Amelogenin p.M1T and p.W4S mutations underlying hypoplastic X-linked amelogenesis imperfecta
about
FAM20A mutations can cause enamel-renal syndrome (ERS).Novel WDR72 mutation and cytoplasmic localizationMMP20 hemopexin domain mutation in amelogenesis imperfectaFAM83H mutations in families with autosomal-dominant hypocalcified amelogenesis imperfectaThe molecular etiologies and associated phenotypes of amelogenesis imperfectaNovel genetic linkage of rat Sp6 mutation to Amelogenesis imperfectaEnamel ribbons, surface nodules, and octacalcium phosphate in C57BL/6 Amelx(-/-) mice and Amelx(+/-) lyonizationDental enamel development: proteinases and their enamel matrix substratesBodyweight assessment of enamelin null miceTarget gene analyses of 39 amelogenesis imperfecta kindredsRecessive Mutations in ACPT, Encoding Testicular Acid Phosphatase, Cause Hypoplastic Amelogenesis ImperfectaENAM Mutations in Autosomal-dominant Amelogenesis ImperfectaAlteration of conserved alternative splicing in AMELX causes enamel defects.Enamel formation genes influence enamel microhardness before and after cariogenic challenge.Genes and related proteins involved in amelogenesis imperfecta.Exclusion of p63 as a candidate gene for autosomal-dominant amelogenesis imperfecta.ENAM mutations with incomplete penetrance.MMP20 active-site mutation in hypomaturation amelogenesis imperfectaOrigin, splicing, and expression of rodent amelogenin exon 8.Phenotype of ENAM mutations is dosage-dependentMolecular genetics of ameloblast cell lineage.Candidate gene strategy reveals ENAM mutations.Current knowledge of tooth development: patterning and mineralization of the murine dentition.MiR-153 Regulates Amelogenesis by Targeting Endocytotic and Endosomal/lysosomal Pathways-Novel Insight into the Origins of Enamel Pathologies.Defining a new candidate gene for amelogenesis imperfecta: from molecular genetics to biochemistry.Deletion of Slc26a1 and Slc26a7 Delays Enamel Mineralization in Mice.Abrogation of epithelial BMP2 and BMP4 causes Amelogenesis Imperfecta by reducing MMP20 and KLK4 expression.Ameloblastin peptide encoded by exon 5 interacts with amelogenin N-terminus.Preparative SDS PAGE as an Alternative to His-Tag Purification of Recombinant AmelogeninThe Importance of Serine Phosphorylation of Ameloblastin on Enamel Formation.Phenotype-genotype correlations in mouse models of amelogenesis imperfecta caused by Amelx and Enam mutations.Dose-Dependent Rescue of KO Amelogenin Enamel by Transgenes in Vivo.Association between AMELX polymorphisms and dental caries in Koreans.A novel missense mutation (p.P52R) in amelogenin gene causing X-linked amelogenesis imperfecta.Exclusion of candidate genes in seven Turkish families with autosomal recessive amelogenesis imperfecta.
P2860
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P2860
Amelogenin p.M1T and p.W4S mutations underlying hypoplastic X-linked amelogenesis imperfecta
description
2004 nî lūn-bûn
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2004 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
2004 թվականի մայիսին 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
Amelogenin p.M1T and p.W4S mut ...... linked amelogenesis imperfecta
@ast
Amelogenin p.M1T and p.W4S mut ...... linked amelogenesis imperfecta
@en
Amelogenin p.M1T and p.W4S mut ...... linked amelogenesis imperfecta
@nl
type
label
Amelogenin p.M1T and p.W4S mut ...... linked amelogenesis imperfecta
@ast
Amelogenin p.M1T and p.W4S mut ...... linked amelogenesis imperfecta
@en
Amelogenin p.M1T and p.W4S mut ...... linked amelogenesis imperfecta
@nl
prefLabel
Amelogenin p.M1T and p.W4S mut ...... linked amelogenesis imperfecta
@ast
Amelogenin p.M1T and p.W4S mut ...... linked amelogenesis imperfecta
@en
Amelogenin p.M1T and p.W4S mut ...... linked amelogenesis imperfecta
@nl
P2093
P2860
P3181
P1476
Amelogenin p.M1T and p.W4S mut ...... linked amelogenesis imperfecta
@en
P2093
C J M Yamada
J P Simmer
J T Wright
R J Feigal
P2860
P304
P3181
P356
10.1177/154405910408300505
P407
P577
2004-05-01T00:00:00Z