ライフサイエンスコーパス: cryopreservation

1 by feeding larvae a proline-augmented diet (cryopreservation).

2 mem) and ATP-production capacities following cryopreservation.

3 s added to the viability of sperm and oocyte cryopreservation.

4 f fertility preservation by embryo or oocyte cryopreservation.

5 ozole and gonadotropins for embryo or oocyte cryopreservation.

6 ensitive cancers undergoing embryo or oocyte cryopreservation.

7 lls retain their phenotypic properties after cryopreservation.

8 after both transformation and recovery from cryopreservation.

9 ained their phenotype and APC function after cryopreservation.

10 transplantation and five who chose stem-cell cryopreservation.

11 apoptotic death of porcine hepatocytes after cryopreservation.

12 t potentially detrimental procedures such as cryopreservation.

13 prove the survival of mammalian cells during cryopreservation.

14 er serum-free conditions for 36 hours before cryopreservation.

15 fetal bovine serum-supplemented media and to cryopreservation.

16 and potential for differentiation even after cryopreservation.

17 est MSC viability and potency are damaged by cryopreservation.

18 d as a promising alternative to conventional cryopreservation.

19 years with a median 5.25 years after embryo cryopreservation.

20 for selection of patients for ovarian tissue cryopreservation.

21 ) expressions were unchanged after 1month of cryopreservation.

22 lied to assess cell envelope integrity after cryopreservation.

23 t to fields as diverse as cloud formation to cryopreservation.

24 Embryo cryopreservation after ovarian stimulation with the letr

25 rd commercial heart valve freezing method of cryopreservation and an ice-free, vitrification method o

26 Despite major advances in tissue cryopreservation and auto-transplantation, reperfusion i

27 Details are included for propagation, cryopreservation and characterization.

28 forward programming, combined with efficient cryopreservation and good manufacturing practice (GMP)-c

29 haemia followed by reperfusion, we show that cryopreservation and intra-myocardial delivery of one bi

30 ferative, less immunogenic, and resistant to cryopreservation and ischemic injury.

31 valuated ROS in zebrafish spermatozoa during cryopreservation and its effect on viability and motilit

32 Cryopreservation and MMF potentially prevent engraftment

33 strong magnetic responsiveness, capacity for cryopreservation and rapid expansion, and the ability to

34 imised and straightforward procedure for the cryopreservation and recovery of both parental and trans

35 e interstitial ice damage that occurs during cryopreservation and subsequently leads to accelerated v

36 ced PSC (iPSC) derivation, colony expansion, cryopreservation and teratoma formation.

37 r mouse strain maintenance, distribution and cryopreservation and training fellowships in mouse patho

38 Cryopreservation and transplantation of gonadal tissue i

39 We aimed to restore fertility by cryopreservation and transplantation of ovarian tissue.

40 egenerative medicine, in vitro drug testing, cryopreservation, and cell isolation/purification.

41 d from resected tumors and biopsies, survive cryopreservation, and exhibit ductal- and disease-stage-

42 em cells has allowed their in vitro culture, cryopreservation, and genetic modification.

43 pplications of IBPs in the food industry, in cryopreservation, and in other technologies are vast, an

44 irst 20 passages of hESC derivation prior to cryopreservation, and that supplementation with either s

45 uction without IL-10 production; (c) ease in cryopreservation; and (d) markedly reduced cost.

46 optosis occurs in porcine hepatocytes during cryopreservation; and 2) mitochondrial injury in this pr

47 ion, large volume apheresis, processing, and cryopreservation appears to be safe in donors with SCT,

48 Sperm and embryo cryopreservation are considered standard practice and ar

49 nd embryo cryopreservation as well as oocyte cryopreservation are considered standard practice and ar

50 perimental data on the state of water during cryopreservation are lacking.

51 Success rates with oocyte cryopreservation are on the rise and begin to approach t

52 rvation techniques, such as semen and embryo cryopreservation, are established and successful in adul

53 as incubation in a physiological medium and cryopreservation, are suboptimal, resulting in significa

54 Sperm and embryo cryopreservation as well as oocyte cryopreservation are

55 urvival in women undergoing embryo or oocyte cryopreservation before adjuvant chemotherapy.

56 In young women, ovarian cortex cryopreservation before gonadotoxic chemotherapy and its

57 ion criteria and were offered ovarian tissue cryopreservation before starting cancer treatment.

58 urther progress is needed before whole-ovary cryopreservation can be considered an option for safegua

59 Conventional frozen cryopreservation (CFC) is currently the gold standard fo

60 quirements are reliable methods for culture, cryopreservation, characterization and quality control.

61 Cryopreservation combined with electron tomography were

62 model showed no adverse effects of vitreous cryopreservation compared with fresh tissue grafts.

