Connexins, Kv-type ion channels, and pannexins have a dominant role in maintaining the potassium ion homeostasis in the cochlea. The cellular background currents are sustained by Kir2.1 ion channels; however, their involvement in the hearing system is less clear. In this study, the mutations of gap junction proteins beta 2 (GJB2), beta 3 (GJB3) and beta 6 (GJB6) were screened in the white Caucasian population in Hungary using gene mapping and immunofluorescence methods from translated proteins of these genes—connexins on blood cells. Expression of connexins and Kir2.1 ion channels was investigated in the blood cells of deaf patients prior to cochlear implantation, and the results show significantly decreased amounts of connexin26 and connex...
Connexin 26 (Cx26) and Cx30 mediate the intercellular exchange of metabolites and ions within the co...
AbstractConnexins are the protein subunits of gap junction channels that allow a direct signaling pa...
K+-recycling defect is a long-standing hypothesis for deafness mechanism of Connexin26 (Cx26, GJB2) ...
Gap junctions play a critical role in hearing and mutations in connexin genes cause a high incidence...
Gap Junction Beta 2 (GJB2) gene mutations are the leading causes of hereditary hearing impairment. T...
peer reviewedCongenital deafness is a very frequent disorder occurring in approximately I in 1000 li...
peer reviewedCongenital deafness is a very frequent disorder occurring in approximately I in 1000 li...
Gap Junction Beta 2 (GJB2) gene mutations are the leading causes of hereditary hearing impairment. T...
Hearing loss due to mutations in the connexin gene family, which encodes gap junctional proteins, is...
AbstractA number of genes responsible for hearing loss are related to ion recycling and homeostasis ...
Several different recessive mutations in the connexin26 (Cx26; β2) gene have been associated with no...
Several different recessive mutations in the connexin26 (Cx26; β2) gene have been associated with no...
peer reviewedIn the cochlea, connexin 26 (Cx26) and connexin 30 (Cx30) co-assemble into two types o...
Gap-junction channels (GJCs) are formed by headto-head association of two hemichannels (HCs, connexi...
Connexin 26 (Cx26) and Cx30 are the two predominant gap junction constituents expressed in the mamma...
Connexin 26 (Cx26) and Cx30 mediate the intercellular exchange of metabolites and ions within the co...
AbstractConnexins are the protein subunits of gap junction channels that allow a direct signaling pa...
K+-recycling defect is a long-standing hypothesis for deafness mechanism of Connexin26 (Cx26, GJB2) ...
Gap junctions play a critical role in hearing and mutations in connexin genes cause a high incidence...
Gap Junction Beta 2 (GJB2) gene mutations are the leading causes of hereditary hearing impairment. T...
peer reviewedCongenital deafness is a very frequent disorder occurring in approximately I in 1000 li...
peer reviewedCongenital deafness is a very frequent disorder occurring in approximately I in 1000 li...
Gap Junction Beta 2 (GJB2) gene mutations are the leading causes of hereditary hearing impairment. T...
Hearing loss due to mutations in the connexin gene family, which encodes gap junctional proteins, is...
AbstractA number of genes responsible for hearing loss are related to ion recycling and homeostasis ...
Several different recessive mutations in the connexin26 (Cx26; β2) gene have been associated with no...
Several different recessive mutations in the connexin26 (Cx26; β2) gene have been associated with no...
peer reviewedIn the cochlea, connexin 26 (Cx26) and connexin 30 (Cx30) co-assemble into two types o...
Gap-junction channels (GJCs) are formed by headto-head association of two hemichannels (HCs, connexi...
Connexin 26 (Cx26) and Cx30 are the two predominant gap junction constituents expressed in the mamma...
Connexin 26 (Cx26) and Cx30 mediate the intercellular exchange of metabolites and ions within the co...
AbstractConnexins are the protein subunits of gap junction channels that allow a direct signaling pa...
K+-recycling defect is a long-standing hypothesis for deafness mechanism of Connexin26 (Cx26, GJB2) ...