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Research 301–330 of 1000+
- Screening for 21-hydroxylase–deficient nonclassic adrenal hyperplasia among hyperandrogenic women: a prospective study
- Association of Topical Minoxidil With Autosomal Recessive Woolly Hair/Hypotrichosis Caused by <i>LIPH</i> Pathogenic Variants
- Modulating the stem cell niche for tissue regeneration
- Physiological and retinoid-induced proliferations of epidermis basal keratinocytes are differently controlled
- Hair follicle stem cell cultures reveal self‐organizing plasticity of stem cells and their progeny
- An Intrinsic Oscillation of Gene Networks Inside Hair Follicle Stem Cells: An Additional Layer That Can Modulate Hair Stem Cell Activities
- Inhibiting the cytosolic function of CXXC5 accelerates diabetic wound healing by enhancing angiogenesis and skin repair
- ROR2 regulates self-renewal and maintenance of hair follicle stem cells
- MANAGEMENT OF ENDOCRINE DISEASE Hyperandrogenic states in women: pitfalls in laboratory diagnosis
- Candidate SNP markers of reproductive potential are predicted by a significant change in the affinity of TATA-binding protein for human gene promoters
- Isoallopregnanolone reduces tic‐like behaviours in the D1 CT ‐7 mouse model of Tourette syndrome
- Androgenic Alopecia Is Associated with Less Dietary Soy, Higher Blood Vanadium and rs1160312 1 Polymorphism in Taiwanese Communities
- Follikelhormone
- Gonads
- Challenges in the Diagnosis of Simple-Virilizing Congenital Adrenal Hyperplasia: A Case Report
- Hyperandrogenism in Adolescent Girls
- The Skin and Subcutaneous Tissues
- Differentiation of Adipose Derived Stem Cells by Stimulating with Extracellular Vesicles Secreted from Dermal Papilla Cells Activated with Osteogenic and Adipogenic Inducers
- Choreographing Immunity in the Skin Epithelial Barrier
- Efficacy and safety of SGLT2 inhibitor on insulin resistance and hyperglycemia in Werner syndrome—A case report
- Hypotrichosis 14: novel variants of the LSS gene in five Chinese families and insights from literature review
- Exploring the efficacy of testosterone undecanoate in male children with 5α‐reductase deficiency
- Epidermal expression of the truncated prelamin A causing Hutchinson-Gilford progeria syndrome: effects on keratinocytes, hair and skin
- Clinical and molecular features in a cohort of Middle Eastern patients with epidermolysis bullosa
- Molecular Genetics of Human Hair Diseases
- Hedgehog Signaling, Keratin 6 Induction, and Sebaceous Gland Morphogenesis
- Identifying 17-β-HSD3 Deficiency in Patients with Karyotype 46,XY Misdiagnosed with Androgen Insensitivity Syndrome: A Pediatric Case Report
- Collodion baby to bathing suit ichthyosis: A 6-year follow-up
- Over-, ectopic-expression of FoxN1 at early life adversely influences lymphopoiesis (HEM3P.280)
- FoxN1 in K14 promoter-driven epithelium is required for generation and maintenance of 3D-thymus medulla and preventing nude phenotype in the skin (36.33)