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Publications by Meili Wei

The Conserved Residue Arg46 in the N-Terminal Heptad Repeat Domain of HIV-1 Gp41 Is Critical for Viral Fusion and Entry

PLoS ONE

Multidisciplinary

2012

English

Related publications

Mutations of Glu560 Within HIV-1 Envelope Glycoprotein N-Terminal Heptad Repeat Region Contribute to Resistance to Peptide Inhibitors of Virus Entry

English

Trimeric Heptad Repeat Synthetic Peptides HR1 and HR2 Efficiently Inhibit HIV-1 Entry

English

Design of Potent Inhibitors of HIV-1 Entry From the Gp41 N-Peptide Region

Proceedings of the National Academy of Sciences of the United States of America

Multidisciplinary

2001

English

Mutations That Increase the Stability of the Post-Fusion Gp41 Conformation of the HIV-1 Envelope Glycoprotein Are Selected by Both an X4 and R5 HIV-1 Virus to Escape Fusion Inhibitors Corresponding to Heptad Repeat 1 of Gp41, but the Gp120 Adaptive Mutations Differ Between the Two Viruses

English

The Heptad Repeat C Domain of the Respiratory Syncytial Virus Fusion Protein Plays a Key Role in Membrane Fusion

English

A Highly Conserved Residue in the C-Terminal Helix of HIV-1 Matrix Is Required for Envelope Incorporation Into Virus Particles

English

Amphipathic Properties of HIV-1 Gp41 Fusion Inhibitors

Current Topics in Medicinal Chemistry

Medicine

Drug Discovery

2011

English

HIV-1 VPR N-Terminal Tagging Affects Alternative Splicing of the Viral Genome

Scientific Reports

Multidisciplinary

2016

English

The Tale of the Long Tail: The Cytoplasmic Domain of HIV-1 Gp41

English

Amanote Research

Discover open access scientific publications

Search, annotate, share and cite publications

Publications by Meili Wei

The Conserved Residue Arg46 in the N-Terminal Heptad Repeat Domain of HIV-1 Gp41 Is Critical for Viral Fusion and Entry

Related publications

Mutations of Glu560 Within HIV-1 Envelope Glycoprotein N-Terminal Heptad Repeat Region Contribute to Resistance to Peptide Inhibitors of Virus Entry

Trimeric Heptad Repeat Synthetic Peptides HR1 and HR2 Efficiently Inhibit HIV-1 Entry

Design of Potent Inhibitors of HIV-1 Entry From the Gp41 N-Peptide Region

Mutations That Increase the Stability of the Post-Fusion Gp41 Conformation of the HIV-1 Envelope Glycoprotein Are Selected by Both an X4 and R5 HIV-1 Virus to Escape Fusion Inhibitors Corresponding to Heptad Repeat 1 of Gp41, but the Gp120 Adaptive Mutations Differ Between the Two Viruses

The Heptad Repeat C Domain of the Respiratory Syncytial Virus Fusion Protein Plays a Key Role in Membrane Fusion

A Highly Conserved Residue in the C-Terminal Helix of HIV-1 Matrix Is Required for Envelope Incorporation Into Virus Particles

Amphipathic Properties of HIV-1 Gp41 Fusion Inhibitors

HIV-1 VPR N-Terminal Tagging Affects Alternative Splicing of the Viral Genome

The Tale of the Long Tail: The Cytoplasmic Domain of HIV-1 Gp41