Expression of microRNAs and isomiRs in the porcine endometrium: implications for gene regulation at the maternal-conceptus interface
Embryo implantation is a complex, synchronized process that requires establishment of a reciprocal dialogue between a receptive endometrium and developing blastocysts. Recently, microRNAs (miRNAs), known to modulate gene expression through post-transcriptional mechanisms, were implicated in regulati...
Gespeichert in:
Veröffentlicht in: | BMC genomics 2015-11, Vol.16 (903), p.906-906, Article 906 |
---|---|
Hauptverfasser: | , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 906 |
---|---|
container_issue | 903 |
container_start_page | 906 |
container_title | BMC genomics |
container_volume | 16 |
creator | Krawczynski, Kamil Bauersachs, Stefan Reliszko, Zaneta P Graf, Alexander Kaczmarek, Monika M |
description | Embryo implantation is a complex, synchronized process that requires establishment of a reciprocal dialogue between a receptive endometrium and developing blastocysts. Recently, microRNAs (miRNAs), known to modulate gene expression through post-transcriptional mechanisms, were implicated in regulation of early pregnancy events including maternal recognition of pregnancy and implantation. To characterize complex transcriptomic changes, expression of miRNAs in pregnant and cyclic endometria collected on days 12, 16 and 20 was analyzed using Illumina deep sequencing and analyzed with bioinformatic pipeline. Moreover, expression profiles of ten genes related to miRNA synthesis and transport such as DROSHA, DGCR8, XPO5, DICER, TARBP2, TNRC6A, and AGO1-4 were determined.
Among genes involved in miRNA transport and synthesis DROSHA, XPO5, DICER1, TARBP, and AGO1 expression was affected by the reproductive status. Moreover, DICER1 and AGO2 proteins were localized in luminal and glandular epithelium with immunofluorescence staining. Several hundred mature, canonical and non-canonical miRNAs were found to be expressed in the endometrial samples. Detailed analysis revealed that miRNA length variants, isomiRs, accounted for the vast majority of defined sequences. Both miRNA and isomiR of miR-140-3p were shown to affect expression of putative targets in endometrial stromal cells in vitro. Computational analysis of putative target genes for miRNAs differentially expressed (DE) between pregnant and cyclic animals resulted in lists of biological processes and regulatory pathways indicating their role in cellular development, cell cycle, immunological response and organismal development. Among predicted target genes for DE miRNAs, vascular endothelial growth factor (VEGF), progesterone and estradiol receptors (PGR, ESR1) and leukemia inhibitory factor (LIF) were found.
This research revealed a repertoire of pregnancy-related miRNAs in porcine endometrium during initial stages of conceptus implantation and during the estrous cycle, and sheds light on mechanisms regulating miRNA-mediated gene expression at the maternal-conceptus interface. |
doi_str_mv | 10.1186/s12864-015-2172-2 |
format | Article |
