Compounds > isoleucine

isoleucine and Adrenal Hyperplasia, Congenital

isoleucine has been researched along with Adrenal Hyperplasia, Congenital in 3 studies

Research

Studies (3)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's2 (66.67)18.2507
2000's1 (33.33)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Ameglio, F; Capoluongo, E; Carrozza, C; Concolino, P; Corsello, S; Lovicu, RM; Minucci, A; Santini, SA; Santonocito, C; Zuppi, C1
Campbell, RD; Partanen, J1
Chiou, SH; Chung, BC; Hu, MC1

Other Studies

3 other study(ies) available for isoleucine and Adrenal Hyperplasia, Congenital

ArticleYear
First case of V281+I172N/V281L CYP21A2 genotype associated with congenital adrenal hyperplasia form. A case report from South Italy.
    Clinical biochemistry, 2007, Volume: 40, Issue:18

    Topics: Adrenal Hyperplasia, Congenital; Adult; Female; Genotype; Humans; Isoleucine; Italy; Male; Polymorphism, Genetic; Siblings; Steroid 21-Hydroxylase; Valine

2007
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