Sentence examples for molecules which promote from inspiring English sources

This review discusses current and emerging virus-based genetic engineering strategies for the delivery of therapeutic molecules which promote skeletal regeneration.

Alternative possibilities for the chemical regulation of cellular processes including selective ion-channel modulators [14] and sequence specific DNA binding molecules (which promote or inhibit the transcription of specific genes), [15] are also being investigated.

Inflammatory cytokines, including IL-1β, TNF-α, and CRP, have been suggested to induce the expression of cellular adhesion molecules, which promote adhesion of leukocytes to the vascular endothelium [68, 69].

Under such conditions, activated Kss1 executes a program that leads to the production of cell adhesion molecules, which promote the adherence of yeast cells and thus effectively transform the organism from vegetative to filamentous growth [15].

These granules, when activated, release chemokines, prostaglandins and small molecules which promote a pro-inflammatory state and leucocyte migration [ 19].

Another possibility explored through in vitro studies is that MeHg influences adhesion molecules, which promote atherosclerosis by attracting white blood cells to the endothelium of the artery (Prozialeck et al. 2002).

The bFGF is a potent angiogenic molecule, which promotes the neovascularization and blood supply to the granulation tissue.

H2S is a gaseous signalling molecule, which promotes vasodilatation (Zhao et al., 2001), exhibits cytoprotective anti-inflammatory properties (Zanardo et al., 2006), protects against cellular damage induced by reperfusion injury (Elrod et al., 2007) or lethal hypoxia (Blackstone and Roth, 2007), and stimulates angiogenesis in the vasculature (Papapetropoulos et al., 2009).

The 'target' molecules for Ran, which promote mitotic spindle assembly, are captured by Importin.

C5a appeared to promote an immunosuppressive microenvironment, as C5aR antagonism attenuated the population of MDSCs, including the granulocytic subpopulation, and expression of several immunosuppressive molecules, most of which promote Treg activity 77: ARG1, CTLA4, IL-6, IL-10, LAG3, and PDL1.

These complex glycan structures are found on different proteins, including an adhesion molecule E-cadherin, which promote cell detachment and invasion (Dennis et al. 2002) and a tissue inhibitor of metalloproteinase-1 in human colon cancer cells, increasing their metastatic potential (Kim et al. 2008).