(Q57922088)

1

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Jason Chan

2

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Qing Shao

3

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Dale W Laird

4

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Jared M. Churko

Journal of Investigative Dermatology

1

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language of work or name

English

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publication date

November 2011

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published in

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volume

131

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issue

11

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page(s)

2197-204

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2197-2204

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exact match

https://scigraph.springernature.com/pub.10.1038/jid.2011.183

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cites work

Gap junction development in the human fetal hair follicle and bulge region

1 reference

https://api.crossref.org/works/10.1038%2FJID.2011.183

7 January 2021

Changing patterns of gap junctional intercellular communication and connexin distribution in mouse epidermis and hair follicles during embryonic development

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https://api.crossref.org/works/10.1038%2FJID.2011.183

7 January 2021

The potency of the fs260 connexin43 mutant to impair keratinocyte differentiation is distinct from other disease-linked connexin43 mutants

1 reference

https://api.crossref.org/works/10.1038%2FJID.2011.183

7 January 2021

Cell-cell communication in the osteoblast/osteocyte lineage.

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https://api.crossref.org/works/10.1038%2FJID.2011.183

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

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https://api.crossref.org/works/10.1038%2FJID.2011.183

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Gap junctions: multifaceted regulators of embryonic cortical development

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A Gja1 missense mutation in a mouse model of oculodentodigital dysplasia

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Oculodentodigital dysplasia

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https://api.crossref.org/works/10.1038%2FJID.2011.183

7 January 2021

A gap junction connexin is required in the vertebrate left-right organizer

1 reference

https://api.crossref.org/works/10.1038%2FJID.2011.183

7 January 2021

Connexins and impulse propagation in the mouse heart

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https://api.crossref.org/works/10.1038%2FJID.2011.183

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

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https://api.crossref.org/works/10.1038%2FJID.2011.183

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Novel Connexin 43 (GJA1) mutation causes oculo-dento-digital dysplasia with curly hair

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The gap junction proteome and its relationship to disease

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https://api.crossref.org/works/10.1038%2FJID.2011.183

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Connexin levels regulate keratinocyte differentiation in the epidermis

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https://api.crossref.org/works/10.1038%2FJID.2011.183

7 January 2021

Fate of connexin43 in cardiac tissue harbouring a disease-linked connexin43 mutant.

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https://api.crossref.org/works/10.1038%2FJID.2011.183

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Label-retaining cells (presumptive stem cells) of mice vibrissae do not express gap junction protein connexin 43.

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https://api.crossref.org/works/10.1038%2FJID.2011.183

7 January 2021

Functional characterization of oculodentodigital dysplasia-associated Cx43 mutants.

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ODDD-linked Cx43 mutants reduce endogenous Cx43 expression and function in osteoblasts and inhibit late stage differentiation.

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Connexin43 plays an important role in lung development.

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https://api.crossref.org/works/10.1038%2FJID.2011.183

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

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https://api.crossref.org/works/10.1038%2FJID.2011.183

7 January 2021

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

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Oculodentodigital dysplasia syndrome. Report of four cases

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A 2-bp deletion in the GJA1 gene is associated with oculo-dento-digital dysplasia with palmoplantar keratoderma

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Skin changes in oculo-dento-digital dysplasia are correlated with C-terminal truncations of connexin 43

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