Pages that link to "Q48918996"

The following pages link to Altered formation of hemichannels and gap junction channels caused by C-terminal connexin-32 mutations (Q48918996):

Displaying 40 items.

• Spot pattern of leopard Danio is caused by mutation in the zebrafish connexin41.8 gene (Q24678383) (← links)
• Gap junctions in inherited human disorders of the central nervous system (Q26823332) (← links)
• Connexin29 is highly expressed in cochlear Schwann cells, and it is required for the normal development and function of the auditory nerve of mice (Q28511260) (← links)
• Voltage opens unopposed gap junction hemichannels formed by a connexin 32 mutant associated with X-linked Charcot-Marie-Tooth disease (Q34021416) (← links)
• Molecular dissection of transjunctional voltage dependence in the connexin-32 and connexin-43 junctions (Q34171264) (← links)
• Intracellular transport, assembly, and degradation of wild-type and disease-linked mutant gap junction proteins (Q34719366) (← links)
• Molecular basis of calcium regulation in connexin-32 hemichannels (Q34794839) (← links)
• Gap junction hemichannels in astrocytes of the CNS. (Q35206708) (← links)
• Connexinopathies: a structural and functional glimpse (Q36031035) (← links)
• High frequency of GJA12/GJC2 mutations in Turkish patients with Pelizaeus-Merzbacher disease (Q36055058) (← links)
• Regulation of ubiquitin-proteasome system mediated degradation by cytosolic stress (Q36095718) (← links)
• Connexin-based gap junction hemichannels: gating mechanisms (Q36162607) (← links)
• Characterization of the structure and intermolecular interactions between the connexin 32 carboxyl-terminal domain and the protein partners synapse-associated protein 97 and calmodulin (Q36201794) (← links)
• Identification of amino acid residues lining the pore of a gap junction channel (Q36323688) (← links)
• Dislocation and degradation from the ER are regulated by cytosolic stress (Q36324141) (← links)
• How do mutations in GJB1 cause X-linked Charcot-Marie-Tooth disease? (Q36368553) (← links)
• Stoichiometry of transjunctional voltage-gating polarity reversal by a negative charge substitution in the amino terminus of a connexin32 chimera (Q36436716) (← links)
• Single-channel SCAM identifies pore-lining residues in the first extracellular loop and first transmembrane domains of Cx46 hemichannels (Q36445008) (← links)
• The gap junction cellular internet: connexin hemichannels enter the signalling limelight (Q36500579) (← links)
• Molecular genetics of X-linked Charcot-Marie-Tooth disease (Q36507155) (← links)
• Mutation Analysis of Gap Junction Protein Beta 1 and Genotype-Phenotype Correlation in X-linked Charcot-Marie-Tooth Disease in Chinese Patients (Q36856529) (← links)
• Connexins and apoptotic transformation (Q36946179) (← links)
• Membrane trafficking in neuronal maintenance and degeneration. (Q37043326) (← links)
• Conformational maturation and post-ER multisubunit assembly of gap junction proteins (Q37175399) (← links)
• X-linked Charcot-Marie-Tooth disease (Q37188598) (← links)
• The C-terminal domain of connexin43 modulates cartilage structure via chondrocyte phenotypic changes (Q37687342) (← links)
• Secondary structural analysis of the carboxyl-terminal domain from different connexin isoforms (Q39707325) (← links)
• Permeation pathway of homomeric connexin 26 and connexin 30 channels investigated by molecular dynamics (Q41432409) (← links)
• Pelizaeus-Merzbacher-like disease is caused not only by a loss of connexin47 function but also by a hemichannel dysfunction (Q41734605) (← links)
• Voltage dependence of ATP secretion in mammalian taste cells (Q41889178) (← links)
• Targeting motifs and functional parameters governing the assembly of connexins into gap junctions (Q41997747) (← links)
• Cx29 and Cx32, two connexins expressed by myelinating glia, do not interact and are functionally distinct (Q42089141) (← links)
• Oligodendrocyte progenitor enrichment in the connexin32 null-mutant mouse. (Q44357331) (← links)
• Prenylation-defective human connexin32 mutants are normally localized and function equivalently to wild-type connexin32 in myelinating Schwann cells. (Q46633766) (← links)
• Four classes of intercellular channels between glial cells in the CNS. (Q47643765) (← links)
• Phosphorylation in the C-terminus of the rat connexin46 (rCx46) and regulation of the conducting activity of the formed connexons (Q48742941) (← links)
• The role of gap junctions in Charcot-Marie-Tooth disease. (Q53809193) (← links)
• What's the Function of Connexin 32 in the Peripheral Nervous System? (Q57176565) (← links)
• Acetylation of C-terminal lysines modulates protein turnover and stability of Connexin-32 (Q58795702) (← links)
• Calmodulin-Mediated Regulation of Gap Junction Channels (Q92662494) (← links)