Page last updated: 2024-11-08

alanine and Amyotonia Congenita

alanine has been researched along with Amyotonia Congenita in 7 studies

Alanine: A non-essential amino acid that occurs in high levels in its free state in plasma. It is produced from pyruvate by transamination. It is involved in sugar and acid metabolism, increases IMMUNITY, and provides energy for muscle tissue, BRAIN, and the CENTRAL NERVOUS SYSTEM.
alanine : An alpha-amino acid that consists of propionic acid bearing an amino substituent at position 2.

Research Excerpts

ExcerptRelevanceReference
"beta-N-Oxalylamino-L-alanine (BOAA) and beta-N-methylamino-L-alanine (BMAA) are chemically related excitant amino acids isolated from the seed of Lathyrus sativus (BOAA) and Cycas circinalis (BMAA), consumption of which has been linked to lathyrism (an upper motor neuron disorder) and Guam amyotrophic lateral sclerosis (ALS), respectively."3.67Discovery and partial characterization of primate motor-system toxins. ( Hugon, J; Ludolph, A; Nunn, PB; Ross, SM; Roy, DN; Schaumburg, HH; Spencer, PS, 1987)

Research

Studies (7)

TimeframeStudies, this research(%)All Research%
pre-19904 (57.14)18.7374
1990's1 (14.29)18.2507
2000's1 (14.29)29.6817
2010's1 (14.29)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Ning, J1
Li, R1
Ren, J1
Zhangsun, D1
Zhu, X1
Wu, Y1
Luo, S1
Tagawa, K1
Ogawa, M1
Kawabe, K1
Yamanaka, G1
Matsumura, T1
Goto, K1
Nonaka, I1
Nishino, I1
Hayashi, YK1
Falk, RE1
Cederbaum, SD1
Blass, JP1
Gibson, GE1
Kark, RA1
Carrel, RE1
Krentz, AJ1
Williams, AC1
Nattrass, M1
Spencer, PS3
Hugon, J1
Ludolph, A1
Nunn, PB3
Ross, SM2
Roy, DN2
Schaumburg, HH1
Seelig, M2
Zagoren, JC1

Other Studies

7 other studies available for alanine and Amyotonia Congenita

ArticleYear
Alanine-Scanning Mutagenesis of α-Conotoxin GI Reveals the Residues Crucial for Activity at the Muscle Acetylcholine Receptor.
    Marine drugs, 2018, Dec-13, Volume: 16, Issue:12

    Topics: Alanine; Amino Acid Sequence; Animals; Conotoxins; Conus Snail; Molecular Docking Simulation; Molecu

2018
Protein and gene analyses of dysferlinopathy in a large group of Japanese muscular dystrophy patients.
    Journal of the neurological sciences, 2003, Jul-15, Volume: 211, Issue:1-2

    Topics: Age of Onset; Alanine; Blotting, Western; Calpain; Cysteine; Cytoskeletal Proteins; DNA Mutational A

2003
Ketonic diet in the management of pyruvate dehydrogenase deficiency.
    Pediatrics, 1976, Volume: 58, Issue:5

    Topics: Alanine; Carbohydrate Metabolism, Inborn Errors; Child; Citrates; Dietary Carbohydrates; Dietary Fat

1976
Abnormal regulation of carbohydrate metabolism in motor neurone disease.
    Diabetes research (Edinburgh, Scotland), 1991, Volume: 16, Issue:2

    Topics: Alanine; Analysis of Variance; Blood Glucose; C-Peptide; Fatty Acids, Nonesterified; Female; Glucose

1991
Discovery and partial characterization of primate motor-system toxins.
    Ciba Foundation symposium, 1987, Volume: 126

    Topics: Alanine; Amino Acids, Diamino; Animals; beta-Alanine; Cyanobacteria Toxins; Humans; Lathyrism; Macac

1987
Stereospecific acute neuronotoxicity of 'uncommon' plant amino acids linked to human motor-system diseases.
    Brain research, 1987, May-05, Volume: 410, Issue:2

    Topics: Alanine; Amino Acids, Diamino; Animals; beta-Alanine; Cells, Cultured; Cyanobacteria Toxins; Isomeri

1987
Detection and characterization of plant-derived amino acid motorsystem toxins in mouse CNS cultures.
    Progress in clinical and biological research, 1987, Volume: 253

    Topics: Alanine; Amino Acids, Diamino; Animals; beta-Alanine; Cell Survival; Cells, Cultured; Central Nervou

1987