arginine has been researched along with Hair Diseases in 4 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 2 (50.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (25.00) | 29.6817 |
| 2010's | 1 (25.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| de Theije, C; Harding, HP; Köhler, SE; Lamers, MC; Lamers, WH; Lindsey, P; Marion, V; Ron, D; Sankaranarayanan, S; van Dijk, P | 1 |
| Ahmad, W; Leal, SM; Lee, K; Naeem, M; Wajid, M | 1 |
| Barrie, H; Cream, JJ; Phillips, ME | 1 |
| Potter, JL; Silvidi, AA; Timmons, GD | 1 |
4 other study(ies) available for arginine and Hair Diseases
| Article | Year |
|---|---|
Arginine deficiency causes runting in the suckling period by selectively activating the stress kinase GCN2.
Topics: Amino Acid Metabolism, Inborn Errors; Animals; Animals, Suckling; Arginase; Arginine; B-Lymphocytes; Growth Hormone; Hair Diseases; Hypoglycemia; Insulin-Like Growth Factor I; Mechanistic Target of Rapamycin Complex 1; Mice; Mice, Knockout; Multiprotein Complexes; Muscular Diseases; Protein Serine-Threonine Kinases; Proteins; Signal Transduction; Syndrome; TOR Serine-Threonine Kinases | 2011 |
A mutation in the hair matrix and cuticle keratin KRTHB5 gene causes ectodermal dysplasia of hair and nail type.
Topics: Arginine; Chromosome Mapping; Chromosomes, Human, Pair 16; Conserved Sequence; Ectodermal Dysplasia; Hair Diseases; Homozygote; Humans; Keratins; Keratins, Hair-Specific; Keratins, Type II; Microsatellite Repeats; Mutation, Missense; Nail Diseases | 2006 |
Arginosuccinic aciduria with pili torti.
Topics: Amino Acid Metabolism, Inborn Errors; Arginine; Argininosuccinic Acid; Female; Hair Diseases; Humans; Infant | 1981 |
Argininosuccinicaciduria: the hair abnormality revisited.
Topics: Amino Acids; Arginine; Argininosuccinic Acid; Child; Cystine; Female; Hair; Hair Diseases; Humans; Renal Aminoacidurias | 1980 |