Pages that link to "Q36323688"
Jump to navigation
Jump to search
The following pages link to Identification of amino acid residues lining the pore of a gap junction channel (Q36323688):
Displaying 50 items.
- The role of connexins in ear and skin physiology - functional insights from disease-associated mutations (Q26827294) (← links)
- Structure of the connexin 26 gap junction channel at 3.5 A resolution (Q27654539) (← links)
- Asymmetric Configurations and N-terminal Rearrangements in Connexin26 Gap Junction Channels (Q27666014) (← links)
- A fully atomistic model of the Cx32 connexon (Q28473231) (← links)
- Defining a minimal motif required to prevent connexin oligomerization in the endoplasmic reticulum (Q28564736) (← links)
- Conductance of connexin hemichannels segregates with the first transmembrane segment (Q30476801) (← links)
- Cosegregation of permeability and single-channel conductance in chimeric connexins (Q30476803) (← links)
- Gap-junction channels dysfunction in deafness and hearing loss (Q30490087) (← links)
- Cardiac conduction is required to preserve cardiac chamber morphology (Q30496345) (← links)
- Analysis of four connexin26 mutant gap junctions and hemichannels reveals variations in hexamer stability (Q33820883) (← links)
- A transient diffusion model yields unitary gap junctional permeabilities from images of cell-to-cell fluorescent dye transfer between Xenopus oocytes (Q34185230) (← links)
- The permeability of gap junction channels to probes of different size is dependent on connexin composition and permeant-pore affinities (Q34186774) (← links)
- SCAM analysis of Panx1 suggests a peculiar pore structure (Q34243032) (← links)
- Tryptophan scanning mutagenesis of the first transmembrane domain of the innexin Shaking-B(Lethal). (Q35556310) (← links)
- Three-dimensional structure of a human connexin26 gap junction channel reveals a plug in the vestibule (Q35830244) (← links)
- Tryptophan Scanning Reveals Dense Packing of Connexin Transmembrane Domains in Gap Junction Channels Composed of Connexin32 (Q35837081) (← links)
- Pore-lining residues identified by single channel SCAM studies in Cx46 hemichannels (Q35892064) (← links)
- Voltage-dependent conformational changes in connexin channels (Q36007904) (← links)
- Connexinopathies: a structural and functional glimpse (Q36031035) (← links)
- Aberrant trafficking of a Leu89Pro connexin32 mutant associated with X-linked dominant Charcot-Marie-Tooth disease (Q36065993) (← links)
- Accessing gap-junction channel structure-function relationships through molecular modeling and simulations (Q36260709) (← links)
- Single-channel SCAM identifies pore-lining residues in the first extracellular loop and first transmembrane domains of Cx46 hemichannels (Q36445008) (← links)
- Connexin channel permeability to cytoplasmic molecules (Q36807032) (← links)
- Molecular modeling and mutagenesis of gap junction channels (Q36831262) (← links)
- Gap junction channel structure in the early 21st century: facts and fantasies (Q36975165) (← links)
- Novel mutations in GJA1 cause oculodentodigital syndrome (Q36987153) (← links)
- Antibodies targeting extracellular domain of connexins for studies of hemichannels (Q37033926) (← links)
- The N-terminal half of the connexin protein contains the core elements of the pore and voltage gates (Q37075368) (← links)
- Site-directed mutagenesis reveals putative regions of protein interaction within the transmembrane domains of connexins (Q37169087) (← links)
- Neurological manifestations of oculodentodigital dysplasia: a Cx43 channelopathy of the central nervous system? (Q37199244) (← links)
- Conformational changes in a pore-forming region underlie voltage-dependent "loop gating" of an unapposed connexin hemichannel (Q37268155) (← links)
- Cell membrane permeabilization via connexin hemichannels in living and dying cells (Q37769339) (← links)
- Structure of the gap junction channel and its implications for its biological functions (Q37801564) (← links)
- A structural and functional comparison of gap junction channels composed of connexins and innexins (Q38942940) (← links)
- Replacement of a single cysteine in the fourth transmembrane region of zebrafish pannexin 1 alters hemichannel gating behavior (Q39809264) (← links)
- Role of the N-terminus in permeability of chicken connexin45.6 gap junctional channels (Q40239792) (← links)
- Mutation of a conserved threonine in the third transmembrane helix of alpha- and beta-connexins creates a dominant-negative closed gap junction channel (Q40331282) (← links)
- Functional expression in Xenopus oocytes of gap-junctional hemichannels formed by a cysteine-less connexin 43. (Q40542865) (← links)
- Diverse pattern of gap junction beta-2 and gap junction beta-4 genes mutations and lack of contribution of DFNB21, DFNB24, DFNB29, and DFNB42 loci in autosomal recessive nonsyndromic hearing loss patients in Hormozgan, Iran (Q41608836) (← links)
- Roles of Met-34, Cys-64, and Arg-75 in the assembly of human connexin 26. Implication for key amino acid residues for channel formation and function. (Q42050108) (← links)
- Characterization of a novel water pocket inside the human Cx26 hemichannel structure (Q42183057) (← links)
- Gating on the outside. (Q42550659) (← links)
- Charges dispersed over the permeation pathway determine the charge selectivity and conductance of a Cx32 chimeric hemichannel (Q42649575) (← links)
- Essential role of a GXXXG motif for membrane channel formation by Helicobacter pylori vacuolating toxin (Q44299992) (← links)
- Permeant-specific gating of connexin 30 hemichannels (Q47689866) (← links)
- Reversible pore block of connexin channels by cyclodextrins (Q47881008) (← links)
- Functional characterization of oculodentodigital dysplasia-associated Cx43 mutants. (Q52569245) (← links)
- Modeling and Validation of Transmembrane Protein Structures (Q57207084) (← links)
- The Structural Context of Disease-causing Mutations in Gap Junctions (Q57207105) (← links)
- Electrical coupling and its channels (Q58616972) (← links)