Back to Rnomics Platform
Open Session
Home
Public data
LGFUS Public Data
PRPF mutations are associated with generalized defects in spliceosome formation and pre-mRNA splicing in patients with retinitis pigmentosa
PRPF8 knockdown in human cell lines Tanackovic et al.
Fluorescence graphs
: APC.F16 APC.R14 / -1 / siPRPF8 global_2|MCF7 (2007-07-13 96hrs) / Well ID 1143363
Copyright ©2008,2017, all rights reserved. 