<HashMap><database>iProX</database><scores/><additional><omics_type>Proteomics</omics_type><submitter>Wu Zhong</submitter><species>Homo Sapiens</species><full_dataset_link>http://www.iprox.org/page/project.html?id=IPX0002279000</full_dataset_link><submitter_email>zhongwu@bmi.ac.cn</submitter_email><submitter_affiliation>National Engineering Research Center for the Emergency Drug, Beijing Institute of Pharmacology and Toxicology.</submitter_affiliation><sample_protocol></sample_protocol><repository>iProX</repository><data_protocol></data_protocol><pubmed_title>Pathological features of COVID-19-associated liver injury-a preliminary proteomics report based on clinical samples.</pubmed_title><pubmed_authors>Leng Ling L, Cao Ruiyuan R, Ma Jie J, Lv Luye L, Li Wei W, Zhu Yunping Y, Wu Zhihong Z, Wang Manli M, Zhou Yiwu Y, Zhong Wu W</pubmed_authors></additional><is_claimable>false</is_claimable><name>Integrated Proteomics Characterization of SARS-CoV-2 Associated Liver Injury</name><description>The high incidence of liver injury in patients with COVID-19 and the need for long-term medication for recovery make it imperative to study the infectivity and pathogenicity of SARS-CoV-2 in the liver. Here, we have identified significant proteomic changes for the first time in the liver of patients with COVID-19 using a quantitative proteomics approach. We detected differential expression levels of several proteins that mediate characteristic cellular host responses elicited by SARS-CoV-2 infection. These findings reveal important molecular mechanisms that may play a key role in the pathogenesis of COVID-19 associated liver diseases and provide a scientific basis for medical intervention strategy and drug target selection.</description><dates><publication>Tue Jun 23 00:00:00 BST 2020</publication></dates><accession>PXD019968</accession><cross_references><TAXONOMY>9606</TAXONOMY><pubmed>33419962</pubmed></cross_references></HashMap>