Source:http://linkedlifedata.com/resource/pubmed/id/15016773
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
4
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pubmed:dateCreated |
2004-3-22
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pubmed:abstractText |
In contrast to the technique of conventional freezing, the vitrification of spermatozoa requires high cooling rates (720 000 degrees K/min), which could be damaging for spermatozoa. The aim of our study was to compare slowly frozen and vitrified spermatozoa in terms of their post-thaw DNA integrity and motility.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Apr
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pubmed:issn |
0268-1161
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
19
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
932-9
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pubmed:dateRevised |
2004-11-17
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pubmed:meshHeading |
pubmed-meshheading:15016773-Cryopreservation,
pubmed-meshheading:15016773-Cryoprotective Agents,
pubmed-meshheading:15016773-DNA Damage,
pubmed-meshheading:15016773-Feasibility Studies,
pubmed-meshheading:15016773-Humans,
pubmed-meshheading:15016773-Male,
pubmed-meshheading:15016773-Semen Preservation,
pubmed-meshheading:15016773-Sperm Motility,
pubmed-meshheading:15016773-Spermatozoa,
pubmed-meshheading:15016773-Time Factors
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pubmed:year |
2004
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pubmed:articleTitle |
DNA integrity and motility of human spermatozoa after standard slow freezing versus cryoprotectant-free vitrification.
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pubmed:affiliation |
Department of Obstetrics and Gynecology, University of Cologne, Kerpener Str. 34, D-50931 Cologne, Germany. jeniaisachenko@yahoo.de
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pubmed:publicationType |
Journal Article,
Evaluation Studies
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