Impaired Spermatogenesis, Muscle, and Erythrocyte Function in U12 Intron Splicing-Defective Zrsr1 Mutant Mice.
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DOI: 10.1016/j.celrep.2018.03.028
Abstract: The U2AF35-like ZRSR1 has been implicated in the recognition of 3' splice site during spliceosome assembly, but ZRSR1 knockout mice do not show abnormal phenotypes. To analyze ZRSR1 function and its precise role in RNA splicing, we… read more here.
Keywords: zrsr1 mutant; intron; mutant mice; mice ... See more keywords