fullrecord | <record><control><sourceid>gale_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_4636777</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A447998025</galeid><sourcerecordid>A447998025</sourcerecordid><originalsourceid>FETCH-LOGICAL-c528t-f927b7c5c6d3cf4a98e4934f2666f75e3f2bc8c671feb42f2be2e1f66dfaa8fd3</originalsourceid><addsrcrecordid>eNptkkFvFSEUhSdGY2v1B7gxJG50Me3AMMC4MHlp2tqkqclT14THXKY0MzAC07R7f7hMX619xrCAe_nOIbmconiLq0OMBTuKmAhGywo3JcGclORZsY8px7li9PmT817xKsbrqsJckOZlsUdYQ1lNyX7x6-R2ChCj9Q55g0arg19friJSrkM2-tGuI7IOpStAkw_aOkDgOj9CCnYePyE7ToPVKmWDiIwPqIeMBOjn4b6JVLoXjypBcGootXcapjQvtrlllIbXxQujhghvHvaD4sfpyffjL-XF17Pz49VFqRsiUmlawjdcN5p1tTZUtQJoW1NDGGOGN1AbstFCM44NbCjJFRDAhrHOKCVMVx8Un7e-07wZodPgUlCDnIIdVbiTXlm5e-Pslez9jczDYpzzbPDhwSD4nzPEJEcbNQyDcuDnKDGvSY1x1YqMvv8HvfbzMoCF4i0TuCX4L9WrAaR1xud39WIqV5TythUVaTJ1-B8qrw7yh3kHxub-juDjjiAzCW5Tr-YY5fm39S6Lt2z--RgDmMd54EouMZPbmMkcM7nETJKsefd0kI-KP7mqfwO4is-H</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1779681921</pqid></control><display><type>article</type><title>Expression of microRNAs and isomiRs in the porcine endometrium: implications for gene regulation at the maternal-conceptus interface</title><source>MEDLINE</source><source>DOAJ Directory of Open Access Journals</source><source>SpringerLink Journals</source><source>EZB-FREE-00999 freely available EZB journals</source><source>PubMed Central</source><source>PubMed Central Open Access</source><source>Springer Nature OA Free Journals</source><creator>Krawczynski, Kamil ; Bauersachs, Stefan ; Reliszko, Zaneta P ; Graf, Alexander ; Kaczmarek, Monika M</creator><creatorcontrib>Krawczynski, Kamil ; Bauersachs, Stefan ; Reliszko, Zaneta P ; Graf, Alexander ; Kaczmarek, Monika M</creatorcontrib><description>Embryo implantation is a complex, synchronized process that requires establishment of a reciprocal dialogue between a receptive endometrium and developing blastocysts. Recently, microRNAs (miRNAs), known to modulate gene expression through post-transcriptional mechanisms, were implicated in regulation of early pregnancy events including maternal recognition of pregnancy and implantation. To characterize complex transcriptomic changes, expression of miRNAs in pregnant and cyclic endometria collected on days 12, 16 and 20 was analyzed using Illumina deep sequencing and analyzed with bioinformatic pipeline. Moreover, expression profiles of ten genes related to miRNA synthesis and transport such as DROSHA, DGCR8, XPO5, DICER, TARBP2, TNRC6A, and AGO1-4 were determined.
Among genes involved in miRNA transport and synthesis DROSHA, XPO5, DICER1, TARBP, and AGO1 expression was affected by the reproductive status. Moreover, DICER1 and AGO2 proteins were localized in luminal and glandular epithelium with immunofluorescence staining. Several hundred mature, canonical and non-canonical miRNAs were found to be expressed in the endometrial samples. Detailed analysis revealed that miRNA length variants, isomiRs, accounted for the vast majority of defined sequences. Both miRNA and isomiR of miR-140-3p were shown to affect expression of putative targets in endometrial stromal cells in vitro. Computational analysis of putative target genes for miRNAs differentially expressed (DE) between pregnant and cyclic animals resulted in lists of biological processes and regulatory pathways indicating their role in cellular development, cell cycle, immunological response and organismal development. Among predicted target genes for DE miRNAs, vascular endothelial growth factor (VEGF), progesterone and estradiol receptors (PGR, ESR1) and leukemia inhibitory factor (LIF) were found.
