Jonathan Abraham, Ph.D.
Affiliations: | 2010 | Harvard University, Cambridge, MA, United States |
Area:
structural cell biologyGoogle:
"Jonathan Abraham"Mean distance: 8.7
Parents
Sign in to add mentorStephen C. Harrison | grad student | 2010 | Harvard | |
(Host Cell Recognition by New World Hemorrhagic Fever Arenaviruses.) |
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Publications
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Shankar S, Pan J, Yang P, et al. (2024) Viral DNA polymerase structures reveal mechanisms of antiviral drug resistance. Cell |
Yang P, Li W, Fan X, et al. (2023) Structural basis for VLDLR recognition by eastern equine encephalitis virus. Biorxiv : the Preprint Server For Biology |
Hickerson BT, Daniels-Wells TR, Payes C, et al. (2022) Host receptor-targeted therapeutic approach to counter pathogenic New World mammarenavirus infections. Nature Communications. 13: 558 |
Nabel KG, Clark SA, Shankar S, et al. (2021) Structural basis for continued antibody evasion by the SARS-CoV-2 receptor binding domain. Science (New York, N.Y.). eabl6251 |
Wellner A, McMahon C, Gilman MSA, et al. (2021) Rapid generation of potent antibodies by autonomous hypermutation in yeast. Nature Chemical Biology |
Ferrero S, Flores MD, Short C, et al. (2021) Antibody-based inhibition of pathogenic New World Hemorrhagic Fever mammarenaviruses by steric occlusion of the human transferrin receptor 1 apical domain. Journal of Virology. JVI0186820 |
Clark SA, Clark LE, Pan J, et al. (2021) SARS-CoV-2 evolution in an immunocompromised host reveals shared neutralization escape mechanisms. Cell |
Koma T, Huang C, Coscia A, et al. (2021) Glycoprotein N-linked glycans play a critical role in arenavirus pathogenicity. Plos Pathogens. 17: e1009356 |
Wellner A, McMahon C, Gilman MSA, et al. (2020) Rapid generation of potent antibodies by autonomous hypermutation in yeast. Biorxiv : the Preprint Server For Biology |
Clark SA, Clark LE, Pan J, et al. (2020) Molecular basis for a germline-biased neutralizing antibody response to SARS-CoV-2. Biorxiv : the Preprint Server For Biology |