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A gene-edited mouse model of limb-girdle muscular dystrophy 2C for testing exon skipping.
Academic Article
Why?
A single nucleotide deletion in exon 2 produces a novel null allele, HLA-DRB1*01:33N.
Academic Article
Why?
Evolution of the intron-exon structure of eukaryotic genes.
Academic Article
Why?
Exon ligation is proofread by the DExD/H-box ATPase Prp22p.
Academic Article
Why?
Exon-skipping therapy: a roadblock, detour, or bump in the road?
Academic Article
Why?
Hidden dangers: a cryptic exon disrupts BRCA2 mRNA.
Academic Article
Why?
Intron-exon structures of eukaryotic model organisms.
Academic Article
Why?
Mouse connexin 45: genomic cloning and exon usage.
Academic Article
Why?
ORESTES are enriched in rare exon usage variants affecting the encoded proteins.
Academic Article
Why?
Structure of a spliceosome remodelled for exon ligation.
Academic Article
Why?
Variants affecting exon skipping contribute to complex traits.
Academic Article
Why?
A bioinformatics analysis of alternative exon usage in human genes coding for extracellular matrix proteins.
Academic Article
Why?
A multiplexed fragment analysis-based assay for detection of JAK2 exon 12 mutations.
Academic Article
Why?
A possible role of exon-shuffling in the evolution of signal peptides of human proteins.
Academic Article
Why?
BRCA2 T2722R is a deleterious allele that causes exon skipping.
Academic Article
Why?
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