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Research 481–510 of 662
- Evidence for Novel Functions of the Keratin Tail Emerging from a Mutation Causing Ichthyosis Hystrix
- Type XVII collagen coordinates proliferation in the interfollicular epidermis
- TRP Channels in Skin Biology and Pathophysiology
- Cytochrome P450: A Target for Drug Development for Skin Diseases
- Unraveling the ECM-Immune Cell Crosstalk in Skin Diseases
- Autosomal-Dominant Woolly Hair Resulting from Disruption of Keratin 74 (KRT74), a Potential Determinant of Human Hair Texture
- Keratin 17 Expression in the Hard Epithelial Context of the Hair and Nail, and its Relevance for the Pachyonychia Congenita Phenotype
- Keratins and disease at a glance
- Prevention and management of dermatological toxicities related to anticancer agents: ESMO Clinical Practice Guidelines☆
- RASopathic Skin Eruptions during Vemurafenib Therapy
- Inherited ichthyoses/generalized Mendelian disorders of cornification
- Mutations in the Desmoglein 4 Gene Underlie Localized Autosomal Recessive Hypotrichosis with Monilethrix Hairs and Congenital Scalp Erosions
- The molecular basis of human keratin disorders
- The Two Functional Keratin 6 Genes of Mouse Are Differentially Regulated and Evolved Independently from Their Human Orthologs
- Directed Expression of Keratin 16 to the Progenitor Basal Cells of Transgenic Mouse Skin Delays Skin Maturation
- A Missense Mutation within the Helix Initiation Motif of the Keratin K71 Gene Underlies Autosomal Dominant Woolly Hair/Hypotrichosis
- Rapidly progressing mycosis fungoides presenting as follicular mucinosis
- A new mutation Rim3 resembling Re den is mapped close to retinoic acid receptor alpha (Rara) gene on mouse Chromosome 11
- Ichthyosis follicularis, alopecia, and photophobia (IFAP) syndrome
- Keratins and skin disease
- New clinico‐genetic classification of trichothiodystrophy
- Alteration of Skin Properties with Autologous Dermal Fibroblasts
- Genetics of Inherited Ichthyoses and Related Diseases
- Phototherapy in Childhood
- Therapeutic Use of Botulinum Neurotoxins in Dermatology: Systematic Review
- Cylindroma as Tumor of Hair Follicle Origin
- Impaired Hair Follicle Morphogenesis and Cycling with Abnormal Epidermal Differentiation in nackt Mice, a Cathepsin L-Deficient Mutation
- Skin Structure, Physiology, and Pathology in Topical and Transdermal Drug Delivery
- Morphologic and molecular characterization of two novel Krt71 (Krt2-6g) mutations: Krt71 rco12 and Krt71 rco13
- Significance of stress keratin expression in normal and diseased epithelia