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Research 91–120 of 777
- The Functional Diversity of Epidermal Keratins Revealed by the Partial Rescue of the Keratin 14 Null Phenotype by Keratin 16
- Endocrine-skin interactions
- Cicatricial (Scarring) Alopecias
- Madarosis
- Newborn infant skin gene expression: Remarkable differences versus adults
- Congenital atrichia and hypotrichosis
- Madarosis, milphosis, eyelash trichomegaly, and dermatochalasis
- Diseases of Periocular Hair
- The Role of Entrepreneurial Leadership and Innovation in the Future of Therapeutic Dermatology
- Atlas of Geriatric Dermatology
- Dermatomyositis Disease in Dogs
- Influence of donor sources and culture media on the histo-morphological quality of human artificial skin models
- Abstracts from the 17th Congress of the European Society for Dermatology and Psychiatry
- Description of skin lesions
- Frequency of Childhood Dermatological Diseases: An Analysis of 8551 Cases
- Subject Index
- Clinical Management in Psychodermatology
- Molecular Genetics of Alopecias
- The spectrum of nephrocutaneous diseases and associations
- Differential diagnosis of alopetia in children and adolescents
- Bloch-Sulzberger Syndrome: A Rare X-Linked Dominant Genetic Disorder in a Newborn
- Nagashima-Type Palmoplantar Keratosis: A Common Asian Type Caused by SERPINB7 Protease Inhibitor Deficiency
- Targeting the Complexity of In Vitro Skin Models: A Review of Cutting-Edge Developments
- The epidermis: rising to the surface
- Genetic disorders of keratin: are scarring alopecias a sub-set?
- The molecular basis of human keratin disorders
- Type XVII collagen coordinates proliferation in the interfollicular epidermis
- Laminin 332 Is Indispensable for Homeostatic Epidermal Differentiation Programs
- Correction of Hair Shaft Defects through Allele-Specific Silencing of Mutant Krt75
- <i>GJB6</i> missense variant in a Labrador Retriever with paw pad hyperkeratosis