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dihydroxyphenylalanine and Genetic Diseases, Inborn

dihydroxyphenylalanine has been researched along with Genetic Diseases, Inborn in 2 studies

Dihydroxyphenylalanine: A beta-hydroxylated derivative of phenylalanine. The D-form of dihydroxyphenylalanine has less physiologic activity than the L-form and is commonly used experimentally to determine whether the pharmacological effects of LEVODOPA are stereospecific.
dopa : A hydroxyphenylalanine carrying hydroxy substituents at positions 3 and 4 of the benzene ring.

Genetic Diseases, Inborn: Diseases that are caused by genetic mutations present during embryo or fetal development, although they may be observed later in life. The mutations may be inherited from a parent's genome or they may be acquired in utero.

Research

Studies (2)

TimeframeStudies, this research(%)All Research%
pre-19901 (50.00)18.7374
1990's1 (50.00)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Anokhina, IP1
Vertinskaia, AG1
Vekshina, NL1
Nebarakova, TP1
Ovchinnikov, IV1
Druzhina, EV1
Ovchinnikova, OI1
Demos, J1
Berthelon, M1

Other Studies

2 other studies available for dihydroxyphenylalanine and Genetic Diseases, Inborn

ArticleYear
[Hereditary alcoholism: some neurochemical and genetic mechanisms].
    Vestnik Rossiiskoi akademii meditsinskikh nauk, 1999, Issue:6

    Topics: 3,4-Dihydroxyphenylacetic Acid; Alcoholism; Alleles; Brain; Dihydroxyphenylalanine; DNA; Genetic Dis

1999
[Enzymology and myopathy. Diagnostic and genetic value of determination of platelet diphenol-oxydase activity].
    Archives francaises de pediatrie, 1972, Volume: 29, Issue:8

    Topics: Adult; Blood Platelets; Catechol Oxidase; Dihydroxyphenylalanine; Electrophoresis; Epinephrine; Fema

1972