![Identification of exon skipping events associated with Alzheimer's disease in the human hippocampus | BMC Medical Genomics | Full Text Identification of exon skipping events associated with Alzheimer's disease in the human hippocampus | BMC Medical Genomics | Full Text](https://media.springernature.com/lw685/springer-static/image/art%3A10.1186%2Fs12920-018-0453-8/MediaObjects/12920_2018_453_Fig1_HTML.png)
Identification of exon skipping events associated with Alzheimer's disease in the human hippocampus | BMC Medical Genomics | Full Text
![Frontiers | Innovative Therapeutic and Delivery Approaches Using Nanotechnology to Correct Splicing Defects Underlying Disease | Genetics Frontiers | Innovative Therapeutic and Delivery Approaches Using Nanotechnology to Correct Splicing Defects Underlying Disease | Genetics](https://www.frontiersin.org/files/Articles/520004/fgene-11-00731-HTML-r1/image_m/fgene-11-00731-g001.jpg)
Frontiers | Innovative Therapeutic and Delivery Approaches Using Nanotechnology to Correct Splicing Defects Underlying Disease | Genetics
![Exon 16–Skipping HER2 as a Novel Mechanism of Osimertinib Resistance in EGFR L858R/T790M–Positive Non–Small Cell Lung Cancer - Journal of Thoracic Oncology Exon 16–Skipping HER2 as a Novel Mechanism of Osimertinib Resistance in EGFR L858R/T790M–Positive Non–Small Cell Lung Cancer - Journal of Thoracic Oncology](https://els-jbs-prod-cdn.jbs.elsevierhealth.com/cms/attachment/393106e7-2deb-450d-a636-6a01d9af7831/gr1.jpg)
Exon 16–Skipping HER2 as a Novel Mechanism of Osimertinib Resistance in EGFR L858R/T790M–Positive Non–Small Cell Lung Cancer - Journal of Thoracic Oncology
Identification of Small Molecule and Genetic Modulators of AON-Induced Dystrophin Exon Skipping by High-Throughput Screening
![Exons 45–55 Skipping Using Mutation-Tailored Cocktails of Antisense Morpholinos in the DMD Gene: Molecular Therapy Exons 45–55 Skipping Using Mutation-Tailored Cocktails of Antisense Morpholinos in the DMD Gene: Molecular Therapy](https://els-jbs-prod-cdn.jbs.elsevierhealth.com/cms/attachment/35054749-ba19-49aa-b5e8-7b47502f83a7/fx1_lrg.jpg)
Exons 45–55 Skipping Using Mutation-Tailored Cocktails of Antisense Morpholinos in the DMD Gene: Molecular Therapy
![Efficacy of Multi-exon Skipping Treatment in Duchenne Muscular Dystrophy Dog Model Neonates: Molecular Therapy Efficacy of Multi-exon Skipping Treatment in Duchenne Muscular Dystrophy Dog Model Neonates: Molecular Therapy](https://els-jbs-prod-cdn.jbs.elsevierhealth.com/cms/attachment/267367a3-2089-42df-983b-228f8fe52a04/gr1_lrg.jpg)
Efficacy of Multi-exon Skipping Treatment in Duchenne Muscular Dystrophy Dog Model Neonates: Molecular Therapy
![Mutations in the SF1-U2AF59-U2AF23 Complex Cause Exon Skipping in Schizosaccharomyces pombe* - Journal of Biological Chemistry Mutations in the SF1-U2AF59-U2AF23 Complex Cause Exon Skipping in Schizosaccharomyces pombe* - Journal of Biological Chemistry](https://els-jbs-prod-cdn.jbs.elsevierhealth.com/cms/attachment/c81004b5-9aa9-492d-b6aa-5da7ce07692e/gr1_lrg.jpg)
Mutations in the SF1-U2AF59-U2AF23 Complex Cause Exon Skipping in Schizosaccharomyces pombe* - Journal of Biological Chemistry
![MET Exon 14 Skipping Alterations in NSCLC: Current Understanding and Therapeutic Advances - touchONCOLOGY MET Exon 14 Skipping Alterations in NSCLC: Current Understanding and Therapeutic Advances - touchONCOLOGY](https://touchoncology.com/wp-content/uploads/sites/2/2020/12/Fig-3-1.jpg)
MET Exon 14 Skipping Alterations in NSCLC: Current Understanding and Therapeutic Advances - touchONCOLOGY
