Sentence examples for cell programmes from inspiring English sources

Not surprisingly, most major pharmaceutical companies now have in-house stem cell programmes, and collaborate with academic groups or purchase hPSC products from commercial suppliers [ 39].

The authors propose that aberrant activation of the Pax7/c-Met pathways may induce formation of ectopic skeletal muscle by encouraging satellite-cell specification at the expense of alternate developmental stem cell programmes.

Bond lengths and bond angles were calculated using refined lattice parameters and fractional coordinates with the help of Powder Cell programme.

As Seoul's stem cell programme faltered, other nations streamlined regulations and aggressively expanded funding for research, Mr Lee said.

It might sound a little strange, given the brand-new stem cell programme, but Ährlund-Richter would like to see more home-grown sources of funding.

To digitise and visualise data, a NIDAQ 6024E board (National Instruments) and Windows Whole Cell Programme software (WinWCP V3.9.1; courtesy of John Dempster, Strathclyde University, Scotland) were used.

It makes no prediction of stem-cell frequency but simply argues that with the correct signals, the stem cell programme can be activated in otherwise non-CSC malignant cells.

Prdm14 is the first germ cell gene to be expressed and plays crucial roles in two successive events characterizing the germ cell programme: reacquisition of pluripotent potential and epigenetic reprogramming (Weber et al., 2010; Yamaji et al., 2008).

Taken together, our results demonstrate that we have identified a set of genes that captures a specific stem cell programme that holds biological and clinical (prognostic) information in breast cancer.

In summary, this analysis shows that the two different CD34low and CD34high leukaemia-propagating subpopulations of B-ALL are indistinguishable with respect to several published self-renewal signatures and that the programme underlying clonal expansion in B-ALL shows only a limited overlap with the stem cell programme of normal haematopoietic and AML stem cells.

To test our hypothesis that the regulatory network that describes leukaemic propagation in B-ALL is different to the stem cell programme in a hierarchical system, we performed a PCA as before but this time using Eppert's 42-gene (48-probe) signature derived from candidate human AML stem cell populations capable of repopulating immunodeficient mice (Eppert et al, 2011).