arginine has been researched along with Abnormalities, Skin in 2 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 1 (50.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 1 (50.00) | 2.80 |
| Authors | Studies |
|---|---|
| Arveiler, B; Bessis, D; Boralevi, F; Lasseaux, E; Leauté-Labrèze, C; Michaud, V; Morice-Picard, F; Plaisant, C; Rezvani, HR; Taieb, A; Trimouille, A | 1 |
| Kanzaki, T; Mori, M; Murakami, T; Noda, T; Saheki, T; Shimada, T; Takiguchi, M; Tashiro, M; Yamamura, K | 1 |
2 other study(ies) available for arginine and Abnormalities, Skin
| Article | Year |
|---|---|
Hereditary Mucoepithelial Dysplasia Results from Heterozygous Variants at p.Arg557 Mutational Hotspot in SREBF1, Encoding a Transcription Factor Involved in Cholesterol Homeostasis.
Topics: Alopecia; Arginine; Cholesterol; DNA Mutational Analysis; Female; Heterozygote; Humans; Keratosis; Lipid Metabolism; Male; Mucous Membrane; Mutation; Pedigree; Polymorphism, Single Nucleotide; Skin; Skin Abnormalities; Sterol Regulatory Element Binding Protein 1 | 2020 |
Normalization of hair growth in sparse fur-abnormal skin and hair (SPF-ASH) mice by introduction of the rat ornithine transcarbamylase (OTC) gene.
Topics: Animals; Arginine; Citrulline; Crosses, Genetic; Disease Models, Animal; Female; Genetic Linkage; Hair; Intestine, Small; Liver; Male; Mice; Mice, Inbred C57BL; Mice, Mutant Strains; Mice, Transgenic; Ornithine Carbamoyltransferase; Ornithine Carbamoyltransferase Deficiency Disease; Orotic Acid; Phenotype; Rats; Skin Abnormalities; X Chromosome | 1994 |