Effect of cooling and warming rate on glycerolized rabbit kidneys.

[1]  M. Taylor,et al.  The effect of ice formation on the function of smooth muscle tissue stored at −21 or −60 °C , 1983 .

[2]  M. Taylor,et al.  Freeze‐substitution and isothermal freeze‐fixation studies to elucidate the pattern of ice formation in smooth muscle at 252 K (‐21°C) , 1982, Journal of microscopy.

[3]  G. Fahy,et al.  Analysis of "solution effects" injury: cooling rate dependence of the functional and morphological sequellae of freezing in rabbit renal cortex protected with dimethyl sulfoxide. , 1981, Cryobiology.

[4]  I. Jacobsen.  Cooling of rabbit kidneys permeated with glycerol to sub-zero temperatures. , 1979, Cryobiology.

[5]  C. A. Walter,et al.  Attempted canine renal cryopreservation using dimethyl sulphoxide helium perfusion and microwave thawing. , 1978, Cryobiology.

[6]  I. B. Jacobsen.  Distribution and removal of glycerol by vascular albumin perfusion in rabbit kidneys. , 1978, Cryobiology.

[7]  I. Jacobsen.  Renal transplantation in the rabbit: a model for preservation studies , 1978, Laboratory animals.

[8]  M. Wusteman,et al.  Transplantation of rabbit kidneys perfused with glycerol solutions at 10 °C , 1978 .

[9]  D. Pegg,et al.  A new solution for initial perfusion of transplant kidneys. , 1978, Scandinavian journal of urology and nephrology.

[10]  P. Robitaille,et al.  Survival of canine kidneys after treatment with dimethyl-sulfoxide, freezing at −80 °C, and thawing by microwave illumination , 1977 .

[11]  C. E. Huggins,et al.  Water transport in a cluster of closely packed erythrocytes at subzero temperatures. , 1977, Cryobiology.

[12]  C. A. Walter,et al.  Structural and functional aspects of biological freezing techniques , 1977, Journal of microscopy.

[13]  C. A. Walter,et al.  HYPOTHERMIC PERFUSION OF RABBIT KIDNEYS WITH SOLUTIONS CONTAINING GELATIN POLYPEPTIDES , 1977, Transplantation.

[14]  D. Pegg,et al.  Perfusion of rabbit kidneys with glycerol solutions at 5 °C , 1976 .

[15]  E. F. Graham,et al.  The effect of freeze rate, duration of phase transition, and warming rate on survival of frozen canine kidneys. , 1976, Cryobiology.

[16]  R. Miller,et al.  Survival of frozen-thawed human red cells as a function of cooling and warming velocities. , 1976, Cryobiology.

[17]  V. Marshall,et al.  72‐HR CANINE KIDNEY PRESERVATION WITHOUT CONTINUOUS PERFUSION , 1976, Transplantation.

[18]  I. Jacobsen,et al.  LDH release into perfusates of preserved kidneys. , 1976, Scandinavian journal of urology and nephrology.

[19]  M. A. Hayat,et al.  Principles and Techniques of Electron Microscopy , 1975 .

[20]  C. A. Walter,et al.  Ultrastructural appearance of freeze-substituted lymphocytes frozen by interrupting rapid cooling with a period at −26°C , 1975 .

[21]  B. Luyet,et al.  Freeze-fixation at high subzero temperatures. , 1972, Cryobiology.

[22]  N. Tryding,et al.  Recommended methods for the determination of four enzymes in blood. , 1974, Scandinavian journal of clinical and laboratory investigation.

[23]  E. F. Graham,et al.  Long-term functional success following freezing of canine kidneys. , 1973, Surgery.

[24]  C. Green,et al.  Renal preservation by hypothermic perfusion. I. The importance of pressure-control. , 1973, Cryobiology.

[25]  D. Pegg.  Perfusion of rabbit kidneys with cryoprotective agents. , 1982, Cryobiology.

[26]  P. Mazur,et al.  Survival of Mouse Embryos Frozen to -196� and -269�C , 1972, Science.

[27]  M. Orloff,et al.  Whole organ preservation. II. Freezing studies. , 1967, Surgery.

[28]  R. Coggeshall,et al.  A SIMPLIFIED LEAD CITRATE STAIN FOR USE IN ELECTRON MICROSCOPY , 1965, The Journal of cell biology.

[29]  P. Mazur.  CAUSES OF INJURY IN FROZEN AND THAWED CELLS. , 1965, Federation proceedings.

[30]  Luyet Bj,et al.  An electron microscope study of the distribution of ice in single muscle fibers frozen rapidly. , 1961 .