alanine has been researched along with Hypergonadotropic Hypogonadism in 3 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.
| Excerpt | Relevance | Reference |
|---|---|---|
| "Reifenstein syndrome is an eponymic term that describes partial androgen-insensitive disorders." | 5.29 | A mutant androgen receptor from patients with Reifenstein syndrome: identification of the function of a conserved alanine residue in the D box of steroid receptors. ( Cato, AC; Denninger, A; Kaspar, F; Klocker, H, 1993) |
| "The affected kindred displays severe hypogonadotropic hypogonadism." | 1.32 | Mutation Ala(171)Thr stabilizes the gonadotropin-releasing hormone receptor in its inactive conformation, causing familial hypogonadotropic hypogonadism. ( de Roux, N; Karges, B; Karges, W; Kühne, R; Ludwig, L; Milgrom, E; Mine, M, 2003) |
| "He had a complete form of idiopathic hypogonadotropic hypogonadism, with descended testes and severe oligospermia but little response to exogenous gonadotropins." | 1.31 | Clinical phenotype and infertility treatment in a male with hypogonadotropic hypogonadism due to mutations Ala129Asp/Arg262Gln of the gonadotropin-releasing hormone receptor. ( Cohen, DP; Layman, LC; Smith, GD; Xie, J, 2002) |
| "Reifenstein syndrome is an eponymic term that describes partial androgen-insensitive disorders." | 1.29 | A mutant androgen receptor from patients with Reifenstein syndrome: identification of the function of a conserved alanine residue in the D box of steroid receptors. ( Cato, AC; Denninger, A; Kaspar, F; Klocker, H, 1993) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 1 (33.33) | 18.2507 |
| 2000's | 2 (66.67) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Layman, LC | 1 |
| Cohen, DP | 1 |
| Xie, J | 1 |
| Smith, GD | 1 |
| Karges, B | 1 |
| Karges, W | 1 |
| Mine, M | 1 |
| Ludwig, L | 1 |
| Kühne, R | 1 |
| Milgrom, E | 1 |
| de Roux, N | 1 |
| Kaspar, F | 1 |
| Klocker, H | 1 |
| Denninger, A | 1 |
| Cato, AC | 1 |
3 other studies available for alanine and Hypergonadotropic Hypogonadism
| Article | Year |
|---|---|
Clinical phenotype and infertility treatment in a male with hypogonadotropic hypogonadism due to mutations Ala129Asp/Arg262Gln of the gonadotropin-releasing hormone receptor.
Topics: Adult; Alanine; Arginine; Aspartic Acid; Chorionic Gonadotropin; Follicle Stimulating Hormone; Genot | 2002 |
Mutation Ala(171)Thr stabilizes the gonadotropin-releasing hormone receptor in its inactive conformation, causing familial hypogonadotropic hypogonadism.
Topics: Adult; Alanine; Binding Sites; Cell Line; Embryo, Mammalian; Gene Expression; Humans; Hydrogen Bondi | 2003 |
A mutant androgen receptor from patients with Reifenstein syndrome: identification of the function of a conserved alanine residue in the D box of steroid receptors.
Topics: Alanine; Amino Acid Sequence; Animals; Base Sequence; Binding Sites; Conserved Sequence; DNA; Humans | 1993 |