Hani Z. Asfour

TL;DR: A brief account of the research reports on the plants and natural compounds with anti-QS potential is given, which have recently received considerable attention as a new source of safe and effective QS inhibitory substances.

TL;DR: In silico analysis suggested that S136A and P764L variants of BRAF could directly or indirectly destabilize the amino acid interactions and hydrogen bond networks thus explain the functional deviations of protein to some extent.

TL;DR: A new cyclodepsipeptide, namely fusaripeptide A, along with three known compounds adenosine (2), 2[(2-hydroxypropionyl)amino]benzamide (3), and cyclopentanol (4), have been isolated, using extensive 1D and 2D NMR and HRESI and GC mass spectral data.

TL;DR: Stable naringenin nanoemulsions were more effective than the NAR solution in reducing Bcl2 expression, while increasing pro-apoptotic Bax and caspase-3 activity and could be a suitable drug delivery system to enhance the effects of NAR in the treatment of lung cancer.

TL;DR: Enhanced rod photoreceptor differentiation, synaptogenesis and light response in response to addition of decellularised matrices from RPE and neural retina as shown herein provide a novel and substantial advance in generation of retinal organoids for drug screening, tissue engineering and regenerative medicine.