机构：[1]Key Laboratory of Medical Molecular Virology (MOE/NHC/CAMS), School of Basic Medical Sciences, Shanghai Medical College, Fudan University, Shanghai 200032, China[2]Laboratory of Virology and Infectious Disease, The Rockefeller University, New York, NY 10065, USA[3]Laboratory of Molecular Immunology, The Rockefeller University, New York, NY 10065, USA[4]Structural Biology Resource Center, The Rockefeller University, New York, NY 10065, USA[5]West China School of Public Health, West China Hospital, Sichuan University, Chengdu 610041, China四川大学华西医院[6]Howard Hughes Medical Institute, The Rockefeller University, New York, NY 10065, USA[7]Division of Gastroenterology and Hepatology, Weill Cornell Medicine, New York, NY 10065, USA
This work
was supported by National Natural Science Foundation of China 31872730
(to Q.W.), the Thousand Talents Plan Youth Program (to Q.W.), and the Program
for Professor of Special Appointment (Eastern Scholar) at Shanghai Institutions
of Higher Learning TP2017010 (to Q.W.). The project was also supported
in part by grant #UL1TR001866 (to Q.W.) from the National Center for
Advancing Translational Sciences (NCATS), National Institutes of Health
(NIH) Clinical and Translational Science Award (CTSA) program; NIH grants
R01AI143295 and R01DK085713 (to C.M.R.), 2U19AI111825-06 (to M.C.N.),
K08DK090576 (to Y.P.J.), and NIH fellowship F32DK107164 (to E.M.). The
project was co-sponsored by the Center for Basic and Translational Research
on Disorders of the Digestive System through the generosity of the Leona M.
and Harry B. Helmsley Charitable Trust (to E.M.). The use of the instruments
in the Rockefeller University Structural Biology Resource Center was made
possible by grant number 1S10RR027037-01 from the National Center for
Research Resources of the NIH. We thank the staff at APS for their support
of remote data collection. This work is based upon research conducted at
the Northeastern Collaborative Access Team beamlines, which are funded
by the National Institute of General Medical Sciences from NIH (P30
GM124165). The Eiger 16M detector on 24-ID-E beam line is funded by a
NIH-ORIP HEI grant (S10OD021527). This research used resources of the
Advanced Photon Source, a U.S. Department of Energy (DOE) Office of Science
User Facility operated for the DOE Office of Science by Argonne National
Laboratory under contract no. DE-AC02-06CH11357. Support was also provided
by the Robertson Therapeutic Development Fund (to Q.W., E.M., and
M.C.N.). M.C.N. is an HHMI Investigator.
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外文
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出版当年[2020]版：
大类|1 区医学
小类|1 区微生物学1 区寄生虫学1 区病毒学
最新[2023]版：
大类|1 区医学
小类|1 区微生物学1 区寄生虫学1 区病毒学
第一作者：
第一作者机构：[1]Key Laboratory of Medical Molecular Virology (MOE/NHC/CAMS), School of Basic Medical Sciences, Shanghai Medical College, Fudan University, Shanghai 200032, China
共同第一作者：
通讯作者：
通讯机构：[2]Laboratory of Virology and Infectious Disease, The Rockefeller University, New York, NY 10065, USA[7]Division of Gastroenterology and Hepatology, Weill Cornell Medicine, New York, NY 10065, USA
推荐引用方式(GB/T 7714)：
Qiao Wang,Eleftherios Michailidis,Yingpu Yu,et al.A Combination of Human Broadly Neutralizing Antibodies against Hepatitis B Virus HBsAg with Distinct Epitopes Suppresses Escape Mutations.[J].Cell host & microbe.2020,28(2):335-349.e6.doi:10.1016/j.chom.2020.05.010.
APA：
Qiao Wang,Eleftherios Michailidis,Yingpu Yu,Zijun Wang,Arlene M. Hurley...&Michel C. Nussenzweig.(2020).A Combination of Human Broadly Neutralizing Antibodies against Hepatitis B Virus HBsAg with Distinct Epitopes Suppresses Escape Mutations..Cell host & microbe,28,(2)
MLA：
Qiao Wang,et al."A Combination of Human Broadly Neutralizing Antibodies against Hepatitis B Virus HBsAg with Distinct Epitopes Suppresses Escape Mutations.".Cell host & microbe 28..2(2020):335-349.e6
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