Sentence examples for molecular expression pattern from inspiring English sources

Tissue microarray technology (TMA) is nowadays considered as a powerful tool for the high-throughput analysis of molecular expression pattern of cancer.

The molecular expression pattern of SLC4A11 correlates with the observed clinical phenotype for autosomal recessive CHED.

Further clinical studies using biomarkers and molecular expression pattern [ 4, 5] should provide a clue to find the appropriate predicting markers or even new therapeutic targets.

There is growing evidence, however, that the molecular expression pattern of cells in the invading front of solid tumours is different from that of cells in the tumour interior.

There is also increasing evidence that the molecular expression pattern in SSc skin is extremely heterogeneous, and that only smaller subsets of patients express increased levels of inflammatory molecules [ 10].

To our knowledge, this is the first study that has determined the genome-wide molecular expression pattern of human chondrocytes in response to stimulation with RASFsn and thus provided comprehensive insight into chondrocyte dysfunction during RA-related destruction of cartilage.

Whole cell patch clamp can be combined with histological, immunochemical and molecular methods (e.g.( [11])) to establish molecular expression patterns, but these techniques offer low yield in vivo.

Cells were stained for extracellular molecular expression patterns using monoclonal antibodies (mAb) against mouse CD3 (PerCP-Cy5-conjugated), DX5 (FITC-conjugated), CD4 (Pacific Blue-conjugated), CD8 (APC-Cy7-conjugated), F4/80 (PE-conjugated) CD69 (PE-conjugated), CD11b (PerCp-Cy5.5-conjugated), Ly6G (PE-Cy7-conjugated), CD86 (APC-conjugated) and isotype controls.

Clearly, identification of the molecular expression patterns of all ion channel and ion exchanger subtypes in myometrial cells of the uterus is essential (e.g. [107]), and marrying such data to precise electrophysiological, pharmacological and simulated profiles (even if initially this is in clonal cells), is required to furnish a complete biophysical characterization of normal uterine function.

Moreover, surgical incisions may introduce trauma, hypoxia, and bleeding that can alter the molecular expression patterns.

While the molecular expression patterns of many genes and proteins in medulloblastoma subgroups have been discerned, subgroup-specific GPCR expression patterns have not previously been investigated.