ライフサイエンスコーパス: in vitro maturation

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

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

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

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

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

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

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

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

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

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

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

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

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

14 Furthermore, in vitro maturation assays demonstrated significant SNP-

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

30 In vitro maturation of oocytes from homozygous mutant mi

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

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

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

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

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

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

37 Using an in vitro maturation reaction containing purified protoxi

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

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

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

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

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

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

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