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Publications by Y. Habara
Splicing Analysis Disclosed a Determinant Single Nucleotide for Exon Skipping Caused by a Novel Intraexonic Four-Nucleotide Deletion in the Dystrophin Gene
Journal of Medical Genetics
Genetics
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Contemporary Retrotransposition of a Novel Non-Coding Gene Induces Exon-Skipping in Dystrophin mRNA
Journal of Human Genetics
Genetics
Personalized Exon Skipping Strategies to Address Clustered Non-Deletion Dystrophin Mutations
Neuromuscular Disorders
Child Health
Neurology
Pediatrics
Perinatology
Genetics
Quantification of PCR Bias Caused by a Single Nucleotide Polymorphism in SMN Gene Dosage Analysis
Journal of Molecular Diagnostics
Forensic Medicine
Pathology
Molecular Medicine
The Silent Mutation Nucleotide 744 G → A, Lys172Lys, in Exon 6 of BRCA2 Results in Exon Skipping
Breast Cancer Research and Treatment
Cancer Research
Oncology
Dynamic ASXL1 Exon Skipping and Alternative Circular Splicing in Single Human Cells
PLoS ONE
Multidisciplinary
Dual Exon Skipping in Myostatin and Dystrophin for Duchenne Muscular Dystrophy
BMC Medical Genomics
Genetics
Nucleotide Sequence of Novel cDNAs Generated by Alternative Splicing of a Rat Thyroid Hormone Receptor Gene Transcript
Nucleic Acids Research
Genetics
A Novel Type 2A Von Willebrand Factor Mutation Located at the Last Nucleotide of Exon 26 (3538G>A) Causes Skipping of 2 Nonadjacent Exons
Blood
Biochemistry
Immunology
Cell Biology
Hematology
Antisense-Induced Exon Skipping and Synthesis of Dystrophin in the MDX Mouse
Proceedings of the National Academy of Sciences of the United States of America
Multidisciplinary
