Restoration of polr1c in early embryogenesis rescues the Type 3 Treacher Collins Syndrome facial malformation phenotype in zebrafish
Page 1 of 1
Restoration of polr1c in early embryogenesis rescues the Type 3 Treacher Collins Syndrome facial malformation phenotype in zebrafish
Jon Moulton Fri Nov 10, 2017 2:06 pm
Kwong EML, Ho JCH, Lau MCC, You M-S, Jiang Y-J, Tse WKF. Restoration of polr1c in early embryogenesis rescues the Type 3 Treacher Collins Syndrome facial malformation phenotype in zebrafish. Am J Pathol. 2017;[Epub ahead of print] doi:10.1016/j.ajpath.2017.10.004
Jon Moulton- Posts : 5721
Join date : 2010-03-12
Age : 62
Location : Philomath, Oregon, USA -
Similar topics» Fishing the Molecular Bases of Treacher Collins Syndrome
» Knockdown of fbxl10/kdm2bb rescues chd7 morphant phenotype in a zebrafish model of CHARGE syndrome
» Cnbp ameliorates Treacher Collins Syndrome craniofacial anomalies through a pathway that involves redox-responsive genes
» Transient Disruption of Adenosine Signaling During Embryogenesis Triggers a Pro-epileptic Phenotype in Adult Zebrafish
» miR-19a replacement rescues cardiac and fin defects in zebrafish model of holt-oram syndrome
» Knockdown of fbxl10/kdm2bb rescues chd7 morphant phenotype in a zebrafish model of CHARGE syndrome
» Cnbp ameliorates Treacher Collins Syndrome craniofacial anomalies through a pathway that involves redox-responsive genes
» Transient Disruption of Adenosine Signaling During Embryogenesis Triggers a Pro-epileptic Phenotype in Adult Zebrafish
» miR-19a replacement rescues cardiac and fin defects in zebrafish model of holt-oram syndrome
Page 1 of 1
Permissions in this forum:
You cannot reply to topics in this forum