Molecular analysis of type II 3 beta-hydroxysteroid dehydrogenase gene in Japanese patients with classical 3 beta-hydroxysteroid dehydrogenase deficiency

Effects of scan parameters on the accuracies of iodine quantification and hounsfield unit values in dual layer dual-energy head and neck computed tomography: A phantom study conducted in a hospital in Japan.

Radiography (London, England : 1995)·2023

Development of a bioassay system for human growth hormone determination with close correlation to immunoassay.

Journal of clinical laboratory analysis·2012

Glycated albumin but not HbA1c reflects glycaemic control in patients with neonatal diabetes mellitus.

Diabetologia·2011

Growth of human pancreatic cancer cells, induced by human pancreatic phospholipase A(2), is mediated via its specific receptor but not via its catalytic property.

International journal of oncology·2011

Measurement of glycated hemoglobin and glycated albumin in umbilical cord: evaluation of the glycemic control indicators in neonates.

Journal of perinatology : official journal of the California Perinatal Association·2010

Partial paternal uniparental disomy of chromosome 6 in monozygotic twins with transient neonatal diabetes mellitus and macroglossia.

Clinical genetics·2010

Parkinson's disease-associated LRRK2 risk variant, G2385R, enhances Rab substrate phosphorylation and impairs neuronal integrity.

Human molecular genetics·2026

Pleiotropy and eQTL analysis identify shared genetic architecture of lipid traits in African-ancestry populations.

Human molecular genetics·2026

Multidisciplinary pathogenicity assessment of congenital hypothyroidism-associated SLC5A5 gene variants.

Human molecular genetics·2026

Molecular basis of mucopolysaccharidosis IVA in a large cohort: genotype-phenotype correlations and reporting of 12 novel GALNS variants.

Human molecular genetics·2026

Shared genetic architecture of schizophrenia and lupus identifies pleiotropic loci with distinct downstream mechanisms.

Human molecular genetics·2026

Motor dysfunction phenotypes in a drosophila model validate DAO as an ALS gene.

Human molecular genetics·2026

Mesenchymal stem cells in ribosomal insufficiency lead to aberrant osteoblastic differentiation and altered hematopoiesis.

Haematologica·2026

Association of Serum Magnesium, Insulin Resistance, and Atherogenic Dyslipidemia in Type 2 Diabetes Mellitus: A Cross-Sectional Analysis.

Annals of African medicine·2026

Intra-Individual Variability of Blood and Urinary Steroid Markers and the Response to Codeine Intake in Healthy Men and Women.

Drug testing and analysis·2026

Fat Embolism Syndrome as Cause of Death in a Multiorgan Donor With Successful Utilization of Thoracic and Abdominal Organs.

Transplantation proceedings·2026

Integrated Diagnostic and Mechanistic Profiling of Moyamoya and Intracranial Atherosclerotic Disease via Serum Metabolic Fingerprinting Based on SCs-ZIF-8@Au Nanomaterials.

ACS applied materials & interfaces·2026

Correlating metabolites, lipids, and N-glycans in murine kidney microstructures via integrative mass spectrometry imaging.

Nature communications·2026

Related Experiment Videos

Molecular analysis of type II 3 beta-hydroxysteroid dehydrogenase gene in Japanese patients with classical 3

Related Concept Videos

Effects of scan parameters on the accuracies of iodine quantification and hounsfield unit values in dual layer dual-energy head and neck computed tomography: A phantom study conducted in a hospital in Japan.

Development of a bioassay system for human growth hormone determination with close correlation to immunoassay.

Glycated albumin but not HbA1c reflects glycaemic control in patients with neonatal diabetes mellitus.

Growth of human pancreatic cancer cells, induced by human pancreatic phospholipase A(2), is mediated via its specific receptor but not via its catalytic property.

Measurement of glycated hemoglobin and glycated albumin in umbilical cord: evaluation of the glycemic control indicators in neonates.

Partial paternal uniparental disomy of chromosome 6 in monozygotic twins with transient neonatal diabetes mellitus and macroglossia.

Parkinson's disease-associated LRRK2 risk variant, G2385R, enhances Rab substrate phosphorylation and impairs neuronal integrity.

Pleiotropy and eQTL analysis identify shared genetic architecture of lipid traits in African-ancestry populations.

Multidisciplinary pathogenicity assessment of congenital hypothyroidism-associated SLC5A5 gene variants.

Molecular basis of mucopolysaccharidosis IVA in a large cohort: genotype-phenotype correlations and reporting of 12 novel GALNS variants.

Shared genetic architecture of schizophrenia and lupus identifies pleiotropic loci with distinct downstream mechanisms.

Motor dysfunction phenotypes in a drosophila model validate DAO as an ALS gene.

Mesenchymal stem cells in ribosomal insufficiency lead to aberrant osteoblastic differentiation and altered hematopoiesis.

Association of Serum Magnesium, Insulin Resistance, and Atherogenic Dyslipidemia in Type 2 Diabetes Mellitus: A Cross-Sectional Analysis.

Intra-Individual Variability of Blood and Urinary Steroid Markers and the Response to Codeine Intake in Healthy Men and Women.

Fat Embolism Syndrome as Cause of Death in a Multiorgan Donor With Successful Utilization of Thoracic and Abdominal Organs.

Integrated Diagnostic and Mechanistic Profiling of Moyamoya and Intracranial Atherosclerotic Disease via Serum Metabolic Fingerprinting Based on SCs-ZIF-8@Au Nanomaterials.

Correlating metabolites, lipids, and N-glycans in murine kidney microstructures via integrative mass spectrometry imaging.

Related Experiment Videos

Molecular analysis of type II 3 beta-hydroxysteroid dehydrogenase gene in Japanese patients with classical 3...

Related Concept Videos

Related Articles

Molecular analysis of type II 3 beta-hydroxysteroid dehydrogenase gene in Japanese patients with classical 3