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Design and characterization of a human monoclonal antibody that modulates mutant connexin 26 hemichannels implicated in deafness and skin disorders

Academic Article
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Overview

authors

  • Xu, L.
  • Carrer, A.
  • Zonta, F.
  • Qu, Z. H.
  • Ma, P. X.
  • Li, S.
  • Ceriani, F.
  • Buratto, D.
  • Crispino, G.
  • Zorzi, V.
  • Ziraldo, G.
  • Bruno, F.
  • Nardin, C.
  • Peres, C.
  • Mazzarda, F.
  • Salvatore, A. M.
  • Raspa, M.
  • Scavizzi, F.
  • Chu, Y. J.
  • Xie, S. C.
  • Yang, X. M.
  • Liao, J.
  • Liu, X.
  • Wang, W.
  • Wang, S. S.
  • Yang, G.
  • Lerner, Richard
  • Mammano, F.

publication date

  • September 2017

journal

  • Frontiers in Molecular Neuroscience  Journal
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Research

keywords

  • antibody library
  • antibody structure
  • cochlea
  • connexins
  • epitope identification
  • keratinocytes
  • syndromic autosomal hereditary deafness
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Identity

PubMed Central ID

  • PMC5615210

International Standard Serial Number (ISSN)

  • 1662-5099

Digital Object Identifier (DOI)

  • 10.3389/fnmol.2017.00298

PubMed ID

  • 29018324
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Additional Document Info

volume

  • 10

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