Cyclophilin involvement in the replication of hepatitis C virus and other viruses
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James Baugh
James M. Baugh received his PhD from the Department of Microbiology at the University of Chicago in 2009, where he interrogated the ubiquitin independent roteasomal degradation pathway. He is now a Research Associate in the laboratory of Dr. Gallay, investigating the mechanism of action for cyclophilin inhibitor-mediated disruption of hepatitis C virus replication.
Philippe Gallay was born in 1963 and received his PhD in 1993 from the Centre Hospitalier Universitaire Vaudois in Lausanne, Switzerland. After completing his postdoctoral training at The Salk Institute for Biological Studies in La Jolla, California, he moved up the road to The Scripps Research Institute and as an Assistant Professor started his own laboratory in the Department of Immunology. Now a full Professor in the Department of Immunology and Microbial Science, Dr. Gallay’s research focuses on the interplay between host factors and two prime human threats – the human immunodeficiency virus (HIV) and the hepatitis C virus (HCV).
©2012 by Walter de Gruyter Berlin Boston
Articles in the same Issue
- Masthead
- Masthead
- Reviews
- Mitophagy: mechanisms, pathophysiological roles, and analysis
- Zinc networks: the cell-specific compartmentalization of zinc for specialized functions
- Cyclophilin involvement in the replication of hepatitis C virus and other viruses
- Minireviews
- TDP-43 in central nervous system development and function: clues to TDP-43-associated neurodegeneration
- Platelet function and thymosin β4
- Exportin T and Exportin 5: tRNA and miRNA biogenesis – and beyond
- Genes and Nucleic Acids
- Biological and molecular analysis of the pathogenic variant C3 of potato spindle tuber viroid (PSTVd) evolved during adaptation to chamomile (Matricaria chamomilla)
- Protein Structure and Function
- Heterologous production and functional and thermodynamic characterization of cation diffusion facilitator (CDF) transporters of mesophilic and hyperthermophilic origin
- Functional characterization of the Mycobacterium tuberculosis zinc metallopeptidase Zmp1 and identification of potential substrates
- Antimicrobial activity of human islet amyloid polypeptides: an insight into amyloid peptides’ connection with antimicrobial peptides
- Cell Biology and Signaling
- Necroptosis modulated by autophagy is a predominant form of melanoma cell death induced by sanguilutine
Articles in the same Issue
- Masthead
- Masthead
- Reviews
- Mitophagy: mechanisms, pathophysiological roles, and analysis
- Zinc networks: the cell-specific compartmentalization of zinc for specialized functions
- Cyclophilin involvement in the replication of hepatitis C virus and other viruses
- Minireviews
- TDP-43 in central nervous system development and function: clues to TDP-43-associated neurodegeneration
- Platelet function and thymosin β4
- Exportin T and Exportin 5: tRNA and miRNA biogenesis – and beyond
- Genes and Nucleic Acids
- Biological and molecular analysis of the pathogenic variant C3 of potato spindle tuber viroid (PSTVd) evolved during adaptation to chamomile (Matricaria chamomilla)
- Protein Structure and Function
- Heterologous production and functional and thermodynamic characterization of cation diffusion facilitator (CDF) transporters of mesophilic and hyperthermophilic origin
- Functional characterization of the Mycobacterium tuberculosis zinc metallopeptidase Zmp1 and identification of potential substrates
- Antimicrobial activity of human islet amyloid polypeptides: an insight into amyloid peptides’ connection with antimicrobial peptides
- Cell Biology and Signaling
- Necroptosis modulated by autophagy is a predominant form of melanoma cell death induced by sanguilutine
