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In line with the Ki-67 analysis on cell proliferation, mTerc+/+ mice exhibited a stronger induction of proliferation markers characterizing the G2/M stage of the cell cycle (phospho-histone 3 (pH 3) and CDC2) compared to G3 mTerc−/− mice (Figure 4C).

To restrict the number of genes and to find potential markers characterizing the rhabdospheres, a metaanalysis with different microarray samples publicly available (hematopoietic, FM95, embryonic skeletal myoblast, mesenchymal stem cells, embryonic stem cells, neuronal cells, glioblastoma cells and patient samples, neurospheres and prostate cancer samples) was implemented.

Next, both fractions were analyzed by Western blotting, investigating the presence of distinct markers characterizing the selective enrichment for the membrane proteins from A2780 cells.

Thus, in two cases of renal carcinomas, arising in bone marrow transplant recipients, some tumor cells showed genetic markers characterizing the healthy donor (Chakraborty et al. 2004; Yilmaz et al. 2005).

The phenotype analysis for expression of surface markers characterizing the multipotent, common lymphoid and myeloid progenitors reveals that short exposure to cytokines, present in the preactivation/transduction medium, favours the expansion of the myeloid subpopulation against the lymphoid one.

Fluorescence-activated cell-sorter scanner (FACS) analysis for the expression of surface markers, characterizing the multipotent, lymphoid and myeloid progenitors (Olweus et al, 1996; Terstappen et al, 1991; Tjonnfjord et al, 1994) shows that CD34+CD38−CD50+, CD34+CD10+ and CD34+CD33+ are 2.4 ± 1.1, 61 ± 4 and 35 ± 3.2%, respectively (Fig 2B).

Similar(54)

Two important chronostratigraphic markers characterize the EMPT, the Jaramillo Subchron (1.070 0.988 Ma) and the Matuyama Brunhes Chron boundary (∼773 ka).

Numerous molecular markers characterize the central stages of the chondrocyte life cycle.

This structural modification represents an exclusive feature of partly or fully sequenced neuropteran mtDNAs and could be a peculiar genomic marker characterizing the entire order Neuroptera.

Evidence based on this molecular marker characterizes the most dynamic phase of pallial morphogenesis in mice, but may not be strictly comparable with earlier reports based on different criteria for anatomical boundaries.

Thus, only one canonical marker specific for the subspecies tularensis may be included and not all markers characterizing subclades of the subspecies.

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