>
                    
                    
                    
                    
                    
This roof paint blocks 97% of sunlight and pulls water from the air
'Venomous' Republican split over Israel hits new low as fiery feud reaches White House
Disease-ridden monkey that escaped from research facility shot dead by vigilante mom protecting...
Hooters returns - founders say survival hinges on uniform change after buying chain...
The 6 Best LLM Tools To Run Models Locally
 Testing My First Sodium-Ion Solar Battery 
A man once paralyzed from the waist down now stands on his own, not with machines or wires,...
Review: Thumb-sized thermal camera turns your phone into a smart tool
Army To Bring Nuclear Microreactors To Its Bases By 2028
Nissan Says It's On Track For Solid-State Batteries That Double EV Range By 2028
Carbon based computers that run on iron
 Russia flies strategic cruise missile propelled by a nuclear engine 
100% Free AC & Heat from SOLAR! Airspool Mini Split AC from Santan Solar | Unboxing & Install 
Engineers Discovered the Spectacular Secret to Making 17x Stronger Cement

An experimental cancer drug that targets a common genetic fault has been shown to shrink tumours by up to 67 per cent in just six weeks.
Scientists tested their newly developed anti-cancer drug AMG 510 on four patients, two of whom saw their tumours shrink. It did not work for the others.
In studies on mice, the treatment helped to shrink, and in some cases eradicate, the growing tumours.
The daily pill works by turning 'off' the KRAS gene. Mutated forms of the genes are permanently trapped 'on', causing cancerous cells to multiply.
This abnormal activity fuels the development of up to 50 per cent of lung cancers, as well as some pancreatic and bowel cancers.
The pharmaceutical company described their findings as a 'milestone' for patients with cancer KRAS-mutant cancers.
The research was led by by pharmaceutical company Amgen Research, based in Thousand Oaks, California.
The findings, published in Nature, are the first to report the effects of inhibiting KRAS with a drug.