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Corrigendum to: Infection of monkeys by simian-human immunodeficiency viruses with transmitted/founder clade C HIV-1 envelopes [Virology 475 (2015) 37-45]

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Date
2015
Authors
Asmal, M
Luedemann, C
Lavine, CL
Mach, LV
Balachandran, H
Brinkley, C
Denny, TN
Lewis, MG
Anderson, H
Pal, R
Sok, D
Le, K
Pauthner, M
Hahn, BH
Shaw, GM
Seaman, MS
Letvin, NL
Burton, DR
Sodroski, JG
Haynes, BF
Santra, S
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(21 total)
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Journal article
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https://hdl.handle.net/10161/13348
Published Version (Please cite this version)
10.1016/j.virol.2015.01.023
Publication Info
Asmal, M; Luedemann, C; Lavine, CL; Mach, LV; Balachandran, H; Brinkley, C; ... Santra, S (2015). Corrigendum to: Infection of monkeys by simian-human immunodeficiency viruses with transmitted/founder clade C HIV-1 envelopes [Virology 475 (2015) 37-45]. Virology. 10.1016/j.virol.2015.01.023. Retrieved from https://hdl.handle.net/10161/13348.
This is constructed from limited available data and may be imprecise. To cite this article, please review & use the official citation provided by the journal.
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Scholars@Duke

Denny

Thomas Norton Denny

Professor in Medicine
Thomas N. Denny, MSc, M.Phil, is the Chief Operating Officer of the Duke Human Vaccine Institute (DHVI), Associate Dean for Duke Research and Discovery @RTP, and a Professor of Medicine in the Department of Medicine at Duke University Medical Center. He is also an Affiliate Member of the Duke Global Health Institute. Previously, he served on the Health Sector Advisory Council of the Duke University Fuquay School of Business. Prior to joining Duke, he was an Associate Professor of Pathology, Labo
Haynes

Barton Ford Haynes

Frederic M. Hanes Distinguished Professor of Medicine
The Haynes lab is studying host innate and adaptive immune responses to the human immunodeficiency virus (HIV), tuberculosis (TB), and influenza in order to find the enabling technology to make preventive vaccines against these three major infectious diseases. Mucosal Immune Responses in Acute HIV Infection The Haynes lab is working to determine why broadly neutralizing antibodies are rarely made in acute HIV infection (AHI), currently a major obstacle in the de
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