(Q36878846)

16 August 2017

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title

Enamel formation and amelogenesis imperfecta (English)

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16 August 2017

Jan C-C Hu

1

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16 August 2017

Yong-Hee P Chun

series ordinal

2

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16 August 2017

Turki Al Hazzazzi

series ordinal

3

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16 August 2017

James P Simmer

series ordinal

4

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16 August 2017

publication date

1 January 2007

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16 August 2017

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16 August 2017

volume

186

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16 August 2017

issue

1

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16 August 2017

page(s)

78-85

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Identification of a nonsense mutation in the amelogenin gene (AMELX) in a family with X-linked amelogenesis imperfecta (AIH1)

16 August 2017

cites work

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Enamelysin (matrix metalloproteinase 20)-deficient mice display an amelogenesis imperfecta phenotype.

21 January 2018

1 reference

The structural biology of the developing dental enamel matrix

21 January 2018

1 reference

Self-assembly of a recombinant amelogenin protein generates supramolecular structures.

21 January 2018

1 reference

Ameloblastin is a cell adhesion molecule required for maintaining the differentiation state of ameloblasts

21 January 2018

1 reference

A new frameshift mutation encoding a truncated amelogenin leads to X-linked amelogenesis imperfecta

21 January 2018

1 reference

A nomenclature for X-linked amelogenesis imperfecta

21 January 2018

1 reference

Identification of the enamelin (g.8344delG) mutation in a new kindred and presentation of a standardized ENAM nomenclature.

21 January 2018

1 reference

Novel ENAM mutation responsible for autosomal recessive amelogenesis imperfecta and localised enamel defects

21 January 2018

1 reference

Mutation in kallikrein 4 causes autosomal recessive hypomaturation amelogenesis imperfecta

21 January 2018

1 reference

MMP-20 mutation in autosomal recessive pigmented hypomaturation amelogenesis imperfecta

21 January 2018

1 reference

A deletion in the amelogenin gene (AMG) causes X-linked amelogenesis imperfecta (AIH1)

21 January 2018

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Human and mouse amelogenin gene loci are on the sex chromosomes

21 January 2018

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Characterisation of molecular defects in X-linked amelogenesis imperfecta (AIH1)

21 January 2018

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A nonsense mutation in the enamelin gene causes local hypoplastic autosomal dominant amelogenesis imperfecta (AIH2).

21 January 2018

1 reference

Mutation of the gene encoding the enamel-specific protein, enamelin, causes autosomal-dominant amelogenesis imperfecta

21 January 2018

1 reference

The cutting-edge of mammalian development; how the embryo makes teeth

21 January 2018

1 reference

Calcium binding of enamel proteins and their derivatives with emphasis on the calcium-binding domain of porcine sheathlin

21 January 2018

1 reference

21 January 2018

Identifiers

DOI

10.1159/000102683

1 reference

release_nn4gztr32zc57onmv24dp4jype

16 August 2017

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/nn4gztr32zc57onmv24dp4jype

mapped directly with Wikidata item

24 November 2022

based on heuristic

1 reference