Zobrazeno 1 - 10
of 105
pro vyhledávání: '"David E. Pegg"'
Autor:
David E. Pegg, Fritz Kleinhans
Publikováno v:
Cryobiology. 72:83-85
Autor:
David E. Pegg, Ying C. Song
Publikováno v:
Tissue and Cell Processing: An Essential Guide, An Essential Guide
Autor:
Ruth M. Warwick, David E. Pegg
Publikováno v:
Cell and Tissue Banking. 8:307-327
Autor:
David E. Pegg
Publikováno v:
Cryobiology. 53:447-451
Publikováno v:
Cryobiology. 52:347-359
Although isolated chondrocytes can be cryopreserved by standard methods, at the present time there is no satisfactory method that will preserve living chondrocytes in situ in surgical grafts, between the time of procurement or manufacture and actual
Autor:
David E, Pegg
Publikováno v:
Methods in molecular biology (Clifton, N.J.). 1257
Cryopreservation is the use of very low temperatures to preserve structurally intact living cells and tissues. Unprotected freezing is normally lethal and this chapter seeks to analyze some of the mechanisms involved and to show how cooling can be us
Autor:
David E. Pegg
Publikováno v:
Human Fertility. 8:231-239
Traditional cryopreservation methods allow ice to form and solute concentrations to rise during the preservation process: both ice and high solute concentrations can cause damage. Cryoprotectants are highly soluble, permeating compounds of low toxici
Publikováno v:
Cell and Tissue Banking. 5:23-36
Skin allografts, derived from cadaveric donors, are widely used for the treatment of burns and ulcers. Prior to use in clinical situations, these allografts are disinfected using a cocktail of antibiotics and then cryopreserved. Unfortunately, this a
Publikováno v:
Physics in Medicine and Biology. 47:2311-2325
A method that has been proposed for the cryopreservation of tissues and organs is to add a cryoprotective agent (CPA) in sufficient concentration to allow vitrification, and to use rapid electromagnetic heating to prevent the formation of ice crystal
Autor:
David E. Pegg
Publikováno v:
Cryobiology. 44:46-53
This paper reports the cryopreservation of an immortalized human endothelial cell line (ECV304), either as a single cell suspension or as a confluent layer on microcarrier beads. Cell suspensions were exposed to 10% w/w dimethyl sulfoxide in a high-p