Components of the heme biosynthetic pathway and mixed function oxidase activity in human fetal tissues

Idiopathic precocious puberty in girls: Psychosexual development.

Journal of youth and adolescence·2013

Erroneous prenatal diagnosis of congenital adrenal hyperplasia owing to a duplication of the CYP21A2 gene.

Journal of perinatology : official journal of the California Perinatal Association·2012

Pregnancy outcomes in women with classical congenital adrenal hyperplasia due to 21-hydroxylase deficiency.

Journal of pediatric endocrinology & metabolism : JPEM·2005

Update on the prenatal diagnosis and treatment of congenital adrenal hyperplasia due to 11beta-hydroxylase deficiency.

Journal of pediatric endocrinology & metabolism : JPEM·2005

The natural history and genotype-phenotype nonconcordance of HLA identical siblings with the same mutations of the 21-hydroxylase gene.

Journal of pediatric endocrinology & metabolism : JPEM·2005

A novel semiquantitative polymerase chain reaction/enzyme digestion-based method for detection of large scale deletions/conversions of the CYP21 gene and mutation screening in Turkish families with 21-hydroxylase deficiency.

The Journal of clinical endocrinology and metabolism·2003

Wogonoside: Pharmacology, molecular targets and therapeutic potential.

Biochemical pharmacology·2026

Mammalian nitrate transport: emerging roles of sialin, chloride channels, aquaporin-6, and the sodium-iodide symporter.

Biochemical pharmacology·2026

Disruption of gut bacteria-derived hydrogen sulfide signaling mediates antibacterial-induced acute anorexia.

Biochemical pharmacology·2026

One ligand, multiple fates: the multi-receptor signaling network of FSTL1 and receptor-selective intervention strategies.

Biochemical pharmacology·2026

Drug failure in diabetic kidney disease: translational barriers, target validation and trial de-risking strategies.

Biochemical pharmacology·2026

Fetuin-A improves knee osteoarthritis by regulating macrophage PD-1 expression to balance M1/M2 polarization.

Biochemical pharmacology·2026

Isotopic Tracing of [13C6]scyllo-Inositol Uncovers Its Incorporation into Phosphatidylinositols in Immortalized Mammalian Cells.

ACS chemical biology·2026

Association Between Serum Ferritin and Glycated Hemoglobin: Experience From the Biochemistry Laboratory of Mohammed VI University Hospital, Oujda.

Cureus·2026

Insights into vitamin C in musculoskeletal physiology and disorders: mechanisms and translational perspectives.

Frontiers in immunology·2026

6-Aminoquinoline/2,5-Dihydroxybenzoic Acid: A Novel Binary Matrix for Enhanced Detection of Monosaccharides and Oligosaccharides in Tissues by MALDI-MSI.

Analytical chemistry·2026

An H2O2-Aldehyde Dehydrogenase 2-Malondialdehyde Axis Underlies Mitochondrial Viscosity Elevation in Hepatic Ischemia-Reperfusion Injury.

Analytical chemistry·2026

[Lithium-induced electrolyte disturbances and catatonia].

Ugeskrift for laeger·2026

Related Experiment Videos

Components of the heme biosynthetic pathway and mixed function oxidase activity in human fetal tissues

Related Concept Videos

Idiopathic precocious puberty in girls: Psychosexual development.

Erroneous prenatal diagnosis of congenital adrenal hyperplasia owing to a duplication of the CYP21A2 gene.

Pregnancy outcomes in women with classical congenital adrenal hyperplasia due to 21-hydroxylase deficiency.

Update on the prenatal diagnosis and treatment of congenital adrenal hyperplasia due to 11beta-hydroxylase deficiency.

The natural history and genotype-phenotype nonconcordance of HLA identical siblings with the same mutations of the 21-hydroxylase gene.

A novel semiquantitative polymerase chain reaction/enzyme digestion-based method for detection of large scale deletions/conversions of the CYP21 gene and mutation screening in Turkish families with 21-hydroxylase deficiency.

Wogonoside: Pharmacology, molecular targets and therapeutic potential.

Mammalian nitrate transport: emerging roles of sialin, chloride channels, aquaporin-6, and the sodium-iodide symporter.

Disruption of gut bacteria-derived hydrogen sulfide signaling mediates antibacterial-induced acute anorexia.

One ligand, multiple fates: the multi-receptor signaling network of FSTL1 and receptor-selective intervention strategies.

Drug failure in diabetic kidney disease: translational barriers, target validation and trial de-risking strategies.

Fetuin-A improves knee osteoarthritis by regulating macrophage PD-1 expression to balance M1/M2 polarization.

Isotopic Tracing of [13C6]scyllo-Inositol Uncovers Its Incorporation into Phosphatidylinositols in Immortalized Mammalian Cells.

Association Between Serum Ferritin and Glycated Hemoglobin: Experience From the Biochemistry Laboratory of Mohammed VI University Hospital, Oujda.

Insights into vitamin C in musculoskeletal physiology and disorders: mechanisms and translational perspectives.

6-Aminoquinoline/2,5-Dihydroxybenzoic Acid: A Novel Binary Matrix for Enhanced Detection of Monosaccharides and Oligosaccharides in Tissues by MALDI-MSI.

An H2O2-Aldehyde Dehydrogenase 2-Malondialdehyde Axis Underlies Mitochondrial Viscosity Elevation in Hepatic Ischemia-Reperfusion Injury.

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Components of the heme biosynthetic pathway and mixed function oxidase activity in human fetal tissues

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