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Research 511–540 of 1000+
- Two Different Mutations in the Same Codon of a Type II Hair Keratin (hHb6) in Patients with Monilethrix
- <i>Msx2</i> Prevents Stratified Squamous Epithelium Formation in the Enamel Organ
- Skin cancer: understanding the journey of transformation from conventional to advanced treatment approaches
- Biological significance of FoxN1 gain-of-function mutations during T and B lymphopoiesis in juvenile mice
- Alopecia Areata: A Review of the Role of Oxidative Stress, Possible Biomarkers, and Potential Novel Therapeutic Approaches
- Novel Mutation in Sjögren-Larsson Syndrome Is Associated With Divergent Neurologic Phenotypes
- Further Insights in Trichothiodistrophy: A Clinical, Microscopic, and Ultrastructural Study of 20 Cases and Literature Review
- Hair and Scalp Disorders in a Tuscan Pediatric Dermatological Outpatient Clinic: A Clinical and Epidemiological Evaluation
- CDH3 gene related hypotrichosis and juvenile macular dystrophy – A case with a novel mutation
- Biallelic Variants in Lanosterol Synthase (LSS) Cause Palmoplantar Keratoderma-Congenital Alopecia Syndrome Type 2
- Ichthyosis with confetti: a rare diagnosis and treatment plan
- Application of Marine Microbial Natural Products in Cosmetics
- Cases Report the Cronkhite-Canada Syndrome
- Therapeutic Effect of Superficial Scalp Hypothermia on Chemotherapy-Induced Alopecia in Breast Cancer Survivors
- P63 targeted deletion under the FOXN1 promoter disrupts pre-and post-natal thymus development, function and maintenance as well as induces severe hair loss
- Nutritional Disorders of the Hair and Their Management
- Loss of Ten1 in mice induces telomere shortening and models human dyskeratosis congenita
- A Kaleidoscope of Keratin Gene Expression and the Mosaic of Its Regulatory Mechanisms
- Key Factors in the Complex and Coordinated Network of Skin Keratinization: Their Significance and Involvement in Common Skin Conditions
- A Homozygous Missense Variant in K25 Underlying Overlapping Phenotype with Woolly Hair and Dental Anomalies
- Relapsing Polychondritis Following Alopecia Areata
- Tissue Engineering in Cosmetics and Dermatology: A New Era of Innovation and Application
- Comparative study of male and female human hair: A microscopic analysis.
- Scarring Alopecia With Coexisting Lichen Planus in a Child: A Rare Phenomenon
- ADULT (acro–dermato–ungual–lacrimal–tooth) syndrome: A case report from India
- XIAP Stabilizes DDRGK1 to Promote ER‐Phagy and Protects Against Noise‐Induced Hearing Loss
- Platelet-Rich Plasma (PRP): Molecular Mechanisms, Actions and Clinical Applications in Human Body
- Phenol in dermatology: updated evidence on efficacy and safety
- Early Skin Biopsy in Conradi‐Hünermann‐Happle Syndrome (X‐Linked Dominant Chondrodysplasia Punctata)
- Segmental analysis of human hair reveals intra-annual variation in 25(OH)D3 concentrations in modern and archaeological individuals