Pages that link to "Q33372114"

The following pages link to Intronic Alus influence alternative splicing (Q33372114):

Displaying 50 items.

• Genome-wide analyses of Epstein-Barr virus reveal conserved RNA structures and a novel stable intronic sequence RNA (Q21266670) (← links)
• Genomic gems: SINE RNAs regulate mRNA production (Q24632289) (← links)
• Expressing genes do not forget their LINEs: transposable elements and gene expression (Q27026309) (← links)
• Identification of small molecule and genetic modulators of AON-induced dystrophin exon skipping by high-throughput screening (Q28472268) (← links)
• Extensive intron gain in the ancestor of placental mammals (Q28732854) (← links)
• Mobile DNA and evolution in the 21st century (Q28748605) (← links)
• Characterizing of functional human coding RNA editing from evolutionary, structural, and dynamic perspectives. (Q30365845) (← links)
• A novel protein isoform of the multicopy human NAIP gene derives from intragenic Alu SINE promoters (Q33458323) (← links)
• Unconstrained mining of transcript data reveals increased alternative splicing complexity in the human transcriptome. (Q33552994) (← links)
• Alu-element insertion in an OPA1 intron sequence associated with autosomal dominant optic atrophy (Q33645574) (← links)
• InvAluable junk: the cellular impact and function of Alu and B2 RNAs (Q33724692) (← links)
• Distributions of Transposable Elements Reveal Hazardous Zones in Mammalian Introns (Q33900826) (← links)
• Interaction of hnRNPA1/A2 and DAZAP1 with an Alu-derived intronic splicing enhancer regulates ATM aberrant splicing (Q33999480) (← links)
• Intronic L1 retrotransposons and nested genes cause transcriptional interference by inducing intron retention, exonization and cryptic polyadenylation (Q34055996) (← links)
• Next-generation sequencing of duplication CNVs reveals that most are tandem and some create fusion genes at breakpoints (Q34460796) (← links)
• Alternative splicing and evolution: diversification, exon definition and function (Q34618555) (← links)
• Genes associated with the cis-regulatory functions of intragenic LINE-1 elements (Q34636635) (← links)
• A conserved alternative splicing event in plants reveals an ancient exonization of 5S rRNA that regulates TFIIIA. (Q34762619) (← links)
• A comparison of 100 human genes using an alu element-based instability model (Q34766196) (← links)
• The polymorphic AluYb8 insertion in the MUTYH gene is associated with reduced type 1 protein expression and reduced mitochondrial DNA content (Q34926190) (← links)
• Oligophrenin-1 (OPHN1), a gene involved in X-linked intellectual disability, undergoes RNA editing and alternative splicing during human brain development (Q35123027) (← links)
• Post-transcriptional exon shuffling events in humans can be evolutionarily conserved and abundant. (Q35493751) (← links)
• The emerging role of RNA editing in plasticity (Q35803384) (← links)
• Staufen1 Regulates Multiple Alternative Splicing Events either Positively or Negatively in DM1 Indicating Its Role as a Disease Modifier (Q35908266) (← links)
• What Can Domesticated Genes Tell Us about the Intron Gain in Mammals? (Q36014539) (← links)
• The role of short RNA loops in recognition of a single-hairpin exon derived from a mammalian-wide interspersed repeat (Q36190201) (← links)
• Distribution of a marker of germline methylation differs between major families of transposon-derived repeats in the human genome (Q36331117) (← links)
• Intergenic Alu exonisation facilitates the evolution of tissue-specific transcript ends. (Q36337749) (← links)
• Transposable Elements in Human Cancer: Causes and Consequences of Deregulation (Q36362814) (← links)
• The identification of switch-like alternative splicing exons among multiple samples with RNA-Seq data (Q36381051) (← links)
• Transcriptome-wide expansion of non-coding regulatory switches: evidence from co-occurrence of Alu exonization, antisense and editing (Q36619854) (← links)
• Transposable elements reveal a stem cell-specific class of long noncoding RNAs (Q36633093) (← links)
• Limited RNA editing in exons of mouse liver and adipose (Q36709919) (← links)
• Identification of the long, edited dsRNAome of LPS-stimulated immune cells. (Q36959149) (← links)
• The intertwining of transposable elements and non-coding RNAs (Q37091800) (← links)
• Impact of retrotransposons in pluripotent stem cells (Q37200472) (← links)
• Linear decay of retrotransposon antisense bias across genes is contingent upon tissue specificity (Q37309338) (← links)
• Transcriptome-wide effects of inverted SINEs on gene expression and their impact on RNA polymerase II activity. (Q37367215) (← links)
• Complex selection on 5' splice sites in intron-rich organisms (Q37417338) (← links)
• Retroelements and their impact on genome evolution and functioning (Q37569864) (← links)
• Alternative splicing: role of pseudoexons in human disease and potential therapeutic strategies. (Q37677072) (← links)
• The transcript repeat element: the human Alu sequence as a component of gene networks influencing cancer (Q37731398) (← links)
• Nonadaptive processes in primate and human evolution (Q37810545) (← links)
• ADAR enzyme and miRNA story: a nucleotide that can make the difference. (Q38164459) (← links)
• Compensatory signals associated with the activation of human GC 5′ splice sites (Q38319037) (← links)
• The determinants of alternative RNA splicing in human cells. (Q38679766) (← links)
• The understanding of circular RNAs as special triggers in carcinogenesis (Q38732302) (← links)
• Alternative splicing: the pledge, the turn, and the prestige : The key role of alternative splicing in human biological systems (Q38735423) (← links)
• Adaptation to Global Change: A Transposable Element-Epigenetics Perspective. (Q38808835) (← links)
• Novel kinin B₁ receptor splice variant and 5'UTR regulatory elements are responsible for cell specific B₁ receptor expression (Q39029345) (← links)