Mapping Systemic Inflammation and Antibody Responses in Multisystem Inflammatory Syndrome in Children (MIS-C) (vol 183, pg 982, 2020)

CELL(2023)

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摘要
(Cell 183, 982–995.e1–e14; November 12, 2020) In our original author list and author contributions section, we inadvertently missed 7 members of the Mount Sinai COVID-19 BioBank team, who have tirelessly worked on collecting and processing thousands of samples, several of which we used in our study. These members (along with their contributions) are Charuta Agashe (organization and management of patient specimens and training of staff), Joanna Grabowska (organization and management of patient specimens), Kai Nie (whole blood processing of immunophenotyping), Neha Karekar (organization and management of patient specimens), Jessica Le Berichel (organization of the Mount Sinai COVID-19 research effort), Hui Xie (Mount Sinai immune core biobanking), and Noam Beckmann (Mount Sinai BioBank co-creator). In this version of the article, we have added all their names and their specific contributions. We apologize for this omission. Mapping Systemic Inflammation and Antibody Responses in Multisystem Inflammatory Syndrome in Children (MIS-C)Gruber et al.CellSeptember 14, 2020In BriefInsights into the cellular and serological immune dysfunction underlying MIS-C, a novel pediatric inflammatory syndrome associated with SARS-CoV-2 infection, reveal potential autoantibodies that may link organ systems relevant to pathology. Full-Text PDF Open Archive
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关键词
COVID-19,Kawasaki-like,MIS-C,PIMS,SARS-CoV-2,autoimmunity,dysfunction,immune,pediatrics
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