Gene therapy rescues cilia defects and restores olfactory function in a mammalian ciliopathy model
Page 1 of 1
Gene therapy rescues cilia defects and restores olfactory function in a mammalian ciliopathy model
Jon Moulton Tue Sep 04, 2012 1:13 pm
McIntyre JC, Davis E, Joiner A, Williams CL, Tsai IC, Jenkins PM, McEwen DP, Zhang L, Escobado J, Thomas S, Szymanska K, Johnson CA, Beales PL, Green ED, Mullikin JC, NISC Comparative Sequencing Program, Sabo A, Muzny DM, Gibbs RA, Attie-Bitach T, Yoder BK, Reed RR, Katsanis N, Martens J. Gene therapy rescues cilia defects and restores olfactory function in a mammalian ciliopathy model. Nat Med. 2012;[Epub ahead of print] doi:/10.1038/nm.2860
Jon Moulton- Posts : 5721
Join date : 2010-03-12
Age : 61
Location : Philomath, Oregon, USA -
Similar topics» Combining Cep290 and Mkks ciliopathy alleles in mice rescues sensory defects and restores ciliogenesis
» miR-19a replacement rescues cardiac and fin defects in zebrafish model of holt-oram syndrome
» MicroRNA 19a replacement partially rescues fin and cardiac defects in zebrafish model of Holt Oram syndrome
» Knockdown of Bardet-Biedl Syndrome Gene BBS9/PTHB1 Leads to Cilia Defects
» Developmental defects and neuromuscular alterations due to mitofusin 2 gene (MFN2) silencing in zebrafish: a new model for Charcot-Marie-Tooth type 2A neuropathy
» miR-19a replacement rescues cardiac and fin defects in zebrafish model of holt-oram syndrome
» MicroRNA 19a replacement partially rescues fin and cardiac defects in zebrafish model of Holt Oram syndrome
» Knockdown of Bardet-Biedl Syndrome Gene BBS9/PTHB1 Leads to Cilia Defects
» Developmental defects and neuromuscular alterations due to mitofusin 2 gene (MFN2) silencing in zebrafish: a new model for Charcot-Marie-Tooth type 2A neuropathy
Page 1 of 1
Permissions in this forum:
You cannot reply to topics in this forum|
|
|