<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>54(1)</volume><submitter>Emery VC</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>The impact of different cytomegalovirus (HCMV) glycoprotein B (gB) genotypes on pathogenesis remains controversial.&lt;h4>Objectives&lt;/h4>To investigate the effect of gB genotypes either as single infections or as part of multiple infections on the early kinetics of response to ganciclovir therapy.&lt;h4>Methods&lt;/h4>Patients (n=239) enrolled in a study of intravenous ganciclovir or valganciclovir for the treatment of HCMV disease were analysed by a gB genotype specific PCR to quantify the amount of each gB genotype present at initiation of therapy (baseline, day 0) and at days 3, 7, 14 and 21 post therapy.&lt;h4>Results and conclusions&lt;/h4>In all gB groups (individual gB genotype infections and mixed genotype infections) there was a biphasic decline in viral load after therapy. Th</pubmed_abstract><journal>Journal of clinical virology : the official publication of the Pan American Society for Clinical Virology</journal><pagination>56-60</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC3328767</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Differential decay kinetics of human cytomegalovirus glycoprotein B genotypes following antiviral chemotherapy.</pubmed_title><pmcid>PMC3328767</pmcid><pubmed_authors>Kumar D</pubmed_authors><pubmed_authors>Asberg A</pubmed_authors><pubmed_authors>Preiksaitis JK</pubmed_authors><pubmed_authors>Rollag H</pubmed_authors><pubmed_authors>Emery VC</pubmed_authors><pubmed_authors>Humar A</pubmed_authors><pubmed_authors>Pescovitz MD</pubmed_authors><pubmed_authors>Jardine AG</pubmed_authors><pubmed_authors>Hartmann A</pubmed_authors><pubmed_authors>Pang X</pubmed_authors><pubmed_authors>Gahlemann CG</pubmed_authors><pubmed_authors>Manuel O</pubmed_authors></additional><is_claimable>false</is_claimable><name>Differential decay kinetics of human cytomegalovirus glycoprotein B genotypes following antiviral chemotherapy.</name><description>&lt;h4>Background&lt;/h4>The impact of different cytomegalovirus (HCMV) glycoprotein B (gB) genotypes on pathogenesis remains controversial.&lt;h4>Objectives&lt;/h4>To investigate the effect of gB genotypes either as single infections or as part of multiple infections on the early kinetics of response to ganciclovir therapy.&lt;h4>Methods&lt;/h4>Patients (n=239) enrolled in a study of intravenous ganciclovir or valganciclovir for the treatment of HCMV disease were analysed by a gB genotype specific PCR to quantify the amount of each gB genotype present at initiation of therapy (baseline, day 0) and at days 3, 7, 14 and 21 post therapy.&lt;h4>Results and conclusions&lt;/h4>In all gB groups (individual gB genotype infections and mixed genotype infections) there was a biphasic decline in viral load after therapy. Th</description><dates><release>2012-01-01T00:00:00Z</release><publication>2012 May</publication><modification>2025-04-18T14:46:42.518Z</modification><creation>2019-03-27T00:52:26Z</creation></dates><accession>S-EPMC3328767</accession><cross_references><pubmed>22410132</pubmed><doi>10.1016/j.jcv.2012.01.015</doi></cross_references></HashMap>