Compounds > 17-alpha-hydroxyprogesterone
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17-alpha-hydroxyprogesterone and Genetic Predisposition

17-alpha-hydroxyprogesterone has been researched along with Genetic Predisposition in 4 studies

Research

Studies (4)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's1 (25.00)29.6817
2010's3 (75.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Brauner, R; David, M; Lecointre, C; Lienhardt-Roussie, A; Menassa, R; Morel, Y; Sulmont, V; Tardy, V1
Biason-Lauber, A; Gueorguieva, I; Lebon-Labich, B; Paris, F; Philibert, P; Pienkowski, C; Stuckens, C; Sultan, C1
Ambroziak, U; Bablok, L; Bar-Andziak, E; Bednarczuk, T; Ginalska-Malinowska, M; Grzechocińska, B; Kamiński, P; Małunowicz, EM; Przedlacki, J1
Day, NE; Dowsett, M; Dunning, AM; Easton, DF; Folkerd, E; Healey, CS; Kelemen, L; Luben, RN; Novik, KL; Ogata, S; Pharoah, PD; Ponder, BA; Tee, L1

Other Studies

4 other study(ies) available for 17-alpha-hydroxyprogesterone and Genetic Predisposition

ArticleYear
Phenotype-genotype correlations of 13 rare CYP21A2 mutations detected in 46 patients affected with 21-hydroxylase deficiency and in one carrier.
    The Journal of clinical endocrinology and metabolism, 2010, Volume: 95, Issue:3

    Topics: 17-alpha-Hydroxyprogesterone; Adrenal Hyperplasia, Congenital; Animals; Blotting, Western; Cells, Cultured; Chlorocebus aethiops; COS Cells; Genetic Association Studies; Genetic Predisposition to Disease; Humans; Mutation; Phenotype; Protein Conformation; Steroid 21-Hydroxylase; Time Factors

2010
Molecular analysis of WNT4 gene in four adolescent girls with mullerian duct abnormality and hyperandrogenism (atypical Mayer-Rokitansky-Küster-Hauser syndrome).
    Fertility and sterility, 2011, Jun-30, Volume: 95, Issue:8

    Topics: 17-alpha-Hydroxyprogesterone; 46, XX Disorders of Sex Development; Abnormalities, Multiple; Adolescent; Androstenedione; beta Catenin; Cell Line, Tumor; Congenital Abnormalities; Dehydroepiandrosterone; DNA Mutational Analysis; Female; Genetic Predisposition to Disease; Heterozygote; Humans; Hyperandrogenism; Kidney; Mullerian Ducts; Mutation; Ovary; Phenotype; Progesterone Reductase; RNA, Messenger; Somites; Spine; Steroid 17-alpha-Hydroxylase; Transfection; Uterus; Vagina; Wnt Proteins; Wnt4 Protein; Young Adult

2011
[Congenital adrenal hyperplasia due to 21-hydroxylase deficiency--management in adults].
    Endokrynologia Polska, 2010, Volume: 61 Suppl 1

    Topics: 17-alpha-Hydroxyprogesterone; Adolescent; Adrenal Hyperplasia, Congenital; Adult; Aged; Androstenedione; Female; Genetic Predisposition to Disease; Genotype; Glucocorticoids; Humans; Male; Middle Aged; Phenotype; Quality of Life; Steroid 21-Hydroxylase; Young Adult

2010
Polymorphisms associated with circulating sex hormone levels in postmenopausal women.
    Journal of the National Cancer Institute, 2004, Jun-16, Volume: 96, Issue:12

    Topics: 17-alpha-Hydroxyprogesterone; Aged; Androstenedione; Aromatase; Aryl Hydrocarbon Hydroxylases; Breast Neoplasms; Case-Control Studies; Catechol O-Methyltransferase; Cytochrome P-450 CYP1B1; England; Estradiol; Estrone; Female; Genetic Predisposition to Disease; Genetic Variation; Genotype; Gonadal Steroid Hormones; Humans; Linear Models; Middle Aged; Odds Ratio; Polymorphism, Single Nucleotide; Postmenopause; Sex Hormone-Binding Globulin; Steroid 17-alpha-Hydroxylase; Testosterone

2004