Mutation in kallikrein 4 causes autosomal recessive hypomaturation amelogenesis imperfecta
about
FAM20A mutations can cause enamel-renal syndrome (ERS).Novel FAM20A mutations in hypoplastic amelogenesis imperfectaAmelotin--a Novel Secreted, Ameloblast-specific ProteinNovel WDR72 mutation and cytoplasmic localizationProtein-mediated enamel mineralizationRegulation of dental enamel shape and hardnessMMP20 hemopexin domain mutation in amelogenesis imperfectaStress response pathways in ameloblasts: implications for amelogenesis and dental fluorosisHuman and mouse enamel phenotypes resulting from mutation or altered expression of AMEL, ENAM, MMP20 and KLK4Phenotypic variation in FAM83H-associated amelogenesis imperfectaMutations in CNNM4 cause Jalili syndrome, consisting of autosomal-recessive cone-rod dystrophy and amelogenesis imperfectaFAM83H mutations in families with autosomal-dominant hypocalcified amelogenesis imperfectaMutations in the beta propeller WDR72 cause autosomal-recessive hypomaturation amelogenesis imperfectaThe molecular etiologies and associated phenotypes of amelogenesis imperfectaA post-classical theory of enamel biomineralization… and why we need oneSpecificity profiling of seven human tissue kallikreins reveals individual subsite preferencesEnamel proteins and proteases in Mmp20 and Klk4 null and double-null miceHypomaturation enamel defects in Klk4 knockout/LacZ knockin miceNovel genetic linkage of rat Sp6 mutation to Amelogenesis imperfectaIdentification of mutations in SLC24A4, encoding a potassium-dependent sodium/calcium exchanger, as a cause of amelogenesis imperfectaEffect of kallikrein 4 loss on enamel mineralization: comparison with mice lacking matrix metalloproteinase 20WDR72 models of structure and function: a stage-specific regulator of enamel mineralizationEnamel defects and ameloblast-specific expression in Enam knock-out/lacz knock-in miceCritical roles for WDR72 in calcium transport and matrix protein removal during enamel maturationEvolution of Klk4 and enamel maturation in eutheriansKallikrein-related peptidase-4 (KLK4): role in enamel formation and revelations from ablated miceDental enamel development: proteinases and their enamel matrix substratesBodyweight assessment of enamelin null miceTarget gene analyses of 39 amelogenesis imperfecta kindredsComparative genomic analysis of the zebra finch degradome provides new insights into evolution of proteases in birds and mammalsRecessive Mutations in ACPT, Encoding Testicular Acid Phosphatase, Cause Hypoplastic Amelogenesis ImperfectaGenes expressed in dental enamel development are associated with molar-incisor hypomineralizationAlteration of conserved alternative splicing in AMELX causes enamel defects.MMP-20 is predominately a tooth-specific enzyme with a deep catalytic pocket that hydrolyzes type V collagenThe amyloid protein APin is highly expressed during enamel mineralization and maturation in rat incisors.Defining the extended substrate specificity of kallikrein 1-related peptidases.Analyses of MMP20 Missense Mutations in Two Families with Hypomaturation Amelogenesis ImperfectaA Fourth KLK4 Mutation Is Associated with Enamel Hypomineralisation and Structural Abnormalities.Evolutionary history of tissue kallikreinsMouse genetic background influences the dental phenotype.
P2860
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P2860
Mutation in kallikrein 4 causes autosomal recessive hypomaturation amelogenesis imperfecta
description
2004 nî lūn-bûn
@nan
2004 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
2004 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
2004年の論文
@ja
2004年論文
@yue
2004年論文
@zh-hant
2004年論文
@zh-hk
2004年論文
@zh-mo
2004年論文
@zh-tw
2004年论文
@wuu
name
Mutation in kallikrein 4 cause ...... ration amelogenesis imperfecta
@ast
Mutation in kallikrein 4 cause ...... ration amelogenesis imperfecta
@en
Mutation in kallikrein 4 cause ...... ration amelogenesis imperfecta
@en-gb
Mutation in kallikrein 4 cause ...... ration amelogenesis imperfecta
@nl
type
label
Mutation in kallikrein 4 cause ...... ration amelogenesis imperfecta
@ast
Mutation in kallikrein 4 cause ...... ration amelogenesis imperfecta
@en
Mutation in kallikrein 4 cause ...... ration amelogenesis imperfecta
@en-gb
Mutation in kallikrein 4 cause ...... ration amelogenesis imperfecta
@nl
prefLabel
Mutation in kallikrein 4 cause ...... ration amelogenesis imperfecta
@ast
Mutation in kallikrein 4 cause ...... ration amelogenesis imperfecta
@en
Mutation in kallikrein 4 cause ...... ration amelogenesis imperfecta
@en-gb
Mutation in kallikrein 4 cause ...... ration amelogenesis imperfecta
@nl
P2093
P921
P3181
P356
P1476
Mutation in kallikrein 4 cause ...... ration amelogenesis imperfecta
@en
P2093
J T Wright
M D Michalec
P3181
P356
10.1136/JMG.2003.017657
P407
P577
2004-07-01T00:00:00Z