Comparative genomic analysis of eutherian connexin genes.Premzl M.Cited forNUCLEOTIDE SEQUENCECategorySequencesSourceUniProtKB unreviewed (TrEMBL)Sci. Rep. 9:16938-16938 (2019)Cited in99+
Connexin32-null mice develop demyelinating peripheral neuropathy.Scherer S.S., Xu Y.T., Nelles E., Fischbeck K., Willecke K., Bone L.J.View abstractCategorySequencesSourceMGI: 95719PubMedEurope PMCGlia 24:8-20 (1998)Mapped to2
Transplacental uptake of glucose is decreased in embryonic lethal connexin26-deficient mice.Gabriel H.D., Jung D., Butzler C., Temme A., Traub O., Winterhager E., Willecke K.View abstractCategoriesSequences, ExpressionSourceMGI: 95719PubMedEurope PMCJ Cell Biol 140:1453-1461 (1998)Mapped to29
Animal models for inherited peripheral neuropathies.Martini R.View abstractCategorySequencesSourceMGI: 95719PubMedEurope PMCJ Anat 191:321-336 (1997)Mapped to7
Connexin32 gene mutations in X-linked dominant Charcot-Marie-Tooth disease (CMTX1).Janssen E.A.M., Kemp S., Hensels G.W., Sie O.G., de Die-Smulders C.E.M., Hoogendijk J.E., de Visser M., Bolhuis P.A.View abstractCategorySequencesSourceMGI: 95719PubMedEurope PMCHum. Genet. 99:501-505 (1997)Cited in1Mapped to2
A second alternative transcript of the gap junction gene connexin32 is expressed in murine Schwann cells and modulated in injured sciatic nerve.Sohl G., Gillen C., Bosse F., Gleichmann M., Muller H.W., Willecke K.View abstractCategorySequencesSourceMGI: 95719PubMedEurope PMCEur J Cell Biol 69:267-275 (1996)Mapped to2
Defective propagation of signals generated by sympathetic nerve stimulation in the liver of connexin32-deficient mice.Nelles E., Butzler C., Jung D., Temme A., Gabriel H.D., Dahl U., Traub O., Stumpel F., Jungermann K.[...], Willecke K.View abstractCategorySequencesSourceMGI: 95719PubMedEurope PMCProc Natl Acad Sci U S A 93:9565-9570 (1996)Mapped to2
Multiple members of the connexin gene family participate in preimplantation development of the mouse.Davies T.C., Barr K.J., Jones D.H., Zhu D., Kidder G.M.View abstractCategoriesSequences, ExpressionSourceMGI: 95719PubMedEurope PMCDev Genet 18:234-243 (1996)Mapped to42
Molecular basis of common hereditary motor and sensory neuropathies in humans and in mouse models.Snipes G.J., Suter U.View abstractCategorySequencesSourceMGI: 95719PubMedEurope PMCBrain Pathol 5:233-247 (1995)Mapped to7
Physical mapping of 2000 kb of the mouse X chromosome in the vicinity of the Xist locus.Cooper P., Keer J.T., McCabe V.M., Hamvas R.M., Brown S.D., Rastan S., Brockdorff N.View abstractCategorySequencesSourceMGI: 95719PubMedEurope PMCGenomics 15:570-575 (1993)Mapped to18
Murine chromosomal location of four class III POU transcription factors.Avraham K.B., Cho B.C., Gilbert D., Fujii H., Okamoto K., Shimazaki T., Ito T., Shoji H., Wakamatsu Y., Kondoh H.View abstractCategorySequencesSourceMGI: 95719PubMedEurope PMCGenomics 18:131-133 (1993)Mapped to36
Genomic organization and chromosomal localization of mouse Eplg2, a gene encoding a binding protein for the receptor tyrosine kinase elk.Fletcher F.A., Renshaw B., Hollingsworth T., Baum P., Lyman S.D., Jenkins N.A., Gilbert D.J., Copeland N.G., Davison B.L.View abstractCategorySequencesSourceMGI: 95719PubMedEurope PMCGenomics 24:127-132 (1994)Cited in1Mapped to10
The murine interleukin-2 receptor gamma chain gene: organization, chromosomal localization and expression in the adult thymus.Disanto J.P., Certain S., Wilson A., Macdonald H.R., Avner P., Fischer A., de Saint Basile G.View abstractCategorySequencesSourceMGI: 95719PubMedEurope PMCEur. J. Immunol. 24:3014-3018 (1994)Cited in1Mapped to60
Structure, chromosomal location, and expression pattern of three mouse genes homologous to the human MAGE genes.De Backer O., Verheyden A.M., Martin B., Godelaine D., De Plaen E., Brasseur R., Avner P., Boon T.View abstractCategoriesSequences, ExpressionSourceMGI: 95719PubMedEurope PMCGenomics 28:74-83 (1995)Cited in3Mapped to51
