Ultra-rapid warming yields high survival of mouse oocytes cooled to -196°c in dilutions of a standard vitrification solution - Wikidata - awgldk - TriplyDB

Ultra-rapid warming yields high survival of mouse oocytes cooled to -196°c in dilutions of a standard vitrification solution

Ultra-rapid warming yields high survival of mouse oocytes cooled to -196°c in dilutions of a standard vitrification solution

http://www.wikidata.org/entity/Q34257090

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Reversible Cryopreservation of Living Cells Using an Electron Microscopy Cryo-Fixation Method Synchrotron X-ray diffraction to detect glass or ice formation in the vitrified bovine cumulus-oocyte complexes and morulae Alginate Hydrogel Microencapsulation Inhibits Devitrification and Enables Large-Volume Low-CPA Cell Vitrification Generation of live piglets from cryopreserved oocytes for the first time using a defined system for in vitro embryo production.Survivals of mouse oocytes approach 100% after vitrification in 3-fold diluted media and ultra-rapid warming by an IR laser pulse Preserving human cells for regenerative, reproductive, and transfusion medicine.Large-volume vitrification of human biopsied and non-biopsied blastocysts: a simple, robust technique for cryopreservation.High survival of mouse oocytes/embryos after vitrification without permeating cryoprotectants followed by ultra-rapid warming with an IR laser pulse.Physical parameters, modeling, and methodological details in using IR laser pulses to warm frozen or vitrified cells ultra-rapidly The crucial role of zona pellucida in cryopreservation of oocytes by vitrification.Vitrification of mouse embryos using the thin plastic strip method.Direct Measurement of Water States in Cryopreserved Cells Reveals Tolerance toward Ice Crystallization.A combination of hydroxypropyl cellulose and trehalose as supplementation for vitrification of human oocytes: a retrospective cohort study.Morphological and functional preservation of pre-antral follicles after vitrification of macaque ovarian tissue in a closed system.Vitrification of immature bovine cumulus-oocyte complexes: effects of cryoprotectants, the vitrification procedure and warming time on cleavage and embryo development The survival of mouse oocytes shows little or no correlation with the vitrification or freezing of the external medium, but the ability of the medium to vitrify is affected by its solute concentration and by the cooling rate.The effect of minimal concentration of ethylene glycol (EG) combined with polyvinylpyrrolidone (PVP) on mouse oocyte survival and subsequent embryonic development following vitrification Intracellular ice and cell survival in cryo-exposed embryonic axes of recalcitrant seeds of Acer saccharinum: an ultrastructural study of factors affecting cell and ice structures.Extreme rapid warming yields high functional survivals of vitrified 8-cell mouse embryos even when suspended in a half-strength vitrification solution and cooled at moderate rates to -196°C.Oocyte vitrification: advances, progress and future goals.Shortened equilibration time can compromise clinical outcomes in human embryo vitrification.Closed vitrification of human oocytes and blastocysts: outcomes from a series of clinical cases.Persistence of Long-Term Memory in Vitrified and Revived Caenorhabditis elegans.Hydroxypropyl cellulose supplementation in vitrification solutions: a prospective study with donor oocytes.Open versus closed oocyte vitrification in an oocyte donation programme: a prospective randomized sibling oocyte study.Improvement in Ovarian Tissue Quality with Supplementation of Antifreeze Protein during Warming of Vitrified Mouse Ovarian Tissue.

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Ultra-rapid warming yields high survival of mouse oocytes cooled to -196°c in dilutions of a standard vitrification solution

http://www.wikidata.org/entity/Q34257090

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2012 nî lūn-bûn

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2012 թուականի Ապրիլին հրատարակուած գիտական յօդուած

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2012 թվականի ապրիլին հրատարակված գիտական հոդված

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2012年の論文

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2012年論文

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2012年論文

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2012年論文

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2012年論文

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2012年論文

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2012年论文

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Ultra-rapid warming yields hig ...... tandard vitrification solution

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http://www.w3.org/2001/XMLSchema#string

Shinsuke Seki

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Vitrification of mouse oocytes using a nylon loop.

Ultra-rapid vitrification of mouse oocytes in low cryoprotectant concentrations

Effect of warming rate on the survival of vitrified mouse oocytes and on the recrystallization of intracellular ice

Vitrification of human single pronuclear oocytes following two approaches to polar body biopsy.

Nucleation and growth of ice crystals inside cultured hepatocytes during freezing in the presence of dimethyl sulfoxide.

Simple, inexpensive attainment and measurement of very high cooling and warming rates.

Survival of mouse oocytes after being cooled in a vitrification solution to -196°C at 95° to 70,000°C/min and warmed at 610° to 118,000°C/min: A new paradigm for cryopreservation by vitrification.

Over 900 oocyte cryopreservation babies born with no apparent increase in congenital anomalies.

Highly efficient vitrification for cryopreservation of human oocytes and embryos: the Cryotop method.

Development into blastocysts of bovine oocytes cryopreserved by ultra-rapid cooling.

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scholarly article

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10.1371/JOURNAL.PONE.0036058

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