Search
for
Sort by
Research 31–60 of 806
- 9. Immunology and Genetics
- Atlas of Geriatric Dermatology
- Substance P in keratosis follicularis spinulosa decalvans
- Hypotrichosis in a child with olmsted syndrome
- A Novel Connexin 26 Mutation in a Patient Diagnosed with Keratitis–Ichthyosis–Deafness Syndrome
- SASH1 Mutations and Hereditary Disorders of Pigmentation: Review of Literature
- Keratin gene mutations in disorders of human skin and its appendages
- Evidence for Novel Functions of the Keratin Tail Emerging from a Mutation Causing Ichthyosis Hystrix
- Activation of TRPV3 Regulates Inflammatory Actions of Human Epidermal Keratinocytes
- Poster Presentations
- Expanding phenotype of hereditary fibrosing poikiloderma with tendon contractures, myopathy, and pulmonary fibrosis caused by FAM111B mutations: Report of an additional family raising the question of cancer predisposition and a short review of early-onset poikiloderma
- Pathogenesis and management of TRPV3-related Olmsted syndrome
- A Rare Case of Keratosis Follicularis Spinulosa Decalvans Affecting a Female Child
- WNT10A mutation causes ectodermal dysplasia by impairing progenitor cell proliferation and KLF4-mediated differentiation
- Keratins as an Inflammation Trigger Point in Epidermolysis Bullosa Simplex
- The Phenotypic and Genotypic Spectra of Ichthyosis With Confetti Plus Novel Genetic Variation in the 3′ End of<i>KRT10</i>
- Key Factors in the Complex and Coordinated Network of Skin Keratinization: Their Significance and Involvement in Common Skin Conditions
- Spontaneous Quick Resolution of Uncombable Hair Syndrome-Like Disease
- Autosomal recessive woolly hair syndrome: a series of eight patients in an Indian population
- WNT Signaling in Disease
- British Association of Dermatologists guidelines on the efficacy and use of acitretin in dermatology
- Keratin 17 Expression in the Hard Epithelial Context of the Hair and Nail, and its Relevance for the Pachyonychia Congenita Phenotype
- The molecular basis of human keratin disorders
- Diseases associated with hidranitis suppurativa: part 2 of a series on hidradenitis
- Ichthyosis with confetti: clinics, molecular genetics and management
- A Mutational Hotspot in the 2B Domain of Human Hair Basic Keratin 6 (hHb6) in Monilethrix Patients
- Genetic Hair Disorders: A Review
- Molecular determinants for the chemical activation of the warmth-sensitive TRPV3 channel by the natural monoterpenoid carvacrol
- Mechanisms of proton inhibition and sensitization of the cation channel TRPV3
- Hair shaft disorders in children – An update