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Hypothesis: Artifacts, Including Spurious Chimeric RNAs with a Short Homologous Sequence, Caused by Consecutive Reverse Transcriptions and Endogenous Random PrimersEvolutionary convergence on highly-conserved 3' intron structures in intron-poor eukaryotes and insights into the ancestral eukaryotic genomeDetection and analysis of alternative splicing in Yarrowia lipolytica reveal structural constraints facilitating nonsense-mediated decay of intron-retaining transcripts.Origin of spliceosomal introns and alternative splicingRisk-Association of DNMT1 Gene Polymorphisms with Coronary Artery Disease in Chinese Han Population.An interactive association of advanced glycation end-product receptor gene four common polymorphisms with coronary artery disease in northeastern Han Chinese.Characterization of NOL7 gene point mutations, promoter methylation, and protein expression in cervical cancer.Associations of Polymorphisms in MTHFR Gene with the Risk of Age-Related Cataract in Chinese Han Population: A Genotype-Phenotype Analysis.Analysis of sequence variability in the macronuclear DNA of Paramecium tetraurelia: a somatic view of the germlineComplex selection on 5' splice sites in intron-rich organisms.Integrin α3β1 controls mRNA splicing that determines Cox-2 mRNA stability in breast cancer cells.Intron retention in mRNA: No longer nonsense: Known and putative roles of intron retention in normal and disease biology.Deep intronic mutations and human disease.Transcriptome profiling using single-molecule direct RNA sequencing.DMD transcripts in CRL-2061 rhabdomyosarcoma cells show high levels of intron retention by intron-specific PCR amplification.Genetic predisposition to ischaemic stroke by RAGE and HMGB1 gene variants in Chinese Han population.The Y Chromosome Modulates Splicing and Sex-Biased Intron Retention Rates in Drosophila.Transcriptional-Readthrough RNAs Reflect the Phenomenon of "A Gene Contains Gene(s)" or "Gene(s) within a Gene" in the Human Genome, and Thus Are Not Chimeric RNAs.Dissecting the Causal Mechanism of X-Linked Dystonia-Parkinsonism by Integrating Genome and Transcriptome Assembly.
P2860
Q26820767-2673D29F-6511-4B40-8054-6B6A31785CDEQ33358666-06F26C23-6ECE-401A-9E9E-90CFD97E94E9Q33614225-052B61FF-6B4B-4CC0-8876-24424A8B7073Q33653714-AD77A708-2F30-419D-BCD2-82D9328513D4Q34834839-9197B18D-E849-4E9D-B066-4820E6BA2C49Q35025330-E86516AF-16EB-4113-B350-B7697ADC4D44Q35613632-8E471163-ABB6-4EF1-8B6F-26793219D1C2Q35874230-6EAA10F6-804B-4354-ADD2-E2B7CDCFD702Q36517951-D14669B6-D378-49C2-B1D4-F246306242D5Q37417338-1F88995B-18B2-446F-8270-58769DAC42ACQ37636578-133BFCEA-A96E-4F1A-88DD-57AD35855FCEQ38650057-4CEF44D0-4238-416F-877B-5E613C0B59E5Q39301532-631319A1-B183-4B7D-94FB-49DE212183ABQ40852574-EF0D5404-BBB8-45B7-9423-1A3E452E8097Q42247648-EEA410A0-5A43-408E-918E-250A7D900530Q47103796-F2732A94-49B8-481A-B216-653013BDED12Q47269686-2444E508-5CCC-4E37-8A0F-40A83281677FQ50027000-00D5FF28-BF59-4C3A-B82D-9D0B12A6A9CAQ52430458-AC3EB132-70CF-4676-9735-02669710E1C2
P2860
description
2008 nî lūn-bûn
@nan
2008 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
2008 թվականի փետրվարին հրատարակված գիտական հոդված
@hy
2008年の論文
@ja
2008年論文
@yue
2008年論文
@zh-hant
2008年論文
@zh-hk
2008年論文
@zh-mo
2008年論文
@zh-tw
2008年论文
@wuu
name
Intron mis-splicing: no alternative?
@ast
Intron mis-splicing: no alternative?
@en
Intron mis-splicing: no alternative?
@nl
type
label
Intron mis-splicing: no alternative?
@ast
Intron mis-splicing: no alternative?
@en
Intron mis-splicing: no alternative?
@nl
prefLabel
Intron mis-splicing: no alternative?
@ast
Intron mis-splicing: no alternative?
@en
Intron mis-splicing: no alternative?
@nl
P2860
P356
P1433
P1476
Intron mis-splicing: no alternative?
@en
P2093
Manuel Irimia
Scott William Roy
P2860
P2888
P356
10.1186/GB-2008-9-2-208
P577
2008-02-19T00:00:00Z
P5875
P6179
1029156108