alanine has been researched along with Disorders of Sex Development in 1 studies
Alanine: A non-essential amino acid that occurs in high levels in its free state in plasma. It is produced from pyruvate by transamination. It is involved in sugar and acid metabolism, increases IMMUNITY, and provides energy for muscle tissue, BRAIN, and the CENTRAL NERVOUS SYSTEM.
alanine : An alpha-amino acid that consists of propionic acid bearing an amino substituent at position 2.
Disorders of Sex Development: In gonochoristic organisms, congenital conditions in which development of chromosomal, gonadal, or anatomical sex is atypical. Effects from exposure to abnormal levels of GONADAL HORMONES in the maternal environment, or disruption of the function of those hormones by ENDOCRINE DISRUPTORS are included.
| Excerpt | Relevance | Reference |
|---|---|---|
| "This disease is a rare form of male pseudohermaphroditism with virilization during puberty." | 1.30 | Homozygous mutation (A228T) in the 5alpha-reductase type 2 gene in a boy with 5alpha-reductase deficiency: genotype-phenotype correlations. ( Aagenaes, O; Knudtzon, J; Magnus, O; Nordenskjöld, A, 1998) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 1 (100.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Nordenskjöld, A | 1 |
| Magnus, O | 1 |
| Aagenaes, O | 1 |
| Knudtzon, J | 1 |
1 other study available for alanine and Disorders of Sex Development
| Article | Year |
|---|---|
Homozygous mutation (A228T) in the 5alpha-reductase type 2 gene in a boy with 5alpha-reductase deficiency: genotype-phenotype correlations.
Topics: Adolescent; Alanine; Cholestenone 5 alpha-Reductase; Disorders of Sex Development; Female; Genotype; | 1998 |