![Exon-Skipping Oligonucleotides Restore Functional Collagen VI by Correcting a Common COL6A1 Mutation in Ullrich CMD: Molecular Therapy - Nucleic Acids Exon-Skipping Oligonucleotides Restore Functional Collagen VI by Correcting a Common COL6A1 Mutation in Ullrich CMD: Molecular Therapy - Nucleic Acids](https://els-jbs-prod-cdn.jbs.elsevierhealth.com/cms/asset/a008992b-a38f-4329-81d9-e9b089118829/fx1.jpg)
Exon-Skipping Oligonucleotides Restore Functional Collagen VI by Correcting a Common COL6A1 Mutation in Ullrich CMD: Molecular Therapy - Nucleic Acids
![Targeting mRNA Splicing as a Potential Treatment for Duchenne Muscular Dystrophy - Ryszard Kole - Discovery Medicine Targeting mRNA Splicing as a Potential Treatment for Duchenne Muscular Dystrophy - Ryszard Kole - Discovery Medicine](https://www.discoverymedicine.com/Ryszard-Kole/files/2012/07/discovery_medicine_no_74_ryszard_kole_figure_1.png)
Targeting mRNA Splicing as a Potential Treatment for Duchenne Muscular Dystrophy - Ryszard Kole - Discovery Medicine
![Splicing defects caused by exonic mutations in PKD1 as a new mechanism of pathogenesis in autosomal dominant polycystic kidney disease. - Abstract - Europe PMC Splicing defects caused by exonic mutations in PKD1 as a new mechanism of pathogenesis in autosomal dominant polycystic kidney disease. - Abstract - Europe PMC](https://europepmc.org/articles/PMC4615196/bin/krnb-12-04-1014291-g001.jpg)
Splicing defects caused by exonic mutations in PKD1 as a new mechanism of pathogenesis in autosomal dominant polycystic kidney disease. - Abstract - Europe PMC
![An Overview of Recent Advances and Clinical Applications of Exon Skipping and Splice Modulation for Muscular Dystrophy and Various Genetic Diseases | SpringerLink An Overview of Recent Advances and Clinical Applications of Exon Skipping and Splice Modulation for Muscular Dystrophy and Various Genetic Diseases | SpringerLink](https://media.springernature.com/original/springer-static/image/chp%3A10.1007%2F978-1-4939-8651-4_2/MediaObjects/439705_1_En_2_Fig1_HTML.png)
An Overview of Recent Advances and Clinical Applications of Exon Skipping and Splice Modulation for Muscular Dystrophy and Various Genetic Diseases | SpringerLink
![HMGA1a Trapping of U1 snRNP at an Authentic 5′ Splice Site Induces Aberrant Exon Skipping in Sporadic Alzheimer's Disease | Molecular and Cellular Biology HMGA1a Trapping of U1 snRNP at an Authentic 5′ Splice Site Induces Aberrant Exon Skipping in Sporadic Alzheimer's Disease | Molecular and Cellular Biology](https://journals.asm.org/cms/10.1128/MCB.00114-10/asset/e494ead8-4516-41e8-9654-6e27c6445a60/assets/graphic/zmb9991085770007.jpeg)
HMGA1a Trapping of U1 snRNP at an Authentic 5′ Splice Site Induces Aberrant Exon Skipping in Sporadic Alzheimer's Disease | Molecular and Cellular Biology
![Molecules | Free Full-Text | Antisense Oligonucleotide-Based Therapy for Neuromuscular Disease | HTML Molecules | Free Full-Text | Antisense Oligonucleotide-Based Therapy for Neuromuscular Disease | HTML](https://www.mdpi.com/molecules/molecules-22-00563/article_deploy/html/images/molecules-22-00563-g002.png)
Molecules | Free Full-Text | Antisense Oligonucleotide-Based Therapy for Neuromuscular Disease | HTML
![A novel splice mutation induces exon skipping of the EXT1 gene in patients with hereditary multiple exostoses A novel splice mutation induces exon skipping of the EXT1 gene in patients with hereditary multiple exostoses](https://www.spandidos-publications.com/article_images/ijo/54/3/IJO-54-03-0859-g03.jpg)