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The Porteus Maze test (PMT) is a psychological test. It is designed to measure psychological planning capacity and foresight. It is a nonverbal test of intelligence. It was developed by University of Hawaii psychology Professor Stanley Porteus. [1] The test consists of a set of mazes for the subject to solve. The mazes are of varying complexity.
In enzymology, a phenol O-methyltransferase (EC 2.1.1.25) is an enzyme that catalyzes the chemical reaction. S-adenosyl-L-methionine + phenol S-adenosyl-L-homocysteine + anisole. Thus, the two substrates of this enzyme are S-adenosyl methionine and phenol, whereas its two products are S-adenosylhomocysteine and anisole.
A typical luminescence optical system consists of a light-tight reading chamber and a PMT detector. Some plate readers use an Analog PMT detector while others have a photon counting PMT detector. Photon Counting is widely accepted as the most sensitive means of detecting luminescence.
Penn State is a win away from the national title game. The No. 6 Nittany Lions jumped out to a 14-0 lead and held on for a 31-14 win over No. 3 Boise State in the Fiesta Bowl. PSU advances to the ...
A New York judge is set to decide this week whether President-elect Donald Trump's criminal conviction on charges involving hush money paid to a porn star should be overturned in light of the U.S ...
Jay Leno is setting the record straight about his recent string of injuries.. The former Tonight Show host, 74, appeared on the Dec. 22 episode of Bill Maher's Club Random podcast to discuss ...
The human brain, particularly the prefrontal cortex, does not reach "full maturity" or "full development" at any particular age (e.g. 16, 18, 21, 25, 30). Changes in structure and myelination of gray matter are recorded to continue with relative consistency all throughout life including until death.
Phosphatidylethanolamine N-methyltransferase (abbreviated PEMT) is a transferase enzyme (EC 2.1.1.17) which converts phosphatidylethanolamine (PE) to phosphatidylcholine (PC) in the liver. [ 5 ] [ 6 ] [ 7 ] In humans it is encoded by the PEMT gene within the Smith–Magenis syndrome region on chromosome 17 .