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Search results 1 to 100 out of 854 for Gjb2

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Type Details Score
Gene
2706 | GJB2
Type: gene
Organism: human
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Gene
407154 | GJB2
Type: gene
Organism: cattle
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Gene
428083 | GJB2
Type: gene
Organism: chicken
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Gene
704224 | GJB2
Type: gene
Organism: macaque, rhesus
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Gene
549738 | gjb2
Type: gene
Organism: frog, western clawed
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Gene
key_33768 | GJB2
Type: gene
Organism: sheep
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Gene
394266 | Gjb2
Type: gene
Organism: rat
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Gene
403570 | GJB2
Type: gene
Organism: dog, domestic
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Gene
467220 | GJB2
Type: gene
Organism: chimpanzee
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Protein Coding Gene
MGI:95720 | Gjb2
Type: protein_coding_gene
Organism: mouse, laboratory
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Publication
18793701 | J:141222
First Author: Inoshita A
Year: 2008
Journal: Neuroscience
Title: Postnatal development of the organ of Corti in dominant-negative Gjb2 transgenic mice.
Volume: 156
Issue: 4
Pages: 1039-47
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Publication
31562289 | J:297127
First Author: Lin X
Year: 2019
Journal: Aging (Albany NY)
Title: Hearing consequences in Gjb2 knock-in mice: implications for human p.V37I mutation.
Volume: 11
Issue: 18
Pages: 7416-7441
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Publication
25801282 | J:222433
First Author: Iizuka T
Year: 2015
Journal: Hum Mol Genet
Title: Perinatal Gjb2 gene transfer rescues hearing in a mouse model of hereditary deafness.
Volume: 24
Issue: 13
Pages: 3651-61
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Publication
21876744 | J:176346
First Author: Crispino G
Year: 2011
Journal: PLoS One
Title: BAAV mediated GJB2 gene transfer restores gap junction coupling in cochlear organotypic cultures from deaf Cx26Sox10Cre mice.
Volume: 6
Issue: 8
Pages: e23279
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Publication
35345836 | J:322799
 
First Author: Liu XZ
Year: 2021
Journal: Front Mol Neurosci
Title: F-Actin Dysplasia Involved in Organ of Corti Deformity in Gjb2 Knockdown Mouse Model.
Volume: 14
Pages: 808553
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Publication
29361521 | J:257514
 
First Author: Chen S
Year: 2018
Journal: Dis Model Mech
Title: Developmental abnormalities in supporting cell phalangeal processes and cytoskeleton in the Gjb2 knockdown mouse model.
Volume: 11
Issue: 2
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Publication
26777423 | J:229983
First Author: García IE
Year: 2016
Journal: J Invest Dermatol
Title: From Hyperactive Connexin26 Hemichannels to Impairments in Epidermal Calcium Gradient and Permeability Barrier in the Keratitis-Ichthyosis-Deafness Syndrome.
Volume: 136
Issue: 3
Pages: 574-83
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Publication
22031297 | J:220589
First Author: Mese G
Year: 2011
Journal: Mol Biol Cell
Title: The Cx26-G45E mutation displays increased hemichannel activity in a mouse model of the lethal form of keratitis-ichthyosis-deafness syndrome.
Volume: 22
Issue: 24
Pages: 4776-86
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Publication
36736132 | J:339417
 
