glutamine has been researched along with Lipodystrophy in 3 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 1 (33.33) | 18.2507 |
| 2000's | 2 (66.67) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Mori, N; Oishi, M; Osaka, S; Sawada, S; Takasu, T; Uchiyama, T; Yamamoto, M | 1 |
| Anderson, CM; Cao, H; Hegele, RA; Jones, DC; Wang, J | 1 |
| Auclair, M; Buendia, B; Capeau, J; Courvalin, JC; Dubosclard, E; Pouchelet, M; Vigouroux, C | 1 |
3 other study(ies) available for glutamine and Lipodystrophy
| Article | Year |
|---|---|
Nasu-Hakola disease. A case accompanied by abnormalities in fatty acid composition of serum total lipids and amino acid analysis.
Topics: Adult; Amino Acids; Biopsy; Brain; Dementia; Fatty Acids; Glutamine; Humans; Lipids; Lipodystrophy; Male; Syndrome; Tomography, X-Ray Computed | 1993 |
Association between nuclear lamin A/C R482Q mutation and partial lipodystrophy with hyperinsulinemia, dyslipidemia, hypertension, and diabetes.
Topics: Adolescent; Adult; Arginine; Diabetes Mellitus; Female; Genetic Variation; Genotype; Glutamine; Humans; Hyperinsulinism; Hyperlipidemias; Hypertension; Lamin Type A; Lamins; Lipodystrophy; Male; Middle Aged; Nuclear Proteins; Pedigree; Point Mutation | 2000 |
Nuclear envelope disorganization in fibroblasts from lipodystrophic patients with heterozygous R482Q/W mutations in the lamin A/C gene.
Topics: Adult; Arginine; Cell Cycle; Cell Nucleus; Cells, Cultured; DNA-Binding Proteins; Female; Fibroblasts; Genetic Carrier Screening; Genetic Variation; Glutamine; Hot Temperature; Humans; Immunoblotting; Lamin Type A; Lamins; Lipodystrophy; Membrane Proteins; Middle Aged; Mutation, Missense; Nuclear Envelope; Nuclear Pore Complex Proteins; Nuclear Proteins; Solubility; Tryptophan | 2001 |