about
The Zinc-Finger Protein SOP1 Is Required for a Subset of the Nuclear Exosome Functions in ArabidopsisCircular RNAs: Novel Regulators of Neuronal DevelopmentControl of human papillomavirus gene expression by alternative splicingStructural insights into Gemin5-guided selection of pre-snRNAs for snRNP assemblyCytoplasmic Drosha activity generated by alternative splicingNeuroblastoma, a Paradigm for Big Data Science in Pediatric Oncology.Identification of a small molecule inhibitor that stalls splicing at an early step of spliceosome activation.Mechanistic determinants of MBNL activityStatistical modeling of isoform splicing dynamics from RNA-seq time series data.Circular RNAs: Biogenesis, Function and Role in Human Diseases.MiasDB: A Database of Molecular Interactions Associated with Alternative Splicing of Human Pre-mRNAs.Splicing analysis of CYP11B1 mutation in a family affected with 11β-hydroxylase deficiency: case report.Identification of a Novel Human E-Cadherin Splice Variant and Assessment of Its Effects Upon EMT-Related Events.Modeling the ferrochelatase c.315-48C modifier mutation for erythropoietic protoporphyria (EPP) in mice.A deep boosting based approach for capturing the sequence binding preferences of RNA-binding proteins from high-throughput CLIP-seq data.A splicing isoform of TEAD4 attenuates the Hippo-YAP signalling to inhibit tumour proliferationExome Sequencing and Prediction of Long-Term Kidney Allograft Function.RNA-binding protein CPEB1 remodels host and viral RNA landscapes.Lessons from non-canonical splicingHigh prevalence of mutations affecting the splicing process in a Spanish cohort with autosomal dominant retinitis pigmentosa.LOX-1 and Its Splice Variants: A New Challenge for Atherosclerosis and Cancer-Targeted Therapies.Jmjd6, a JmjC Dioxygenase with Many Interaction Partners and Pleiotropic FunctionsHemopoietic-specific Sf3b1-K700E knock-in mice display the splicing defect seen in human MDS but develop anemia without ring sideroblasts.An atlas of alternative splicing profiles and functional associations reveals new regulatory programs and genes that simultaneously express multiple major isoforms.Transcriptome Profiling in Human Diseases: New Advances and PerspectivesNovel promoters and coding first exons in DLG2 linked to developmental disorders and intellectual disability.The RNA-binding protein caper is required for sensory neuron development in Drosophila melanogaster.Transcriptional Signatures of Aging.RBM25 is a global splicing factor promoting inclusion of alternatively spliced exons and is itself regulated by lysine mono-methylation.Ptbp2 Controls an Alternative Splicing Network Required for Cell Communication during Spermatogenesis.Alternative splicing: the pledge, the turn, and the prestige : The key role of alternative splicing in human biological systems.ELAVL2-regulated transcriptional and splicing networks in human neurons link neurodevelopment and autism.Systematic Computational Identification of Variants That Activate Exonic and Intronic Cryptic Splice Sites.Cajal body function in genome organization and transcriptome diversity.Mutational Spectrum of MYO15A and the Molecular Mechanisms of DFNB3 Human Deafness.The roles of RNA processing in translating genotype to phenotypeSplicing factor gene mutations in hematologic malignancies.Alternative splicing and the evolution of phenotypic novelty.Intersections of post-transcriptional gene regulatory mechanisms with intermediary metabolism.Random Splicing of Several Exons Caused by a Single Base Change in the Target Exon of CRISPR/Cas9 Mediated Gene Knockout.
P2860
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P2860
description
2015 nî lūn-bûn
@nan
2015年の論文
@ja
2015年論文
@yue
2015年論文
@zh-hant
2015年論文
@zh-hk
2015年論文
@zh-mo
2015年論文
@zh-tw
2015年论文
@wuu
2015年论文
@zh
2015年论文
@zh-cn
name
RNA mis-splicing in disease.
@en
type
label
RNA mis-splicing in disease.
@en
prefLabel
RNA mis-splicing in disease.
@en
P2860
P356
P1476
RNA mis-splicing in disease.
@en
P2093
Marina M Scotti
P2860
P2888
P356
10.1038/NRG.2015.3
P577
2015-11-23T00:00:00Z
P6179
1039700013