63 Assess the effects of cryopreservation (cryo) and vitrification (vitro) on the

64 breast surgery enables earlier initiation of cryopreservation cycles and chemotherapy and, when appro

65 gen and processed cells were infused without cryopreservation daily for 4 consecutive days.

66 Although cryopreservation decreased hepatocyte viability, individ

67 als using cryopreserved sperm (p < 0.05); 3) cryopreservation did not affect settlement success, as l

68 ere ice growth control is necessary, such as cryopreservation, food storage, and anti-icing.

69 ast elimination; and (4) an optional step of cryopreservation for the storage of the excess of cells.

70 tal growth is a major problem in cell/tissue cryopreservation for transplantation, transfusion and ba

71 have a wide range of applications including cryopreservation, frost protection, and as models in bio

72 Cryopreservation has been adopted as a method for long-t

73 extra embryos (if embryos are set aside for cryopreservation, higher quality embryos may have been a

74 Ice-free cryopreservation (IFC) already demonstrated matrix struc

75 Cryopreservation in 5% dimethyl sulfoxide/6% pentastarch

76 nburgh selection criteria for ovarian tissue cryopreservation in girls and young women with cancer to

77 s embryo cryopreservation in women and sperm cryopreservation in men before the initiation of cancer-

78 rving fertility in this population is embryo cryopreservation in women and sperm cryopreservation in

79 sh to delay childbearing, which makes oocyte cryopreservation increasingly popular to overcome an age

80 For men, semen cryopreservation is a simple way of preserving reproduct

81 Cryopreservation is a well-established technique used fo

82 Sperm cryopreservation is an effective but underused method to

83 Cryopreservation is an important conservation tool, whic

84 However, cryopreservation is associated with a loss of hepatocyte

85 Because long-term cryopreservation is critical for CB banking and transpla

86 The mechanism of cell death during cryopreservation is incompletely understood, but may inv

87 For prepubertal boys, testicular biopsy cryopreservation is offered in some centres, but how tha

88 Although prechemotherapy sperm cryopreservation is recommended, treatment with microdis

89 vation of ovarian tissue is an option if egg cryopreservation is ruled out.

90 The current state-of-the-art method of cryopreservation is the addition of large amounts of org

91 Ovarian-tissue cryopreservation is used to preserve fertility in childr

92 Among the three defined cryopreservation media (PBS, 7H9, and 7H9 plus glycerol)

93 liquid nitrogen (LN2), because commonly used cryopreservation media containing cell membrane permeati

94 The ice-free cryopreservation method demonstrated significant reducti

95 better fertility preservation, but the best cryopreservation method is unknown.

96 e donors make it mandatory to use an optimal cryopreservation method that allows maximal recovery and

97 the practicability of a promising long-term cryopreservation method that completely eliminates the n

98 cification is influenced by two factors, the cryopreservation method used and immunogenicity.

99 A glycerol-based cryopreservation method was also tested.

100 A cryopreservation method was established to optimize sour

101 To be an effective restoration tool, the cryopreservation methods and husbandry to produce new of

102 Alternative cryopreservation methods that avoid ice formation may im

103 Current red-blood-cell cryopreservation methods utilize bulk volumes, causing c

104 Using modifications of established cryopreservation methods we developed MSC that retain >9

105 Both egg and ovarian tissue cryopreservation might be ready for application to the p

106 This implies that suboptimal cryopreservation might not cause severe damage to the ce

107 CBU potency is typically assessed before cryopreservation, neglecting changes in potency occurrin

108 hipathic helix and that it enhances the DMSO cryopreservation of adherent cell lines.

109 oprotective agent (CPA) is necessary for the cryopreservation of articular cartilage.

110 The vitrification solutions used in the cryopreservation of biological samples aim to minimize t

111 Current long term cryopreservation of cell stocks routinely requires the u

112 The cryopreservation of cells, tissue and organs is fundamen

113 They have potential for the cryopreservation of cells, tissues, and organs, as well

114 bservation of cellular structures as well as cryopreservation of cells.

115 is and Acropora millepora and found that: 1) cryopreservation of coral sperm reduced sperm motility a

116 Cryopreservation of cortex ovarian tissue before antican

117 e technological importance especially in the cryopreservation of donor cells and tissue, but native a

118 The application of these polymers to the cryopreservation of donor cells is also introduced.

119 Cryopreservation of eggs or ovarian tissue to preserve f

120 Options for fertility preservation include cryopreservation of embryos or oocytes before chemothera

121 native-immediate in vitro fertilisation with cryopreservation of embryos-is not always appropriate.

