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These results, obtained by using biochemical methods, were also confirmed by using the FRET technique (bottom boxes).
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Prenatal testing is preferably done by genetic analyses, but biochemical methods are also available for cases where the mutation in the ABCD1 gene has not been established.
Numerous experimental methods are also being developed to explore the range of possible biochemical reactions.
Recently, the directed evolution methods are also used to change the elasticity (kinetic property of κ i ) and will be useful techniques for biochemical circuit design [ 34- 36].
Paraffin methods are also questionable.
We began with 12 evolutionary and biochemical features (see Methods), which were also tested in the original EvoD model [ 23] that is built for diagnosing disease variants.
The following biochemical tests were also done; Fasting Blood Glucose (FBG) (glucose oxidase method – Hitachi 704 chemical auto-analyzer), Glycosylated haemoglobin (HPLC technique) and urine microalbumin.
Serum biochemical analyses were also conducted.
BMD and biochemical markers were also measured.
Individual biochemical variables were also recorded.
Hematological and biochemical tests were also performed.
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