(Q57922088)

1

0 references

Jason Chan

2

0 references

Qing Shao

3

0 references

Dale W Laird

4

0 references

Jared M. Churko

Journal of Investigative Dermatology

1

0 references

language of work or name

English

0 references

publication date

November 2011

0 references

published in

0 references

volume

131

0 references

issue

11

0 references

page(s)

2197-204

0 references

2197-2204

0 references

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

1 reference

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.

1 reference

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

7 January 2021

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

1 reference

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

7 January 2021

Gap junctions: multifaceted regulators of embryonic cortical development

1 reference

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

7 January 2021

A Gja1 missense mutation in a mouse model of oculodentodigital dysplasia

1 reference

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

7 January 2021

Oculodentodigital dysplasia

1 reference

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

1 reference

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

7 January 2021

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

1 reference

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

7 January 2021

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

1 reference

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

7 January 2021

The gap junction proteome and its relationship to disease

1 reference

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

7 January 2021

Connexin levels regulate keratinocyte differentiation in the epidermis

1 reference

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.

1 reference

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

7 January 2021

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

1 reference

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

7 January 2021

Functional characterization of oculodentodigital dysplasia-associated Cx43 mutants.

1 reference

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

7 January 2021

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

1 reference

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

7 January 2021

Connexin43 plays an important role in lung development.

1 reference

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

7 January 2021

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

1 reference

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

1 reference

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

7 January 2021

Oculodentodigital dysplasia syndrome. Report of four cases

1 reference

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

7 January 2021

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

1 reference

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

7 January 2021

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

1 reference

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

7 January 2021