First Author: Peres C
Year: 2023
Journal: EBioMedicine
Title: Antibody gene transfer treatment drastically improves epidermal pathology in a keratitis ichthyosis deafness syndrome model using male mice.
Volume: 89
Pages: 104453
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Publication
19047647 | J:142084
First Author: Ortolano S
Year: 2008
Journal: Proc Natl Acad Sci U S A
Title: Coordinated control of connexin 26 and connexin 30 at the regulatory and functional level in the inner ear.
Volume: 105
Issue: 48
Pages: 18776-81
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Publication
22142852 | J:180311
First Author: Qu Y
Year: 2012
Journal: Biochem Biophys Res Commun
Title: Early developmental expression of connexin26 in the cochlea contributes to its dominate functional role in the cochlear gap junctions.
Volume: 417
Issue: 1
Pages: 245-50
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Publication
22098503 | J:184162
First Author: Lynn BD
Year: 2011
Journal: Eur J Neurosci
Title: Ablation of connexin30 in transgenic mice alters expression patterns of connexin26 and connexin32 in glial cells and leptomeninges.
Volume: 34
Issue: 11
Pages: 1783-93
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Publication
17702002 | J:124146
First Author: Qu Y
Year: 2007
Journal: J Comp Neurol
Title: Analysis of connexin subunits required for the survival of vestibular hair cells.
Volume: 504
Issue: 5
Pages: 499-507
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Publication
17227867 | J:119517
First Author: Ahmad S
Year: 2007
Journal: Proc Natl Acad Sci U S A
Title: Restoration of connexin26 protein level in the cochlea completely rescues hearing in a mouse model of human connexin30-linked deafness.
Volume: 104
Issue: 4
Pages: 1337-41
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Publication
26439696 | J:303036
First Author: Stewart MK
Year: 2015
Journal: Oncotarget
Title: Cx26 knockout predisposes the mammary gland to primary mammary tumors in a DMBA-induced mouse model of breast cancer.
Volume: 6
Issue: 35
Pages: 37185-99
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Publication
31034913 | J:289715
 
First Author: Xie L
Year: 2019
Journal: Neurochem Int
Title: Reduced postnatal expression of cochlear Connexin26 induces hearing loss and affects the developmental status of pillar cells in a dose-dependent manner.
Volume: 128
Pages: 196-205
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Publication
35308122 | J:338593
 
First Author: Sun L
Year: 2022
Journal: Front Cell Neurosci
Title: Failure Of Hearing Acquisition in Mice With Reduced Expression of Connexin 26 Correlates With the Abnormal Phasing of Apoptosis Relative to Autophagy and Defective ATP-Dependent Ca(2+) Signaling in Kölliker's Organ.
Volume: 16
Pages: 816079
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Publication
30199819 | J:267859
 
First Author: Fetoni AR
Year: 2018
Journal: Redox Biol
Title: Cx26 partial loss causes accelerated presbycusis by redox imbalance and dysregulation of Nfr2 pathway.
Volume: 19
Pages: 301-317
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Publication
26965868 | J:269202
 
First Author: Green KL
Year: 2016
Journal: Sci Rep
Title: ACEMg Diet Supplement Modifies Progression of Hereditary Deafness.
Volume: 6
Pages: 22690
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Publication
26927086 | J:290005
First Author: Zhou XX
Year: 2016
Journal: Int J Mol Sci
Title: Reduced Connexin26 in the Mature Cochlea Increases Susceptibility to Noise-Induced Hearing Lossin Mice.
Volume: 17
Issue: 3
Pages: 301
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Publication
20926451 | J:166732
First Author: Schütz M
Year: 2011
Journal: Hum Mol Genet
Title: The connexin26 S17F mouse mutant represents a model for the human hereditary keratitis-ichthyosis-deafness syndrome.
Volume: 20
Issue: 1
Pages: 28-39
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Publication
36753545 | J:339757
First Author: Liu LM
Year: 2023
Journal: Sci Adv
Title: Cx26 heterozygous mutations cause hyperacusis-like hearing oversensitivity and increase susceptibility to noise.
Volume: 9
Issue: 6
Pages: eadf4144
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Publication
19712724 | J:155138
First Author: Minekawa A
Year: 2009
Journal: Neuroscience
Title: Cochlear outer hair cells in a dominant-negative connexin26 mutant mouse preserve non-linear capacitance in spite of impaired distortion product otoacoustic emission.
Volume: 164
Issue: 3
Pages: 1312-9
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Publication
28779115 | J:288216
First Author: Crispino G
Year: 2017
Journal: Sci Rep
Title: In vivo genetic manipulation of inner ear connexin expression by bovine adeno-associated viral vectors.
Volume: 7
Issue: 1
Pages: 6567
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Publication
18508043 | J:137725
First Author: Bartholin L
Year: 2008
Journal: Dev Biol
Title: Maternal Tgif is required for vascularization of the embryonic placenta.
Volume: 319
Issue: 2
Pages: 285-97
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Publication
30518746 | J:315629
First Author: Chen S
Year: 2018
Journal: Cell Death Dis
Title: The spatial distribution pattern of Connexin26 expression in supporting cells and its role in outer hair cell survival.
Volume: 9
Issue: 12
Pages: 1180
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Publication
25251605 | J:218449
 
