399) le to induce a multitude of specific gene expression changes during senescence and d |
400) Gene expression changes of basic fibroblast gro |
401) Gene expression changes were analysed using qua |
402) Using gene expression data and pathway signatures, we |
403) Gene expression data indicate that EPCs, or the |
404) Analysis of publicly available expression data suggests that the two Arab |
405) After deriving an expression for I(D;R) in terms of sensitiv |
406) atients, indicating increased AdipoR1mRNA expression for a similar AMPKα1 expressio |
407) diagnostic test performance and derive an expression for channel capacity in terms o |
408) ibitor increased Math1 and decreased Hes1 expression, indicating Notch signaling reg |
409) ar numbers of ISCs, but had reduced Math1 expression, indicating a suppressed secret |
410) inhibitors increased both Math1 and Muc2 expression, indicating an ability to promo |
411) Meanwhile, there was IL-17 receptor expression on CD133(+)CSLCs derived from A |
412) CD44 and RANKL expression on protein level was correlated |
413) arch has shown the influence of emotional expression on psychological and physical w |
414) relative increase in Homer2 versus Homer1 expression via Homer1c overexpression or H |
415) omagnetic field induced osteogenic marker expression via bone morphogenetic protein, |
416) acetylation, DACi can interfere with gene expression via miRNA pathways. |
417) Runx2 gene expression, alkaline phosphatase (ALP) act |
418) omagnetic field increased osteogenic gene expression, alkaline phosphate activity an |
419) molecular markers that show differential expression between distinct sample groups. |
420) and pipelines for detecting differential expression between sample groups in a prac |
421) - and time-dependent increase in Gadd45α expression, but Nano-TiO2 did not. |
422) ar redox homeostasis and to regulate gene expression, but these processes remain poo |
423) ion of adult stem cells and analysed gene expression, cell proliferation and extrace |
424) luding induction of genetic damages, gene expression, cell transformation, prolifera |
425) sent study was to investigate STAT5A gene expression during early bovine embryogenes |
426) aim of the current work was to study the expression during early development of bot |
427) uman T cell line, with a maximal level of expression from 1.5 to 2.5 h after exposur |
428) cant decline in the level of SCGB1A1 mRNA expression from 16 to 144 h post-ovulation |
429) Furthermore, its expression increased during tumor progress |
430) t abundance was initially lower, but mRNA expression increased significantly at 72 a |
431) NA-exposed nymphs did not increase Lsspok expression level, but almost completely re |
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