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Polydisperse molecular architecture of connexin 26/30 heteromeric hemichannels revealed by atomic force microscopy imaging

The Journal of biological chemistry, 2020-12, Vol.295 (49), p.16499-16509

2020

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Structure of native lens connexin 46/50 intercellular channels by cryo-EM

Nature (London), 2018-12, Vol.564 (7736), p.372-377

2018

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A pore locus in the E1 domain differentially regulates Cx26 and Cx30 hemichannel function

The Journal of general physiology, 2024-11, Vol.156 (11)

2024

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An Ala/Glu difference in E1 of Cx26 and Cx30 contributes to their differential anionic permeabilities

The Journal of general physiology, 2024-11, Vol.156 (11)

2024

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Expression and Functionality of Connexin-Based Channels in Human Liver Cancer Cell Lines

International journal of molecular sciences, 2021-11, Vol.22 (22), p.12187

2021

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Subcellular Localization of Connexin 26 in Cardiomyocytes and in Cardiomyocyte-Derived Extracellular Vesicles

Molecules (Basel, Switzerland), 2021-11, Vol.26 (21), p.6726

2021

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Cx26 partial loss causes accelerated presbycusis by redox imbalance and dysregulation of Nfr2 pathway

Redox biology, 2018-10, Vol.19, p.301-317

2018

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Connexin-Based Channel Activity Is Not Specifically Altered by Hepatocarcinogenic Chemicals

International journal of molecular sciences, 2021-10, Vol.22 (21), p.11724

2021

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Modeling gap junction beta 2 gene-related deafness with human iPSC

Human molecular genetics, 2021-07, Vol.30 (15), p.1429-1442

2021

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Structures of wild-type and a constitutively closed mutant of connexin26 shed light on channel regulation by CO 2

eLife, 2024-06, Vol.13

2024

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Tricellular adherens junctions provide a cell surface delivery platform for connexin 26/30 oligomers in the cochlea

Hearing research, 2021-02, Vol.400, p.108137-108137, Article 108137

2021

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Transforming Growth Factor Beta 1 Drives a Switch in Connexin Mediated Cell-to-Cell Communication in Tubular Cells of the Diabetic Kidney

Cellular physiology and biochemistry, 2018-04, Vol.45 (6), p.2369-2388

2018

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Heart and liver connexin expression related to the first stage of aging: A study on naturally aged animals

Acta histochemica, 2020-12, Vol.122 (8), p.151651-151651, Article 151651

2020

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Identification of homozygous mutations for hearing loss

Gene, 2021-04, Vol.778, p.145464-145464, Article 145464

2021

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Microarray-based screening system identifies temperature-controlled activity of Connexin 26 that is distorted by mutations

Scientific reports, 2019-09, Vol.9 (1), p.13543-12, Article 13543

2019

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PUPIL enables mapping and stamping of transient electrical connectivity in developing nervous systems

Cell reports (Cambridge), 2021-10, Vol.37 (3), p.109853-109853, Article 109853

2021

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Analysis of miRNA-mRNA Interaction Network Reveals Gap Junction Beta 2 as a Potential Candidate Gene Involved in Psoriatic Hearing Loss Pathogenesis

Combinatorial chemistry & high throughput screening, 2021-01, Vol.24 (7), p.976-985

2021

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Genomic and transcriptomic characterization of desmoplastic small round cell tumors

Genes chromosomes & cancer, 2021-09, Vol.60 (9), p.595-603

2021

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Revertant mosaicism repairs skin lesions in a patient with keratitis-ichthyosis-deafness syndrome by second-site mutations in connexin 26

Human molecular genetics, 2017-03, Vol.26 (6), p.1070-1077

2017

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Generation of hiPSC line UMi030-A from an individual with the hearing loss-related GJB2 mutation c.109G > A

Stem cell research, 2022-01, Vol.58, p.102599-102599, Article 102599

2022

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Precise control of ion channel and gap junction expression is required for patterning of the regenerating axolotl limb

The International journal of developmental biology, 2020, Vol.64 (10-11-12), p.485-494

2020

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The Expression of Connexin 26 Regulates the Radiosensitivity of Hepatocellular Carcinoma Cells through a Mitogen-Activated Protein Kinases Signal Pathway

International journal of molecular sciences, 2022-11, Vol.23 (23), p.14644

2022

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Computational Studies of Molecular Permeation through Connexin26 Channels

Biophysical journal, 2016-02, Vol.110 (3), p.584-599

2016

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The p.Gly130Val mutation in the GJB2 gene: A familiar case of autosomal dominant non-syndromic hearing loss

International journal of pediatric otorhinolaryngology, 2019-12, Vol.127, p.109653-109653, Article 109653

2019

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Concatenation of Human Connexin26 (hCx26) and Human Connexin46 (hCx46) for the Analysis of Heteromeric Gap Junction Hemichannels and Heterotypic Gap Junction Channels

International journal of molecular sciences, 2018-09, Vol.19 (9), p.2742

2018

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Polydisperse molecular architecture of connexin 26/30 heteromeric hemichannels revealed by atomic force microscopy imaging

Structure of native lens connexin 46/50 intercellular channels by cryo-EM

A pore locus in the E1 domain differentially regulates Cx26 and Cx30 hemichannel function

An Ala/Glu difference in E1 of Cx26 and Cx30 contributes to their differential anionic permeabilities

Expression and Functionality of Connexin-Based Channels in Human Liver Cancer Cell Lines

Subcellular Localization of Connexin 26 in Cardiomyocytes and in Cardiomyocyte-Derived Extracellular Vesicles

Cx26 partial loss causes accelerated presbycusis by redox imbalance and dysregulation of Nfr2 pathway

Connexin-Based Channel Activity Is Not Specifically Altered by Hepatocarcinogenic Chemicals

Modeling gap junction beta 2 gene-related deafness with human iPSC

Structures of wild-type and a constitutively closed mutant of connexin26 shed light on channel regulation by CO 2

Tricellular adherens junctions provide a cell surface delivery platform for connexin 26/30 oligomers in the cochlea

Transforming Growth Factor Beta 1 Drives a Switch in Connexin Mediated Cell-to-Cell Communication in Tubular Cells of the Diabetic Kidney

Heart and liver connexin expression related to the first stage of aging: A study on naturally aged animals

Identification of homozygous mutations for hearing loss

Microarray-based screening system identifies temperature-controlled activity of Connexin 26 that is distorted by mutations

PUPIL enables mapping and stamping of transient electrical connectivity in developing nervous systems

Analysis of miRNA-mRNA Interaction Network Reveals Gap Junction Beta 2 as a Potential Candidate Gene Involved in Psoriatic Hearing Loss Pathogenesis

Genomic and transcriptomic characterization of desmoplastic small round cell tumors

Revertant mosaicism repairs skin lesions in a patient with keratitis-ichthyosis-deafness syndrome by second-site mutations in connexin 26

Generation of hiPSC line UMi030-A from an individual with the hearing loss-related GJB2 mutation c.109G > A

Precise control of ion channel and gap junction expression is required for patterning of the regenerating axolotl limb

The Expression of Connexin 26 Regulates the Radiosensitivity of Hepatocellular Carcinoma Cells through a Mitogen-Activated Protein Kinases Signal Pathway

Computational Studies of Molecular Permeation through Connexin26 Channels

The p.Gly130Val mutation in the GJB2 gene: A familiar case of autosomal dominant non-syndromic hearing loss

Concatenation of Human Connexin26 (hCx26) and Human Connexin46 (hCx46) for the Analysis of Heteromeric Gap Junction Hemichannels and Heterotypic Gap Junction Channels

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