First Author: Chang Q
Year: 2015
Journal: Neurobiol Dis
Title: Timed conditional null of connexin26 in mice reveals temporary requirements of connexin26 in key cochlear developmental events before the onset of hearing.
Volume: 73
Pages: 418-27
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Publication
21813206 | J:187503
First Author: Degen J
Year: 2011
Journal: Eur J Cell Biol
Title: Connexin32 can restore hearing in connexin26 deficient mice.
Volume: 90
Issue: 10
Pages: 817-24
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Publication
37368868 | J:337478
First Author: Kersbergen CJ
Year: 2023
Journal: PLoS Biol
Title: Preservation of developmental spontaneous activity enables early auditory system maturation in deaf mice.
Volume: 21
Issue: 6
Pages: e3002160
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Publication
28077706 | J:238404
First Author: Johnson SL
Year: 2017
Journal: J Neurosci
Title: Connexin-Mediated Signaling in Nonsensory Cells Is Crucial for the Development of Sensory Inner Hair Cells in the Mouse Cochlea.
Volume: 37
Issue: 2
Pages: 258-268
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Publication
26490746 | J:239951
 
First Author: Zhu Y
Year: 2015
Journal: Sci Rep
Title: Connexin26 gap junction mediates miRNA intercellular genetic communication in the cochlea and is required for inner ear development.
Volume: 5
Pages: 15647
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Publication
24732355 | J:219459
First Author: Chen J
Year: 2014
Journal: Biochem Biophys Res Commun
Title: Deafness induced by Connexin 26 (GJB2) deficiency is not determined by endocochlear potential (EP) reduction but is associated with cochlear developmental disorders.
Volume: 448
Issue: 1
Pages: 28-32
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Publication
19673007 | J:187353
First Author: Sun Y
Year: 2009
Journal: J Comp Neurol
Title: Connexin30 null and conditional connexin26 null mice display distinct pattern and time course of cellular degeneration in the cochlea.
Volume: 516
Issue: 6
Pages: 569-79
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Publication
1849321 | J:11099
First Author: Hsieh CL
Year: 1991
Journal: Somat Cell Mol Genet
Title: Distribution of genes for gap junction membrane channel proteins on human and mouse chromosomes.
Volume: 17
Issue: 2
Pages: 191-200
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Publication
24333301 | J:206835
 
First Author: Takada Y
Year: 2014
Journal: Hear Res
Title: Connexin 26 null mice exhibit spiral ganglion degeneration that can be blocked by BDNF gene therapy.
Volume: 309
Pages: 124-35
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Publication
26232528 | J:315404
 
First Author: Lee MY
Year: 2015
Journal: Hear Res
Title: Mice with conditional deletion of Cx26 exhibit no vestibular phenotype despite secondary loss of Cx30 in the vestibular end organs.
Volume: 328
Pages: 102-12
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Publication
19047635 | J:178055
First Author: Anselmi F
Year: 2008
Journal: Proc Natl Acad Sci U S A
Title: ATP release through connexin hemichannels and gap junction transfer of second messengers propagate Ca2+ signals across the inner ear.
Volume: 105
Issue: 48
Pages: 18770-5
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Publication
28823936 | J:259579
 
First Author: Mei L
Year: 2017
Journal: Neurobiol Dis
Title: A deafness mechanism of digenic Cx26 (GJB2) and Cx30 (GJB6) mutations: Reduction of endocochlear potential by impairment of heterogeneous gap junctional function in the cochlear lateral wall.
Volume: 108
Pages: 195-203
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Publication
20510229 | J:165759
First Author: Chiu HS
Year: 2010
Journal: Dev Biol
Title: Comparative gene expression analysis of genital tubercle development reveals a putative appendicular Wnt7 network for the epidermal differentiation.
Volume: 344
Issue: 2
Pages: 1071-87
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Publication
26035172 | J:233555
 
