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
: C1orf16.F8 C1orf16.R8 / -1 / siPRPF8 global_1|MCF7 (2007-07-13 96hrs) / Well ID 1143380
Copyright ©2008,2017, all rights reserved. 