<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Piewbang C</submitter><funding>Thailand Science Research and Innovation</funding><funding>The Second Century Fund (C2F), Chulalongkorn University</funding><funding>Ratchadapisek Somphot Fund for Postdoctoral Fellowship, Chulalongkorn University</funding><funding>National Research Council of Thailand</funding><funding>Thailand Research Fund</funding><funding>Joint Funding of External Research Project, Ratchadaphiseksomphot Endowment Fund and Veterinary Science Research Fund</funding><funding>Thailand Science Research and Innovation Fund (TSRI)</funding><pagination>1648-1659</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9511090</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>36(5)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Whether domestic cat hepadnavirus (DCH) infection is associated with clinical disease remains to be determined.&lt;h4>Objectives&lt;/h4>To determine the relationship between DCH detection, hematology, serum bichemistry and liver histology in DCH-positive cats.&lt;h4>Animals&lt;/h4>One thousand twenty-two cats in Thailand without concurrent diseases and not undergoing treatments adversely affecting the liver.&lt;h4>Methods&lt;/h4>Retrospective cross-sectional study. Samples derived from cats with concurrent virus detection were excluded. DCH detection was determined in blood and fresh-frozen liver by quantitative polymerase chain reaction (qPCR) and further investigated in liver sections showing histological parenchymal disorders (HPD) and normal liver (HNL) using in situ hybridization (IS</pubmed_abstract><journal>Journal of veterinary internal medicine</journal><pubmed_title>Domestic cat hepadnavirus associated with hepatopathy in cats: A retrospective study.</pubmed_title><pmcid>PMC9511090</pmcid><funding_grant_id>PHD/0021/256</funding_grant_id><funding_grant_id>NRCT5-RGJ63001-013</funding_grant_id><funding_grant_id>CU_FRB640001_01_31_2</funding_grant_id><funding_grant_id>NRCT5‐RGJ63001‐013</funding_grant_id><funding_grant_id>N42A650553</funding_grant_id><funding_grant_id>N41A640175</funding_grant_id><funding_grant_id>RES_65_005_31_005</funding_grant_id><pubmed_authors>Piewbang C</pubmed_authors><pubmed_authors>Tummaruk P</pubmed_authors><pubmed_authors>Dankaona W</pubmed_authors><pubmed_authors>Yostawonkul J</pubmed_authors><pubmed_authors>Sirivisoot S</pubmed_authors><pubmed_authors>Poonsin P</pubmed_authors><pubmed_authors>Kasantikul T</pubmed_authors><pubmed_authors>Lacharoje S</pubmed_authors><pubmed_authors>Techangamsuwan S</pubmed_authors></additional><is_claimable>false</is_claimable><name>Domestic cat hepadnavirus associated with hepatopathy in cats: A retrospective study.</name><description>&lt;h4>Background&lt;/h4>Whether domestic cat hepadnavirus (DCH) infection is associated with clinical disease remains to be determined.&lt;h4>Objectives&lt;/h4>To determine the relationship between DCH detection, hematology, serum bichemistry and liver histology in DCH-positive cats.&lt;h4>Animals&lt;/h4>One thousand twenty-two cats in Thailand without concurrent diseases and not undergoing treatments adversely affecting the liver.&lt;h4>Methods&lt;/h4>Retrospective cross-sectional study. Samples derived from cats with concurrent virus detection were excluded. DCH detection was determined in blood and fresh-frozen liver by quantitative polymerase chain reaction (qPCR) and further investigated in liver sections showing histological parenchymal disorders (HPD) and normal liver (HNL) using in situ hybridization (IS</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Sep</publication><modification>2026-07-14T17:11:14.803Z</modification><creation>2025-02-19T01:21:30.295Z</creation></dates><accession>S-EPMC9511090</accession><cross_references><pubmed>36054642</pubmed><doi>10.1111/jvim.16525</doi></cross_references></HashMap>