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1  that these manifest in nonuniform ice after vitrification.
2 scale coral fragments via mL-scale isochoric vitrification.
3 trol of the thickness of the sample prior to vitrification.
4 tion by six orders of magnitude and promotes vitrification.
5 e T = 7 particles are too fragile to survive vitrification.
6 design of improved methods for bovine oocyte vitrification.
7 ions without the need for crystallization or vitrification.
8 dual stresses that accumulate during polymer vitrification.
9 p toward our understanding of the physics of vitrification.
10 lear-cut transition in local energies during vitrification.
11 s modulus, in agreement with stiffening upon vitrification.
12  the conditions of crystal growth or protein vitrification.
13 ration, but fast enough to prevent immediate vitrification.
14 ase Tc retention in glass waste forms during vitrification.
15  also observed when glycine was added during vitrification.
16  engineered to minimize heterogeneity during vitrification.
17 peratures to exhibit a considerable state of vitrification.
18 ent filter paper against the specimen before vitrification.
19  decreasing the propensity for intracellular vitrification.
20 nables automated, fast, and blot-free sample vitrification.
21 cial markers into the sample and (ii) sample vitrification.
22 in a near-native, 'frozen-hydrated' state by vitrification.
23  is much smaller than the estimated time for vitrification (1 x 10(-4) second).
24 new insight into understanding the origin of vitrification and describing mesoscopic order-disorder t
25 f live mammalian biospecimens-slow freezing, vitrification and hypothermic storage-limit the biomedic
26                                              Vitrification and laser warming (300 V, 10 ms pulse widt
27 tive of this study was to develop a suitable vitrification and laser warming protocol for larvae of t
28 to most toxic), and larvae were subjected to vitrification and laser warming using 2 M EG + 1 M PG an
29 tate, suggesting an intimate connection with vitrification and locally favored structures inhibiting
30 cryopreservation agent VS55 before and after vitrification and nanowarming and that achieve high-temp
31  Upon cooling, pressurised materials undergo vitrification and networks exhibit comparative mechanica
32 tion of novel developments, including oocyte vitrification and oocyte maturation in vitro, has result
33 s glycerol or dimethyl sulfoxide, to promote vitrification and prevent ice formation.
34 ing and unloading conditions and methods for vitrification and rewarming (VR).
35                            This study tested vitrification and rewarming in 0.5-3 L volumes using cry
36 as a proof-of-concept that human organ scale vitrification and rewarming is physically possible, ther
37 esent study was to compare the efficiency of vitrification and slow freezing techniques for the cryop
38            Experiment 2 aimed to compare the vitrification and slow freezing techniques in the follow
39          With the recent successes in oocyte vitrification and storage, clear metrics are needed to d
40 o settle upon warming, and suggests that the vitrification and ultra-fast laser warming approach may
41 ed oocyte; however, the addition of ffEVs to vitrification and/or thawing media enhanced the ability
42 sition from liquid to vitrified solid (i.e., vitrification) and the levitation of droplets on liquid
43  thickness control of the foam film prior to vitrification, and for some specimens enhances orientati
44 formulated mCPAs are suitable for perfusion, vitrification, and nanowarming of whole organs with mini
45                               We show that a vitrification approach to storing vascular tissue result
46         Instead, both direct interaction and vitrification are required.
47 MP-7 and C3a, showing promise for isothermal vitrification as a safe, efficient, and low-cost alterna
48 lution experiences either crystallization or vitrification as being cooled, yet the mechanism of this
49 permeate the cells and promote intracellular vitrification (as is almost universally believed), or be
50 , and endothelial function was evident after vitrification at -110 degrees C.
51 nd Pt-based metallic glasses and study their vitrification behavior and atomic mobility.
52 ibution, beam-induced motion, and suboptimal vitrification can compromise data quality.
53 M, rapid and efficient methods for assessing vitrification conditions in situ are required for the ac
54 ests that reducing osmotic stress induced by vitrification could improve the development of vitrified
55                          Cryopreservation by vitrification could transform fields ranging from organ
56                            Organ banking via vitrification could transform transplantation, but has n
57 ells and subcellular regions of interest for vitrification, cryo-focused ion beam (cryo-FIB) milling,
58 val using Custodiol HTK solution, even after vitrification, cryostorage in liquid nitrogen for 1 week
59 also shows great control over the reversible vitrification-crystallization processes, suggesting its
60 which was constructed using the freezing and vitrification curve and values characterizing the condit
61 ced states using an automated blot-free grid vitrification device - the SPT Labtech chameleon.
