Subtype-specific alternative splicing events in breast cancer identified by large-scale data analysis
Phylogenetic comparison and splice site conservation of the animal SMNDC1 gene family
GPATCH11 variants cause mis-splicing and early-onset retinal dystrophy with neurological impairment
A newly identified gene Ahed plays essential roles in haematopoiesis through RNA splicing
Autistic traits in myotonic dystrophy type 1 due to MBNL inhibition and RNA mis-splicing
A newly identified spliceosomal protein Ahed is essential for homeostasis of the epidermis
CTNNBIP1-CLSTN1 Functions as a Housekeeping Chimeric RNA, and Regulates Cell Proliferation through SERPINE2
Tumor heterogeneity and prognostic impact of the aberrant splicing burden of colorectal cancers
Short and long-read whole genome sequencing explains most undiagnosed Autosomal Dominant Polycystic Kidney Disease
Loss of function of ADNP by an intragenic inversion: towards an out-of frame start codon mechanism