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dc.contributor.authorKleppe, Lene
dc.contributor.authorEdvardsen, Rolf Brudvik
dc.contributor.authorFurmanek, Tomasz
dc.contributor.authorAndersson, Eva
dc.contributor.authorSkaftnesmo, Kai Ove
dc.contributor.authorThyri Segafredo, Frida
dc.contributor.authorWargelius, Anna Sofie Troedsson
dc.date.accessioned2020-10-22T12:56:41Z
dc.date.available2020-10-22T12:56:41Z
dc.date.created2020-08-16T13:17:24Z
dc.date.issued2020
dc.identifier.citationBMC Genomics. 2020, 21:99 1-15.en_US
dc.identifier.issn1471-2164
dc.identifier.urihttps://hdl.handle.net/11250/2684552
dc.description.abstractSustainability challenges are currently hampering an increase in salmon production. Using sterile salmon can solve problems with precocious puberty and genetic introgression from farmed escapees to wild populations. Recently sterile salmon was produced by knocking out the germ cell-specific dead end (dnd). Several approaches may be applied to inhibit Dnd function, including gene knockout, knockdown or immunization. Since it is challenging to develop a successful treatment against a gene product already existing in the body, alternative targets are being explored. Germ cells are surrounded by, and dependent on, gonadal somatic cells. Targeting genes essential for the survival of gonadal somatic cells may be good alternative targets for sterility treatments. Our aim was to identify and characterize novel germ cell and gonadal somatic factors in Atlantic salmon.en_US
dc.language.isoengen_US
dc.titleTranscriptomic analysis of dead end knockout testis reveals germ cell and gonadal somatic factors in Atlantic salmonen_US
dc.typePeer revieweden_US
dc.typeJournal articleen_US
dc.description.versionpublishedVersionen_US
dc.source.pagenumber1-15en_US
dc.source.volume21:99en_US
dc.source.journalBMC Genomicsen_US
dc.identifier.doi10.1186/s12864-020-6513-4
dc.identifier.cristin1823488
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1


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