Compounds > glutamic acid

glutamic acid and Genetic Diseases

glutamic acid has been researched along with Genetic Diseases in 6 studies

Research

Studies (6)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's2 (33.33)18.2507
2000's4 (66.67)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Ahmad, R; Blackinton, J; Cookson, MR; Greggio, E; Lakshminarasimhan, M; Raza, AS; Thomas, KJ; Wilson, MA1
Baitei, EY; Raef, H; Shi, Y; Zou, M1
Eisen, AA1
Casadesús, J; D'Ari, R1
Hikasa, Y; Inaba, M; Kagota, K; Matsuu, A; Ono, K; Sato, K; Suwa, Y1
Berg, K; Darin, N; Kyllerman, M; Martinsson, T; Oldfors, A; Tajsharghi, H; Wahlstrom, J1

Reviews

1 review(s) available for glutamic acid and Genetic Diseases

ArticleYear
Amyotrophic lateral sclerosis. A multifactorial disease.
    Advances in neurology, 1995, Volume: 68

    Topics: Amyotrophic Lateral Sclerosis; Genetic Diseases, Inborn; Glutamic Acid; Humans; Nerve Growth Factors; Risk Factors; Second Messenger Systems

1995

Other Studies

5 other study(ies) available for glutamic acid and Genetic Diseases

ArticleYear
Formation of a stabilized cysteine sulfinic acid is critical for the mitochondrial function of the parkinsonism protein DJ-1.
    The Journal of biological chemistry, 2009, Mar-06, Volume: 284, Issue:10

    Topics: Amino Acid Substitution; Animals; Cell Line, Tumor; Cysteine; Genetic Diseases, Inborn; Glutamic Acid; Humans; Intracellular Signaling Peptides and Proteins; Mice; Mitochondrial Proteins; Mutation; Oncogene Proteins; Oxidation-Reduction; Parkinson Disease; Protein Deglycase DJ-1; Sulfinic Acids

2009
Genotype-phenotype correlation in a family with primary cortisol resistance: possible modulating effect of the ER22/23EK polymorphism.
    European journal of endocrinology, 2008, Volume: 158, Issue:4

    Topics: Adrenal Gland Diseases; Adult; Amino Acid Substitution; Arginine; Family; Genetic Diseases, Inborn; Genotype; Glutamic Acid; Heterozygote; Homozygote; Humans; Hydrocortisone; Lysine; Male; Phenotype; Polymorphism, Genetic; Receptors, Glucocorticoid

2008
Underground metabolism.
    BioEssays : news and reviews in molecular, cellular and developmental biology, 1998, Volume: 20, Issue:2

    Topics: Alanine; Biological Evolution; Energy Metabolism; Enzymes; Genetic Diseases, Inborn; Glutamic Acid; Phenotype; Substrate Specificity; Sulfides

1998
Inherited defects of sodium-dependent glutamate transport mediated by glutamate/aspartate transporter in canine red cells due to a decreased level of transporter protein expression.
    The Journal of biological chemistry, 2000, Mar-03, Volume: 275, Issue:9

    Topics: Amino Acid Sequence; Amino Acid Transport System X-AG; Animals; ATP-Binding Cassette Transporters; Biological Transport; Bone Marrow Cells; Brain; Cloning, Molecular; Dogs; Erythrocytes; Genetic Diseases, Inborn; Glutamic Acid; Japan; Kinetics; Microinjections; Molecular Sequence Data; Mutation; Oocytes; Pedigree; RNA, Messenger; Sequence Alignment; Xenopus

2000
Autosomal dominant myopathy: missense mutation (Glu-706 --> Lys) in the myosin heavy chain IIa gene.
    Proceedings of the National Academy of Sciences of the United States of America, 2000, Dec-19, Volume: 97, Issue:26

    Topics: Adult; Amino Acid Sequence; Animals; Child; Female; Genetic Diseases, Inborn; Glutamic Acid; Humans; Lysine; Male; Microscopy, Electron; Middle Aged; Molecular Sequence Data; Molecular Structure; Muscular Diseases; Mutation, Missense; Myosin Heavy Chains; Myosins; NADH Tetrazolium Reductase; Pedigree; Staining and Labeling

2000