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Effects of various combinations of cryoprotectants and cooling speed on the survival and further development of mouse oocytes after vitrification |
Soo Kyung Cha, Bo Yeun Kim, Mi Kyung Kim, You Shin Kim, Woo Sik Lee, Tae Ki Yoon, Dong Ryul Lee |
Clin Exp Reprod Med. 2011;38(1):24-30. Published online March 31, 2011 DOI: https://doi.org/10.5653/cerm.2011.38.1.24 |
Effects of various combinations of cryoprotectants and cooling speed on the survival and further development of mouse oocytes after vitrification High survival of mouse oocytes/embryos after vitrification without permeating cryoprotectants followed by ultra-rapid warming with an IR laser pulse 79. Mouse oocytes exhibit nearly 90% survival after cooling to −196°C in diluted vitrification solutions, provided that they are warmed at exceedingly high rates Survival of porcine GV and M II-oocytes after exposure to cryoprotectants and cooling to 10 °C 96. Effects of using slush nitrogen (SN2) and various cryoprotectants (CPA) compositions/concentrations on vitrification of mouse germinal vesicle (GV)—and metaphase II (MII)—oocytes 92. The dominance of warming rate over cooling rate in the survival of mouse oocytes subjected to a vitrification procedure The dominance of warming rate over cooling rate in the survival of mouse oocytes subjected to a vitrification procedure 037 Relative importance of cooling and warming rate in obtaining high survivals of mouse oocytes and embryos after vitrification Effects of L Carnitine and Cryoprotectants on Viability Rate of Immature Buffalo Oocytes in vitro After Vitrification Cryopreservation of rabbit semen: Comparing the effects of different cryoprotectants, cryoprotectant-free vitrification, and the use of albumin plus osmoprotectants on sperm survival and fertility after standard vapor freezing and vitrification |