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Somatic Mutations in the Connexin 40 Gene (GJA5) in Atrial Fibrillation

The New England journal of medicine, 2006-06, Vol.354 (25), p.2677-2688

2006

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Novel Germline GJA5/Connexin40 Mutations Associated with Lone Atrial Fibrillation Impair Gap Junctional Intercellular Communication

Human mutation, 2013-04, Vol.34 (4), p.603-609

2013

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The Role of Amino Terminus of Mouse Cx50 in Determining Transjunctional Voltage-Dependent Gating and Unitary Conductance

Biophysical journal, 2010-10, Vol.99 (7), p.2077-2086

2010

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Structure and functional studies of N-terminal Cx43 mutants linked to oculodentodigital dysplasia

Molecular biology of the cell, 2012-09, Vol.23 (17), p.3312-3321

2012

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The severity of mammary gland developmental defects is linked to the overall functional status of Cx43 as revealed by genetically modified mice

Biochemical journal, 2013-01, Vol.449 (2), p.401-413

2013

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Human dermal fibroblasts derived from oculodentodigital dysplasia patients suggest that patients may have wound-healing defects

Human mutation, 2011-04, Vol.32 (4), p.456-466

2011

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Differential Potency of Dominant Negative Connexin43 Mutants in Oculodentodigital Dysplasia

The Journal of biological chemistry, 2007-06, Vol.282 (26), p.19190-19202

2007

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Functional Characterization of a GJA1 Frameshift Mutation Causing Oculodentodigital Dysplasia and Palmoplantar Keratoderma

The Journal of biological chemistry, 2006-10, Vol.281 (42), p.31801-31811

2006

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Pannexin 1 and pannexin 3 are glycoproteins that exhibit many distinct characteristics from the connexin family of gap junction proteins

Journal of cell science, 2007-11, Vol.120 (21), p.3772-3783

2007

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Oculodentodigital Dysplasia-causing Connexin43 Mutants Are Non-functional and Exhibit Dominant Effects on Wild-type Connexin43

The Journal of biological chemistry, 2005-03, Vol.280 (12), p.11458-11466

2005

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A mechanism of gap junction docking revealed by functional rescue of a human-disease-linked connexin mutant

Journal of cell science, 2013-07, Vol.126 (Pt 14), p.3113-3120

2013

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Asparagine 175 of Connexin32 Is a Critical Residue for Docking and Forming Functional Heterotypic Gap Junction Channels with Connexin26

The Journal of biological chemistry, 2011-06, Vol.286 (22), p.19672-19681

2011

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The Canonical WNT2 Pathway and FSH Interact to Regulate Gap Junction Assembly in Mouse Granulosa Cells

Biology of reproduction, 2013-08, Vol.89 (2), p.39-39

2013

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D‐Aspartate and NMDA, but not L‐aspartate, block AMPA receptors in rat hippocampal neurons

British journal of pharmacology, 2005-06, Vol.145 (4), p.449-459

2005

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A Gja1 missense mutation in a mouse model of oculodentodigital dysplasia

Development (Cambridge), 2005-10, Vol.132 (19), p.4375-4386

2005

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A gap junction docking mechanism revealed by functional rescue of a human disease-linked connexin mutant

Journal of cell science, 2013-01

2013

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

Cardiovascular research, 2008-12, Vol.80 (3), p.385-395

2008

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Sodium–hydrogen exchange inhibition attenuates glycoside-induced hypertrophy in rat ventricular myocytes

Cardiovascular research, 2010-01, Vol.85 (1), p.79-89

2010

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D-Serine inhibits AMPA receptor-mediated current in rat hippocampal neurons

Canadian journal of physiology and pharmacology, 2007-05, Vol.85 (5), p.546-555

2007

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Functional Characterization of Oculodentodigital Dysplasia-Associated Cx43 Mutants

Cell communication & adhesion, 2005-01, Vol.12 (5-6), p.279-292

2005

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Size Selectivity Between Gap Junction Channels Composed of Different Connexins

Cell communication & adhesion, 2001, Vol.8 (4-6), p.187-192

2001

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Hydrogen Bonds at the Docking Interface are Critical for Functional Gap Junction Channel Formation of Cx26 and Cx32

Biophysical journal, 2013-01, Vol.104 (2), p.43a-43a

2013

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Molecular Mechanisms Governing Cx26/Cx32 Heterotypic Docking and Functional Gap Junction Channel Formation

Biophysical journal, 2012-01, Vol.102 (3), p.107a-107a

2012

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The Canonical WNT2 Pathway and FSH Interact to Regulate Gap Junction Assembly in Mouse Granulosa Cells1

Biology of reproduction, 2013-08, Vol.89 (2)

2013

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Asparagine175 of Cx32 is a Critical Residue for Docking and Forming Functional Heterotypic Gap Junction Channels with Cx26

Biophysical journal, 2011-02, Vol.100 (3), p.563a-563a

2011

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Somatic Mutations in the Connexin 40 Gene (GJA5) in Atrial Fibrillation

Novel Germline GJA5/Connexin40 Mutations Associated with Lone Atrial Fibrillation Impair Gap Junctional Intercellular Communication

The Role of Amino Terminus of Mouse Cx50 in Determining Transjunctional Voltage-Dependent Gating and Unitary Conductance

Structure and functional studies of N-terminal Cx43 mutants linked to oculodentodigital dysplasia

The severity of mammary gland developmental defects is linked to the overall functional status of Cx43 as revealed by genetically modified mice

Human dermal fibroblasts derived from oculodentodigital dysplasia patients suggest that patients may have wound-healing defects

Differential Potency of Dominant Negative Connexin43 Mutants in Oculodentodigital Dysplasia

Functional Characterization of a GJA1 Frameshift Mutation Causing Oculodentodigital Dysplasia and Palmoplantar Keratoderma

Pannexin 1 and pannexin 3 are glycoproteins that exhibit many distinct characteristics from the connexin family of gap junction proteins

Oculodentodigital Dysplasia-causing Connexin43 Mutants Are Non-functional and Exhibit Dominant Effects on Wild-type Connexin43

A mechanism of gap junction docking revealed by functional rescue of a human-disease-linked connexin mutant

Asparagine 175 of Connexin32 Is a Critical Residue for Docking and Forming Functional Heterotypic Gap Junction Channels with Connexin26

The Canonical WNT2 Pathway and FSH Interact to Regulate Gap Junction Assembly in Mouse Granulosa Cells

D‐Aspartate and NMDA, but not L‐aspartate, block AMPA receptors in rat hippocampal neurons

A Gja1 missense mutation in a mouse model of oculodentodigital dysplasia

A gap junction docking mechanism revealed by functional rescue of a human disease-linked connexin mutant

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

Sodium–hydrogen exchange inhibition attenuates glycoside-induced hypertrophy in rat ventricular myocytes

D-Serine inhibits AMPA receptor-mediated current in rat hippocampal neurons

Functional Characterization of Oculodentodigital Dysplasia-Associated Cx43 Mutants

Size Selectivity Between Gap Junction Channels Composed of Different Connexins

Hydrogen Bonds at the Docking Interface are Critical for Functional Gap Junction Channel Formation of Cx26 and Cx32

Molecular Mechanisms Governing Cx26/Cx32 Heterotypic Docking and Functional Gap Junction Channel Formation

The Canonical WNT2 Pathway and FSH Interact to Regulate Gap Junction Assembly in Mouse Granulosa Cells1

Asparagine175 of Cx32 is a Critical Residue for Docking and Forming Functional Heterotypic Gap Junction Channels with Cx26

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