J
Jeffrey S. Glenn
Researcher at Stanford University
Publications - 184
Citations - 9120
Jeffrey S. Glenn is an academic researcher from Stanford University. The author has contributed to research in topics: Virus & Hepatitis C virus. The author has an hindex of 49, co-authored 175 publications receiving 7186 citations. Previous affiliations of Jeffrey S. Glenn include University of California, San Francisco & Boston Children's Hospital.
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Journal ArticleDOI
A mouse-adapted model of SARS-CoV-2 to test COVID-19 countermeasures.
Kenneth H. Dinnon,Sarah R. Leist,Alexandra Schäfer,Caitlin E. Edwards,David R. Martinez,Stephanie A. Montgomery,Ande West,Boyd Yount,Yixuan J. Hou,Lily E. Adams,Kendra Gully,Ariane J. Brown,Emily Huang,Matthew D. Bryant,Ingrid Choong,Jeffrey S. Glenn,Jeffrey S. Glenn,Lisa E. Gralinski,Timothy P. Sheahan,Ralph S. Baric +19 more
TL;DR: A model in mouse using a species-adapted virus recapitulates features of SARS-CoV-2 infection and age-related disease pathogenesis in humans, and provides a model system for rapid evaluation of medical countermeasures against coronavirus disease 2019 (COVID-19).
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Structural Linkage between Ligand Discrimination and Receptor Activation by Type I Interferons
Christoph Thomas,Ignacio Moraga,Doron Levin,Peter O. Krutzik,Yulia Podoplelova,Angelica Trejo,Choongho Lee,Ganit Yarden,Susan E. Vleck,Jeffrey S. Glenn,Garry P. Nolan,Jacob Piehler,Gideon Schreiber,K. Christopher Garcia +13 more
TL;DR: Functional differences between IFNs are linked to their respective receptor recognition chemistries, in concert with a ligand-induced conformational change in IFNAR1, that collectively control signal initiation and complex stability, ultimately regulating differential STAT phosphorylation profiles, receptor internalization rates, and downstream gene expression patterns.
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Identification of a prenylation site in delta virus large antigen
TL;DR: Mutation of Cys211 in the CXXX box of the large antigen abolished both prenylation and particle formation, suggesting that this site is important for virion morphogenesis.
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Six RNA Viruses and Forty-One Hosts: Viral Small RNAs and Modulation of Small RNA Repertoires in Vertebrate and Invertebrate Systems
Poornima Parameswaran,Ella H. Sklan,Courtney Wilkins,Trever B. Burgon,Melanie A. Samuel,Rui Lu,K. Mark Ansel,Vigo Heissmeyer,Shirit Einav,William T. Jackson,Tammy Doukas,Suman Marie Paranjape,Charlotta Polacek,Flávia Barreto dos Santos,Roxana Jalili,Farbod Babrzadeh,Baback Gharizadeh,Dirk Grimm,Mark A. Kay,Satoshi Koike,Peter Sarnow,Mostafa Ronaghi,Shou-Wei Ding,Eva Harris,Marie Chow,Michael S. Diamond,Karla Kirkegaard,Jeffrey S. Glenn,Andrew Fire +28 more
TL;DR: Multiplexed high-throughput sequencing is used to characterize changes in small RNA populations that occur during viral infection in animal cells, defining vsRNAs as one possible component of the interplay between animal viruses and their hosts.
Journal ArticleDOI
Discovery of a hepatitis C target and its pharmacological inhibitors by microfluidic affinity analysis
Shirit Einav,Doron Gerber,Paul D. Bryson,Ella H. Sklan,Menashe Elazar,Sebastian J. Maerkl,Sebastian J. Maerkl,Jeffrey S. Glenn,Stephen R. Quake +8 more
TL;DR: It is shown that HCV NS4B binds RNA and that this binding is specific for the 3′ terminus of the negative strand of the viral genome with a dissociation constant (Kd) of ∼3.4 nM.