(Q36841898)

16 August 2017

1 reference

title

Developmental biology and genetics of dental malformations (English)

1 reference

16 August 2017

developmental biology

1 reference

Jan C-C Hu

1

1 reference

PubMed ID

17552940

16 August 2017

James P Simmer

series ordinal

2

1 reference

16 August 2017

1 May 2007

1 reference

Orthodontics & Craniofacial Research

16 August 2017

1 reference

16 August 2017

10

1 reference

16 August 2017

2

1 reference

16 August 2017

45-52

1 reference

Signalling networks regulating dental development

16 August 2017

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-6343.2007.00384.X

Tooth and jaw: molecular mechanisms of patterning in the first branchial arch

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-6343.2007.00384.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-6343.2007.00384.X

Msx1 deficient mice exhibit cleft palate and abnormalities of craniofacial and tooth development

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-6343.2007.00384.X

A human MSX1 homeodomain missense mutation causes selective tooth agenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-6343.2007.00384.X

Mutation of PAX9 is associated with oligodontia

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-6343.2007.00384.X

Mutations in AXIN2 cause familial tooth agenesis and predispose to colorectal cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-6343.2007.00384.X

X-linked anhidrotic (hypohidrotic) ectodermal dysplasia is caused by mutation in a novel transmembrane protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-6343.2007.00384.X

The anhidrotic ectodermal dysplasia gene (EDA) undergoes alternative splicing and encodes ectodysplasin-A with deletion mutations in collagenous repeats

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-6343.2007.00384.X

Cell lineage of primary and secondary enamel knots

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-6343.2007.00384.X

A proposed classification for heritable human dentine defects with a description of a new entity

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-6343.2007.00384.X

DSPP mutation in dentinogenesis imperfecta Shields type II

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-6343.2007.00384.X

Dentinogenesis imperfecta 1 with or without progressive hearing loss is associated with distinct mutations in DSPP

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-6343.2007.00384.X

Mutation of the signal peptide region of the bicistronic gene DSPP affects translocation to the endoplasmic reticulum and results in defective dentine biomineralization

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-6343.2007.00384.X

Clinical, histopathologic, and genetic investigation in two large families with dentinogenesis imperfecta type II.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-6343.2007.00384.X

Mutational hot spot in the DSPP gene causing dentinogenesis imperfecta type II.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-6343.2007.00384.X

Dentin phosphoprotein compound mutation in dentin sialophosphoprotein causes dentinogenesis imperfecta type III.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-6343.2007.00384.X

Dentin sialophosphoprotein knockout mouse teeth display widened predentin zone and develop defective dentin mineralization similar to human dentinogenesis imperfecta type III.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-6343.2007.00384.X

Identification of a mutation in DLX3 associated with tricho-dento-osseous (TDO) syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-6343.2007.00384.X

DLX3 mutation associated with autosomal dominant amelogenesis imperfecta with taurodontism

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-6343.2007.00384.X

The structural biology of the developing dental enamel matrix

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-6343.2007.00384.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-6343.2007.00384.X

Molecular cloning and mRNA tissue distribution of a novel matrix metalloproteinase isolated from porcine enamel organ

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-6343.2007.00384.X

MMP-20 mutation in autosomal recessive pigmented hypomaturation amelogenesis imperfecta

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-6343.2007.00384.X

Mutation in kallikrein 4 causes autosomal recessive hypomaturation amelogenesis imperfecta

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-6343.2007.00384.X

Hypophosphatasia and the role of alkaline phosphatase in skeletal mineralization

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-6343.2007.00384.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-6343.2007.00384.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-6343.2007.00384.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-6343.2007.00384.X

Amelogenesis imperfecta phenotype-genotype correlations with two amelogenin gene mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-6343.2007.00384.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-6343.2007.00384.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-6343.2007.00384.X

Genetic, clinical and molecular analysis of a family affected by amelogenesis imperfecta

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-6343.2007.00384.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-6343.2007.00384.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-6343.2007.00384.X

10.1111/J.1601-6343.2007.00384.X

21 January 2018

Identifiers

DOI

1 reference

16 August 2017

1 reference

PubMed ID

17552940