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Research 421–450 of 783
- Inherited disorders of the skin in human and mouse: from development to differentiation.
- Inherited Disorders of Corneocyte Proteins
- Structure and Development of the Skin and Cutaneous Appendages
- Does dry skin indicate defective epidermal permeability barrier?
- Keratin gene mutations in disorders of human skin and its appendages
- Trichothiodystrophy
- A null mutation in the cystatin M/E gene of ichq mice causes juvenile lethality and defects in epidermal cornification
- Harlequin fetus with abnormal lamellar granules and giant mitochondria
- The skin landscape in diabetes mellitus. Focus on dermocosmetic management
- Efficient In Vitro Transfection of Human Keratinocytes with an Adenovirus-Enhanced Receptor-Mediated System
- Biochemical examination of fetal skin biopsy specimens obtained by fetoscopy: Use of the method for analysis of keratins and filaggrin
- A Case of IFAP Syndrome with Severe Atopic Dermatitis
- Formation of the cornified envelope
- