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Mihail Sadoveanu Neamul Soimarestilor 11.pdf


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www.publiciatii.ro/categoria/mihail-sadoveanu-neamul-soimarestilor Category:Romanian writers Category:1947 births Category:1996 deaths Category:Romanian essayists Category:Romanian journalists Category:Romanian novelists Category:Romanian dramatists and playwrights Category:Romanian translators Category:Romanian satirists Category:20th-century novelists Category:20th-century essayists Category:20th-century Romanian dramatists and playwrightsCYP21A2 polymorphisms in Indian patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency. P450 cholesterol side-chain cleavage (P450scc) deficiency is one of the causes of congenital adrenal hyperplasia. P450c21 is the enzyme that converts cholesterol to pregnenolone in the adrenal cortex. 21-hydroxylase deficiency is characterized by reduced adrenal steroidogenesis due to impairment in the 21-hydroxylase enzyme. We have studied the CYP21A2 gene for the IVS2n+1G>A (T293-->C) polymorphism in a population of 90 Indian children with salt-losing congenital adrenal hyperplasia due to 21-hydroxylase deficiency. The wild-type homozygote has been shown to be associated with a salt-losing form of the disease. The IVS2n+1G>A polymorphism was found to be absent in this population. In addition to this, a newly discovered single nucleotide polymorphism (SNP), 5'GATA in the gene promoter region, was found in all the patients, whereas this SNP was not present in the wild-type population. The SNP 5'GATA could be used to confirm the diagnosis of 21-hydroxylase deficiency and to identify the molecular defect in cases of congenital adrenal hyperplasia with no history of treatment or no response to treatment.Q: Slidify element from hidden to visible, using a timer I have the following layout for my web page: The




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Mihail Sadoveanu Neamul Soimarestilor 11.pdf

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