arginine has been researched along with De Morsier Syndrome in 1 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 1 (100.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Asensio, JL; Cañada, J; de la Mata, I; Garcia, JL; González, C; Jiménez-Barbero, J; Menéndez, M | 1 |
1 other study(ies) available for arginine and De Morsier Syndrome
Article | Year |
---|---|
The impact of R53C mutation on the three-dimensional structure, stability, and DNA-binding properties of the human Hesx-1 homeodomain.
Topics: Amino Acid Sequence; Animals; Arginine; Base Sequence; Basic Helix-Loop-Helix Transcription Factors; Circular Dichroism; Cysteine; DNA; Drosophila Proteins; Genes, Homeobox; Homeodomain Proteins; Humans; Kinetics; Models, Molecular; Molecular Sequence Data; Nuclear Magnetic Resonance, Biomolecular; Point Mutation; Protein Binding; Protein Structure, Secondary; Protein Structure, Tertiary; Septo-Optic Dysplasia; Thermodynamics; Transcription Factor HES-1 | 2002 |