Connexin32 Promotes the Activation of Foxo3a to Ameliorate Diabetic Nephropathy <i>via</i> Inhibiting the Polyubiquitination and Degradation of Sirt1.Li S., Xiao H., Sun X., Chen Z., Lin Z., Li C., Zeng J., Xu Z., Cheng Y., Huang H.View abstractAnnotationConnexin32 Promotes the Activation of Foxo3a to Ameliorate Diabetic Nephropathy via Inhibiting the Polyubiquitination and Degradation of Sirt1.CategorySequencesSourceGeneRif: 14618PubMedEurope PMCAntioxid Redox Signal 39:241-261 (2023)Mapped to4
Connexin32 ameliorates epithelial-to-mesenchymal-transition in diabetic renal tubular via inhibiting NOX4.Sun X., Xiao H., Li S., Chen R., Lin Z., Yang Y., Chen Z., Deng L., Huang H.View abstractAnnotationConnexin32 ameliorates epithelial-to-mesenchymal-transition in diabetic renal tubular via inhibiting NOX4.CategorySequencesSourceGeneRif: 14618, MGI: 95719PubMedEurope PMCPharmacol Res 176:106084-106084 (2022)Mapped to9
SkM1 and Cx32 improve conduction in canine myocardial infarcts yet only SkM1 is antiarrhythmic.Boink G.J., Lau D.H., Shlapakova I.N., Sosunov E.A., Anyukhovsky E.P., Driessen H.E., Dun W., Chen M., Danilo P. Jr.[...], Rosen M.R.View abstractAnnotationCx32 therapy improves gap junctional conductance results in larger infarct size and no antiarrhythmic efficacy.CategorySequencesSourceGeneRif: 14618PubMedEurope PMCCardiovasc Res 94:450-459 (2012)Mapped to2
Connexin32 can restore hearing in connexin26 deficient mice.Degen J., Schutz M., Dicke N., Strenzke N., Jokwitz M., Moser T., Willecke K.View abstractAnnotationCx32 can functionally replace Cx26 in the mouse cochlea resulting in almost normal hearingCategorySequencesSourceGeneRif: 14618, MGI: 95719PubMedEurope PMCEur J Cell Biol 90:817-824 (2011)Mapped to15
PITX2c is expressed in the adult left atrium, and reducing Pitx2c expression promotes atrial fibrillation inducibility and complex changes in gene expression.Kirchhof P., Kahr P.C., Kaese S., Piccini I., Vokshi I., Scheld H.H., Rotering H., Fortmueller L., Laakmann S.[...], Brown N.A.View abstractCategoriesFunction, SequencesSourceMGI: 95719PubMedEurope PMCCirc Cardiovasc Genet 4:123-133 (2011)Mapped to99+
Developmental regulation of gap junction gene expression during mouse embryonic development.Nishi M., Kumar N.M., Gilula N.B.View abstractCategoriesSequences, ExpressionSourceMGI: 95719PubMedEurope PMCDev. Biol. 146:117-130 (1991)Cited in3Mapped to12
Characterization of a murine gene expressed from the inactive X chromosome.Borsani G., Tonlorenzi R., Simmler M.C., Dandolo L., Arnaud D., Capra V., Grompe M., Pizzuti A., Muzny D.[...], Ballabio A.View abstractCategorySequencesSourceMGI: 95719PubMedEurope PMCNature 351:325-329 (1991)Mapped to52
Six genes of the human connexin gene family coding for gap junctional proteins are assigned to four different human chromosomes.Willecke K., Jungbluth S., Dahl E., Hennemann H., Heynkes R., Grzeschik K.H.View abstractCategorySequencesSourceMGI: 95719PubMedEurope PMCEur J Cell Biol 53:275-280 (1990)Mapped to18
Distribution of genes for gap junction membrane channel proteins on human and mouse chromosomes.Hsieh C.L., Kumar N.M., Gilula N.B., Francke U.View abstractCategorySequencesSourceMGI: 95719PubMedEurope PMCSomat Cell Mol Genet 17:191-200 (1991)Mapped to20
Identification of connexin36 in gap junctions between neurons in rodent locus coeruleus.Rash J.E., Olson C.O., Davidson K.G., Yasumura T., Kamasawa N., Nagy J.I.View abstractCategoriesSequences, ExpressionSourceMGI: 95719PubMedEurope PMCNeuroscience 147:938-956 (2007)Mapped to8
The transcriptional landscape of the mammalian genome.Carninci P., Kasukawa T., Katayama S., Gough J., Frith M.C., Maeda N., Oyama R., Ravasi T., Lenhard B.[...], Hayashizaki Y.View abstractCategorySequencesSourceMGI: 95719PubMedEurope PMCScience 309:1559-1563 (2005)Cited in99+16Mapped to99+