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List of works by Donglin Bai

A Gja1 missense mutation in a mouse model of oculodentodigital dysplasia

scientific article

A dominant loss-of-function GJA1 (Cx43) mutant impairs parturition in the mouse

scientific article

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

scientific article published on 17 May 2013

An atrial-fibrillation-linked connexin40 mutant is retained in the endoplasmic reticulum and impairs the function of atrial gap-junction channels

scientific article published on 13 March 2014

Asparagine 175 of connexin32 is a critical residue for docking and forming functional heterotypic gap junction channels with connexin26.

scientific article published on 8 April 2011

Aspartic acid residue D3 critically determines Cx50 gap junction channel transjunctional voltage-dependent gating and unitary conductance

scientific article

Atrial fibrillation-linked GJA5/connexin40 mutants impaired gap junctions via different mechanisms

scientific article published on 19 March 2014

Atrial fibrillation-linked germline GJA5/connexin40 mutants showed an increased hemichannel function

scientific article

Autosomal recessive GJA1 (Cx43) gene mutations cause oculodentodigital dysplasia by distinct mechanisms

scientific article published on 19 April 2013

Bicuculline-insensitive GABA-gated Cl- channels in the larval nervous system of the moth Manduca sexta

scientific article

Charge at the 46th residue of connexin 50 is crucial for the gap-junctional unitary conductance and transjunctional voltage-dependent gating

scientific article published on 25 September 2014

Crucial motifs and residues in the extracellular loops influence the formation and specificity of connexin docking.

scientific article

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

scientific article

Differential potency of dominant negative connexin43 mutants in oculodentodigital dysplasia

scientific article published on 9 April 2007

Engineered Cx26 variants established functional heterotypic Cx26/Cx43 and Cx26/Cx40 gap junction channels

scientific article published on 17 March 2016

Engineered Cx40 variants increased docking and function of heterotypic Cx40/Cx43 gap junction channels

scientific article published on 25 November 2015

Extracellular domains play different roles in gap junction formation and docking compatibility.

scientific article published on February 2014

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

scientific article

Functional Characterization of Novel Atrial Fibrillation-Linked GJA5 (Cx40) Mutants

scientific article

Functional Characterization of aGJA1Frameshift Mutation Causing Oculodentodigital Dysplasia and Palmoplantar Keratoderma

scientific article published in Journal of Biological Chemistry

Functional characterization of oculodentodigital dysplasia-associated Cx43 mutants

scientific article published in July 2005

Functional roles of the amino terminal domain in determining biophysical properties of Cx50 gap junction channels

scientific article published on 18 December 2013

GABAB receptor modulation of rapid inhibitory and excitatory neurotransmission from subfornical organ and other afferents to median preoptic nucleus neurons.

scientific article published on 18 February 2004

Heterotypic connexin50/connexin50 mutant gap junction channels reveal interactions between two hemichannels during transjunctional voltage-dependent gating

scientific article

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

scientific article

In vivo analysis of undocked connexin43 gap junction hemichannels in ovarian granulosa cells

scientific article published on 30 October 2007

Non-ionotropic cross-talk between AMPA and NMDA receptors in rodent hippocampal neurones

scientific article published in August 2002

Novel GermlineGJA5/Connexin40 Mutations Associated with Lone Atrial Fibrillation Impair Gap Junctional Intercellular Communication ⬇️

scientific article published on April 1, 2013

Oculodentodigital dysplasia-causing connexin43 mutants are non-functional and exhibit dominant effects on wild-type connexin43.

scientific article published on 10 January 2005

Oogenesis defects in a mutant mouse model of oculodentodigital dysplasia

scientific article published on 23 February 2009

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

scientific article

Patch-clamp study reveals that the importance of connexin43-mediated gap junctional communication for ovarian folliculogenesis is strain specific in the mouse

scientific article published on 31 August 2005

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

scientific journal article

Specific functional pathologies of Cx43 mutations associated with oculodentodigital dysplasia

scientific article

Structural analysis of key gap junction domains--Lessons from genome data and disease-linked mutants.

scientific article

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

scientific article

The First Extracellular Domain Plays an Important Role in Unitary Channel Conductance of Cx50 Gap Junction Channels

scientific article published in December 2015

The G60S Cx43 mutant enhances keratinocyte proliferation and differentiation

article

The canonical WNT2 pathway and FSH interact to regulate gap junction assembly in mouse granulosa cells

scientific article published on 22 August 2013

The distribution and functional properties of Pelizaeus-Merzbacher-like disease-linked Cx47 mutations on Cx47/Cx47 homotypic and Cx47/Cx43 heterotypic gap junctions

scientific article published in June 2013

The role of amino terminus of mouse Cx50 in determining transjunctional voltage-dependent gating and unitary conductance

scientific article published on October 2010

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

scientific article

Variants with increased negative electrostatic potential in the Cx50 gap junction pore increased unitary channel conductance and magnesium modulation

scientific article published on 06 November 2018

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