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113
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Simple
- ... the body's ability to break down the simple sugar glucose, which is the primary energy source ... in cells known as glycolysis. During glycolysis, the simple sugar glucose is broken down to produce energy. ...
- ... disorder that affects how the body processes a simple sugar called galactose. A small amount of galactose ... diet. These enzymes break down galactose into another simple sugar, glucose, and other molecules that the body ...
- ... classic forms, known as the salt-wasting and simple virilizing types. The third type is called the ... salt-wasting type is the most severe, the simple virilizing type is less severe, and the non- ...
- ... called disaccharides because they are made of two simple sugars. Disaccharides are broken down into simple sugars during digestion. Sucrose is broken down into ...
- ... are outbursts of sound. Some motor tics are simple and involve only one muscle group. Simple motor tics, such as rapid eye blinking, shoulder ... appear later than motor tics, also can be simple or complex. Simple vocal tics include grunting, sniffing, ...
- ... pathway that produces sialic acid, which is a simple sugar that attaches to the ends of more ... sialic acid. As a result, less of this simple sugar is available to attach to molecules on ...
- ... because they are each made up of two simple sugar molecules. Disaccharides must be broken down into simple sugar molecules to be used by the body. ... is to break down sucrose and maltose into simple sugars so that they can be absorbed by ...
- ... many complex traits, handedness does not have a simple pattern of inheritance. Children of left-handed parents ... IC. Genome-wide association study of handedness excludes simple genetic models. Heredity (Edinb). 2014 Mar;112(3): ...
- ... and mildest feature of the GEFS+ spectrum is simple febrile seizures, which begin in infancy and usually ... may not fit into the classical diagnosis of simple febrile seizures, FS+, or Dravet syndrome.Family members ...
- ... in a completely nonfunctional enzyme. People with the simple virilizing type of this condition have CYP21A2 gene ... novel point mutations in the CYP21 gene causing simple virilizing forms of congenital adrenal hyperplasia due to ...
