about
Human and mouse enamel phenotypes resulting from mutation or altered expression of AMEL, ENAM, MMP20 and KLK4FAM83H mutations in families with autosomal-dominant hypocalcified amelogenesis imperfectaEnamel defects and ameloblast-specific expression in Enam knock-out/lacz knock-in miceDoes enamelin have pleiotropic effects on organs other than the teeth? Lessons from a phenotyping screen of two enamelin-mutant mouse linesKallikrein-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 miceA mutation in the mouse Amelx tri-tyrosyl domain results in impaired secretion of amelogenin and phenocopies human X-linked amelogenesis imperfectaEnamel protein regulation and dental and periodontal physiopathology in MSX2 mutant miceCharacterization of periodontal structures of enamelin-null mice.Genomic characterization of mutant laboratory mouse strains by exome sequencing and annotation lift-over.Consequences for enamel development and mineralization resulting from loss of function of ameloblastin or enamelin.Phenotype-genotype correlations in mouse models of amelogenesis imperfecta caused by Amelx and Enam mutations.Matrix Gla protein inhibition of tooth mineralization.
P2860
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P2860
description
article
@en
im August 2007 veröffentlichter wissenschaftlicher Artikel
@de
wetenschappelijk artikel
@nl
наукова стаття, опублікована в серпні 2007
@uk
name
A Mutation in the Enamelin Gene in a Mouse Model
@en
A Mutation in the Enamelin Gene in a Mouse Model
@nl
type
label
A Mutation in the Enamelin Gene in a Mouse Model
@en
A Mutation in the Enamelin Gene in a Mouse Model
@nl
prefLabel
A Mutation in the Enamelin Gene in a Mouse Model
@en
A Mutation in the Enamelin Gene in a Mouse Model
@nl
P2093
P2860
P1476
A mutation in the enamelin gene in a mouse model
@en
P2093
P2860
P304
P356
10.1177/154405910708600815
P407
P577
2007-08-01T00:00:00Z