From the transcription of genes involved in ectodermal dysplasias to the understanding of associated dental anomalies. (Q36425832)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23239958%20AND%20SRC:MED&resulttype=core&format=json

20 February 2020

title

From the transcription of genes involved in ectodermal dysplasias to the understanding of associated dental anomalies (English)

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20 February 2020

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20 February 2020

V Laugel-Haushalter

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20 February 2020

A Langer

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20 February 2020

J Marrie

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20 February 2020

V Fraulob

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20 February 2020

B Schuhbaur

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20 February 2020

M Koch-Phillips

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20 February 2020

P Dollé

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20 February 2020

publication date

27 September 2012

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20 February 2020

published in

Molecular syndromology

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20 February 2020

volume

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20 February 2020

issue

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20 February 2020

page(s)

158-168

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Cardio-facio-cutaneous syndrome: does genotype predict phenotype?

20 February 2020

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A hypermorphic IkappaBalpha mutation is associated with autosomal dominant anhidrotic ectodermal dysplasia and T cell immunodeficiency

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30 September 2017

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30 September 2017

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30 September 2017

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30 September 2017

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30 September 2017

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IkappaBalpha deficiency results in a sustained NF-kappaB response and severe widespread dermatitis in mice

30 September 2017

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30 September 2017

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30 September 2017

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30 September 2017

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28 June 2018

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28 June 2018

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28 June 2018

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21 September 2018

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Ectodermal dysplasias: clinical and molecular review.

21 September 2018

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Heterozygous N-terminal deletion of IkappaBalpha results in functional nuclear factor kappaB haploinsufficiency, ectodermal dysplasia, and immune deficiency.

21 September 2018

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Interferon regulatory factor 6 (IRF6) and fibroblast growth factor receptor 1 (FGFR1) contribute to human tooth agenesis.

21 September 2018

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The genetic basis of tooth development and dental defects.

21 September 2018

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Germline mutations in genes within the MAPK pathway cause cardio-facio-cutaneous syndrome

21 September 2018

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Developmental expression analysis of the mouse and chick orthologues of IRF6: the gene mutated in Van der Woude syndrome.

21 September 2018

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Orphanet, an information site on rare diseases

21 September 2018

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Aberrant gene expression in epithelial cells of mixed odontogenic tumors

21 September 2018

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Developing teeth as biomarker of dioxin exposure.

21 September 2018

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Quantification of taurodontism: interests in the early diagnosis of hypohidrotic ectodermal dysplasia

21 September 2018

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12 December 2020

[Information on rare diseases: the Orphanet project]

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12 December 2020

Gene/environment relations in the development of tooth anomalies

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12 December 2020

[Amoxicillin may be a cause of enamel hypomineralization]

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12 December 2020

A new gene, EVC2, is mutated in Ellis-van Creveld syndrome

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12 December 2020

IRF6 mutations in mixed isolated familial clefting

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12 December 2020

Identifiers

DOI

10.1159/000342833

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23239958%20AND%20SRC:MED&resulttype=core&format=json

20 February 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23239958%20AND%20SRC:MED&resulttype=core&format=json

20 February 2020

PubMed publication ID

23239958

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23239958%20AND%20SRC:MED&resulttype=core&format=json