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Research 241–270 of 597
- The adverse effects of commonly used medications on male fertility: a comprehensive review
- Dynamic immunomodulatory nanoarchitectonics: Rewiring tissue regenerative microenvironment via intelligent regulation
- Inflammatory Skin Disease in Latin America: Treatment Challenges and Opportunities
- Obesity in Adults: Position Statement of Polish Association for the Study on Obesity, Polish Association of Endocrinology, Polish Association of Cardiodiabetology, Polish Psychiatric Association, Section of Metabolic and Bariatric Surgery of the Association of Polish Surgeons, and the College of Family Physicians in Poland
- Autosomal-Dominant Woolly Hair Resulting from Disruption of Keratin 74 (KRT74), a Potential Determinant of Human Hair Texture
- Mutations in SNRPE, which Encodes a Core Protein of the Spliceosome, Cause Autosomal-Dominant Hypotrichosis Simplex
- Development of Woolly Hair and Hairlessness in a CRISPR−Engineered Mutant Mouse Model with KRT71 Mutations
- Mesenchymal–epithelial interactions during hair follicle morphogenesis and cycling
- Localisation and regulation of cholesterol transporters in the human hair follicle: mapping changes across the hair cycle
- The Well-Forgotten Old: Platelet-Rich Plasma in Modern Anti-Aging Therapy
- Hair follicle-specific keratins and their diseases
- Synthesis of porcine pCLCA2 protein during late differentiation of keratinocytes of epidermis and hair follicle inner root sheath
- The Roles of Non-coding RNA in the Development and Regeneration of Hair Follicles: Current Status and Further Perspectives
- Effect of N-acetylcysteine on hair follicle changes in mouse model of cyclophosphamide-induced alopecia: histological and biochemical study
- Trichohyalin, an intermediate filament-associated protein of the hair follicle.
- Systemic Absorption and Pharmacokinetics of Five Novel Topical Dermatologic Agents: A Review
- 448 Challenges of securing insurance approval for oral tofacitinib treatment of alopecia areata: A multi-institutional retrospective review
- Inherited Disorders of the Hair
- Abstracts from the Symposium on the Pathophysiology of Hair Growth Organized by the Institute of Dermatology at the Royal Society of Medicine, 29 October 1987
- APCDD1 is a novel Wnt inhibitor mutated in hereditary hypotrichosis simplex
- Loose Anagen Hair as a Cause of Hereditary Hair Loss in Children
- Congenital hair loss disorders: Rare, but not too rare
- Molecular Genetics of Alopecias
- Perspectives and Challenges of Hair Analysis
- Recent advances in the molecular mechanisms determining tissue sensitivity to glucocorticoids: novel mutations, circadian rhythm and ligand-induced repression of the human glucocorticoid receptor
- Utilizing the hair follicle to dissect the regulation and autocrine/paracrine activities of prolactin in humans
- Metabolism and skin diseases
- Sexually dimorphic sail feathers in the Mandarin duck as a model for lifelong developmental modulation
- Ozone and procaine increase secretion of platelet-derived factors in platelet-rich plasma
- Generalised Glucocorticoid Resistance