435) ring the last decade showed that the gene expression profiling can be the biomarker |
436) Many gene expression profiling have been found and r |
437) ally linked as a tetramer, inhibited gene expression regulation by chondrocalcin, su |
438) ed regions that were associated with gene expression regulation during carcinogenesi |
439) and complete lack of smooth muscle actin expression that has only been reported onc |
440) MicroRNAs are negative regulators of gene expression that have been shown to be esse |
441) .5%) of African-Barbadian men lacked DARC expression, whereas almost three-fifths (5 |
442) g through epigenetic inhibition of BRCA-1 expression, whereas dietary antagonists of |
443) o term because of abnormal imprinted gene expression, which is not regulated by Mend |
444) ssing cells reduced BCL6 mRNA and protein expression, which is sufficient to induce |
445) Furthermore, knockdown of POU5F1B expression with a short hairpin RNA confir |
446) the SCCF2 cells had increased COX-2 mRNA expression with bone conditioned medium. |
447) tudy demonstrates that upregulation of NO expression within adult stem cells differe |
448) (P = 0.002) and also associated with VEGF expression within malignant CMT (P = 0.043 |
449) β3 release and adenoviral-mediated shRNA expression (LV-T + Ad-sh) generally de |
450) ween FBP1 and c-Myc (P = 0.005) and Ki-67 expression (P = 0.009). |
451) High FBP1 expression (located in cell nuclei) was ob |
452) ed hippocampal beclin1 and increased Bcl2 expression (mimicking schizophrenia and no |
453) ive breast carcinomas, we examined TGFBR2 expression (n=252) and phosphorylation lev |
454) the largest displacement for each facial expression (∼11-14 mm). |
455) In translational control of gene expression, R12 repeats is known to intera |
456) fects of β-NF at the level of transcript expression, a 6K microarray analysis was e |
457) of viability and specific neuronal marker expression allowed assessment that the cor |
458) Disruption of RP58 expression alters the differentiation of i |
459) In combination with global gene expression analysis, 91 of these ST-DMRs w |
460) s new molecular endpoints, including gene expression, as suitable tools that, comple |
461) Furthermore, manipulation of SALL4 expression can affect drug sensitivity of |
462) e study revealed that CAF-specific TGFBR2 expression correlated with improved recurr |
463) PGE2 expression declined over time in group C b |
464) the second postnatal week, while the α5 expression declines later in development w |
465) ussing on the dynamical influence of gene expression delays in morphogen-based Turin |
466) stigated the correlation between KIT gene expression determined by immunohistochemis |
467) We also analyzes the expression dynamics of several conserved s |
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