122 One marker for embryo quality is cryopreservation of extra embryos (if embryos are set as

123 rnal age, number of embryos transferred, and cryopreservation of extra, nontransferred embryos (an in

124 From derivation to cryopreservation of fully characterized initial stocks t

125 The successful cryopreservation of hBTSCs facilitates establishment of

126 Cryopreservation of hematopoietic stem cells (HSCs) and

127 After collection and cryopreservation of hematopoietic stem cells, 15 patient

128 ng demand for successful, efficient means of cryopreservation of hepatocytes.

129 Vitrification is now the main route to the cryopreservation of human and animal oocytes and preimpl

130 his methodology, including the technique for cryopreservation of human tissue, will allow multiple (s

131 of M. tuberculosis complex strains to study cryopreservation of M. tuberculosis complex cells in div

132 Cryopreservation of mature oocytes is also becoming more

133 Successful cryopreservation of most multicompartmental biological s

134 ld woman underwent a right oophorectomy with cryopreservation of ovarian cortical strips before recei

135 For young women, cryopreservation of ovarian cortical tissue with later r

136 Cryopreservation of ovarian tissue has been selectively

137 Cryopreservation of ovarian tissue is an option if egg c

138 This natural cryopreservation of plant tissue over many thousands of

139 -DL-Asp-fluoromethylketone (ZVAD-fmk) during cryopreservation of porcine hepatocytes.

140 wed include processing of testicular tissue, cryopreservation of retrieved spermatozoa, in-vitro matu

141 to antifreeze (glyco)proteins to enhance the cryopreservation of sheep and human red blood cells.

142 actical value, for example, for the possible cryopreservation of stem cells from boys undergoing trea

143 Our results show that cryopreservation of testicular tissue from prepubescent

144 tients are offered fertility preservation by cryopreservation of the ovarian cortex.

145 s required to design optimized protocols for cryopreservation of tissue.

146 d soft biomaterials and is of great value to cryopreservation of tissues, hyperthermia or cryogenic,

147 etal bovine serum (FBS) can provide reliable cryopreservation of various kinds of human and porcine p

148 examined whether antioxidants might improve cryopreservation of zebrafish sperm.

149 Herein we examine the effect of cryopreservation on human MSC viability, immunomodulator

150 The influence of cryopreservation on PBPC was tested in vitro by enumerat

151 plored the effects of lethal irradiation and cryopreservation on TALL-104 cell viability and lytic ef

152 141 of the 376 patients who were not offered cryopreservation; one of these patients had developed pr

153 pared to slow freezing and may be a valuable cryopreservation option.

154 As its use preceded development of either cryopreservation or cell culture, the vaccine strain was

155 regarded as experimental (eg, ovarian tissue cryopreservation, pharmacological protection against gon

156 We show that the cryopreservation procedure is equally applicable to the

157 Further, the cryopreservation procedure kept sensitivity unaltered fo

158 The development of cryopreservation procedures for tissues has proven to be

159 nerating viable pregnancies or surviving the cryopreservation process are also a viable source of hES

160 when viability is maintained throughout the cryopreservation process, MSC retain their therapeutic p

161 e modified to improve the reliability of the cryopreservation process, perhaps using a different cryo

162 Cryopreservation protocols have been developed that mini

163 Thus, the addition of trehalose to cryopreservation protocols leads to previously unobtaina

164 There are improved cryopreservation protocols, but these need further refin

165 Ice-free cryopreservation, referred to as vitrification, is recei

166 sment of cellular response to IL-6 following cryopreservation revealed a similar pattern of up-regula

167 In contrast, damage caused during cryopreservation significantly affects the overall tensi

168 ients who had successfully undergone ovarian cryopreservation, six had developed premature ovarian in

169 onments, and plays a central role in various cryopreservation techniques; its formation is observed o

170 ents who met the criteria for ovarian tissue cryopreservation than for those who did not (15-year pro

171 Together with the possibility of cryopreservation this shall foster diffusion and exploit

172 s (ICCs) were more pronounced: recovery from cryopreservation was 94%, compared with 42% without treh

173 stimulation (OS) for FP by oocyte or embryo cryopreservation was performed.

174 The efficacy of cryopreservation was quantified by microbiological cultu

175 t of reducing the variability in mouse sperm cryopreservation, we examined whether antioxidants might

176 ls with their respective water states during cryopreservation, we found that survival is less depende

177 Recovery of adult islets after cryopreservation with 300 mmol/l trehalose was 92 vs. 58

178 ion and an ice-free, vitrification method of cryopreservation with fresh controls in a subcutaneous,

179 Ovarian tissue cryopreservation with later reimplantation has been show

180 ic polymer-based approach for red-blood-cell cryopreservation without the need for any (toxic) organi

181 ing and the number of samples needed to make cryopreservation worthwhile.