Page last updated: 2024-08-17

aspartic acid and Basedow Disease

aspartic acid has been researched along with Basedow Disease in 3 studies

Research

Studies (3)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's1 (33.33)18.2507
2000's1 (33.33)29.6817
2010's1 (33.33)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Ardito, M; De Groot, AS; De Groot, LJ; Inaba, H; Martin, W1
Danielsen, ER; Dock, J; Elberling, TV; Feldt-Rasmussen, U; Hørding, M; Perrild, H; Rasmussen, AK; Thomsen, C; Waldemar, G1
Bengtsson, M; Heldin, NE; Kinch, A; Schuppert, F; Simanainen, J; Westermark, B; Westermark, K; Winsa, B1

Other Studies

3 other study(ies) available for aspartic acid and Basedow Disease

ArticleYear
The role of glutamic or aspartic acid in position four of the epitope binding motif and thyrotropin receptor-extracellular domain epitope selection in Graves' disease.
    The Journal of clinical endocrinology and metabolism, 2010, Volume: 95, Issue:6

    Topics: Amino Acid Substitution; Animals; Antigen Presentation; Aspartic Acid; Epitopes; Extracellular Space; Glutamic Acid; Graves Disease; HLA Antigens; HLA-DR Antigens; HLA-DR3 Antigen; HLA-DR7 Antigen; Humans; Immunization; Lymphocytes; Mice; Receptors, Thyrotropin

2010
Reduced parietooccipital white matter glutamine measured by proton magnetic resonance spectroscopy in treated graves' disease patients.
    The Journal of clinical endocrinology and metabolism, 2008, Volume: 93, Issue:8

    Topics: Adult; Aspartic Acid; Choline; Dipeptides; Female; Glutamic Acid; Glutamine; Graves Disease; Humans; Inositol; Magnetic Resonance Spectroscopy; Male; Middle Aged; Occipital Lobe; Parietal Lobe; Prospective Studies

2008
Analysis of mutations in exon 1 of the human thyrotropin receptor gene: high frequency of the D36H and P52T polymorphic variants.
    Thyroid : official journal of the American Thyroid Association, 1999, Volume: 9, Issue:1

    Topics: Alleles; Amino Acid Substitution; Aspartic Acid; Exons; Female; Gene Frequency; Genetic Testing; Graves Disease; Heterozygote; Histidine; Humans; Male; Mutation; Polymorphism, Single-Stranded Conformational; Proline; Receptors, Thyrotropin; Restriction Mapping; Threonine

1999