This research revealed a repertoire of pregnancy-related miRNAs in porcine endometrium during initial stages of conceptus implantation and during the estrous cycle, and sheds light on mechanisms regulating miRNA-mediated gene expression at the maternal-conceptus interface.</description><identifier>ISSN: 1471-2164</identifier><identifier>EISSN: 1471-2164</identifier><identifier>DOI: 10.1186/s12864-015-2172-2</identifier><identifier>PMID: 26546342</identifier><language>eng</language><publisher>England: BioMed Central Ltd</publisher><subject>Analysis ; Animals ; Endometrium - metabolism ; Female ; Gene expression ; Gene Expression Regulation - genetics ; Genomics ; Health aspects ; Influence ; MicroRNA ; MicroRNAs - genetics ; Pregnancy ; Pregnant women ; Stromal Cells - metabolism ; Swine ; Vascular endothelial growth factor ; Vascular Endothelial Growth Factor A - metabolism</subject><ispartof>BMC genomics, 2015-11, Vol.16 (903), p.906-906, Article 906</ispartof><rights>COPYRIGHT 2015 BioMed Central Ltd.</rights><rights>Copyright BioMed Central 2015</rights><rights>Krawczynski et al. 2015</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c528t-f927b7c5c6d3cf4a98e4934f2666f75e3f2bc8c671feb42f2be2e1f66dfaa8fd3</citedby><cites>FETCH-LOGICAL-c528t-f927b7c5c6d3cf4a98e4934f2666f75e3f2bc8c671feb42f2be2e1f66dfaa8fd3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4636777/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4636777/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,860,881,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26546342$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Krawczynski, Kamil</creatorcontrib><creatorcontrib>Bauersachs, Stefan</creatorcontrib><creatorcontrib>Reliszko, Zaneta P</creatorcontrib><creatorcontrib>Graf, Alexander</creatorcontrib><creatorcontrib>Kaczmarek, Monika M</creatorcontrib><title>Expression of microRNAs and isomiRs in the porcine endometrium: implications for gene regulation at the maternal-conceptus interface</title><title>BMC genomics</title><addtitle>BMC Genomics</addtitle><description>Embryo implantation is a complex, synchronized process that requires establishment of a reciprocal dialogue between a receptive endometrium and developing blastocysts. Recently, microRNAs (miRNAs), known to modulate gene expression through post-transcriptional mechanisms, were implicated in regulation of early pregnancy events including maternal recognition of pregnancy and implantation. To characterize complex transcriptomic changes, expression of miRNAs in pregnant and cyclic endometria collected on days 12, 16 and 20 was analyzed using Illumina deep sequencing and analyzed with bioinformatic pipeline. Moreover, expression profiles of ten genes related to miRNA synthesis and transport such as DROSHA, DGCR8, XPO5, DICER, TARBP2, TNRC6A, and AGO1-4 were determined.
Among genes involved in miRNA transport and synthesis DROSHA, XPO5, DICER1, TARBP, and AGO1 expression was affected by the reproductive status. Moreover, DICER1 and AGO2 proteins were localized in luminal and glandular epithelium with immunofluorescence staining. Several hundred mature, canonical and non-canonical miRNAs were found to be expressed in the endometrial samples. Detailed analysis revealed that miRNA length variants, isomiRs, accounted for the vast majority of defined sequences. Both miRNA and isomiR of miR-140-3p were shown to affect expression of putative targets in endometrial stromal cells in vitro. Computational analysis of putative target genes for miRNAs differentially expressed (DE) between pregnant and cyclic animals resulted in lists of biological processes and regulatory pathways indicating their role in cellular development, cell cycle, immunological response and organismal development. Among predicted target genes for DE miRNAs, vascular endothelial growth factor (VEGF), progesterone and estradiol receptors (PGR, ESR1) and leukemia inhibitory factor (LIF) were found.
