Pages that link to "Q36818243"
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The following pages link to Intron self-complementarity enforces exon inclusion in a yeast pre-mRNA (Q36818243):
Displaying 50 items.
- Rates of spontaneous mutation (Q24548000) (← links)
- Role of RNA structure in regulating pre-mRNA splicing (Q24631714) (← links)
- Exonization of AluYa5 in the human ACE gene requires mutations in both 3' and 5' splice sites and is facilitated by a conserved splicing enhancer. (Q24811113) (← links)
- Intronic binding sites for hnRNP A/B and hnRNP F/H proteins stimulate pre-mRNA splicing (Q25256959) (← links)
- Cross-kingdom patterns of alternative splicing and splice recognition (Q27486159) (← links)
- RNA polymerase II conducts a symphony of pre-mRNA processing activities (Q28221126) (← links)
- Ligand-induced sequestering of branchpoint sequence allows conditional control of splicing (Q33319324) (← links)
- Correlation between the secondary structure of pre-mRNA introns and the efficiency of splicing in Saccharomyces cerevisiae. (Q33355848) (← links)
- Conserved secondary structures in Aspergillus (Q33356008) (← links)
- Intronic Alus influence alternative splicing (Q33372114) (← links)
- Epistatic interactions modulate the evolution of mammalian mitochondrial respiratory complex components (Q33467118) (← links)
- Ultraconserved elements in insect genomes: a highly conserved intronic sequence implicated in the control of homothorax mRNA splicing (Q33841561) (← links)
- Rare autosomal recessive cardiac valvular form of Ehlers-Danlos syndrome results from mutations in the COL1A2 gene that activate the nonsense-mediated RNA decay pathway. (Q33909884) (← links)
- A computational analysis of sequence features involved in recognition of short introns (Q33944374) (← links)
- Multiple splicing defects in an intronic false exon (Q33965191) (← links)
- Evidence for splice site pairing via intron definition in Schizosaccharomyces pombe (Q33966195) (← links)
- The iStem, a long-range RNA secondary structure element required for efficient exon inclusion in the Drosophila Dscam pre-mRNA. (Q34150831) (← links)
- Widespread selection for local RNA secondary structure in coding regions of bacterial genes (Q34227414) (← links)
- The adenosine deaminase gene polymorphism is associated with chronic heart failure risk in Chinese (Q34358729) (← links)
- Genome-wide bioinformatic and molecular analysis of introns in Saccharomyces cerevisiae (Q34361753) (← links)
- RNA structure replaces the need for U2AF2 in splicing (Q34501702) (← links)
- detectIR: a novel program for detecting perfect and imperfect inverted repeats using complex numbers and vector calculation (Q34542425) (← links)
- Microsatellites in different eukaryotic genomes: survey and analysis (Q35028489) (← links)
- The association of ADORA2A and ADORA2B polymorphisms with the risk and severity of chronic heart failure: a case-control study of a northern Chinese population (Q35138929) (← links)
- ATP can be dispensable for prespliceosome formation in yeast (Q35185397) (← links)
- Compensatory evolution of a precursor messenger RNA secondary structure in the Drosophila melanogaster Adh gene (Q36161161) (← links)
- Long-range RNA pairings contribute to mutually exclusive splicing (Q36406311) (← links)
- Eukaryotic TPP riboswitch regulation of alternative splicing involving long-distance base pairing (Q36684878) (← links)
- Competition between pre-mRNAs for the splicing machinery drives global regulation of splicing (Q37166231) (← links)
- RNA structure in splicing: An evolutionary perspective (Q37238025) (← links)
- Alternative splicing of U2AF1 reveals a shared repression mechanism for duplicated exons (Q37577401) (← links)
- Intronic features that determine the selection of the 3' splice site. (Q38027121) (← links)
- Modulation of exon skipping by high-affinity hnRNP A1-binding sites and by intron elements that repress splice site utilization (Q38325989) (← links)
- Role and convergent evolution of competing RNA secondary structures in mutually exclusive splicing (Q38917777) (← links)
- Identification of a novel element required for processing of intron-encoded box C/D small nucleolar RNAs in Saccharomyces cerevisiae (Q39451064) (← links)
- Conserved sequence elements associated with exon skipping (Q39744420) (← links)
- Secondary structure is required for 3' splice site recognition in yeast (Q39826068) (← links)
- Introns regulate the production of ribosomal proteins by modulating splicing of duplicated ribosomal protein genes (Q39946569) (← links)
- RNA structure is a key regulatory element in pathological ATM and CFTR pseudoexon inclusion events (Q40117572) (← links)
- A stem structure in fibroblast growth factor receptor 2 transcripts mediates cell-type-specific splicing by approximating intronic control elements (Q40407732) (← links)
- Multiple 5'-untranslated exons in the nuclear respiratory factor 1 gene span 47 kb and contribute to transcript heterogeneity and translational efficiency (Q40947007) (← links)
- The position of yeast snoRNA-coding regions within host introns is essential for their biosynthesis and for efficient splicing of the host pre-mRNA. (Q41500554) (← links)
- Effects of CYP3A4 polymorphisms on the plasma concentration of voriconazole. (Q41595490) (← links)
- Uncoupling yeast intron recognition from transcription with recursive splicing (Q41961425) (← links)
- High-affinity hnRNP A1 binding sites and duplex-forming inverted repeats have similar effects on 5' splice site selection in support of a common looping out and repression mechanism (Q41993441) (← links)
- Conservation and regulation of alternative splicing by dynamic inter- and intra-intron base pairings in Lepidoptera 14-3-3ξ pre-mRNAs (Q42013056) (← links)
- Perturbation of transcription elongation influences the fidelity of internal exon inclusion in Saccharomyces cerevisiae. (Q42038332) (← links)
- Identification of splicing silencers and enhancers in sense Alus: a role for pseudoacceptors in splice site repression (Q42124182) (← links)
- Transcription and proper splicing of a mammalian gene in yeast (Q47868691) (← links)
- A PLP splicing abnormality is associated with an unusual presentation of PMD. (Q48480596) (← links)