, and the maturation of murine and porcine enamel. | Q35763516 | ||
| Binding of amelogenin to MMP-9 and their co-expression in developing mouse teeth | Q36285362 | ||
| Ameloblastin is a cell adhesion molecule required for maintaining the differentiation state of ameloblasts | Q36322570 | ||
| Novel KLK4 and MMP20 mutations discovered by whole-exome sequencing | Q36623188 | ||
| High-resolution electron microscope study of human enamel crystallites: size, shape, and growth | Q36661105 | ||
| Molecular cloning and mRNA tissue distribution of a novel matrix metalloproteinase isolated from porcine enamel organ | Q36842172 | ||
| Enamel formation and amelogenesis imperfecta | Q36878846 | ||
| Kallikrein-related peptidases | Q37111311 | ||
| Mutations in MMP9 and MMP13 determine the mode of inheritance and the clinical spectrum of metaphyseal anadysplasia | Q37301193 | ||
| DPPI may activate KLK4 during enamel formation. | Q37341921 | ||
| MMP20 and KLK4 activation and inactivation interactions in vitro | Q37701902 | ||
| High-resolution electron-microscopic study of the relationship between human enamel and dentin crystals at the dentinoenamel junction | Q39547475 | ||
| Cleavage site specificity of MMP-20 for secretory-stage ameloblastin. | Q39713540 | ||
| Proteolytic enzyme activity in porcine immature enamel | Q40539191 | ||
| Proteolytic Enzyme in Porcine Immature Enamel | Q40576454 | ||
| Enamel rod formation in the monkey observed by scanning electron microscopy | Q41245151 | ||
| Length and shape of enamel crystals | Q41573622 | ||
| Transient amorphous calcium phosphate in forming enamel | Q41817996 | ||
| Identification and characterization of enamel proteinases isolated from developing enamel. Amelogeninolytic serine proteinases are associated with enamel maturation in pig | Q41840311 | ||
| Human amelogenesis. I: High resolution electron microscopy study of ribbon-like crystals | Q41996443 | ||
| Mmp-20 and Klk4 cleavage site preferences for amelogenin sequences | Q42566135 | ||
| Enamelysin and kallikrein-4 mRNA expression in developing mouse molars | Q44121741 | ||
| Porcine kallikrein-4 activation, glycosylation, activity, and expression in prokaryotic and eukaryotic hosts. | Q44382063 | ||
| The intramembrane protease SPPL2A is critical for tooth enamel formation | Q45349053 | ||
| How do enamelysin and kallikrein 4 process the 32-kDa enamelin? | Q46281887 | ||
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 240 | |
| P577 | publication date | 2014-07-04 | |
| P1433 | published in | Frontiers in Physiology | Q2434141 |
| P1476 | title | Kallikrein-related peptidase-4 (KLK4): role in enamel formation and revelations from ablated mice | |
| P478 | volume | 5 |
| Q33734821 | A Fourth KLK4 Mutation Is Associated with Enamel Hypomineralisation and Structural Abnormalities |
| Q39596733 | Buffering of protons released by mineral formation during amelogenesis in mice |
| Q64058391 | Comparative Genomics Reveals the Genetic Mechanisms of Musk Secretion and Adaptive Immunity in Chinese Forest Musk Deer |
| Q90679084 | Constitutive activation of β-catenin in ameloblasts leads to incisor enamel hypomineralization |
| Q33729357 | Disruption of Steroid Axis, a New Paradigm for Molar Incisor Hypomineralization (MIH). |
| Q90361822 | ENAM Gene Variation in Students Exposed to Different Fluoride Concentrations |
| Q37603164 | Enamel and dental anomalies in latent-transforming growth factor beta-binding protein 3 mutant mice. |
| Q39638110 | Full Spectrum of Postnatal Tooth Phenotypes in a Novel Irf6 Cleft Lip Model |
| Q57168734 | Identifying Candidate Biomarkers for Pleomorphic Adenoma: A Case-Control Study |
| Q36923743 | Maturation stage enamel malformations in Amtn and Klk4 null mice |
| Q35585269 | Mutations in the latent TGF-beta binding protein 3 (LTBP3) gene cause brachyolmia with amelogenesis imperfecta. |
| Q50580266 | Novel MMP20 and KLK4 Mutations in Amelogenesis Imperfecta. |
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