62 ces for anaerobic grid preparation involve a vitrification device located in an anoxic chamber, which
63                           Here, we present a vitrification device with highly automated sample handli
64  quartzite sand positively influenced by the vitrification during the pyrolysis of the galvanic sludg
65 d cryoprotectant (CPA) significantly impacts vitrification efficiency of bovine oocytes.
66 s the raw building material that governs the vitrification efficiency.
67                                  In general, vitrification entails a large temperature difference bet
68 ification experiments, we observed that such vitrification events are accompanied by a Leidenfrost ph
69                               In our droplet vitrification experiments, we observed that such vitrifi
70                                              Vitrification (glass formation) is a potential method fo
71 ocated at random to slow freezing (n = 6) or vitrification group (n = 6).
72                          Cryopreservation by vitrification has far-reaching implications.
73 cessful in adults, and development of oocyte vitrification has greatly improved the potential to cryo
74 t a high percentage of mouse oocytes survive vitrification in media that contain only half the usual
75 orphology, mechanics, and function following vitrification in nanoliter volumes is developed using a
76                                       Embryo vitrification is a standard procedure in assisted reprod
77                   Additionally, we find that vitrification is accompanied by a bulk material strength
78 is review we present evidence that, although vitrification is indeed required, it is not in itself su
79                          Such intramolecular vitrification is likely to be found in molecules in whic
80                                              Vitrification is now the main route to the cryopreservat
81 glycerol molar concentration ~ 18%, at which vitrification is possible with no crystallization on rap
82  It has been suggested that glass formation (vitrification) is in itself sufficient to stabilize dry
83    Ice-free cryopreservation, referred to as vitrification, is receiving increased attention in the h
84 lows, including milling thick specimens with vitrification issues, specimens with preferred orientati
85 ntrast, we observe pronounced size dependent vitrification kinetics in micrometer-sized glasses, whic
86 heless, design rules for crystallization and vitrification kinetics still lack predictive power.
87 h the assemblies jam, since both jamming and vitrification lead to a solid-like behavior of the assem
88                         Results suggest that vitrification maintains both elastic and viscous compone
89                             We conclude that vitrification may be more effective than slow freezing f
90  method of cryopreservation and an ice-free, vitrification method of cryopreservation with fresh cont
91               Here, we introduce a blot-free vitrification method that uses free-standing surfactant-
92              We adopt and modify a thin film vitrification method to preserve the sensitive yet criti
93 ctrospun lyoprotectant matrix and isothermal vitrification methodology for non-cryogenic stabilizatio
94 es, which cannot be achieved by conventional vitrification methods, and thus allows for exploring new
95 ntally a threshold droplet radius during the vitrification of a cryoprotectant droplet in the presenc
96                                          The vitrification of a liquid occurs when ice crystal format
97 t emulsion-based process that exploits rapid vitrification of a thixotropic medium to manufacture div
98                                              Vitrification of aqueous nanodroplets yields nanodomains
99                                              Vitrification of C. parvum oocysts in larger volumes wil
100                   For cryo-preservation, the vitrification of cells is believed to be mandatory for c
101                     A major roadblock to the vitrification of cells is the requirement of high concen
102 on study to create conditions for successful vitrification of metallic liquid germanium.
103 re we report an experimental approach to the vitrification of monatomic metallic liquids by achieving
104  adding glycine, an organic osmolyte, during vitrification of mouse germinal vesicle stage oocyte and
105  However, the findings we report here on the vitrification of mouse oocytes are not in accord with th
106 terials that were studied in relation to the vitrification of nuclear waste.
107 t a streamlined approach that allows for the vitrification of oxygen-sensitive proteins in reduced st
108 trated with experimental results obtained by vitrification of protein suspensions, lipid vesicles, ba
109                                          The vitrification of pure water is compared with that of mol
110                     Experimentally, however, vitrification of single-element metallic liquids is noto
111                         These data show that vitrification of the additive is not sufficient to affec
112 ents to constrain conditions that led to the vitrification of the inner wall rocks in the hillfort at
113  quartzite sand to the sludge influences the vitrification of the material.
114    We find that both ice crystallization and vitrification of the nanodroplets lead to demixing of pu
115        We aimed to compare slow freezing and vitrification of whole ovary for fertility preservation
116  revealed the short-term negative impacts of vitrification on embryo and fetal development and the lo
117                               The effects of vitrification on T(m) are explained using the two-dimens
118 d to explore the effects of mouse blastocyst vitrification on the phenotype of vitrified-warmed blast
119 ic states can be preserved rapidly by either vitrification or chemical fixation.