This research revealed a repertoire of pregnancy-related miRNAs in porcine endometrium during initial stages of conceptus implantation and during the estrous cycle, and sheds light on mechanisms regulating miRNA-mediated gene expression at the maternal-conceptus interface.</description><subject>Analysis</subject><subject>Animals</subject><subject>Endometrium - metabolism</subject><subject>Female</subject><subject>Gene expression</subject><subject>Gene Expression Regulation - genetics</subject><subject>Genomics</subject><subject>Health aspects</subject><subject>Influence</subject><subject>MicroRNA</subject><subject>MicroRNAs - genetics</subject><subject>Pregnancy</subject><subject>Pregnant women</subject><subject>Stromal Cells - metabolism</subject><subject>Swine</subject><subject>Vascular endothelial growth factor</subject><subject>Vascular Endothelial Growth Factor A - metabolism</subject><issn>1471-2164</issn><issn>1471-2164</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNptkkFvFSEUhSdGY2v1B7gxJG50Me3AMMC4MHlp2tqkqclT14THXKY0MzAC07R7f7hMX619xrCAe_nOIbmconiLq0OMBTuKmAhGywo3JcGclORZsY8px7li9PmT817xKsbrqsJckOZlsUdYQ1lNyX7x6-R2ChCj9Q55g0arg19friJSrkM2-tGuI7IOpStAkw_aOkDgOj9CCnYePyE7ToPVKmWDiIwPqIeMBOjn4b6JVLoXjypBcGootXcapjQvtrlllIbXxQujhghvHvaD4sfpyffjL-XF17Pz49VFqRsiUmlawjdcN5p1tTZUtQJoW1NDGGOGN1AbstFCM44NbCjJFRDAhrHOKCVMVx8Un7e-07wZodPgUlCDnIIdVbiTXlm5e-Pslez9jczDYpzzbPDhwSD4nzPEJEcbNQyDcuDnKDGvSY1x1YqMvv8HvfbzMoCF4i0TuCX4L9WrAaR1xud39WIqV5TythUVaTJ1-B8qrw7yh3kHxub-juDjjiAzCW5Tr-YY5fm39S6Lt2z--RgDmMd54EouMZPbmMkcM7nETJKsefd0kI-KP7mqfwO4is-H</recordid><startdate>20151106</startdate><enddate>20151106</enddate><creator>Krawczynski, Kamil</creator><creator>Bauersachs, Stefan</creator><creator>Reliszko, Zaneta P</creator><creator>Graf, Alexander</creator><creator>Kaczmarek, Monika M</creator><general>BioMed Central Ltd</general><general>BioMed Central</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>ISR</scope><scope>3V.</scope><scope>7QP</scope><scope>7QR</scope><scope>7SS</scope><scope>7TK</scope><scope>7U7</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7P</scope><scope>P64</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20151106</creationdate><title>Expression of microRNAs and isomiRs in the porcine endometrium: implications for gene regulation at the maternal-conceptus interface</title><author>Krawczynski, Kamil ; Bauersachs, Stefan ; Reliszko, Zaneta P ; Graf, Alexander ; Kaczmarek, Monika M</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c528t-f927b7c5c6d3cf4a98e4934f2666f75e3f2bc8c671feb42f2be2e1f66dfaa8fd3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Analysis</topic><topic>Animals</topic><topic>Endometrium - metabolism</topic><topic>Female</topic><topic>Gene expression</topic><topic>Gene Expression Regulation - genetics</topic><topic>Genomics</topic><topic>Health aspects</topic><topic>Influence</topic><topic>MicroRNA</topic><topic>MicroRNAs - genetics</topic><topic>Pregnancy</topic><topic>Pregnant women</topic><topic>Stromal Cells - metabolism</topic><topic>Swine</topic><topic>Vascular endothelial growth factor</topic><topic>Vascular Endothelial Growth Factor A - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Krawczynski, Kamil</creatorcontrib><creatorcontrib>Bauersachs, Stefan</creatorcontrib><creatorcontrib>Reliszko, Zaneta P</creatorcontrib><creatorcontrib>Graf, Alexander</creatorcontrib><creatorcontrib>Kaczmarek, Monika M</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Gale In Context: Science</collection><collection>ProQuest Central (Corporate)</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Neurosciences Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Biological Science Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>BMC genomics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Krawczynski, Kamil</au><au>Bauersachs, Stefan</au><au>Reliszko, Zaneta P</au><au>Graf, Alexander</au><au>Kaczmarek, Monika M</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Expression of microRNAs and isomiRs in the porcine endometrium: implications for gene regulation at the maternal-conceptus interface</atitle><jtitle>BMC genomics</jtitle><addtitle>BMC Genomics</addtitle><date>2015-11-06</date><risdate>2015</risdate><volume>16</volume><issue>903</issue><spage>906</spage><epage>906</epage><pages>906-906</pages><artnum>906</artnum><issn>1471-2164</issn><eissn>1471-2164</eissn><abstract>Embryo implantation is a complex, synchronized process that requires establishment of a reciprocal dialogue between a receptive endometrium and developing blastocysts. Recently, microRNAs (miRNAs), known to modulate gene expression through post-transcriptional mechanisms, were implicated in regulation of early pregnancy events including maternal recognition of pregnancy and implantation. To characterize complex transcriptomic changes, expression of miRNAs in pregnant and cyclic endometria collected on days 12, 16 and 20 was analyzed using Illumina deep sequencing and analyzed with bioinformatic pipeline. Moreover, expression profiles of ten genes related to miRNA synthesis and transport such as DROSHA, DGCR8, XPO5, DICER, TARBP2, TNRC6A, and AGO1-4 were determined.
