Phenotype-genotype correlations in mouse models of amelogenesis imperfecta caused by Amelx and Enam mutations (Q43081816)

13 November 2017

Phenotype-genotype correlations in mouse models of amelogenesis imperfecta caused by Amelx and Enam mutations (English)

1 reference

13 November 2017

amelogenesis imperfecta

1 reference

Martin John Barron

3

0 references

author name string

Thomas Liam Coxon

series ordinal

1

1 reference

13 November 2017

Alan Henry Brook

series ordinal

2

1 reference

13 November 2017

Richard Nigel Smith

series ordinal

4

1 reference

13 November 2017

language of work or name

1 reference

28 June 2012

1 reference

13 November 2017

1 reference

13 November 2017

196

1 reference

13 November 2017

5

1 reference

13 November 2017

420-430

1 reference

A mutation in the mouse Amelx tri-tyrosyl domain results in impaired secretion of amelogenin and phenocopies human X-linked amelogenesis imperfecta

13 November 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3718574

Consequences for enamel development and mineralization resulting from loss of function of ameloblastin or enamelin

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3718574

Amelogenin in cranio-facial development: the tooth as a model to study the role of amelogenin during embryogenesis.

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3718574

Human and mouse enamel phenotypes resulting from mutation or altered expression of AMEL, ENAM, MMP20 and KLK4

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3718574

The in vitro and in vivo validation of a mobile non-contact camera-based digital imaging system for tooth colour measurement.

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3718574

A review of tooth colour and whiteness

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3718574

Defining new dental phenotypes using 3-D image analysis to enhance discrimination and insights into biological processes

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3718574

Quantification and variation in experimental studies of morphogenesis

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3718574

Mouse models of tooth abnormalities

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3718574

The clinical measurement of tooth colour and stain

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3718574

Enamel formation and amelogenesis imperfecta

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3718574

The molecular etiologies and associated phenotypes of amelogenesis imperfecta

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3718574

X-chromosome inactivation: a hypothesis linking ontogeny and phylogeny

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3718574

Enamelin (Enam) is essential for amelogenesis: ENU-induced mouse mutants as models for different clinical subtypes of human amelogenesis imperfecta (AI)

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3718574

Amelogenin p.M1T and p.W4S mutations underlying hypoplastic X-linked amelogenesis imperfecta

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3718574

Gene action in the X-chromosome of the mouse (Mus musculus L.)

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3718574

Relationship of phenotype and genotype in X-linked amelogenesis imperfecta

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3718574

Subunit structures in hydroxyapatite crystal development in enamel: implications for amelogenesis imperfecta

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3718574

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

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3718574

Amelogenesis imperfecta phenotype-genotype correlations with two amelogenin gene mutations

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3718574

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

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3718574

Amelogenin-deficient mice display an amelogenesis imperfecta phenotype

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3718574

Atomic force microscopy studies of crystal surface topology during enamel development

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3718574

Optical profilometric study of changes in surface roughness of enamel during in vitro demineralization

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3718574

Measuring agreement in method comparison studies

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3718574

Partial expression of sex-linked recessive amelogenesis imperfecta in females compatible with the Lyon hypothesis

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3718574

Analysis of crystallite shape in rat incisor enamel

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3718574

Sample size requirements for reliability studies

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3718574

An image analysis system for the determination of tooth dimensions from study casts: comparison with manual measurements of mesio-distal diameter.

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3718574

Statistical methods for assessing agreement between two methods of clinical measurement

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3718574

Human and mouse amelogenin gene loci are on the sex chromosomes

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3718574

A model for development and evolution of complex morphological structures

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3718574

The human enamel protein gene amelogenin is expressed from both the X and the Y chromosomes

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3718574

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

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3718574

A scanning electron microscope study of aberrations in the prism pattern of rat incisor inner enamel

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3718574

The genetic basis of tooth development and dental defects.

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3718574

A Mutation in the Enamelin Gene in a Mouse Model

15 August 2018

1 reference

Crossref

https://api.crossref.org/works/10.1159%2F000336440

X-ray microtomographic study of mineral distribution in enamel of mandibular rat incisors

21 January 2018

1 reference

12 December 2020

Location and first appearance of rat incisor pigmentation

1 reference

12 December 2020

Changes in the protein components of rat incisor enamel during tooth development

1 reference

12 December 2020

A method for sampling the stages of amelogenesis on mandibular rat incisors using the molars as a reference for dissection

1 reference

12 December 2020

Transgenic mice that express normal and mutated amelogenins

1 reference

12 December 2020

Identifiers

DOI

10.1159/000336440

1 reference

release_rgcv6n344rgalifatoxg2yycui

13 November 2017

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/rgcv6n344rgalifatoxg2yycui

24 November 2022

mapped directly with Wikidata item

1 reference

13 November 2017

PubMed publication ID

22759786

1 reference