Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Amy E Walker"'
Autor:
Cinzia Ambrosi, Amy E Walker, Adam D Depriest, Angela C Cone, Connie Lu, John Badger, I Martha Skerrett, Gina E Sosinsky
Publikováno v:
PLoS ONE, Vol 8, Iss 8, p e70916 (2013)
Human Connexin26 gene mutations cause hearing loss. These hereditary mutations are the leading cause of childhood deafness worldwide. Mutations in gap junction proteins (connexins) can impair intercellular communication by eliminating protein synthes
Externí odkaz:
https://doaj.org/article/281d61dfc0ad4f86a660875601fecdc1
Autor:
John Badger, Amy E. Walker, Gina E. Sosinsky, Connie Lu, Adam D. DePriest, I. Martha Skerrett, Angela C. Cone, Cinzia Ambrosi
Publikováno v:
PLoS ONE, Vol 8, Iss 8, p e70916 (2013)
PLoS ONE
PLoS ONE
Human Connexin26 gene mutations cause hearing loss. These hereditary mutations are the leading cause of childhood deafness worldwide. Mutations in gap junction proteins (connexins) can impair intercellular communication by eliminating protein synthes
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::88e99fb672aea2d28928983030669eae
http://europepmc.org/articles/PMC3744544?pdf=render
http://europepmc.org/articles/PMC3744544?pdf=render
Publikováno v:
Biophysical Journal. 102:106a
Connexins (Cx) assemble to form the intercellular communication channels in gap junctions (GJs). Mutations in Connexin26 (Cx26) that cause childhood pre-lingual deafness are found in human populations around the globe. Types of defect resulting from
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::435d1eee82502ff6dfc7243c054fbdaf
https://doi.org/10.1016/j.bpj.2011.11.598
https://doi.org/10.1016/j.bpj.2011.11.598