C. Tipper

发表

Role of TRIM5α RING Domain E3 Ubiquitin Ligase Activity in Capsid Disassembly, Reverse Transcription Blockade, and Restriction of Simian Immunodeficiency Virus

J. Sodroski, Christopher H. Tipper, Jonghwan Kim, 2011, Journal of Virology.

Mus spicilegus Endogenous Retrovirus HEMV Uses Murine Sodium-Dependent Myo-Inositol Transporter 1 as a Receptor

J. Coffin, Christopher H. Tipper, C. Tipper, 2012, Journal of Virology.

Characterization of Hortulanus Endogenous Murine Leukemia Virus, an Endogenous Provirus That Encodes an Infectious Murine Leukemia Virus of a Novel Subgroup

J. Coffin, Christopher H. Tipper, C. Tipper, 2005, Journal of Virology.

Elimination of defective alpha-factor pheromone receptors

Y. Li, Christopher H. Tipper, D. Jenness, 1997, Molecular and cellular biology.

Elimination of Defective a -Factor Pheromone Receptors

Li Yu, Christopher H. Tipper, D. Jenness, 1997 .

Adeno-Associated Virus Gene Therapy for Liver Disease

L. Kattenhorn, K. Clark, T. Wright, 2016, Human gene therapy.

Yeast Mutants Affecting Possible Quality Control of Plasma Membrane Proteins

Christopher H. Tipper, D. Jenness, Yu Li, 1999, Molecular and Cellular Biology.

Enhanced Autointegration in Hyperstable Simian Immunodeficiency Virus Capsid Mutants Blocked after Reverse Transcription

J. Sodroski, Christopher H. Tipper, C. Tipper, 2013, Journal of Virology.

Brefeldin A's effects on endosomes, lysosomes, and the TGN suggest a general mechanism for regulating organelle structure and membrane traffic

J. Lippincott-Schwartz, L. Orci, R. Klausner, 1991, Cell.

The Requirement for Cellular Transportin 3 (TNPO3 or TRN-SR2) during Infection Maps to Human Immunodeficiency Virus Type 1 Capsid and Not Integrase

Kenneth A. Matreyek, A. Engelman, I. Oztop, 2009, Journal of Virology.

Contribution of Glutamine Residues in the Helix 4-5 Loop to Capsid-Capsid Interactions in Simian Immunodeficiency Virus of Macaques

J. Sodroski, Christopher H. Tipper, C. Tipper, 2014, Journal of Virology.

Characterization of Adeno-Associated Viral Vector-Mediated Human Factor VIII Gene Therapy in Hemophilia A Mice.

Lili Wang, James M. Wilson, K. Clark, 2017, Human gene therapy.