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Research 631–660 of 1000+
- Resting no more: re‐defining telogen, the maintenance stage of the hair growth cycle
- Molecular evolution of the keratin associated protein gene family in mammals, role in the evolution of mammalian hair
- The Skin Microbiome: Current Landscape and Future Opportunities
- Testosterone and doping control
- An Autosomal Recessive Form of Monilethrix Is Caused by Mutations in DSG4: Clinical Overlap with Localized Autosomal Recessive Hypotrichosis
- Self-Activated Electrical Stimulation for Effective Hair Regeneration <i>via</i> a Wearable Omnidirectional Pulse Generator
- Epidermal stem cells and skin tissue engineering in hair follicle regeneration
- Safety of testosterone treatment in postmenopausal women
- Aging of the hair follicle pigmentation system
- A small multigene hydroxyproline-O-galactosyltransferase family functions in arabinogalactan-protein glycosylation, growth and development in Arabidopsis
- Local heroes or villains: tissue-resident memory T cells in human health and disease
- The Modulatable Stem Cell Niche: Tissue Interactions during Hair and Feather Follicle Regeneration
- Meta-analysis identifies novel risk loci and yields systematic insights into the biology of male-pattern baldness
- Hirsutism, Normal Androgens and Diagnosis of PCOS
- Physiological Regeneration of Skin Appendages and Implications for Regenerative Medicine
- “Sebocytes’ makeup” - Novel mechanisms and concepts in the physiology of the human sebaceous glands
- Does prostaglandin D<sub>2</sub> hold the cure to male pattern baldness?
- Androgens and ovarian function: translation from basic discovery research to clinical impact
- The prostamide‐related glaucoma therapy, bimatoprost, offers a novel approach for treating scalp alopecias
- Hair-Growth Potential of Ginseng and Its Major Metabolites: A Review on Its Molecular Mechanisms
- Follicular mucinosis: A detailed morphologic and immunopathologic study
- Hyperandrogenism in polycystic ovarian syndrome and role of CYP gene variants: a review
- A Variable Monilethrix Phenotype Associated With a Novel Mutation, Glu402Lys, in the Helix Termination Motif of the Type II Hair Keratin hHb1
- Myotonic Dystrophy—A Progeroid Disease?
- Frequency, severity and related factors of androgenetic alopecia in dermatology outpatient clinic: hospital-based cross-sectional study in Turkey
- Madarosis: A marker of many Maladies
- Intravital imaging of host–parasite interactions in skin and adipose tissues
- Revisiting the role of melatonin in human melanocyte physiology: A skin context perspective
- Genetic Hair Disorders: A Review
- Hirsutism: diagnosis and treatment