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James McSwiggen

Researcher at Sirna Therapeutics

Publications -  160
Citations -  7841

James McSwiggen is an academic researcher from Sirna Therapeutics. The author has contributed to research in topics: Nucleic acid & Small interfering RNA. The author has an hindex of 41, co-authored 159 publications receiving 7816 citations.

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Patent

RNA INTERFERENCE MEDIATED INHIBITION OF GENE EXPRESSION USING CHEMICALLY MODIFIED SHORT INTERFERING NUCLEIC ACID (siNA)

TL;DR: In this article, the authors present methods and reagents useful for modulating gene expression in various applications such as therapeutic, diagnostic, target assessment and genome discovery applications, which relates to synthetic chemically modified small nucleic acid molecules capable of mediating RNA interference (RNAi) to a target NCA sequence, such as short interfering nucleic acids (siNA), short interfering RNA (siRNA).
Patent

RNA interference mediated inhibition of adenosine A1 receptor (ADORA1) gene expression using short interfering RNA

TL;DR: In this article, the authors present methods and reagents useful in modulating adenosine A1 receptor (ADORA1) gene expression in a variety of applications, including use in therapeutic, diagnostic, target validation, and genomic discovery applications.
Journal ArticleDOI

Activity of stabilized short interfering RNA in a mouse model of hepatitis B virus replication

TL;DR: These experiments establish the strong impact that siRNAs can have on the extent of HBV infection and underscore the importance of stabilization of siRNA against nuclease degradation.
Patent

Method and reagent for inhibiting viral replication.

TL;DR: In this article, a diagram of an enzymatic RNA molecule in the hammerhead motif is presented, in the motif of a hairpin, hepatitis delta virus, group I intron or RNaseP-like RNA.
Journal ArticleDOI

Chemical Modification of Hammerhead Ribozymes: CATALYTIC ACTIVITY AND NUCLEASE RESISTANCE

TL;DR: A systematic study of selectively modified, 36-mer hammerhead ribozymes has resulted in the identification of a generic, catalytically active and nuclease stable ribozyme motif containing 5 ribose residues, 29-30 2-O-Me nucleotides, 1-2 other 2′-modified nucleotide at positions U4 and U7, and a 3′-3′-linked nucleotide “cap.”