نتایج جستجو برای: 17α

تعداد نتایج: 979  

Journal: :Biochemistry 2014
Piotr J Mak Michael C Gregory Stephen G Sligar James R Kincaid

An important function of steroidogenic cytochromes P450 is the transformation of cholesterol to produce androgens, estrogens, and the corticosteroids. The activities of cytochrome P450c17 (CYP17) are essential in sex hormone biosynthesis, with severe developmental defects being a consequence of deficiency or mutations. The first reaction catalyzed by this multifunctional P450 is the 17α-hydroxy...

2002
Shao-Hung Yen Hung-Te Chen

Background: 17α-hydroxylase deficiency is a rare cause of congenital adrenal hyperplasia and endocrine hypertension. Only around 124 cases were reported in literature. Case: A 35-year-old Taiwanese female presented with severe hypertension (220/130 mmHg), absence of secondary sexual characteristics and primary amenorrhea. Chromosome study revealed 46XX karyotye. The laboratory data revealed hyp...

2013
Seong-Rip Oh Hyeong-Cheol Kang Chi-Hoon Lee Sang-Woo Hur Young-Don Lee

To understand the sex reversal characteristics in the longtooth grouper (Epinephelus bruneus), this study examined the sex reversal and artificial masculinization of wild caught E. bruneus reared in indoor rearing tank after a 17α-methyltestosterone injection. To domesticate a broodstock, 64 wild caught E. bruneus, between 47.0 to 110.0 cm in total length and from 1.5 to 21.4 kg in body weight,...

2016
Hajar Azarin Mohammad Reza Imanpour Mohammad Sadegh Aramli

The in vitro effect of 17α, 20β-Dihydroxyprogesterone on the maturation of Persian sturgeon (Acipenser persicus) oocytes for 7, 10, 12, 24 and 30th hours of incubation were investigated. Blood serum, testosterone (T), progesterone (P4) and 17-β estradiol concentrations were measured using enzyme-linked immuno-sorbent assay (ELISA). The oocytes were incubated in SIS, RM2, L-15 and PSACF media in...

Journal: :Genetics and molecular research : GMR 2015
H Xiao H Zhang T Li D Wu L T Qin T Wang B Zhang S X Liao

We determined whether a child with 17α-hydroxylase/17, 20-lyase deficiency possessed the sex-determining region (SRY) gene, and examined the mutations present in the CYP17A1 gene that led to 17α-hydroxylase/17, 20-lyase deficiency. In the child, karyotype analysis was performed and polymerase chain reaction analysis and electrophoretic techniques were used to identify the SRY gene. A total of 5...

2015
Poonam Singh Sanjeev Kumar Jain

Background: Antepartum hemorrhage and placenta previa effects majority of pregnant women endangering their life both maternal and fetal. Symptomatic placenta previa are being treated with tocolytic agents. Progesterone is the most common used drug for the preservation of pregnancy and aids in the extension of pregnancy. Materials and Methods: A 80 patients were randomly assigned to two groups u...

2011
Daw-Yang Hwang Chi-Chih Hung Felix G. Riepe Richard J. Auchus Alexandra E. Kulle Paul-Martin Holterhus Mei-Chyn Chao Mei-Chuan Kuo Shang-Jyh Hwang Hung-Chun Chen

17α-Hydroxylase/17, 20-lyase deficiency (17OHD) is an autosomal recessive disease causing congenital adrenal hyperplasia and a rare cause of hypertension with hypokalemia. The CYP17A1 gene mutation leads to 17OHD and its clinical features. We described an 18 y/o female with clinical features of 17α-hydroxylase/17, 20-lyase deficiency and characterized the functional consequences of an intronic ...

Journal: :Arquivos brasileiros de endocrinologia e metabologia 2010
Daiane Rodrigues Barbosa Belgini Maricilda Palandi de Mello Maria Tereza Matias Baptista Daniel Minutti de Oliveira Fernanda Canova Denardi Heraldo Mendes Garmes Oswaldo da Rocha Grassiotto Cristina Laguna Benetti Pinto Antonia Paula Marques-de-Faria Andréa Trevas Maciel-Guerra Gil Guerra-Júnior

In 2004, Costa-Santos and cols. reported 24 patients from 19 Brazilian families with 17α-hydroxylase deficiency and showed that p.W406R and p.R362C corresponded to 50% and 32% of CYP17A1 mutant alleles, respectively. The present report describes clinical and molecular data of six patients from three inbred Brazilian families with 17α-hydroxlyse deficiency. All patients had hypogonadism, amenorr...

Journal: :The American journal of physiology 1997
Shayla L Waters Gary W Miller Michael D Aleo Rick G Schnellmann

Diverse γ-aminobutyric acid (GABAA) receptor modulators exhibited novel cytoprotective effects and mechanisms of action in rabbit renal proximal tubules subjected to mitochondrial inhibition (antimycin A) or hypoxia. Cytoprotective potencies (50% effective concentration, EC50) were 0.3 nM allopregnanolone (AP) > 0.4 nM 17α-OH-allopregnanolone (17α-OH-AP) > 30 nM dehydroepiandrosterone sulfate (...

1996
William L. Gale Martin S. Fitzpatrick Carl B. Schreck

One of the most common techniques for producing mono-sex populations is steroid-induced sex inversion. This involves the administration of synthetic androgens (to produce male populations) or estrogens (to produce female populations). Several methods of steroid administration are possible, including injection, microencapsulation, feeding of steroid, and immersion of fry in steroid solutions. Th...

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