asparagine and Congenital Adrenal Hyperplasia

asparagine has been researched along with Congenital Adrenal Hyperplasia in 3 studies

Research

Studies (3)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	2 (66.67)	18.2507
2000's	1 (33.33)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Balogh, K; Belema, B; Bertalan, R; Borgulya, G; Fekete, G; Gergics, P; Gláz, E; Luczay, A; Majnik, J; Nagy, ZZ; Németh, J; Patócs, A; Rácz, K; Sereg, M; Sólyom, J; Szabó, V; Szappanos, A; Toke, J; Török, D; Tóth, M; Tulassay, Z	1
Campbell, RD; Partanen, J	1
Chiou, SH; Chung, BC; Hu, MC	1

Reviews

1 review(s) available for asparagine and Congenital Adrenal Hyperplasia

Article	Year
[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; Glucocorticoids; Humans; Lasers, Excimer; Male; Mutation; Ocular Hypertension; Phenotype; Photorefractive Keratectomy; Polymorphism, Genetic; Protein Isoforms; Receptors, Glucocorticoid; Retrospective Studies; Serine	2006

Article

Year

[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; Glucocorticoids; Humans; Lasers, Excimer; Male; Mutation; Ocular Hypertension; Phenotype; Photorefractive Keratectomy; Polymorphism, Genetic; Protein Isoforms; Receptors, Glucocorticoid; Retrospective Studies; Serine

2006

Other Studies

2 other study(ies) available for asparagine and Congenital Adrenal Hyperplasia

Article	Year
Substitution of Ile-172 to Asn in the steroid 21-hydroxylase B (P450c21B) gene in a Finnish patient with the simple virilizing form of congenital adrenal hyperplasia. Human genetics, 1991, Volume: 87, Issue:6 Topics: Adrenal Hyperplasia, Congenital; Asparagine; Base Sequence; Child; Cloning, Molecular; DNA; Finland; Humans; Isoleucine; Male; Molecular Sequence Data; Mutation; Polymerase Chain Reaction; Steroid 21-Hydroxylase	1991
A missense mutation at Ile172----Asn or Arg356----Trp causes steroid 21-hydroxylase deficiency. The Journal of biological chemistry, 1990, Feb-25, Volume: 265, Issue:6 Topics: Adolescent; Adrenal Hyperplasia, Congenital; Arginine; Asparagine; Base Sequence; Codon; DNA; Female; Genes; Humans; Isoleucine; Molecular Sequence Data; Mutation; Oligonucleotide Probes; Plasmids; Reference Values; Restriction Mapping; Steroid 21-Hydroxylase; Steroid Hydroxylases; Transfection; Tryptophan	1990

Article

Year

Substitution of Ile-172 to Asn in the steroid 21-hydroxylase B (P450c21B) gene in a Finnish patient with the simple virilizing form of congenital adrenal hyperplasia.

Human genetics, 1991, Volume: 87, Issue:6

Topics: Adrenal Hyperplasia, Congenital; Asparagine; Base Sequence; Child; Cloning, Molecular; DNA; Finland; Humans; Isoleucine; Male; Molecular Sequence Data; Mutation; Polymerase Chain Reaction; Steroid 21-Hydroxylase

1991

A missense mutation at Ile172----Asn or Arg356----Trp causes steroid 21-hydroxylase deficiency.

The Journal of biological chemistry, 1990, Feb-25, Volume: 265, Issue:6

Topics: Adolescent; Adrenal Hyperplasia, Congenital; Arginine; Asparagine; Base Sequence; Codon; DNA; Female; Genes; Humans; Isoleucine; Molecular Sequence Data; Mutation; Oligonucleotide Probes; Plasmids; Reference Values; Restriction Mapping; Steroid 21-Hydroxylase; Steroid Hydroxylases; Transfection; Tryptophan

1990