Richard B. Waring

Affiliations: 
Temple University, Philadelphia, PA, United States 
Area:
Molecular Biology, Genetics, Cell Biology
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"Richard Waring"
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Publications

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Burg L, Palmer N, Kikhi K, et al. (2018) Conditional mutagenesis by oligonucleotide-mediated integration of loxP sites in zebrafish. Plos Genetics. 14: e1007754
Burg L, Zhang K, Bonawitz T, et al. (2016) Internal epitope tagging informed by relative lack of sequence conservation. Scientific Reports. 6: 36986
Brown TA, Ray JA, Waring RB, et al. (2013) A mitochondrial reading frame which may code for a second form of ATPase subunit 9 in Aspergillus nidulans. Current Genetics. 8: 489-92
Bolduc JM, Spiegel PC, Chatterjee P, et al. (2003) Structural and biochemical analyses of DNA and RNA binding by a bifunctional homing endonuclease and group I intron splicing factor. Genes & Development. 17: 2875-88
Geese WJ, Kwon YK, Wen X, et al. (2003) In vitro analysis of the relationship between endonuclease and maturase activities in the bi-functional group I intron-encoded protein, I-AniI. European Journal of Biochemistry / Febs. 270: 1543-54
Geese WJ, Waring RB. (2001) A comprehensive characterization of a group IB intron and its encoded maturase reveals that protein-assisted splicing requires an almost intact intron RNA. Journal of Molecular Biology. 308: 609-22
Ho Y, Waring RB. (1999) The maturase encoded by a group I intron from Aspergillus nidulans stabilizes RNA tertiary structure and promotes rapid splicing. Journal of Molecular Biology. 292: 987-1001
Hur M, Geese WJ, Waring RB. (1997) Self-splicing activity of the mitochondrial group-I introns from Aspergillus nidulans and related introns from other species. Current Genetics. 32: 399-407
Ho Y, Kim SJ, Waring RB. (1997) A protein encoded by a group I intron in Aspergillus nidulans directly assists RNA splicing and is a DNA endonuclease. Proceedings of the National Academy of Sciences of the United States of America. 94: 8994-9
Hur M, Waring RB. (1996) Two group I introns with a C.G basepair at the 5' splice-site instead of the very highly conserved U.G basepair: is selection post-translational? Nucleic Acids Research. 23: 4466-70
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