F
Fei Gao
Researcher at Stanford University
Publications - 8
Citations - 1120
Fei Gao is an academic researcher from Stanford University. The author has contributed to research in topics: Lipidome & White adipose tissue. The author has an hindex of 7, co-authored 8 publications receiving 632 citations.
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Journal ArticleDOI
High-resolution proteomic and lipidomic analysis of exosomes and microvesicles from different cell sources.
Reka A. Haraszti,Marie-Cecile Didiot,Ellen Sapp,John D. Leszyk,Scott A. Shaffer,Hannah E. Rockwell,Fei Gao,Niven R. Narain,Marian DiFiglia,Michael A. Kiebish,Neil Aronin,Anastasia Khvorova +11 more
TL;DR: High-resolution lipidomic and proteomic analyses of exosomes and MVs derived by differential ultracentrifugation from 3 different cell types: U87 glioblastoma cells, Huh7 hepatocellular carcinoma cells and human bone marrow-derived mesenchymal stem cells are reported.
Journal ArticleDOI
The cold-induced lipokine 12,13-diHOME promotes fatty acid transport into brown adipose tissue
Matthew D. Lynes,Luiz O. Leiria,Morten Lundh,Morten Lundh,Alexander Bartelt,Farnaz Shamsi,Tian Lian Huang,Hirokazu Takahashi,Michael F. Hirshman,Christian Schlein,Alexandra Lee,Lisa A. Baer,Francis J. May,Fei Gao,Niven R. Narain,Emily Y. Chen,Michael A. Kiebish,Aaron M. Cypess,Matthias Blüher,Laurie J. Goodyear,Gökhan S. Hotamisligil,Kristin I. Stanford,Yu-Hua Tseng +22 more
TL;DR: It is shown that the lipid 12, 13-dihydroxy-9Z-octadecenoic acid (12,13-diHOME) is a stimulator of BAT activity, and that its levels are negatively correlated with body-mass index and insulin sensitivity, and this data suggest that 12,13 -diHOME, or a functional analog, could be developed as a treatment for metabolic disorders.
Journal ArticleDOI
Systems vaccinology of the BNT162b2 mRNA vaccine in humans.
Prabhu S. Arunachalam,Madeleine K D Scott,Thomas Hagan,Thomas Hagan,Chunfeng Li,Yupeng Feng,Florian Wimmers,Lilit Grigoryan,Meera Trisal,Venkata Viswanadh Edara,Lilin Lai,Sarah Esther Chang,Allan Feng,Shaurya Dhingra,Mihir Shah,Alexandra S. Lee,Sharon Chinthrajah,Sayantani B. Sindher,Vamsee Mallajosyula,Fei Gao,Natalia Sigal,Sangeeta Kowli,Sheena Gupta,Kathryn L. Pellegrini,Gregory K. Tharp,Sofia Maysel-Auslender,Sydney Hamilton,Hadj Aoued,Kevin Hrusovsky,Mark Roskey,Steven E. Bosinger,Steven E. Bosinger,Holden T. Maecker,Scott D. Boyd,Mark M. Davis,Paul J. Utz,Mehul S. Suthar,Purvesh Khatri,Kari C. Nadeau,Kari C. Nadeau,Bali Pulendran +40 more
TL;DR: In this article, the authors used a system vaccinology approach to comprehensively profile the innate and adaptive immune responses of 56 healthy volunteers who were vaccinated with the Pfizer-BioNTech mRNA vaccine (BNT162b2).
Journal ArticleDOI
Lipidomic Adaptations in White and Brown Adipose Tissue in Response to Exercise Demonstrate Molecular Species-Specific Remodeling
Francis J. May,Lisa A. Baer,Adam C. Lehnig,Kawai So,Emily Y. Chen,Fei Gao,Niven R. Narain,Liubov V. Gushchina,Aubrey L. Rose,Andrea I. Doseff,Michael A. Kiebish,Laurie J. Goodyear,Kristin I. Stanford +12 more
TL;DR: Exercise-induced changes to the scWAT and BAT lipidome are highly specific to certain molecular lipid species, indicating that changes in tissue lipid content reflect selective remodeling in scWat and BAT of both phospholipids and glycerol lipids in response to exercise training, thus providing a comprehensive resource for future studies of lipid metabolism pathways.
Posted ContentDOI
mRNA vaccination compared to infection elicits an IgG-predominant response with greater SARS-CoV-2 specificity and similar decrease in variant spike recognition
Katharina Roeltgen,Sandra C. A. Nielsen,Prabhu S. Arunachalam,Fan Yang,Ramona A. Hoh,Oliver F. Wirz,Alexandra S. Lee,Fei Gao,Vamsee Mallajosyula,Chunfeng Li,Emily Haraguchi,Massa J. Shoura,James L. Wilbur,Jacob N. Wohlstadter,Mark M. Davis,Mark M. Davis,Benjamin A. Pinsky,George Sigal,Bali Pulendran,Kari C. Nadeau,Scott D. Boyd +20 more
TL;DR: In this paper, the authors compare the magnitude and breadth of antibodies targeting SARS-CoV-2, SARS CoV2 variants of concern, and endemic coronaviruses, in vaccinees and infected patients.