First Author: Chen J
Year: 2015
Journal: Sci Rep
Title: Pannexin1 channels dominate ATP release in the cochlea ensuring endocochlear potential and auditory receptor potential generation and hearing.
Volume: 5
Pages: 10762
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Protein Coding Gene
MGP_CAROLIEiJ_G0019345 | -
Type: protein_coding_gene
Organism: Mus caroli
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Protein Coding Gene
MGP_129S1SvImJ_G0021402 | -
Type: protein_coding_gene
Organism: mouse, laboratory
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Protein Coding Gene
MGP_AJ_G0021363 | -
Type: protein_coding_gene
Organism: mouse, laboratory
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Protein Coding Gene
MGP_AKRJ_G0021338 | -
Type: protein_coding_gene
Organism: mouse, laboratory
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Protein Coding Gene
MGP_BALBcJ_G0021366 | -
Type: protein_coding_gene
Organism: mouse, laboratory
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Protein Coding Gene
MGP_C3HHeJ_G0021145 | -
Type: protein_coding_gene
Organism: mouse, laboratory
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Protein Coding Gene
MGI_C57BL6J_95720 | -
Type: protein_coding_gene
Organism: mouse, laboratory
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Protein Coding Gene
MGP_C57BL6NJ_G0021805 | -
Type: protein_coding_gene
Organism: mouse, laboratory
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Protein Coding Gene
MGP_CASTEiJ_G0020663 | -
Type: protein_coding_gene
Organism: mouse, laboratory
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Protein Coding Gene
MGP_CBAJ_G0021112 | -
Type: protein_coding_gene
Organism: mouse, laboratory
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Protein Coding Gene
MGP_DBA2J_G0021233 | -
Type: protein_coding_gene
Organism: mouse, laboratory
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Protein Coding Gene
MGP_FVBNJ_G0021214 | -
Type: protein_coding_gene
Organism: mouse, laboratory
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Protein Coding Gene
MGP_LPJ_G0021308 | -
Type: protein_coding_gene
Organism: mouse, laboratory
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Protein Coding Gene
MGP_NODShiLtJ_G0021242 | -
Type: protein_coding_gene
Organism: mouse, laboratory
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Protein Coding Gene
MGP_NZOHlLtJ_G0021829 | -
Type: protein_coding_gene
Organism: mouse, laboratory
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Protein Coding Gene
MGP_PWKPhJ_G0020406 | -
Type: protein_coding_gene
Organism: mouse, laboratory
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Protein Coding Gene
MGP_WSBEiJ_G0020715 | -
Type: protein_coding_gene
Organism: mouse, laboratory
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Protein Coding Gene
MGP_PahariEiJ_G0030363 | -
Type: protein_coding_gene
Organism: Mus pahari
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Protein Coding Gene
MGP_SPRETEiJ_G0020239 | -
Type: protein_coding_gene
Organism: Mus spretus
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Publication
21714813 | J:177941
First Author: Nagy JI
Year: 2011
Journal: Eur J Neurosci
Title: Connexin26 expression in brain parenchymal cells demonstrated by targeted connexin ablation in transgenic mice.
Volume: 34
Issue: 2
Pages: 263-71
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Publication
12121617 | J:77823
First Author: Cohen-Salmon M
Year: 2002
Journal: Curr Biol
Title: Targeted ablation of connexin26 in the inner ear epithelial gap junction network causes hearing impairment and cell death.
Volume: 12
Issue: 13
Pages: 1106-11
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Publication
24491564 | J:218582
First Author: Chen S
Year: 2014
Journal: Biochem Biophys Res Commun
Title: Down regulated connexin26 at different postnatal stage displayed different types of cellular degeneration and formation of organ of Corti.
Volume: 445
Issue: 1
Pages: 71-7
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Publication
16740338 | J:115078
First Author: Ott T
Year: 2006
Journal: Eur J Cell Biol
Title: Ablation of gap junctional communication in hepatocytes of transgenic mice does not lead to disrupted cellular homeostasis or increased spontaneous tumourigenesis.
Volume: 85
Issue: 8
Pages: 717-28
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Publication
27959894 | J:256797
First Author: Chan DK
Year: 2016
Journal: PLoS One
Title: Sound-Induced Intracellular Ca2+ Dynamics in the Adult Hearing Cochlea.
Volume: 11
Issue: 12
Pages: e0167850
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Publication
24988191 | J:218935
First Author: Stewart MK
Year: 2014
Journal: PLoS One
Title: Mammary gland specific knockdown of the physiological surge in Cx26 during lactation retains normal mammary gland development and function.
Volume: 9
Issue: 7
Pages: e101546
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Publication
25451287 | J:221450
 
