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aspartic acid and Muscular Dystrophy, Duchenne

aspartic acid has been researched along with Muscular Dystrophy, Duchenne in 2 studies

Aspartic Acid: One of the non-essential amino acids commonly occurring in the L-form. It is found in animals and plants, especially in sugar cane and sugar beets. It may be a neurotransmitter.
aspartic acid : An alpha-amino acid that consists of succinic acid bearing a single alpha-amino substituent
L-aspartic acid : The L-enantiomer of aspartic acid.

Muscular Dystrophy, Duchenne: An X-linked recessive muscle disease caused by an inability to synthesize DYSTROPHIN, which is involved with maintaining the integrity of the sarcolemma. Muscle fibers undergo a process that features degeneration and regeneration. Clinical manifestations include proximal weakness in the first few years of life, pseudohypertrophy, cardiomyopathy (see MYOCARDIAL DISEASES), and an increased incidence of impaired mentation. Becker muscular dystrophy is a closely related condition featuring a later onset of disease (usually adolescence) and a slowly progressive course. (Adams et al., Principles of Neurology, 6th ed, p1415)

Research

Studies (2)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's2 (100.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Vulin, A1
Wein, N1
Strandjord, DM1
Johnson, EK1
Findlay, AR1
Maiti, B1
Howard, MT1
Kaminoh, YJ1
Taylor, LE1
Simmons, TR1
Ray, WC1
Montanaro, F1
Ervasti, JM1
Flanigan, KM1
Doorenweerd, N1
Hooijmans, M1
Schubert, SA1
Webb, AG1
Straathof, CS1
van Zwet, EW1
van Buchem, MA1
Verschuuren, JJ1
Hendriksen, JG1
Niks, EH1
Kan, HE1

Other Studies

2 other studies available for aspartic acid and Muscular Dystrophy, Duchenne

ArticleYear
The ZZ domain of dystrophin in DMD: making sense of missense mutations.
    Human mutation, 2014, Volume: 35, Issue:2

    Topics: Actins; Animals; Aspartic Acid; Cysteine; Dystroglycans; Dystrophin; Genetic Variation; Humans; Mice

2014
Proton Magnetic Resonance Spectroscopy Indicates Preserved Cerebral Biochemical Composition in Duchenne Muscular Dystrophy Patients.
    Journal of neuromuscular diseases, 2017, Volume: 4, Issue:1

    Topics: Adolescent; Aquaporin 4; Aspartic Acid; Brain; Case-Control Studies; Cerebellum; Child; Choline; Cre

2017
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