Pages that link to "Q33886651"
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The following pages link to Cell-free synthesis and assembly of connexins into functional gap junction membrane channels (Q33886651):
Displaying 50 items.
- Dynamic trafficking and delivery of connexons to the plasma membrane and accretion to gap junctions in living cells (Q24533504) (← links)
- Life cycle of connexins in health and disease (Q24541428) (← links)
- Posttranslational modifications in connexins and pannexins (Q26825229) (← links)
- Gap junctions (Q26850591) (← links)
- Cxs and Panx- hemichannels in peripheral and central chemosensing in mammals (Q26859920) (← links)
- Divergent effects of two sequence variants of GJB3 (G12D and R32W) on the function of connexin 31 in vitro (Q28191724) (← links)
- Analysis of gap junction assembly using mutated connexins detected in Charcot-Marie-Tooth X-linked disease (Q28646227) (← links)
- Biological and biophysical properties of vascular connexin channels (Q30436052) (← links)
- In vitro motility of liver connexin vesicles along microtubules utilizes kinesin motors (Q30501622) (← links)
- Function of Shaker potassium channels produced by cell-free translation upon injection into Xenopus oocytes (Q30531727) (← links)
- Recent advances in producing and selecting functional proteins by using cell-free translation (Q31972407) (← links)
- Expression of a mitochondrial progesterone receptor (PR-M) in leiomyomata and association with increased mitochondrial membrane potential (Q33570062) (← links)
- Intracellular trafficking pathways in the assembly of connexins into gap junctions. (Q33855593) (← links)
- A novel missense mutation in the connexin30 causes nonsyndromic hearing loss (Q33952479) (← links)
- Gap junctions. (Q34020827) (← links)
- Zonula occludens-1 alters connexin43 gap junction size and organization by influencing channel accretion (Q34148181) (← links)
- Different ionic selectivities for connexins 26 and 32 produce rectifying gap junction channels (Q34171884) (← links)
- Gap junctions and connexin hemichannels underpin hemostasis and thrombosis. (Q34243239) (← links)
- Co-translational association of cell-free expressed membrane proteins with supplied lipid bilayers (Q34282941) (← links)
- Mutation R184Q of connexin 26 in hearing loss patients has a dominant-negative effect on connexin 26 and connexin 30 (Q34329503) (← links)
- A truncated progesterone receptor (PR-M) localizes to the mitochondrion and controls cellular respiration (Q34631310) (← links)
- Human connexin disorders of the skin (Q34685630) (← links)
- Two Drosophila innexins are expressed in overlapping domains and cooperate to form gap-junction channels (Q34735076) (← links)
- Sharing signals: connecting lung epithelial cells with gap junction channels. (Q34958828) (← links)
- A novel mutation in the connexin 29 gene may contribute to nonsyndromic hearing loss (Q35010482) (← links)
- Different domains are critical for oligomerization compatibility of different connexins. (Q35656804) (← links)
- Missense mutations in GJB2 encoding connexin-26 cause the ectodermal dysplasia keratitis-ichthyosis-deafness syndrome (Q35764888) (← links)
- Trafficking of gap junction channels at a vertebrate electrical synapse in vivo (Q35807635) (← links)
- Vascular gap junctions and implications for hypertension (Q35956825) (← links)
- Molecular mechanisms regulating formation, trafficking and processing of annular gap junctions (Q36031604) (← links)
- Cardiac Cx43, Cx40 and Cx45 co-assembling: involvement of connexins epitopes in formation of hemichannels and Gap junction channels (Q36260704) (← links)
- Physiological role of gap-junctional hemichannels. Extracellular calcium-dependent isosmotic volume regulation (Q36327016) (← links)
- Pathways and control of connexin oligomerization. (Q36401843) (← links)
- Pathological significance of intracytoplasmic connexin proteins: implication in tumor progression (Q36893654) (← links)
- Genetic diseases of junctions. (Q37002828) (← links)
- Conformational maturation and post-ER multisubunit assembly of gap junction proteins (Q37175399) (← links)
- The M34A mutant of Connexin26 reveals active conductance states in pore-suspending membranes (Q37445738) (← links)
- Membrane protein synthesis in cell-free systems: from bio-mimetic systems to bio-membranes (Q38220437) (← links)
- The electrical synapse: Molecular complexities at the gap and beyond. (Q39124530) (← links)
- Cell-free expression of a functional pore-only sodium channel. (Q40637180) (← links)
- Aggregated DsRed-tagged Cx43 and over-expressed Cx43 are targeted to lysosomes in human breast cancer cells (Q40725246) (← links)
- Green fluorescent protein changes the conductance of connexin 43 (Cx43) hemichannels reconstituted in planar lipid bilayers (Q40734152) (← links)
- Comparative analysis and application of fluorescent protein-tagged connexins (Q40827204) (← links)
- Deficient assembly and function of gap junctions in Trf1, a trafficking mutant of the human liver-derived cell line HuH-7. (Q40933340) (← links)
- A cataract-causing connexin 50 mutant is mislocalized to the ER due to loss of the fourth transmembrane domain and cytoplasmic domain (Q41262299) (← links)
- Heteromerization of innexin gap junction proteins regulates epithelial tissue organization in Drosophila (Q41769604) (← links)
- Functional analysis of a nonsyndromic hearing loss-associated mutation in the transmembrane II domain of the GJC3 gene (Q41838330) (← links)
- Synthesis and assembly of connexins in vitro into homomeric and heteromeric functional gap junction hemichannels. (Q41897817) (← links)
- Targeting motifs and functional parameters governing the assembly of connexins into gap junctions (Q41997747) (← links)
- A carboxyl terminal domain of connexin43 is critical for gap junction plaque formation but not for homo- or hetero-oligomerization (Q42144773) (← links)