glutamine has been researched along with Genetic Diseases in 3 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 2 (66.67) | 18.2507 |
| 2000's | 1 (33.33) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Battaglia, M; Bosticardo, M; Casati, A; Cavazzana-Calvo, M; Facchetti, F; Frascoli, L; Gougeon, ML; Grassi, F; Lemercier, B; Marrella, V; Notarangelo, LD; Poliani, PL; Ravanini, M; Roncarolo, MG; Rucci, F; Vezzoni, P; Villa, A | 1 |
| Perutz, M | 1 |
| Perutz, MF | 1 |
2 review(s) available for glutamine and Genetic Diseases
| Article | Year |
|---|---|
Polar zippers: their role in human disease.
Topics: Amino Acid Sequence; Animals; Ascaris; Genetic Diseases, Inborn; Glutamine; Hemoglobins; Humans; Lupus Erythematosus, Systemic; Molecular Sequence Data; Nervous System Diseases; Repetitive Sequences, Nucleic Acid; Ribonucleoproteins, Small Nuclear | 1994 |
Glutamine repeats and inherited neurodegenerative diseases: molecular aspects.
Topics: Genetic Diseases, Inborn; Glutamine; Models, Molecular; Mutation; Nervous System Diseases; Nucleic Acid Conformation; Protein Structure, Secondary; Recombination, Genetic; Repetitive Sequences, Nucleic Acid | 1996 |
1 other study(ies) available for glutamine and Genetic Diseases
| Article | Year |
|---|---|
A hypomorphic R229Q Rag2 mouse mutant recapitulates human Omenn syndrome.
Topics: Amino Acid Substitution; Animals; Arginine; Cells, Cultured; Disease Models, Animal; DNA-Binding Proteins; Genetic Diseases, Inborn; Glutamine; Humans; Immune Tolerance; Immunologic Deficiency Syndromes; Mice; Mice, Inbred C57BL; Mice, Mutant Strains; Mice, Transgenic; Mutagenesis, Site-Directed | 2007 |