Knockdown of fbxl10/kdm2bb rescues chd7 morphant phenotype in a zebrafish model of CHARGE syndrome
Page 1 of 1
Knockdown of fbxl10/kdm2bb rescues chd7 morphant phenotype in a zebrafish model of CHARGE syndrome
Jon Moulton Mon Aug 05, 2013 12:43 pm
Balow SA, Pierce LX, Zentner GE, Conrad PA, Davis S, Sabaawy HE, McDermott BM, Scacheri PC. Knockdown of fbxl10/kdm2bb rescues chd7 morphant phenotype in a zebrafish model of CHARGE syndrome. Dev Biol. 2013; doi:10.1016/j.ydbio.2013.07.026
Jon Moulton- Posts : 5721
Join date : 2010-03-12
Age : 61
Location : Philomath, Oregon, USA -
Similar topics» Role of Chd7 in Zebrafish: A Model for CHARGE Syndrome
» Restoration of polr1c in early embryogenesis rescues the Type 3 Treacher Collins Syndrome facial malformation phenotype in zebrafish
» Etiology and functional validation of gastrointestinal motility dysfunction in a zebrafish model of CHARGE syndrome
» miR-19a replacement rescues cardiac and fin defects in zebrafish model of holt-oram syndrome
» Neurologic and ocular phenotype in Pitt-Hopkins syndrome and a zebrafish model
» Restoration of polr1c in early embryogenesis rescues the Type 3 Treacher Collins Syndrome facial malformation phenotype in zebrafish
» Etiology and functional validation of gastrointestinal motility dysfunction in a zebrafish model of CHARGE syndrome
» miR-19a replacement rescues cardiac and fin defects in zebrafish model of holt-oram syndrome
» Neurologic and ocular phenotype in Pitt-Hopkins syndrome and a zebrafish model
Page 1 of 1
Permissions in this forum:
You cannot reply to topics in this forum|
|
|