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Research 151–180 of 1000+
- Vitamin D, Lipid Metabolism and Prostate Cancer
- Editorial: Exploring innovative therapies for rare inflammatory skin diseases
- Prevalence of MMP-1 rs1799750 Polymorphism in Androgenetic Alopecia: A Cross-Sectional Study in an Indonesia Population
- Androgen effects on the skin
- Mucocutaneous Manifestations of Endocrine Disorders
- The Androgen Excess and PCOS Society criteria for the polycystic ovary syndrome: the complete task force report
- Congenital Adrenal Hyperplasia
- Nonclassic Congenital Adrenal Hyperplasia
- Congenital adrenal hyperplasia
- Clinical analysis of 78 patients with non-classical 21-hydroxylase deficiency
- Candidate SNP markers of reproductive potential are predicted by a significant change in the affinity of TATA-binding protein for human gene promoters
- Causality of Aging Hallmarks
- The Skin and Subcutaneous Tissues
- UNCONVENTIONAL PROTEIN SECRETION OF KERATIN 75 BY AMELOBLASTS IN VIVO
- Gonads
- Nonclassic adrenal hyperplasia
- Challenges in the Diagnosis of Simple-Virilizing Congenital Adrenal Hyperplasia: A Case Report
- Autologous Platelet Concentrates in Periodontology : Science, Concept, Protocols and Clinical Applications
- Differentiation of Adipose Derived Stem Cells by Stimulating with Extracellular Vesicles Secreted from Dermal Papilla Cells Activated with Osteogenic and Adipogenic Inducers
- Analysis of the function of ADAM17 in iRhom2 curly-bare and tylosis with esophageal cancer mutant mice
- Reduced plakoglobin increases the risk of sodium current defects and atrial conduction abnormalities in response to androgenic anabolic steroid abuse
- Two novel <i>BTD</i> mutations causing profound biotinidase deficiency in a Chinese patient
- New CDH3 mutation in the first Spanish case of hypotrichosis with juvenile macular dystrophy, a case report
- Ruxolitinib Rescues Multiorgan Clinical Autoimmunity in Patients with APS-1
- Human Hair Growth Deficiency Is Linked to a Genetic Defect in the Phospholipase Gene <i>LIPH</i>
- Clinical features and genetic analysis of acrodermatitis enteropathica in an ethnic minority infant from Western China: a case report and literature review
- Exploring the efficacy of testosterone undecanoate in male children with 5α‐reductase deficiency
- Phenotypic Variability of c.436delC DCAF17 Gene Mutation in Woodhouse-Sakati Syndrome
- Highlights of Gene and Cell Therapy for Epidermolysis Bullosa and Ichthyosis
- PNKP is required for maintaining the integrity of progenitor cell populations in adult mice