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Research 391–420 of 753
- Pediatric Inpatients Requesting Dermatology Consultation in a Tertiary Care Hospital: Retrospective Analysis of 614 Patients
- Prevalence of Skin Diseases in Pediatric Patients Admitted to Cerrahpaşa Medical Faculty Dermatology and Venereal Diseases Outpatient Clinic Between 2014-2017
- Skin Disorders
- Vitamins
- Nagashima-Type Palmoplantar Keratosis: A Common Asian Type Caused by SERPINB7 Protease Inhibitor Deficiency
- Homozygous Dominant Missense Mutation in Keratin 17 Leads to Alopecia in Addition to Severe Pachyonychia Congenita
- Type XVII collagen coordinates proliferation in the interfollicular epidermis
- Genetic disorders of keratin: are scarring alopecias a sub-set?
- Laminin 332 Is Indispensable for Homeostatic Epidermal Differentiation Programs
- The epidermis: rising to the surface
- The molecular basis of human keratin disorders
- Targeting the Complexity of In Vitro Skin Models: A Review of Cutting-Edge Developments
- Keratins: the hair shaft's backbone revealed
- Fibroblasts become fat to reduce scarring
- KLHL24-Mediated Hair Follicle Stem Cells Structural Disruption Causes Alopecia
- Research Techniques Made Simple: Zebrafish Models for Human Dermatologic Disease
- Skin applications of cannabidiol: sources, effects, delivery systems, marketed formulations and safety
- 75392 Psychosocial Burden of Severe Pediatric Alopecia Areata and Strategies for Mitigation: A Narrative Evidence Synthesis
- The Role of EAAT4 in Epidermal Differentiation and Calcium Homeostasis during Aging
- Genes of Congenital Dermatologic Disorders in Dogs—A Review
- Skin fragility in the wild-derived, inbred mouse strain Mus pahari/EiJ
- Faculty Opinions recommendation of Loss of desmocollin 3 in mice leads to epidermal blistering.
- 155 Exploring perceived quality of life in middle- to old-aged patients with inherited ichthyosis: a qualitative study
- Deregulated expression of c-Myc depletes epidermal stem cells
- Evidence for Novel Functions of the Keratin Tail Emerging from a Mutation Causing Ichthyosis Hystrix
- The Two Functional Keratin 6 Genes of Mouse Are Differentially Regulated and Evolved Independently from Their Human Orthologs
- Structure and function of skin, hair and nails
- A new mutation Rim3 resembling Re den is mapped close to retinoic acid receptor alpha (Rara) gene on mouse Chromosome 11
- Unmet Medical Needs in Chronic, Non-communicable Inflammatory Skin Diseases
- Therapeutic Use of Botulinum Neurotoxins in Dermatology: Systematic Review