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Research 391–420 of 1000+
- The involvement of androgens in human hair growth
- Hair aging and anti-aging
- From Hair-Pulling to Trichobezoars and Rapunzel Syndrome: A Comprehensive Review of Trichotillomania
- Recent Advances in Understanding of the Etiopathogenesis, Diagnosis, and Management of Hair Loss Diseases
- Laminin-511 is an epithelial message promoting dermal papilla development and function during early hair morphogenesis
- Hormonal regulation in male androgenetic alopecia—Sex hormones and beyond: Evidence from recent genetic studies
- α3β1-integrin regulates hair follicle but not interfollicular morphogenesis in adult epidermis
- Hair and scalp disorders
- mTOR signaling promotes stem cell activation via counterbalancing BMP-mediated suppression during hair regeneration
- Planar cell polarity-dependent and independent functions in the emergence of tissue-scale hair follicle patterns
- Normal and Aging Hair Biology and Structure ‘Aging and Hair'
- Hair loss and its management in children
- Alopecia Areata: A tissue specific autoimmune disease of the hair follicle
- Diagnosis and management of hair loss in children
- A Complex Clinical Situation in Polycystic Ovary Syndrome: HAIR‐AN Syndrome ‘‘Case Report’’
- Hair follicle stem cells and the collapse of self-tolerance in alopecia: the interplay of barrier function, the microbiome, and immunity
- Male pattern hair loss: Taking one for the team: The selfless gene
- Aging of hair
- Prevalence and Predictors of Premature Graying of Hair Before the Age of 30: A Cross‐Sectional Study in Saudi Arabia
- Diagnosis and treatment of isolated autosomal recessive woolly hair/hypotrichosis
- Rapp-Hodgkin syndrome: A review of the aspects of hair and hair color
- Associaton of Insulin Resistance Linked Diseases and Hair Loss in Elderly Men. Finnish Population-based Study
- CCDC22 and CCDC93, two potential retriever-interacting proteins, are required for root and root hair growth in Arabidopsis
- Novel D323G mutation of <i>DSG4</i> gene in a girl with localized autosomal recessive hypotrichosis clinically overlapped with monilethrix
- Genetically modified laboratory mice with sebaceous glands abnormalities
- Keratin disorders: from gene to therapy
- Deficiency of the human cysteine protease inhibitor cystatin M/E causes hypotrichosis and dry skin
- Disruption of P2RY5, an orphan G protein–coupled receptor, underlies autosomal recessive woolly hair
- New case of trichorinophalangeal syndrome-like phenotype with a de novo t(2;8)(p16.1;q23.3) translocation which does not disrupt the TRPS1 gene
- Autosomal recessive monilethrix: Novel variants of the <i>DSG4</i> gene in three Chinese families