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Research 301–330 of 834
- Steroid Biomarkers and Genetic Studies Reveal Inactivating Mutations in Hexose-6-Phosphate Dehydrogenase in Patients with Cortisone Reductase Deficiency
- Beyond Expectations
- Androgen receptors and their biology
- Recent advances in the molecular mechanisms determining tissue sensitivity to glucocorticoids: novel mutations, circadian rhythm and ligand-induced repression of the human glucocorticoid receptor
- The Inflammatory Caspases-1 and -11 Mediate the Pathogenesis of Dermatitis in Sharpin-Deficient Mice
- Nonclassic adrenal hyperplasia
- How to diagnose a lipodystrophy syndrome
- Identification of the Rat Rex Mutation as a 7-bp Deletion at Splicing Acceptor Site of the Krt71 Gene
- Primary cicatricial alopecia: Recent advances in understanding and management
- Trichoscopy in Hair Shaft Disorders
- Prognosis and Management of Congenital Hair Shaft Disorders with Fragility—Part I
- Generation of Cashmere Goats Carrying an <i>EDAR</i> Gene Mutant Using CRISPR-Cas9-Mediated Genome Editing
- Hairless is a nuclear receptor corepressor essential for skin function
- Diagnostic approach to low‐renin hypertension
- Analysis of hidradenitis suppurativa–linked mutations in four genes and the effects of PSEN1-P242LfsX11 on cytokine and chemokine expression in macrophages
- Testosterone levels in relation to oral contraceptive use and the androgen receptor CAG and GGC length polymorphisms in healthy young women
- The Genetics of Human Skin Disease
- Unraveling the Molecular Mechanisms of Hair and Nail Genodermatoses
- Analysis of the FGF gene family provides insights into aquatic adaptation in cetaceans
- The inconsistent regulation of HOXC13 on different keratins and the regulation mechanism on HOXC13 in cashmere goat (Capra hircus)
- Roles of Wnt7a in embryo development, tissue homeostasis, and human diseases
- What′s new in cicatricial alopecia?
- Congenital adrenal hyperplasia
- Characterization of X‐linked hypohidrotic ectodermal dysplasia (XL‐HED) hair and sweat gland phenotypes using phototrichogram analysis and live confocal imaging
- Prognosis and Management of Congenital Hair Shaft Disorders without Fragility—Part II
- Localisation and regulation of cholesterol transporters in the human hair follicle: mapping changes across the hair cycle
- Dermatopathology and molecular genetics
- Dermatologic manifestations of endocrine disorders
- Congenital atrichia and hypotrichosis
- The role of aquaporins in polycystic ovary syndrome – A way towards a novel drug target in PCOS