ライフサイエンスコーパス: totipotent

1 ll (2C) embryos in which the blastomeres are totipotent.

2 Most stem cells are not totipotent.

3 velopment, gametes are reprogramed to become totipotent.

4 maintaining high rates of DNA synthesis, are totipotent.

5 itions, that is, conversion of the oocyte to totipotent 2-cell blastomeres, compaction, and blastocys

6 caste fate, and (e) breeding conflicts among totipotent adults.

7 o environmental mutagens and plant cells are totipotent, an understanding of RNR function in plants i

8 Totipotent and differentiated cells exhibited similar in

9 Whereas Oct3/4 is expressed in totipotent and pluripotent cells in the mouse life cycle

10 complexes are essential for formation of the totipotent and pluripotent cells of the early embryo.

11 to host embryos is the key feature of murine totipotent and pluripotent cells.

12 1) Sox2(+) /Pax6(+) stem-like cells that are totipotent and self-renew over the long term, 2) Ascl1(+

13 generally considered pluripotent rather than totipotent because of the failure to detect germline cel

14 red oocytes for optimal progression into the totipotent blastocysts.

15 This finding demonstrates the totipotent capacity of bryophytes, the ability of a cell

16 inner cell mass (ICM) are the descendants of totipotent cells and can differentiate into any cell typ

17 Totipotent cells in early embryos are progenitors of all

18 pring were produced following aggregation of totipotent cells of the four-cell embryos.

19 scription factor associated with potentially totipotent cells.

20 Thus, zebrafish achieve a totipotent chromatin state at ZGA through paternal genom

21 ticellular organisms can be regenerated from totipotent differentiated somatic cell or nuclear founde

22 ay for the induction of erythroid cells from totipotent ectoderm of the embryo.

23 taining the molecular characteristics of the totipotent egg and early embryo.

24 al and a naive paternal genome to generate a totipotent embryo.

25 friable embryogenic callus from which highly totipotent embryogenic suspension cultures could be esta

26 Totipotent embryonic stem (ES) cells are infected with a

27 the murine beta-globin locus was analyzed in totipotent embryonic stem cells and in differentiated ce

28 It was found that s-SHIP is expressed in totipotent embryonic stem cells to the exclusion of the

29 osteopontin enhancer, which is expressed in totipotent embryonic stem cells.

30 hese findings raise caution about the use of totipotent ESCs in cell transplantation therapy, because

31 Genes activated in mouse totipotent F9 teratocarcinoma cells solely by activation

32 transcriptional gene regulation preserve the totipotent genome of germ cells through generations.

33 Higher eukaryotes must adapt a totipotent genome to specialized cell types with stable

34 ell tumors (GCTs) arise by transformation of totipotent germ cells.

35 Totipotent germline blastomeres in Caenorhabditis elegan

36 uires the engraftment of genetically altered totipotent hematopoietic stem cells (THSCs).

37 family of zinc finger proteins, expressed in totipotent hemopoietic cells as well as in myeloid proge

38 vidual, otherwise indistinguishable cells of totipotent human embryos, primordial germ cells, and sta

39 surrounded efforts to undertake research on totipotent human stem cells.

40 The totipotent mouse embryonic stem (ES) cell is known to di

41 Differentiation of totipotent mouse embryonic stem (ES) cells to various ly

42 as a result of generation of GRP cells from totipotent neuroepithelial stem cells, of O2A/OPCs from

43 entage of adult or differentiated cells have totipotent nuclei, and a much higher percentage of cells

44 ese data suggest that the cell lines exhibit totipotent potential and that BMP4 can prime human PSCs

45 ound tissue identity is first specified from totipotent precursor cells in the embryo.

46 allowing differentiated gametes to unleash a totipotent program following fertilization.

47 nion at fertilization, their genomes drive a totipotent program, giving rise to a complete embryo as

48 The immortal and totipotent properties of the germ line depend on determi

49 n oocytes can reprogram somatic cells into a totipotent state enabling animal cloning through somatic

50 Why does a totipotent state linger within the inner cell mass of mo

51 germ cells (PGCs) marks the beginning of the totipotent state.

52 research using human embryos as a source of totipotent stem cells can secure broad public support if

53 Totipotent stem cells have the potential to differentiat

54 Renewal of totipotent stem cells in the germline and cellular diffe

55 z1- or Rfz2-specific chimera leads, in these totipotent stem cells, to some differential activation o

56 rate the integration of a functional gene in totipotent stem cells.

57 es, similar to what is seen with features of totipotent two-cell blastomeres.

58 rements accompany the transition from motile totipotent unicellular organisms to multicellular organi

59 During gastrulation, PGCs remain totipotent while surrounding cells in the vegetal mass b

60 unique form of eusocial polyphenism in that totipotent workers can differentiate into either soldier

61 transforms a differentiated germ cell into a totipotent zygote capable of somatic development.

62 ession is essential for the development of a totipotent zygote into an embryo with defined cell linea

63 ty to transition from differentiated cell to totipotent zygote is unknown.

64 mechanisms regulate the transition from the totipotent zygote to pluripotent primitive ectoderm cell

65 eprogrammed after fertilization to produce a totipotent zygote with the potential to generate a new o