High Developmental Rates of Mouse Oocytes Cryopreserved by an Optimized Vitrification Protocol: The Effects of Cryoprotectants, Calcium and Cumulus Cells
Author:
Affiliation:
1. Laboratory of Animal Reproduction, School of Veterinary Medicine, Azabu University, Sagamihara 252-5201, Japan
2. Graduate School of Veterinary Science, Azabu University, Sagamihara 252-5201, Japan
Publisher
Japanese Society of Animal Reproduction
Subject
Animal Science and Zoology
Link
https://www.jstage.jst.go.jp/article/jrd/57/6/57_11-066H/_pdf
Reference33 articles.
1. 1. Mazur P, Leibo SP, Seidel GE Jr Cryopreservation of the germplasm of animals used in biological and medical research: importance, impact, status, and future directions. Biol Reprod 2008; 78: 2-12.
2. 2. Zhou GB, Li N. Cryopreservation of porcine oocytes: recent advances. Mol Hum Reprod 2009; 15: 279-285.
3. 3. Rall WF, Fahy GM. Ice-free cryopreservation of mouse embryos at -196 degrees C by vitrification. Nature 1985; 313: 573-575.
4. 4. Kuwayama M. Highly efficient vitrification for cryopreservation of human oocytes. Theriogenology 2007; 67: 73-80.
5. 5. Parkening TA, Chang MC. Effects of cooling rates and maturity of the animal on the recovery and fertilization of frozen-thawed rodent eggs. Biol Reprod 1977; 17: 527-531.
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