Results 181 to 190 of about 35,670 (271)

An element regulating adrenal-specific steroid 21-hydroxylase expression is located within the slp gene.

, 1992
David S. Milstone, Sunil K. Shaw, K L Parker, Moshe Szyf, J G Seidman   +4 more
openalex   +1 more source

T Cell Responses to Steroid Cytochrome P450 21-Hydroxylase in Patients with Autoimmune Primary Adrenal Insufficiency [PDF]

, 2009
Eirik Bratland, Beate Skinningsrud, Dag E. Undlien, Edna Mozes, Eystein S. Husebye   +4 more
openalex   +1 more source

Common genetic variants of the human steroid 21-hydroxylase gene (CYP21A2) are related to differences in circulating hormone levels. [PDF]

PLoS One, 2014
Doleschall M, Szabó JA, Pázmándi J, Szilágyi Á, Koncz K, Farkas H, Tóth M, Igaz P, Gláz E, Prohászka Z, Korbonits M, Rácz K, Füst G, Patócs A.   +13 more
europepmc   +1 more source

Determination of 14 steroid hormones in amniotic fluid (AF): its usefulness in the antenatal diagnosis of 21-hydroxylase deficiency [PDF]

, 1981
Maguelone G. Forest, E de Peretti, Annick Lecoq, M David, J Bertrand   +4 more
openalex   +1 more source

Guidelines for Diagnosing Steroid 21-Hydroxylase Deficiency

Clinical Pediatric Endocrinology, 1999
Toyozo Umehashi, Masaru Fukushi, Satoshi Kusuda, Katsuhiko Tachibana, Seizo Suwa, Yoshio Igarashi, Sumitaka Saisho, Ichiro Yokota, Kenji Fujieda   +8 more
openaire   +2 more sources

Response to Letter to the Editor: "Congenital Adrenal Hyperplasia Due to Steroid 21-Hydroxylase Deficiency: An Endocrine Society Clinical Practice Guideline".

J Clin Endocrinol Metab, 2019
Speiser PW, Auchus RJ, Merke DP, Miller WL, White PC.   +4 more
europepmc   +1 more source

151 DIACNOSIS OF 21-HYDROXYLASE DEPFICIENCY (21-HD) BY DETERMINATION OF SALIVARY STEROIDS [PDF]

, 1988
B.J. Otten, Joop Rijken, C B A Stoelinga, Theo Benraad, J. L. Van den Brande   +4 more
openalex   +1 more source

Pro-453 to Ser mutation in CYP21 is associated with nonclassic steroid 21-hydroxylase deficiency. [PDF]

, 1992
David Owerbach, Lowell S. Sherman, A L Ballard, Ricardo Azziz   +3 more
openalex   +1 more source

Mutations of P450c21 (steroid 21-hydroxylase) at Cys428, Val281, and Ser268 result in complete, partial, or no loss of enzymatic activity, respectively. [PDF]

, 1991
Da Wu, Bon‐chu Chung
openalex   +1 more source

An Androgen Receptor Gene Mutation (E653K) in a Family with Congenital Adrenal Hyperplasia due to Steroid 21-Hydroxylase Deficiency as well as in Partial Androgen Insensitivity [PDF]

, 2002
Yvonne Lundberg Giwercman
openalex   +2 more sources