ライフサイエンスコーパス: in vitro maturation

1 logy as well as metabolism of the COC during in vitro maturation.

2 led those of HDMECs, indicating a process of in vitro maturation.

3 o effect on the progression of meiosis after in vitro maturation.

4 handling, electrophysiological functions and in vitro maturation.

5 y changes once blood dendritic cells undergo in vitro maturation.

6 complete set of changes in gene expression, in vitro maturation.

7 that rAd28 and rAd35 infected and led to the in vitro maturation and activation of both human and mou

8 cells preceding nuclear transfer, as well as in vitro maturation and activation of oocytes and in vit

9 added to cell culture profoundly affect the in vitro maturation and function of monocyte-derived den

10 rker into these microspores and hence, after in vitro maturation and in situ fertilisation, for the g

11 neered skin after in vivo grafting with both in vitro maturation and normal human skin.

12 Here we describe the in vitro maturation and selection of mouse and human T c

13 Likewise, in-vitro maturation and xenografting are experimental an

14 the ability to fire action potentials after in vitro maturation as well as after in vivo transplanta

15 e C-terminal extension, we used an enzymatic in vitro maturation assay that allows synthesizing funct

16 Furthermore, in vitro maturation assays demonstrated significant SNP-

17 Together with in vitro maturation assays, these findings shed light on

18 mete cryosurvival and the ability to undergo in vitro maturation, cat oocytes were vitrified using th

19 nt (EP2(-/-)) macrophages exhibited enhanced in vitro maturation compared with wild-type cells, as ev

20 confers mouse progenitor B cell self renewal in vitro, maturation defects in vivo and B-ALL with eith

21 We delineated distinct phases of in vitro maturation during reprogramming of human neuron

22 s that packaged exogenous MYP are capable of in vitro maturation, fertilization, and early developmen

23 We comprehensively phenotyped hPSC-CMs after in vitro maturation for 20 and 40 days on either PDMS or

24 By means of in vitro maturation in the presence of (15)N- and (13)C-

25 We conclude that in vitro maturation is not a requirement for effective m

26 quine cumulus-oocyte complexes (COCs) during in vitro maturation (IVM), as determined using a combina

27 y competent metaphase II (MII) oocytes after in vitro maturation (IVM).

28 the influence of cyclosporine A (CsA) on the in vitro maturation of DC, and on the nuclear translocat

29 Interestingly, in vivo and in vitro maturation of DCs did not enhance GPI presentat

30 In addition, StII-induced in vitro maturation of dendritic cells might be supporti

31 li iron-sulfur carrier protein NfuA supports in vitro maturation of fully active [FeFe]-hydrogenase,

32 However, it is problem that in vitro maturation of hepatoblasts is insufficient in t

33 entiation, few studies have demonstrated the in vitro maturation of hiPSC-derived hepatic progenitor

34 To understand the mechanisms regulating the in vitro maturation of hPSC-derived hepatocytes, we deve

35 Addition of IL-10 during in vitro maturation of human monocyte-derived DCs with i

36 HTMSNs exhibit a higher level of uptake and in vitro maturation of immune cells including dendritic

37 we show that AQP-1 is partially lost during in vitro maturation of mouse reticulocytes and that it i

38 omains of NifU are shown to be competent for in vitro maturation of nitrogenase component proteins, a

39 In vitro maturation of oocytes from homozygous mutant mi

40 In vitro maturation of oocytes may be offered as an emer

41 In vitro maturation of PBDC resulted in median 3- and 41

42 mains in isolation (TAC:CD3epsilon) promotes in vitro maturation of Scid.adh, whereas engagement of C

43 Using a recently developed technique for in vitro maturation of sea urchin oocytes, we analyzed t

44 have developed a highly efficient system for in vitro maturation of secreting B lymphocytes and plasm

45 In vitro maturation of such Spb4-enriched pre-60S partic

46 Here, we show that PGRN stimulates the in vitro maturation of the lysosomal aspartyl protease c

47 , cryopreservation of retrieved spermatozoa, in-vitro maturation of germ cells and microinjection of

48 Prolonged in vitro maturation presents a major challenge to stem c

49 sotopically labeled via a recently developed in vitro maturation procedure allowing advanced electron

50 Inclusion of NfuA in the in vitro maturation process improves its efficacy by del

51 Using an in vitro maturation reaction containing purified protoxi

52 ts and protoxin peptides as substrates in an in vitro maturation reaction dependent upon HlyC and acy

53 Skeletal muscle cells undergo in vitro maturation resulting in myotube formation and s

54 roinflammatory cytokines, and do not require in vitro maturation to act as potent APCs.

55 obe the components involved in the deficient in vitro maturation towards fully functional beta-cells.

56 e origin and frequency of indels seen during in vitro maturation were similar to that in vivo.

57 pothesis is that CD3epsilon fails to promote in vitro maturation when in the context of an Ab-engaged

58 In vitro maturation with purified maturation enzymes has