242 results on '"Seki, Shinsuke"'
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2. Streamlined and quantitative detection of chimerism using digital PCR
3. Vitrification of medaka whole testis with a trehalose-containing solution and production of medaka individuals derived from the vitrified cells
4. TIGIT mediates activation-induced cell death of ILC2s during chronic airway allergy
5. Production of the medaka derived from vitrified whole testes by germ cell transplantation
6. Vitrification of one-cell rat embryos in cryotubes by small-volume vitrification and rapid warming
7. 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
8. Cryobiological properties of immature zebrafish oocytes assessed by their ability to be fertilized and develop into hatching embryos
9. 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
10. The dominance of warming rate over cooling rate in the survival of mouse oocytes subjected to a vitrification procedure
11. Intracellular ice formation in yeast cells vs. cooling rate: Predictions from modeling vs. experimental observations by differential scanning calorimetry
12. Formation of extracellular and intracellular ice during warming of vitrified mouse morulae and its effect on embryo survival
13. Kinetics and activation energy of recrystallization of intracellular ice in mouse oocytes subjected to interrupted rapid cooling
14. Small-volume vitrification and rapid warming yield high survivals of one-cell rat embryos in cryotubes
15. Cryoprotectant permeability of aquaporin-3 expressed in Xenopus oocytes
16. Expression of aquaporin-3 improves the permeability to water and cryoprotectants of immature oocytes in the medaka ( Oryzias latipes)
17. Japanese flounder ( Paralichthys olivaceus) embryos are difficult to cryopreserve by vitrification
18. Extra- and intra-cellular ice formation in Stage I and II Xenopus laevis oocytes
19. Extra- and intracellular ice formation in mouse oocytes
20. Water- and cryoprotectant-permeability of mature and immature oocytes in the medaka ( Oryzias latipes)
21. Mechanism Of Immature Pig Oocyte Injury At A Low Temperature
22. Vitrification Of Mouse And Rabbit Zygotes; Effect Of Rapid Warming
23. Characteristic features of newly established specific pathogen-free albino large rabbit (JW-AKT): Comparison with Japanese White and New Zealand White rabbits
24. Vitrification of one-cell mouse embryos in cryotubes
25. The CCR4-NOT deadenylase complex controls Atg7-dependent cell death and heart function
26. The temperature and type of intracellular ice formation in preimplantation human embryos
27. Conservation of the medaka bio-resources by cryopreservation of germ cells
28. Production of the medaka derived from vitrified whole testes by germ cell transplantation
29. Production of the medaka derived from vitrified whole testes by germ cell transplantation
30. Intracellular ice formation in mouse zygotes and early morulae vs. cooling rate and temperature-experimental vs. theory
31. Production of viable trout offspring derived from frozen whole fish
32. Simple, inexpensive attainment and measurement of very high cooling and warming rates
33. Comparison between the temperatures of intracellular ice formation in fresh mouse oocytes and embryos and those previously subjected to a vitrification procedure
34. The present status of trolling of the Biwa salmon Oncorhynchus masou subsp. Lake Biwa, assessed by obligatory reporting by recreational anglers
35. 091 Aquaporin 9 plays a significant role in the channel-dependent movement of Me2SO and acetamide in mouse morulae
36. 070 Production of donor-derived offspring by allogenic transplantation of cryopreserved spermatogonia in medaka
37. A Trial to Cryopreserve Immature Medaka (Oryzias latipes) Oocytes after Enhancing Their Permeability by Exogenous Expression of Aquaporin 3
38. Corrigendum to “Simple, inexpensive attainment and measurement of very high cooling and warming rates” [Cryobiology 61 (2010) 231–233]
39. The Role of Aquaporin 9 in the Movement of DMSO and Acetamide in Mouse Morulae.
40. Ultra-Rapid Warming Yields High Survival of Mouse Oocytes Cooled to −196°C in Dilutions of a Standard Vitrification Solution
41. Developmental ability of vitrified mouse oocytes expressing water channels
42. 87. The triad of evidence that intracellular ice is the cause of death in COS-7 tissue culture cells rapidly cooled to −70°C. (I): The observed occurrence of intracellular ice as a function of temperature and cooling rate
43. Functional survival of mouse oocytes and 8-cell embryos after vitrification in 1×, 0.75×, 0.5×, and 0.33× EAFS vitrification media and warming at an exceedingly high rate of 117,500°C/min
44. 88. The triad of evidence that intracellular ice is the cause of death in COS-7 tissue culture cells rapidly cooled to −70°C. (II): Comparison between the computed occurrence of intracellular ice as a function of temperature and cooling rate and the observed relationship
45. Pathway for the Movement of Water and Cryoprotectants in Bovine Oocytes and Embryos1
46. Effect of the expression of aquaporins 1 and 3 in mouse oocytes and compacted eight-cell embryos on the nucleation temperature for intracellular ice formation
47. Stability of mouse oocytes at −80 °C: the role of the recrystallization of intracellular ice
48. 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
49. Developmental Ability of Vitrified Mouse Oocytes Expressing Water Channels
50. オーステナイトステンレス鋼溶接部の機械的性質に及ぼす超音波振動の影響
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