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Structural Studies of N-Terminal Mutants of Connexin 26 and Connexin 32 Using (1)H NMR Spectroscopy
Alterations in gap junctions underlie the etiologies of syndromic deafness (KID) and Charcot-Marie Tooth disease (CMTX). Functional gap junctions are composed of connexin molecules with N-termini containing a flexible turn around G12, inserting the N-termini into the channel pore allowing voltage ga...
Tallennettuna:
| Julkaisussa: | Arch Biochem Biophys |
|---|---|
| Päätekijät: | , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
2016
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5051353/ https://ncbi.nlm.nih.gov/pubmed/27378082 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.abb.2016.06.019 |
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