2006 - Fellow of the American Association for the Advancement of Science (AAAS)
His primary areas of study are Molecular biology, RNA, Interferon, Protein kinase R and Biochemistry. His Molecular biology study incorporates themes from Complementary DNA, RNA silencing, Adenosine deaminase, Exon and EIF-2 kinase. His RNA study integrates concerns from other disciplines, such as Virology and Cell biology.
His Interferon study combines topics in areas such as Virus, Cell culture, Recombinant DNA and Interferon regulatory factors. Protein kinase R is a subfield of Protein kinase A that Charles E. Samuel investigates. Within one scientific family, Charles E. Samuel focuses on topics pertaining to RNA-binding protein under ADAR, and may sometimes address concerns connected to Fusion protein.
Charles E. Samuel mainly focuses on Molecular biology, Interferon, RNA, Protein kinase R and Virology. Charles E. Samuel combines subjects such as Messenger RNA, Adenosine deaminase, Protein kinase A and Biochemistry with his study of Molecular biology. Charles E. Samuel has researched Interferon in several fields, including Cell culture, Gene, Mutant and Phosphorylation.
His RNA study frequently involves adjacent topics like Cell biology. His Protein kinase R research incorporates themes from Transcription, EIF-2 kinase and Gene expression. His research in RNA editing intersects with topics in RNA-dependent RNA polymerase, Polymerase and Ribosome.
Charles E. Samuel spends much of his time researching Molecular biology, RNA, Protein kinase R, Interferon and RNA silencing. The various areas that he examines in his Molecular biology study include Stress granule, Cytopathic effect, Transcription and Adenosine deaminase. His RNA research integrates issues from Virus and Cell biology.
His Cell biology course of study focuses on Adenosine and Gene silencing, RNA splicing and Interferon regulatory factors. His Protein kinase R research is multidisciplinary, incorporating elements of EIF-2 kinase and Protein biosynthesis. His Cell culture research extends to the thematically linked field of Interferon.
His main research concerns Molecular biology, RNA, Interferon, RNA editing and Protein kinase R. His Molecular biology research is multidisciplinary, incorporating perspectives in Virus and Viral replication. His study connects Cell biology and RNA.
His work focuses on many connections between Interferon and other disciplines, such as Stress granule, that overlap with his field of interest in EIF-2 kinase. His study in RNA editing is interdisciplinary in nature, drawing from both Polymerase and Ribosome. His Protein kinase R study introduces a deeper knowledge of Protein kinase A.
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Antiviral Actions of Interferons
Charles E. Samuel.
Clinical Microbiology Reviews (2001)
Interferons and their actions.
Sidney Pestka;Jerome A. Langer;Kathryn C. Zoon;Charles E. Samuel.
Annual Review of Biochemistry (1987)
Antiviral actions of interferon interferon-regulated cellular proteins and their surprisingly selective antiviral activities
Charles E. Samuel.
Virology (1991)
Expression and Regulation by Interferon of a Double-Stranded- RNA-Specific Adenosine Deaminase from Human Cells: Evidence for Two Forms of the Deaminase
J B Patterson;C E Samuel.
Molecular and Cellular Biology (1995)
The eIF-2 alpha protein kinases, regulators of translation in eukaryotes from yeasts to humans.
C E Samuel.
Journal of Biological Chemistry (1993)
Adenovirus VAI RNA antagonizes the antiviral action of interferon by preventing activation of the interferon-induced eIF-2α kinase
Jan Kitajewski;Robert J. Schneider;Brian Safer;Susan M. Munemitsu.
Cell (1986)
cDNA structures and regulation of two interferon-induced human Mx proteins.
M Aebi;J Fäh;N Hurt;C E Samuel.
Molecular and Cellular Biology (1989)
The role of gamma interferon in antimicrobial immunity.
Ronit Shtrichman;Charles E Samuel.
Current Opinion in Microbiology (2001)
Dynamic landscape and regulation of RNA editing in mammals
Meng How Tan;Qin Li;Raghuvaran Shanmugam;Robert Piskol.
Nature (2017)
Human RNA-specific adenosine deaminase ADAR1 transcripts possess alternative exon 1 structures that initiate from different promoters, one constitutively active and the other interferon inducible
Cyril X. George;Charles E. Samuel.
Proceedings of the National Academy of Sciences of the United States of America (1999)
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