PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
27872312-3	2016	Here, we describe an innovative approach for targeting mast cells in vitro and in vivo using antisense oligonucleotide-mediated exon skipping of the beta-subunit of the high-affinity IgE receptor (FcepsilonRIbeta) to eliminate surface high-affinity IgE receptor (FcepsilonRI) expression and function, rendering mast cells unresponsive to IgE-mediated activation.	Oligonucleotides	103-118	Fc epsilon receptor Ia	Homo sapiens	197-208