Among genes involved in miRNA transport and synthesis DROSHA, XPO5, DICER1, TARBP, and AGO1 expression was affected by the reproductive status. Moreover, DICER1 and AGO2 proteins were localized in luminal and glandular epithelium with immunofluorescence staining. Several hundred mature, canonical and non-canonical miRNAs were found to be expressed in the endometrial samples. Detailed analysis revealed that miRNA length variants, isomiRs, accounted for the vast majority of defined sequences. Both miRNA and isomiR of miR-140-3p were shown to affect expression of putative targets in endometrial stromal cells in vitro. Computational analysis of putative target genes for miRNAs differentially expressed (DE) between pregnant and cyclic animals resulted in lists of biological processes and regulatory pathways indicating their role in cellular development, cell cycle, immunological response and organismal development. Among predicted target genes for DE miRNAs, vascular endothelial growth factor (VEGF), progesterone and estradiol receptors (PGR, ESR1) and leukemia inhibitory factor (LIF) were found.
This research revealed a repertoire of pregnancy-related miRNAs in porcine endometrium during initial stages of conceptus implantation and during the estrous cycle, and sheds light on mechanisms regulating miRNA-mediated gene expression at the maternal-conceptus interface.</abstract><cop>England</cop><pub>BioMed Central Ltd</pub><pmid>26546342</pmid><doi>10.1186/s12864-015-2172-2</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1471-2164 |
ispartof | BMC genomics, 2015-11, Vol.16 (903), p.906-906, Article 906 |
issn | 1471-2164 1471-2164 |
language | eng |
recordid | cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_4636777 |
source | MEDLINE; DOAJ Directory of Open Access Journals; SpringerLink Journals; EZB-FREE-00999 freely available EZB journals; PubMed Central; PubMed Central Open Access; Springer Nature OA Free Journals |
subjects | Analysis Animals Endometrium - metabolism Female Gene expression Gene Expression Regulation - genetics Genomics Health aspects Influence MicroRNA MicroRNAs - genetics Pregnancy Pregnant women Stromal Cells - metabolism Swine Vascular endothelial growth factor Vascular Endothelial Growth Factor A - metabolism |
title | Expression of microRNAs and isomiRs in the porcine endometrium: implications for gene regulation at the maternal-conceptus interface |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-10T13%3A49%3A30IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Expression%20of%20microRNAs%20and%20isomiRs%20in%20the%20porcine%20endometrium:%20implications%20for%20gene%20regulation%20at%20the%20maternal-conceptus%20interface&rft.jtitle=BMC%20genomics&rft.au=Krawczynski,%20Kamil&rft.date=2015-11-06&rft.volume=16&rft.issue=903&rft.spage=906&rft.epage=906&rft.pages=906-906&rft.artnum=906&rft.issn=1471-2164&rft.eissn=1471-2164&rft_id=info:doi/10.1186/s12864-015-2172-2&rft_dat=%3Cgale_pubme%3EA447998025%3C/gale_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1779681921&rft_id=info:pmid/26546342&rft_galeid=A447998025&rfr_iscdi=true |