Related references
Note: Only part of the references are listed.The conditional connexin43G138R mouse mutant represents a new model of hereditary oculodentodigital dysplasia in humans
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Gating properties of heterotypic gap junction channels formed of connexins 40, 43, 45
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Skin changes in oculo-dento-digital dysplasia are correlated with C-terminal truncations of connexin 43
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Connexin30.2 containing gap junction channels decelerate impulse propagation through the atrioventricular node
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A Gja1 missense mutation in a mouse model of oculodentodigital dysplasia
AM Flenniken et al.
DEVELOPMENT (2005)
Novel GJA1 mutations in patients with oculo-dento-digital dysplasia (ODDD)
P Debeer et al.
EUROPEAN JOURNAL OF MEDICAL GENETICS (2005)
Connexin phosphorylation as a regulatory event linked to gap junction internalization and degradation
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BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES (2005)
Functional characterization of connexin43 mutations found in patients with oculodentodigital dysplasia
J Shibayama et al.
CIRCULATION RESEARCH (2005)
Oculodentodigital dysplasia-causing connexin43 mutants are non-functional and exhibit dominant effects on wild-type connexin43
W Roscoe et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2005)
A 2-bp deletion in the GJA1 gene is associated with oculo-dento-digital dysplasia with palmoplantar keratoderma
MAM van Steensel et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2005)
Remodelling of gap junctions and connexin expression in heart disease
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Functional role of connexin43 gap junction channels in adult mouse heart assessed by inducible gene deletion
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Alterations of intercellular communication in neonatal cardiac myocytes from connexin43 null mice
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Connexin43 phosphorylation at S368 is acute during S and G2/M and in response to protein kinase C activation
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JOURNAL OF CELL SCIENCE (2003)
Connexin 43 (GJA1) mutations cause the pleiotropic phenotype of oculodentodigital dysplasia
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AMERICAN JOURNAL OF HUMAN GENETICS (2003)
Up-regulation of connexin45 in heart failure
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Gap junction remodeling and cardiac arrhythmogenesis: cause or coincidence?
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Conduction slowing and sudden arrhythmic death in mice with cardiac-restricted inactivation of connexin43
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Altered connexin expression in human congestive heart failure
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Conditional gene targeting of connexin43: Exploring the consequences of gap junction remodeling in the heart
DE Gutstein et al.
CELL COMMUNICATION AND ADHESION (2001)
Regulation of gap junctions by phosphorylation of connexins
PD Lampe et al.
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS (2000)
Gap junctions in cardiovascular disease
HJ Jongsma et al.
CIRCULATION RESEARCH (2000)