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      <dc:title>Sex-sorted bovine spermatozoa and DNA damage: I. Static features</dc:title>
      <dc:creator>Gosálvez Berenguer, Jaime</dc:creator>
      <dc:creator>Ramírez, Miguel Ángel</dc:creator>
      <dc:creator>López Fernández, Carmen</dc:creator>
      <dc:creator>Crespo Castejón, Francisco</dc:creator>
      <dc:creator>Evans, Michael</dc:creator>
      <dc:creator>Kjelland, Michael</dc:creator>
      <dc:creator>Moreno, Juan Francisco</dc:creator>
      <dc:description>This study examined the static response of Spermatozoa DNA Fragmentation (SDF) after sex selection in bulls using a MoFlo® SX (Beckman Coulter, Miami FL) spermatozoa sorter to produce three different subpopulations: 1) Spermatozoa bearing X- chromosomes with a purity of 95%, 2) Spermatozoa bearing Y-chromosomes with a purity of 95%, and 3) non-viable spermatozoa. The static response of SDF refers to the baseline values observed for DNA damage when analyzed pre- and post sex-sorting. Results showed that while the baseline level SDF in pre-sorted bull spermatozoa samples ranged from 5.3% to 11% with an average of 7.9% ± 2.1%, the level of SDF obtained in X- and Y-chromosome sorted samples was much lower (3.1% ± 1.9%) and statistical differences were obtained after comparing both groups (P &lt; 0.01). Spermatozoa containing a fragmented DNA molecule tend to be accumulated in the non-viable subpopulation. The baseline SDF level in X- and Y-chromosome sorted subpopulations is reduced, by 63% on average when compared to the values obtained in the neat semen sample. Different bulls exhibit unique SDF reduction efficiencies via the X- and Y-chromosome sex selection process.</dc:description>
      <dc:date>2024-01-31T19:40:22Z</dc:date>
      <dc:date>2024-01-31T19:40:22Z</dc:date>
      <dc:date>2011</dc:date>
      <dc:type>journal article</dc:type>
      <dc:identifier>Gosálvez J, Ramirez MA, López-Fernández C, Crespo F, Evans KM, Kjelland ME, Moreno JF. Sex-sorted bovine spermatozoa and DNA damage: I. Static features. Theriogenology. 2011 Jan 15;75(2):197-205</dc:identifier>
      <dc:identifier>0093-691X</dc:identifier>
      <dc:identifier>10.1016/j.theriogenology.2010.08.006</dc:identifier>
      <dc:identifier>https://hdl.handle.net/20.500.14352/97424</dc:identifier>
      <dc:identifier>https://doi.org/10.1016/j.theriogenology.2010.08.006</dc:identifier>
      <dc:identifier>20932559</dc:identifier>
      <dc:identifier>https://pubmed.ncbi.nlm.nih.gov/20932559/</dc:identifier>
      <dc:language>eng</dc:language>
      <dc:relation>BFU 2007-66340/BFI</dc:relation>
      <dc:rights>http://creativecommons.org/licenses/by-nc-nd/4.0/</dc:rights>
      <dc:rights>restricted access</dc:rights>
      <dc:rights>Attribution-NonCommercial-NoDerivatives 4.0 International</dc:rights>
      <dc:publisher>Elsevier</dc:publisher>
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