First Author: Zhu Y
Year: 2015
Journal: Neuroscience
Title: Connexin26 (GJB2) deficiency reduces active cochlear amplification leading to late-onset hearing loss.
Volume: 284
Pages: 719-29
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Publication
18308698 | J:135639
First Author: Marx-Stoelting P
Year: 2008
Journal: Toxicol Sci
Title: Tumor promotion in liver of mice with a conditional Cx26 knockout.
Volume: 103
Issue: 2
Pages: 260-7
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Publication
22975134 | J:189014
First Author: Liang C
Year: 2012
Journal: Neurosci Lett
Title: Cell degeneration is not a primary causer for Connexin26 (GJB2) deficiency associated hearing loss.
Volume: 528
Issue: 1
Pages: 36-41
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Publication
33505961 | J:341879
 
First Author: Xu K
Year: 2020
Journal: Front Cell Dev Biol
Title: Local Macrophage-Related Immune Response Is Involved in Cochlear Epithelial Damage in Distinct Gjb2-Related Hereditary Deafness Models.
Volume: 8
Pages: 597769
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Publication
32958814 | J:346709
First Author: van de Wiel J
Year: 2020
Journal: Commun Biol
Title: Connexin26 mediates CO(2)-dependent regulation of breathing via glial cells of the medulla oblongata.
Volume: 3
Issue: 1
Pages: 521
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Publication
26070424 | J:223754
First Author: Bosen F
Year: 2015
Journal: FEBS Lett
Title: Altered epidermal lipid processing and calcium distribution in the KID syndrome mouse model Cx26S17F.
Volume: 589
Issue: 15
Pages: 1904-10
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Publication
36699003 | J:346040
 
First Author: Abbott AC
Year: 2022
Journal: Front Cell Dev Biol
Title: Expression of KID syndromic mutation Cx26S17F produces hyperactive hemichannels in supporting cells of the organ of Corti.
Volume: 10
Pages: 1071202
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Publication
28569788 | J:314310
First Author: Press E
Year: 2017
Journal: Cell Death Dis
Title: Disease-linked connexin26 S17F promotes volar skin abnormalities and mild wound healing defects in mice.
Volume: 8
Issue: 6
Pages: e2845
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Publication
10751667 | J:62241
First Author: Frenz CM
Year: 2000
Journal: Brain Res Brain Res Rev
Title: Immunolocalization of connexin 26 in the developing mouse cochlea.
Volume: 32
Issue: 1
Pages: 172-80
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Publication
8014476 | J:19346
First Author: Monaghan P
Year: 1994
Journal: J Histochem Cytochem
Title: Rapid modulation of gap junction expression in mouse mammary gland during pregnancy, lactation, and involution.
Volume: 42
Issue: 7
Pages: 931-8
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Publication
9139825 | J:47816
First Author: Kelsell DP
Year: 1997
Journal: Nature
Title: Connexin 26 mutations in hereditary non-syndromic sensorineural deafness.
Volume: 387
Issue: 6628
Pages: 80-3
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Publication
14681042 | J:135603
First Author: Bakirtzis G
Year: 2003
Journal: Cell Commun Adhes
Title: The effects of a mutant connexin 26 on epidermal differentiation.
Volume: 10
Issue: 4-6
Pages: 359-64
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GXD Expression
GXD Expression
   
Probe: MGI:2665049
Assay Type: RT-PCR
Annotation Date: 2003-07-11
Strength: Absent
Sex: Not Specified
Emaps: EMAPS:360411
Stage: TS01
Assay Id: MGI:2665071
Age: embryonic day 0.5
Image: 2
Specimen Label: 1-cell
Detected: false
Specimen Num: 2
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GXD Expression
GXD Expression
   
Probe: MGI:2665049
Assay Type: RT-PCR
Annotation Date: 2003-07-11
Strength: Present
Sex: Not Specified
Emaps: EMAPS:1684628
Stage: TS28
Assay Id: MGI:2665071
Age: postnatal adult
Image: 2
Specimen Label: Liver
Detected: true
Specimen Num: 9
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GXD Expression
GXD Expression
   
Probe: MGI:2665049
Assay Type: RT-PCR
Annotation Date: 2003-07-11
Strength: Absent
Sex: Not Specified
Emaps: EMAPS:1610528
Stage: TS28
Assay Id: MGI:2665071
Age: postnatal adult
Image: 2
Specimen Label: Heart
Detected: false
Specimen Num: 10
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GXD Expression
GXD Expression
   
