Identification of Alternative Splicing Events Associated with Paratuberculosis in Dairy Cattle Using Multi-Tissue RNA Sequencing Data. 
 PMID:35328051
                                    
                                
                                    Detection and Functional Verification of Noncanonical Splice Site Mutations in Hereditary Deafness. 
 PMID:34956325
                                    
                                
                                    Applications and potentials of nanopore sequencing in the (epi)genome and (epi)transcriptome era. 
 PMID:34901902
                                    
                                
                                    Alternative Splicing: A New Cause and Potential Therapeutic Target in Autoimmune Disease. 
 PMID:34484216
                                    
                                
                                    Lithium increases mitochondrial respiration in iPSC-derived neural precursor cells from lithium responders. 
 PMID:34075196
                                    
                                
                                    Computational Methods for Identifying Similar Diseases. 
 PMID:31678735
                                    
                                
                                    More than a messenger: Alternative splicing as a therapeutic target. 
 PMID:31271898
                                    
                                
                                    A Novel Heterozygous Intronic Mutation in the FBN1 Gene Contributes to FBN1 RNA Missplicing Events in the Marfan Syndrome. 
 PMID:30003093
                                    
                                
                                    Mycobacterium tuberculosis H37Rv infection regulates alternative splicing in Macrophages. 
 PMID:29433383
                                    
                                
                                    Integration of mRNP formation and export. 
 PMID:28314893
                                    
                                
                                    LOX-1 and Its Splice Variants: A New Challenge for Atherosclerosis and Cancer-Targeted Therapies. 
 PMID:28146073
                                    
                                
                                    RNA splicing during terminal erythropoiesis. 
 PMID:28118223
                                    
                                
                                    Fusing literature and full network data improves disease similarity computation. 
 PMID:27578323
                                    
                                
                                    Nuclear poly(A)-binding protein aggregates misplace a pre-mRNA outside of SC35 speckle causing its abnormal splicing. 
 PMID:27507886
                                    
                                
                                    Recruitment of the NineTeen Complex to the activated spliceosome requires AtPRMT5. 
 PMID:27114555
                                    
                                
                                    Alternative Splicing in CKD. 
 PMID:26763787
                                    
                                
                                    Defective control of pre-messenger RNA splicing in human disease. 
 PMID:26728853
                                    
                                
                                    Modulators of alternative splicing as novel therapeutics in cancer. 
 PMID:26468443
                                    
                                
                                    Single-Molecule Pull-Down FRET to Dissect the Mechanisms of Biomolecular Machines. 
 PMID:26068753
                                    
                                
                                    SMN2 splice modulators enhance U1-pre-mRNA association and rescue SMA mice. 
 PMID:26030728
                                    
                                
                                    Coupling and coordination in gene expression processes with pre-mRNA splicing. 
 PMID:25768347
                                    
                                
                                    Pre-mRNA splicing is facilitated by an optimal RNA polymerase II elongation rate. 
 PMID:25452276
                                    
                                
                                    In silico prediction of splice-altering single nucleotide variants in the human genome. 
 PMID:25416802
                                    
                                
                                    SemFunSim: a new method for measuring disease similarity by integrating semantic and gene functional association. 
 PMID:24932637
                                    
                                
                                    A meta-analysis of somatic mutations from next generation sequencing of 241 melanomas: a road map for the study of genes with potential clinical relevance. 
 PMID:24755198
                                    
                                
                                    Oncogenic alternative splicing switches: role in cancer progression and prospects for therapy. 
 PMID:24285959
                                    
                                
                                    SIDD: a semantically integrated database towards a global view of human disease. 
 PMID:24146757
                                    
                                
                                    Alternative splicing and its impact as a cancer diagnostic marker. 
 PMID:23105933
                                    
                                
                                    Life on two tracks. 
 PMID:22917184
                                    
                                
                                    Nucleoside analog studies indicate mechanistic differences between RNA-editing adenosine deaminases. 
 PMID:22885375
                                    
                                
                                    Identifying disease mutations in genomic medicine settings: current challenges and how to accelerate progress. 
 PMID:22830651