The nature and origin of the soluble protein in human amniotic fluid

The AS/AGU rat: a spontaneous model of disruption and degeneration in the nigrostriatal dopaminergic system.

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A novel homozygous nonsense mutations E135* in the type II 3beta-hydroxysteroid dehydrogenase gene in a girl with salt-losing congenital adrenal hyperplasia. Mutations in brief no. 168. Online.

Human mutation·2000

Phenotypic variability and origins of mutations in the gene encoding 3beta-hydroxysteroid dehydrogenase type II.

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Genomics·1999

Local cerebral glucose utilization in the AS/AGU rat: a mutant with movement disorders.

The European journal of neuroscience·1998

Glucocorticoid receptor polymorphism in genetic hypertension.

Journal of molecular endocrinology·1998

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Biological reviews of the Cambridge Philosophical Society·2026

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Hot and cold deserts as eco-evolutionary arenas for understanding plant resistance to multiple abiotic stressors.

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A global meta-analysis of non-lethal mammal browsing control in forests.

Biological reviews of the Cambridge Philosophical Society·2026

Land birds on atolls: diversity, origin, and function.

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Beyond bulk physics: Interfacial and confinement effects in aqueous microdroplets.

Reports on progress in physics. Physical Society (Great Britain)·2026

Asymmetric post-equilibrium displacement between Congo Red and Alizarin Red S reveals secondary-release risk during competitive adsorption.

Journal of hazardous materials·2026

Reversible Cystine Disulfide Scaffolding Enables Carbonyl Sulfide-Mediated Intramolecular Peptide Bond Formation via Cyclocystine: Implications for Prebiotic Chemistry.

Chemistry (Weinheim an der Bergstrasse, Germany)·2026

CFD-DEM Investigation of Spout Stabilization by Large-Particle Addition.

ACS omega·2026

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ACS omega·2026

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Chemical science·2026

Related Experiment Videos

The nature and origin of the soluble protein in human amniotic fluid

Related Concept Videos

The AS/AGU rat: a spontaneous model of disruption and degeneration in the nigrostriatal dopaminergic system.

A novel homozygous nonsense mutations E135* in the type II 3beta-hydroxysteroid dehydrogenase gene in a girl with salt-losing congenital adrenal hyperplasia. Mutations in brief no. 168. Online.

Phenotypic variability and origins of mutations in the gene encoding 3beta-hydroxysteroid dehydrogenase type II.

Cloning, expression, and physical mapping of the 3beta-hydroxysteroid dehydrogenase gene cluster (HSD3BP1-HSD3BP5) in human.

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Reversible Cystine Disulfide Scaffolding Enables Carbonyl Sulfide-Mediated Intramolecular Peptide Bond Formation via Cyclocystine: Implications for Prebiotic Chemistry.

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The nature and origin of the soluble protein in human amniotic fluid

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