<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>9(3)</volume><submitter>Selokar NL</submitter><pubmed_abstract>Somatic cells were isolated from cryopreserved semen of 4 buffalo bulls, 3 of which had died over 10 years earlier, and were established in culture. The cells expressed cytokeratin-18, keratin and vimentin indicating that they were of epithelial origin. The cells were used as nuclear donors for hand-made cloning for producing buffalo embryos. The blastocyst rate and quality, as indicated by apoptotic index, were comparable among embryos produced using cells obtained from fresh or frozen-thawed semen or those obtained from conventional cell sources such as skin. Examination of the epigenetic status revealed that the global level of H3K27me3 but not that of H3K9/14ac and H4K5ac differed significantly (P&lt;0.05) among cloned embryos from different bulls. The relative mRNA abundance of HDAC1, DN</pubmed_abstract><journal>PloS one</journal><pagination>e90755</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC3948694</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Hope for restoration of dead valuable bulls through cloning using donor somatic cells isolated from cryopreserved semen.</pubmed_title><pmcid>PMC3948694</pmcid><pubmed_authors>Selokar NL</pubmed_authors><pubmed_authors>Saini M</pubmed_authors><pubmed_authors>Palta P</pubmed_authors><pubmed_authors>Chauhan MS</pubmed_authors><pubmed_authors>Manik R</pubmed_authors><pubmed_authors>Singla SK</pubmed_authors></additional><is_claimable>false</is_claimable><name>Hope for restoration of dead valuable bulls through cloning using donor somatic cells isolated from cryopreserved semen.</name><description>Somatic cells were isolated from cryopreserved semen of 4 buffalo bulls, 3 of which had died over 10 years earlier, and were established in culture. The cells expressed cytokeratin-18, keratin and vimentin indicating that they were of epithelial origin. The cells were used as nuclear donors for hand-made cloning for producing buffalo embryos. The blastocyst rate and quality, as indicated by apoptotic index, were comparable among embryos produced using cells obtained from fresh or frozen-thawed semen or those obtained from conventional cell sources such as skin. Examination of the epigenetic status revealed that the global level of H3K27me3 but not that of H3K9/14ac and H4K5ac differed significantly (P&lt;0.05) among cloned embryos from different bulls. The relative mRNA abundance of HDAC1, DN</description><dates><release>2014-01-01T00:00:00Z</release><publication>2014</publication><modification>2025-04-20T02:46:53.618Z</modification><creation>2019-03-26T23:24:04Z</creation></dates><accession>S-EPMC3948694</accession><cross_references><pubmed>24614586</pubmed><doi>10.1371/journal.pone.0090755</doi></cross_references></HashMap>