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Research 91–120 of 1000+
- Disorders of the skin appendages
- Diseases of Periocular Hair
- Nonclassic adrenal hyperplasia
- Variant 1859G→A (Arg620Gln) of the “Hairless” Gene: Absence of Association with Papular Atrichia or Androgenetic Alopecia
- Cystatin M/E Variant Causes Autosomal Dominant Keratosis Follicularis Spinulosa Decalvans by Dysregulating Cathepsins L and V
- Congenital Adrenal Hyperplasia
- Novel mutations in the keratin-74 (KRT74) gene underlie autosomal dominant woolly hair/hypotrichosis in Pakistani families
- Congenital atrichia associated with nevus flammeus: A rare association
- Relationship of a Novel c.429delC Deletion in Hairless Gene HR with Alopecia in Two Families from Southern Punjab, Pakistan
- Investigating the role of keratin proteins and microbial associations in hereditary and pathogenic alopecia
- Eyebrow and Eyelash Alopecia: A Clinical Review
- The Biology and Genomics of Human Hair Follicles: A Focus on Androgenetic Alopecia
- Focused Review on Metal Nanoparticles in Hair Regeneration and Alopecia: Insights into Mechanisms, Assessment Techniques, Toxicity, Regulatory and Intellectual Property Perspectives
- Alopecia in Children
- Study of the Thyroid Profile of Patients with Alopecia
- Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- Genetic screening of non-classic CAH females with hyperandrogenemia identifies a novel CYP11B1 gene mutation
- Gene-knockout mice with abnormal epidermal and hair follicular development
- Acrodermatitis enteropathica in the pediatric population: a literature review of real-world studies
- Epidermal expression of the truncated prelamin A causing Hutchinson-Gilford progeria syndrome: effects on keratinocytes, hair and skin
- Genetic Hair Disorders: A Review
- The Role of Sex and Gender in Dermatology - From Pathogenesis to Clinical Implications
- Hairless Suppresses Vitamin D Receptor Transactivation in Human Keratinocytes
- When Rare Meets Risky: Clouston Syndrome with Cutaneous Squamous Cell Carcinoma
- Cell death in skin function, inflammation, and disease
- Sphingolipid metabolism orchestrates establishment of the hair follicle stem cell compartment
- Hair & Cutaneous Development
- Oral Presentations
- Does D matter? The role of vitamin D in hair disorders and hair follicle cycling