serine has been researched along with Adrenal Hyperplasia, Congenital in 7 studies
Serine: A non-essential amino acid occurring in natural form as the L-isomer. It is synthesized from GLYCINE or THREONINE. It is involved in the biosynthesis of PURINES; PYRIMIDINES; and other amino acids.
serine : An alpha-amino acid that is alanine substituted at position 3 by a hydroxy group.
Adrenal Hyperplasia, Congenital: A group of inherited disorders of the ADRENAL GLANDS, caused by enzyme defects in the synthesis of cortisol (HYDROCORTISONE) and/or ALDOSTERONE leading to accumulation of precursors for ANDROGENS. Depending on the hormone imbalance, congenital adrenal hyperplasia can be classified as salt-wasting, hypertensive, virilizing, or feminizing. Defects in STEROID 21-HYDROXYLASE; STEROID 11-BETA-HYDROXYLASE; STEROID 17-ALPHA-HYDROXYLASE; 3-beta-hydroxysteroid dehydrogenase (3-HYDROXYSTEROID DEHYDROGENASES); TESTOSTERONE 5-ALPHA-REDUCTASE; or steroidogenic acute regulatory protein; among others, underlie these disorders.
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 3 (42.86) | 18.2507 |
| 2000's | 4 (57.14) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Miller, WL | 4 |
| Barbaro, M | 1 |
| Lajic, S | 1 |
| Baldazzi, L | 1 |
| Balsamo, A | 1 |
| Pirazzoli, P | 1 |
| Cicognani, A | 1 |
| Wedell, A | 1 |
| Cacciari, E | 1 |
| Majnik, J | 1 |
| Patócs, A | 1 |
| Balogh, K | 1 |
| Luczay, A | 1 |
| Török, D | 1 |
| Szabó, V | 1 |
| Borgulya, G | 1 |
| Gergics, P | 1 |
| Szappanos, A | 1 |
| Bertalan, R | 1 |
| Belema, B | 1 |
| Toke, J | 1 |
| Sereg, M | 1 |
| Nagy, ZZ | 1 |
| Sólyom, J | 1 |
| Tóth, M | 1 |
| Gláz, E | 1 |
| Rácz, K | 1 |
| Németh, J | 1 |
| Fekete, G | 1 |
| Tulassay, Z | 1 |
| Auchus, RJ | 1 |
| Geller, DH | 1 |
| Owerbach, D | 1 |
| Sherman, L | 1 |
| Ballard, AL | 1 |
| Azziz, R | 1 |
| Lin, D | 1 |
| Harikrishna, JA | 1 |
| Moore, CC | 1 |
| Jones, KL | 1 |
4 reviews available for serine and Adrenal Hyperplasia, Congenital
| Article | Year |
|---|---|
Androgen biosynthesis from cholesterol to DHEA.
Topics: Adrenal Glands; Adrenal Hyperplasia, Congenital; Androgens; Animals; Cholesterol; Cholesterol Side-C | 2002 |
Disorders of androgen synthesis--from cholesterol to dehydroepiandrosterone.
Topics: Adrenal Cortex; Adrenal Hyperplasia, Congenital; Androgens; Cholesterol; Cholesterol Side-Chain Clea | 2005 |
[Nucleotide sequence variants of the glucocorticoid receptor gene and their significance in determining glucocorticoid sensitivity].
Topics: Adenoma; Adrenal Gland Neoplasms; Adrenal Hyperplasia, Congenital; Asparagine; Base Sequence; Female | 2006 |
The regulation of 17,20 lyase activity.
Topics: Adrenal Hyperplasia, Congenital; Amino Acid Sequence; Animals; Binding Sites; Cytochrome P-450 Enzym | 1997 |
3 other studies available for serine and Adrenal Hyperplasia, Congenital
| Article | Year |
|---|---|
Functional analysis of two recurrent amino acid substitutions in the CYP21 gene from Italian patients with congenital adrenal hyperplasia.
Topics: Adolescent; Adrenal Hyperplasia, Congenital; Amino Acid Substitution; Animals; Child; Child, Prescho | 2004 |
Pro-453 to Ser mutation in CYP21 is associated with nonclassic steroid 21-hydroxylase deficiency.
Topics: Adrenal Hyperplasia, Congenital; Base Sequence; DNA; Female; Humans; Molecular Sequence Data; Point | 1992 |
Missense mutation serine106----proline causes 17 alpha-hydroxylase deficiency.
Topics: Adolescent; Adrenal Hyperplasia, Congenital; Alleles; Base Sequence; Blotting, Northern; Blotting, S | 1991 |