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1 the induction of KDR(+) PDGFRa(+) CPCs from human ES cells.
2 were morphologically indistinguishable from human ES cells.
3 aling is required to sustain self-renewal of human ES cells.
4 of FGF signaling to support self-renewal of human ES cells.
5 sion of NO signaling components in mouse and human ES cells.
6 ed shortly thereafter by their derivation of human ES cells.
7 k of autoregulatory and feedforward loops in human ES cells.
8 hlighted known differences between mouse and human ES cells.
9 stablished for mouse ES cells work poorly in human ES cells.
10 e development of homologous recombination in human ES cells.
11 ansplantation of neural precursor cells from human ES cells.
13 is hypermethylated and largely repressed in human ES cells and derived trophoblast cell lines, as we
14 and H3K27me3) of ChIP sequencing datasets in human ES cells and eight pairs in murine ES cells, and p
15 of cortical neuroepithelial stem cells from human ES cells and human iPS cells was dependent on reti
16 3 gene signature transcriptionally resembles human ES cells and in vitro cultured GBM stem cells, and
18 surface markers and genes that characterize human ES cells, and maintain the developmental potential
20 s recombination is an essential technique if human ES cells are to fulfill their promise as a basic r
22 tion of these factors at promoter regions in human ES cells, Boyer et al. demonstrate frequent promot
23 mpared gene expression profiles of mouse and human ES cells by immunocytochemistry, RT-PCR, and membr
24 Although efficient methods for production of human ES cells by somatic nuclear transfer must be devel
28 o, in contrast to their murine counterparts, human ES cells cannot be cloned efficiently from single
32 reakthroughs in somatic nuclear transfer and human ES cell derivation have produced a flurry of new a
36 onstrated endothelial differentiation within human ES cell-derived aggregates using VEGF loaded MPs.
37 Surface-modified scaffolds were seeded with human ES cell-derived cardiomyocytes and cultured in vit
38 ansplantation into the neonatal mouse brain, human ES cell-derived neural precursors were incorporate
40 in human embryonic stem (ES) cells and four human ES-cell-derived lineages, we uncover extensive chr
46 Selection for CD34(+) cells derived from human ES cells enriches for hematopoietic colony-forming
47 nce of acetylated histone H3K56 (H3K56ac) in human ES cells (ESCs) correlates positively with the bin
49 , STELLAR and OCT4, whereas undifferentiated human ES cells expressed these genes along with the germ
50 CNT could aid efforts to generate autologous human ES cells for regenerative applications, as donated
52 High, stable transfection efficiencies in human ES cells have been difficult to achieve, and, in p
53 Significant differences between mouse and human ES cells have hampered the development of homologo
56 tion of a unique stem cell phenotype by both human ES cells (hESCs) and induced pluripotent stem cell
58 to identify cardiovascular progenitors from human ES cells (hESCs) that can functionally integrate i
60 20q11.21, including three genes expressed in human ES cells, ID1, BCL2L1 and HM13, occurred in >20% o
62 two factor-induced human iPS cells resemble human ES cells in pluripotency, global gene expression p
63 results demonstrate that differentiation of human ES cells into EBs in vitro results in formation of
64 in combination with the success in deriving human ES cell-like induced pluripotent stem (iPS) cells
65 ocumented and recent research has shown that human ES cell lines can be derived in vitro, this review
66 on profiles showed that the five independent human ES cell lines clustered tightly together, reflecti
71 in H1 cells was similar to that of two other human ES cell lines tested (line I-6 and clonal line-H9.
73 mors, we compared the expression profiles of human ES cell lines, human germ cell tumor cell lines an
82 ch, based on the physical characteristics of human ES cells, that we used to successfully target HPRT
87 ranscriptional profiles of three pluripotent human ES cells to those of isolated inner cell mass (ICM
89 ferentiated hematopoietic cells derived from human ES cells under these conditions also express norma
90 quantified the abundances of these codes as human ES cells undergo differentiation to reveal strikin
91 insights into transcriptional regulation of human ES cells, we have identified OCT4, SOX2, and NANOG
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