Page last updated: 2024-11-08

serine and Adrenal Hyperplasia, Congenital

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.

Research

Studies (7)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's3 (42.86)18.2507
2000's4 (57.14)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Miller, WL4
Barbaro, M1
Lajic, S1
Baldazzi, L1
Balsamo, A1
Pirazzoli, P1
Cicognani, A1
Wedell, A1
Cacciari, E1
Majnik, J1
Patócs, A1
Balogh, K1
Luczay, A1
Török, D1
Szabó, V1
Borgulya, G1
Gergics, P1
Szappanos, A1
Bertalan, R1
Belema, B1
Toke, J1
Sereg, M1
Nagy, ZZ1
Sólyom, J1
Tóth, M1
Gláz, E1
Rácz, K1
Németh, J1
Fekete, G1
Tulassay, Z1
Auchus, RJ1
Geller, DH1
Owerbach, D1
Sherman, L1
Ballard, AL1
Azziz, R1
Lin, D1
Harikrishna, JA1
Moore, CC1
Jones, KL1

Reviews

4 reviews available for serine and Adrenal Hyperplasia, Congenital

ArticleYear
Androgen biosynthesis from cholesterol to DHEA.
    Molecular and cellular endocrinology, 2002, Dec-30, Volume: 198, Issue:1-2

    Topics: Adrenal Glands; Adrenal Hyperplasia, Congenital; Androgens; Animals; Cholesterol; Cholesterol Side-C

2002
Disorders of androgen synthesis--from cholesterol to dehydroepiandrosterone.
    Medical principles and practice : international journal of the Kuwait University, Health Science Centre, 2005, Volume: 14 Suppl 1

    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].
    Orvosi hetilap, 2006, Nov-05, Volume: 147, Issue:44

    Topics: Adenoma; Adrenal Gland Neoplasms; Adrenal Hyperplasia, Congenital; Asparagine; Base Sequence; Female

2006
The regulation of 17,20 lyase activity.
    Steroids, 1997, Volume: 62, Issue:1

    Topics: Adrenal Hyperplasia, Congenital; Amino Acid Sequence; Animals; Binding Sites; Cytochrome P-450 Enzym

1997

Other Studies

3 other studies available for serine and Adrenal Hyperplasia, Congenital

ArticleYear
Functional analysis of two recurrent amino acid substitutions in the CYP21 gene from Italian patients with congenital adrenal hyperplasia.
    The Journal of clinical endocrinology and metabolism, 2004, Volume: 89, Issue:5

    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.
    Molecular endocrinology (Baltimore, Md.), 1992, Volume: 6, Issue:8

    Topics: Adrenal Hyperplasia, Congenital; Base Sequence; DNA; Female; Humans; Molecular Sequence Data; Point

1992
Missense mutation serine106----proline causes 17 alpha-hydroxylase deficiency.
    The Journal of biological chemistry, 1991, Aug-25, Volume: 266, Issue:24

    Topics: Adolescent; Adrenal Hyperplasia, Congenital; Alleles; Base Sequence; Blotting, Northern; Blotting, S

1991