2013 - Fellow of the American Association for the Advancement of Science (AAAS)
His primary areas of study are Virology, Virus, Capsid, Reverse transcriptase and Viral protein. Christopher Aiken has included themes like Virus Integration, Cell culture and Point mutation in his Virology study. His work on Simian immunodeficiency virus, Murine leukemia virus and Infectivity as part of general Virus study is frequently connected to Pseudotyping, therefore bridging the gap between diverse disciplines of science and establishing a new relationship between them.
His work investigates the relationship between Capsid and topics such as Biophysics that intersect with problems in Random hexamer. His Reverse transcriptase study which covers Virus Uncoating that intersects with Transcription, TRIM5alpha and In vitro. His research investigates the connection between Viral protein and topics such as Cryo-electron microscopy that intersect with problems in Hydrophobic effect, Capsomere and Crystallography.
His primary scientific interests are in Capsid, Virology, Cell biology, Virus and Mutant. His Capsid study combines topics from a wide range of disciplines, such as Reverse transcriptase, Biophysics and Cypa, Cyclophilin A, Molecular biology. His Virology research is multidisciplinary, incorporating elements of Cell culture and Nuclear transport.
In his study, Protease is strongly linked to Cleavage, which falls under the umbrella field of Cell biology. In the field of Virus, his study on Murine leukemia virus, Vesicular stomatitis virus and Viral life cycle overlaps with subjects such as Pseudotyping. His research in Mutant intersects with topics in Mutation, Phenotype, DNA and Cell nucleus.
His scientific interests lie mostly in Capsid, Cell biology, Reverse transcriptase, Mutant and Biophysics. Within the field of Virus and Virology Christopher Aiken studies Capsid. He interconnects HEK 293 cells, Wild type, In vitro and DNA in the investigation of issues within Cell biology.
He focuses mostly in the field of Reverse transcriptase, narrowing it down to matters related to DNA synthesis and, in some cases, Retrovirus, Endogeny and Viral replication. Christopher Aiken combines subjects such as Viral life cycle and Viral protein with his study of Mutant. His work deals with themes such as RNA, Recombinant DNA, Small molecule and Random hexamer, which intersect with Biophysics.
Christopher Aiken mainly investigates Capsid, Virus, Mutant, Cell biology and Biophysics. His Capsid study necessitates a more in-depth grasp of Virology. The various areas that he examines in his Virus study include Reverse transcriptase, Phenotype, Interferon, DNA and Peptide sequence.
His Reverse transcriptase research incorporates themes from Viral life cycle, Viral protein and Recombinant DNA. His work carried out in the field of Mutant brings together such families of science as RNA, Innate immune system, Small molecule and Cell nucleus. His Biophysics research includes elements of Cypa, Capsomere, Protein structure and Random hexamer.
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Nef induces CD4 endocytosis: requirement for a critical dileucine motif in the membrane-proximal CD4 cytoplasmic domain.
Christopher Aiken;Jason Konner;Nathaniel R. Landau;Marc E. Lenburg;Marc E. Lenburg.
Cell (1994)
Mature HIV-1 capsid structure by cryo-electron microscopy and all-atom molecular dynamics
Gongpu Zhao;Juan R. Perilla;Ernest L. Yufenyuy;Ernest L. Yufenyuy;Xin Meng.
Nature (2013)
Vif is crucial for human immunodeficiency virus type 1 proviral DNA synthesis in infected cells.
U. Von Schwedler;Jinping Song;C. Aiken;D. Trono.
Journal of Virology (1993)
Formation of a Human Immunodeficiency Virus Type 1 Core of Optimal Stability Is Crucial for Viral Replication
Brett M. Forshey;Uta von Schwedler;Wesley I. Sundquist;Christopher Aiken.
Journal of Virology (2002)
Nef stimulates human immunodeficiency virus type 1 proviral DNA synthesis.
C Aiken;D Trono.
Journal of Virology (1995)
Pseudotyping human immunodeficiency virus type 1 (HIV-1) by the glycoprotein of vesicular stomatitis virus targets HIV-1 entry to an endocytic pathway and suppresses both the requirement for Nef and the sensitivity to cyclosporin A.
Christopher Aiken.
Journal of Virology (1997)
HIV-1 infection of nondividing cells: C-terminal tyrosine phosphorylation of the viral matrix protein is a key regulator
Philippe Gallay;Simon Swingler;Christopher Aiken;Didier Trono.
Cell (1995)
Assembly Properties of the Human Immunodeficiency Virus Type 1 CA Protein
Barbie K. Ganser-Pornillos;Uta K. von Schwedler;Kirsten M. Stray;Christopher Aiken.
Journal of Virology (2004)
Escape from the dominant HLA-B27-restricted cytotoxic T-lymphocyte response in Gag is associated with a dramatic reduction in human immunodeficiency virus type 1 replication.
Arne Schneidewind;Mark A. Brockman;Mark A. Brockman;Ruifeng Yang;Rahma I. Adam.
Journal of Virology (2007)
Structural convergence between Cryo-EM and NMR reveals intersubunit interactions critical for HIV-1 capsid function.
In-Ja L. Byeon;Xin Meng;Jinwon Jung;Gongpu Zhao.
Cell (2009)
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