<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Sethi S</submitter><funding>European Research Council</funding><funding>NCI NIH HHS</funding><pagination>1123-1136</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6551791</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>30(6)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>In membranous nephropathy (MN), which is characterized by deposition of immune complexes along the glomerular basement membrane (GBM), phospholipase A2 receptor (PLA2R) and thrombospondin type 1 domain-containing 7A are target antigens in approximately 70% and 1%-5% of cases of primary MN, respectively. In other cases of primary MN and in secondary MN, the target antigens are unknown.&lt;h4>Methods&lt;/h4>We studied 224 cases of biopsy-proven PLA2R-negative MN and 102 controls (including 47 cases of PLA2R-associated MN) in pilot and discovery cohorts. We also evaluated 48 cases of PLA2R-negative presumed primary MN and lupus MN in a validation cohort. We used laser microdissection and mass spectrometry to identify new antigens, which were localized by immunohistochemistry.&lt;h4></pubmed_abstract><journal>Journal of the American Society of Nephrology : JASN</journal><pubmed_title>Exostosin 1/Exostosin 2-Associated Membranous Nephropathy.</pubmed_title><pmcid>PMC6551791</pmcid><funding_grant_id>322947</funding_grant_id><funding_grant_id>P30 CA015083</funding_grant_id><pubmed_authors>Specks U</pubmed_authors><pubmed_authors>Sethi S</pubmed_authors><pubmed_authors>Gross L</pubmed_authors><pubmed_authors>Madden BJ</pubmed_authors><pubmed_authors>Ronco P</pubmed_authors><pubmed_authors>Debiec H</pubmed_authors><pubmed_authors>Charlesworth MC</pubmed_authors><pubmed_authors>Ravindran A</pubmed_authors><pubmed_authors>Hummel AM</pubmed_authors><pubmed_authors>Fervenza FC</pubmed_authors></additional><is_claimable>false</is_claimable><name>Exostosin 1/Exostosin 2-Associated Membranous Nephropathy.</name><description>&lt;h4>Background&lt;/h4>In membranous nephropathy (MN), which is characterized by deposition of immune complexes along the glomerular basement membrane (GBM), phospholipase A2 receptor (PLA2R) and thrombospondin type 1 domain-containing 7A are target antigens in approximately 70% and 1%-5% of cases of primary MN, respectively. In other cases of primary MN and in secondary MN, the target antigens are unknown.&lt;h4>Methods&lt;/h4>We studied 224 cases of biopsy-proven PLA2R-negative MN and 102 controls (including 47 cases of PLA2R-associated MN) in pilot and discovery cohorts. We also evaluated 48 cases of PLA2R-negative presumed primary MN and lupus MN in a validation cohort. We used laser microdissection and mass spectrometry to identify new antigens, which were localized by immunohistochemistry.&lt;h4></description><dates><release>2019-01-01T00:00:00Z</release><publication>2019 Jun</publication><modification>2025-04-04T07:57:42.484Z</modification><creation>2025-04-04T07:57:42.484Z</creation></dates><accession>S-EPMC6551791</accession><cross_references><pubmed>31061139</pubmed><doi>10.1681/asn.2018080852</doi><doi>10.1681/ASN.2018080852</doi></cross_references></HashMap>