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Minigene
EYS Mutations and Implementation of Minigene Assay for Variant
Cellular Minigene Models for the Study of Allelic Expression of the Tau Gene and Its Role in Progressive Supranuclear Palsy
Splicing Inhibition of U2AF Leads to Alternative Exon Skipping
An Inhibitory Intron to a Stimulatory Intron by Alteration of the Splice Donor Sequence
Independence Between Pre-Mrna Splicing and De Novo DNA Methylation in an Isogenic Minigene Resource
Splicing Inhibition of U2AF Leads to Alternative Exon Skipping
Use of Minigene Systems to Dissect Alternative Splicing Elements
Cell-Based Splicing of Minigenes
Identification of Pathogenic Gene Mutations in LMNA and MYBPC3 That Alter RNA Splicing
Splicing: Going in Circles
Hybrid Minigene Splicing Assay Verifies the Pathogenicity of a Novel
Using Positional Distribution to Identify Splicing Elements and Predict Pre-Mrna Processing Defects in Human Genes
The Conserved 39 End Domain of U6atac Snrna Can Direct U6 Snrna to the Minor Spliceosome
Regulation of Alternative Splicing in the Generation of Isoforms
Cell Type-Restricted Activity of Hnrnpm Promotes Breast Cancer Metastasis Via Regulating Alternative Splicing
Splicing Defects in the CFTR Gene: Minigene Analysis of Two Mutations, 1811+1GNC and 1898+3ANG
The RNA-Binding Protein AKAP8 Suppresses Tumor Metastasis by Antagonizing EMT-Associated Alternative Splicing
Aberrant Splicing of U12-Type Introns Is the Hallmark of ZRSR2 Mutant Myelodysplastic Syndrome
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Splicing Analysis of Exonic OCRL Mutations Causing Lowe Syndrome Or Dent-2 Disease
Dual Fluorescence Splicing Reporter Minigene Identifies an Antisense
An Exonic Splicing Silencer Represses Spliceosome Assembly After ATP-Dependent Exon Recognition
Short Technical Reports Minigene Reporter for Identification And
Aberrant Splicing of Tau Pre-Mrna Caused by Intronic Mutations
An Engineered U1 Snrnp Redefines SMN1 Exon 7 Carrying a Pathogenic Mutation at the Splice Donor Site
Exon Skipping Via Chimeric Antisense U1 Snrnas to Correct Retinitis Pigmentosa Gtpase- 2 Regulator (RPGR) Splice Defect
(Hnrnps) in Cellular Processes: Focus on Hnrnp E1's Multifunctional Regulatory Roles
A CRISPR RNA-Binding Protein Screen Reveals Regulators of RUNX1 Isoform Generation
Regulation of Alternative Splicing and Its Connections to Cancer
Hybrid Minigene Assay: an Efficient Tool to Characterize Mrna
Exonic CLDN16 Mutations Associated with Familial Hypomagnesemia With
Contribution of Bioinformatics Predictions and Functional Splicing Assays to the Interpretation of Unclassified Variants of the BRCA Genes
RNA-Targeted Therapies and High-Throughput Screening Methods