(Q50784279)

19 March 2018

title

Cleft lip in oculodentodigital dysplasia suggests novel roles for connexin43. (English)

1 reference

19 March 2018

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Amano K

1

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19 March 2018

Ishiguchi M

2

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19 March 2018

Aikawa T

3

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19 March 2018

Kimata M

4

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19 March 2018

Kishi N

5

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19 March 2018

Fujimaki T

6

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19 March 2018

Murakami A

7

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19 March 2018

Kogo M

8

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19 March 2018

language of work or name

English

0 references

publication date

1 July 2012

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19 March 2018

Journal of Dental Research

published in

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19 March 2018

volume

91

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19 March 2018

issue

7 Suppl

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19 March 2018

page(s)

38S-44S

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19 March 2018

Mutations in BMP4 cause eye, brain, and digit developmental anomalies: overlap between the BMP4 and hedgehog signaling pathways

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Cleft lip and palate: understanding genetic and environmental influences

21 January 2018

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The conditional connexin43G138R mouse mutant represents a new model of hereditary oculodentodigital dysplasia in humans.

21 January 2018

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Loss of connexin43-mediated gap junctional coupling in the mesenchyme of limb buds leads to altered expression of morphogens in mice

21 January 2018

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A Gja1 missense mutation in a mouse model of oculodentodigital dysplasia

21 January 2018

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Slow ventricular conduction in mice heterozygous for a connexin43 null mutation

21 January 2018

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A case of oculodentodigital dysplasia syndrome with novel GJA1 gene mutation.

21 January 2018

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Complete sequencing shows a role for MSX1 in non-syndromic cleft lip and palate

21 January 2018

1 reference

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Fetal genetic risk of isolated cleft lip only versus isolated cleft lip and palate: a subphenotype analysis using two population-based studies of orofacial clefts in Scandinavia

21 January 2018

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Gap junction remodeling and cardiac arrhythmogenesis in a murine model of oculodentodigital dysplasia.

21 January 2018

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Mutations in IRF6 cause Van der Woude and popliteal pterygium syndromes

21 January 2018

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Expression and function of connexins in the epidermis, analyzed with transgenic mouse mutants

21 January 2018

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Peters Plus syndrome is caused by mutations in B3GALTL, a putative glycosyltransferase

21 January 2018

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Endothelial cell-specific knockout of connexin 43 causes hypotension and bradycardia in mice

21 January 2018

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Defective epidermal barrier in neonatal mice lacking the C-terminal region of connexin43.

21 January 2018

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TFAP2A mutations result in branchio-oculo-facial syndrome

21 January 2018

1 reference

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Connexin 43 (GJA1) mutations cause the pleiotropic phenotype of oculodentodigital dysplasia

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0022034512447952

GJA1 mutations, variants, and connexin 43 dysfunction as it relates to the oculodentodigital dysplasia phenotype

21 January 2018

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https://api.crossref.org/works/10.1177%2F0022034512447952

Cardiac malformation in neonatal mice lacking connexin43.

21 January 2018

1 reference

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Protein kinase C spatially and temporally regulates gap junctional communication during human wound repair via phosphorylation of connexin43 on serine368.

21 January 2018

1 reference

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Familial risk of oral clefts by morphological type and severity: population based cohort study of first degree relatives

21 January 2018

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Mutations of PVRL1, encoding a cell-cell adhesion molecule/herpesvirus receptor, in cleft lip/palate-ectodermal dysplasia

21 January 2018

1 reference

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MSX1 mutation is associated with orofacial clefting and tooth agenesis in humans

21 January 2018

1 reference

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Heart defects in connexin43-deficient mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0022034512447952

Interferon regulatory factor 6 (IRF6) gene variants and the risk of isolated cleft lip or palate

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0022034512447952

21 January 2018

Identifiers

DOI

10.1177/0022034512447952

1 reference

19 March 2018

release_2jdomeebyjgmvhxpb56xxkxczq

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/2jdomeebyjgmvhxpb56xxkxczq

mapped directly with Wikidata item

24 November 2022

based on heuristic

1 reference

19 March 2018