120 ce formation, but a promising alternative is vitrification, or the rapid cooling of organs to a stabl
121 obin and myoglobin at temperatures below the vitrification point of the surrounding solvent.
122   The formation of glassy material occurs by vitrification, preventing crystallization and promoting
123  in the vitrification solution EAFS 10/10 to vitrification procedures using a broad range of cooling
124 handling of frozen-hydrated samples from the vitrification process to low temperature imaging for sca
125 nt bud-freezing, slow-cooling, and (droplet-)vitrification protocols have been developed, but few are
126                                  Whole ovary vitrification provides better follicular survival compar
127 e feed-to-glass conversion affects the waste vitrification rate in an electric glass melter.
128 k strengthening was the desired effect, then vitrification represents an Iron Age technology that fai
129 tions that approximate the widely used plant vitrification solution 2.
130 se of solutions containing a single CPA, the vitrification solution causes the bilayer to thin and be
131  DOPC-beta-sitosterol bilayers solvated in a vitrification solution containing glycerol, ethylene gly
132            We subjected mouse oocytes in the vitrification solution EAFS 10/10 to vitrification proce
133  ms pulse width, 2 mm beam diameter) using a vitrification solution of 2 M EG + 1 M PG, 40% w/v Ficol
134 btained using increasing concentrations of a vitrification solution of the latest generation (VM3) an
135      A decrease in the amount of DMSO in the vitrification solution with a corresponding increase in
136 ition temperature [Formula: see text] of the vitrification solution, a property which, given the narr
137                                          The vitrification solution, which presented the highest memb
138                                   Nearly all vitrification solutions contain both permeating and non-
139 insights to inform design of next-generation vitrification solutions that minimize thermal cracking r
140                                          The vitrification solutions used in the cryopreservation of
141 and of chemistries represented within common vitrification solutions, is seldom investigated in therm
142 , and form the basis for the optimization of vitrification solutions.
143                                              Vitrification studies on the high solids system at subze
144                     The advantage of stepped vitrification (SV) is avoiding ice crystal nucleation, w
145 ature (about -125 degrees C), at which point vitrification takes place, arresting further changes ove
146 rom eggs cryopreserved with the Kuwayama egg vitrification technique for non-medical (social) indicat
147                   Here, we leverage advanced vitrification techniques to overcome the preferential de
148 sition (33 to 70 degrees C), and a very high vitrification temperature (up to 250 degrees C).
149 n both groups but significantly higher after vitrification than after slow freezing (0.3% +/- 0.5% vs
150     Recent technical advances include sample vitrification that faithfully preserves molecular struct
151    Furthermore, glycine addition during both vitrification/thawing and maturation further enhanced th
152 howed that glycine supplementation in either vitrification/thawing or maturation medium significantly
153                                       During vitrification, the granular wall rocks partially melt, s
154                                       Unlike vitrification, the lineal packing of the NPs in the netw
155             MicroED experiments, from sample vitrification to final structure, can take anywhere from
156                        The time elapsed from vitrification to warming was comparable between patients
157 lize cryopreserved oocytes and the time from vitrification to warming.
158                                              Vitrification upon cooling of the liquid phase gives ris
159 has been demonstrated to undergo melting and vitrification upon cooling.
160 ily produced in situ by spatially addressing vitrification using common patterning tools--useful for
161 for cryopreservation of C. parvum oocysts by vitrification using custom high aspect ratio specimen co
162 cterized the departure from equilibrium upon vitrification via the non-equilibrium index; water-like
163 s the effects of cryopreservation (cryo) and vitrification (vitro) on the viscoelastic properties of
164 igher at 40 and 60 but lower at 80 MPa after vitrification-warming in the treated groups than control
165 optimized convective cooling, and successful vitrification was confirmed via visual inspection, therm
166                                              Vitrification was obtained using increasing concentratio
167 yopreservation of Cryptosporidium oocysts by vitrification was recently achieved, the method is restr
168                    The compounding effect of vitrification when applied to two distinct stages (oocyt
169                               The ability of vitrification when crossing the glass transition tempera
170 solvents may be due to a density increase on vitrification which reduces the volume of bulk solvent t
171  formation during cooling can be achieved by vitrification, which is defined as solidification in an
172 omprehensive understanding of confined water vitrification with potential implications for numerous a

 
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