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Research 31–60 of 1000+
- Correction of ornithine transcarbamylase (OTC) deficiency in spf‐ash mice by introduction of rat OTC gene
- Ocular aspects in biotinidase deficiency Clinical and genetic original studies
- OsUEV1B, an Ubc enzyme variant protein, is required for phosphate homeostasis in rice
- Different effects of phospholipase Dζ2 and non‐specific phospholipase C4 on lipid remodeling and root hair growth in Arabidopsis response to phosphate deficiency
- Does <i>myo</i>-inositol oxygenase, the only enzyme to catalyze <i>myo</i>-inositol <i>in vivo</i>, play a role in the etiology of polycystic ovarian syndrome?
- Molecular, immunological, enzymatic and biochemical studies of coproporphyrinogen oxidase deficiency in a family with hereditary coproporphyria.
- Retinol Esterification by DGAT1 Is Essential for Retinoid Homeostasis in Murine Skin
- Common Forms of Congenital Adrenal Hyperplasia
- Biotinidase Deficiency: Prevalence, Impact And Management Strategies.
- Cyclic Alopecia and Abnormal Epidermal Cornification in Zdhhc13 -Deficient Mice Reveal the Importance of Palmitoylation in Hair and Skin Differentiation
- Biotin - facts and hopes
- 9 Role of 5α-reductase in health and disease
- Skin Signs due to Starvation
- Cutaneous Retinoic Acid Levels Determine Hair Follicle Development and Downgrowth
- Zinc: An overview and therapeutic uses in dermatology
- Severe Skin Permeability Barrier Dysfunction in Knockout Mice Deficient in a Fatty Acid ω-Hydroxylase Crucial to Acylceramide Production
- Structural basis for the catalysis and inhibition of human steroid 5α‐reductase 2
- Biotinidase Deficiency and Seizures
- Severe Zinc Deficiency in Male and Female Rats
- LPA-producing enzyme PA-PLA<sub>1</sub>α regulates hair follicle development by modulating EGFR signalling
- Congenital Copper Deficiency: Copper Therapy and Dopamine‐β‐Hydroxylase Activity in the Mottled (Brindled) Mouse
- Virilism and Ectopic Expression of HSD17B5 in Mature Cystic Teratoma
- Fast Motions in 5 Alpha Reductase and Its Impact on Enzyme Kinetics
- Approaching fertility in congenital adrenal hyperplasia: exploring P30L mutation-induced 21-hydroxylase deficiency with a presentation between non-classical and simple virilizing phenotypes. A case report
- Testosterone Deficiency is Not Protective Against the Development of Adenocarcinoma of the Prostate in a Type 1 Diabetic Patient
- Biotinidase Deficiency: A Treatable Neurometabolic Disorder- A Case Report
- Disorders linked to insufficient androgen action in male children
- 5α-Metabolism in Finasteride-Treated Subjects and Male Pseudohermaphrodites with Inherited 5α-Reductase Deficiency
- Urinary 5-ene-steroid excretion in non-classical congenital adrenal hyperplasia due to 3β-hydroxysteroid dehydrogenase deficiency (NC-3BHSD)
- 5-Alpha reductase deficiency