Probe: MGI:2664894
Assay Type: Nuclease S1
Annotation Date: 2003-07-11
Strength: Present
Sex: Not Specified
Emaps: EMAPS:1684628
Stage: TS28
Assay Id: MGI:2665096
Age: postnatal adult
Image: 4
Specimen Label: Liver
Detected: true
Specimen Num: 3
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GXD Expression
GXD Expression
   
Probe: MGI:2664894
Assay Type: Nuclease S1
Annotation Date: 2003-07-11
Strength: Absent
Sex: Not Specified
Emaps: EMAPS:1610528
Stage: TS28
Assay Id: MGI:2665096
Age: postnatal adult
Image: 4
Specimen Label: heart
Detected: false
Specimen Num: 4
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GXD Expression
GXD Expression
   
Probe: MGI:2664894
Assay Type: Nuclease S1
Annotation Date: 2003-07-11
Strength: Present
Sex: Not Specified
Emaps: EMAPS:3526928
Stage: TS28
Assay Id: MGI:2665117
Age: embryonic day 5.5
Image: 6
Specimen Label: 5.5p.c.
Detected: true
Specimen Num: 3
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GXD Expression
GXD Expression
   
Probe: MGI:2664894
Assay Type: Nuclease S1
Annotation Date: 2003-07-11
Strength: Present
Sex: Not Specified
Emaps: EMAPS:160427
Stage: TS07
Assay Id: MGI:2665117
Age: embryonic day 5.5
Image: 6
Specimen Label: 5.5p.c.
Detected: true
Specimen Num: 3
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GXD Expression
GXD Expression
   
Probe: MGI:2664894
Assay Type: Nuclease S1
Annotation Date: 2003-07-11
Strength: Present
Sex: Not Specified
Emaps: EMAPS:3526928
Stage: TS28
Assay Id: MGI:2665117
Age: embryonic day 6.5
Image: 6
Specimen Label: 6.5
Detected: true
Specimen Num: 4
•
•
•
•
•
GXD Expression
GXD Expression
   
Probe: MGI:2664894
Assay Type: Nuclease S1
Annotation Date: 2003-07-11
Strength: Present
Sex: Not Specified
Emaps: EMAPS:160429
Stage: TS09
Assay Id: MGI:2665117
Age: embryonic day 6.5
Image: 6
Specimen Label: 6.5
Detected: true
Specimen Num: 4
•
•
•
•
•
GXD Expression
GXD Expression
   
Probe: MGI:2664894
Assay Type: Nuclease S1
Annotation Date: 2003-07-11
Strength: Present
Sex: Not Specified
Emaps: EMAPS:3526928
Stage: TS28
Assay Id: MGI:2665117
Age: embryonic day 7.5
Image: 6
Specimen Label: 7.5
Detected: true
Specimen Num: 5
•
•
•
•
•
GXD Expression
GXD Expression
   
Probe: MGI:2664894
Assay Type: Nuclease S1
Annotation Date: 2003-07-11
Strength: Present
Sex: Not Specified
Emaps: EMAPS:1604211
Stage: TS11
Assay Id: MGI:2665117
Age: embryonic day 7.5
Image: 6
Specimen Label: 7.5
Detected: true
Specimen Num: 5
•
•
•
•
•
GXD Expression
GXD Expression
   
Probe: MGI:2664894
Assay Type: Nuclease S1
Annotation Date: 2003-07-11
Strength: Present
Sex: Not Specified
Emaps: EMAPS:3526928
Stage: TS28
Assay Id: MGI:2665117
Age: embryonic day 9.5
Image: 6
Specimen Label: 9.5
Detected: true
Specimen Num: 6
•
•
•
•
•
GXD Expression
GXD Expression
   
Probe: MGI:2664894
Assay Type: Nuclease S1
Annotation Date: 2003-07-11
Strength: Present
Sex: Not Specified
Emaps: EMAPS:1604215
Stage: TS15
Assay Id: MGI:2665117
Age: embryonic day 9.5
Image: 6
Specimen Label: 9.5
Detected: true
Specimen Num: 6
•
•
•
•
•




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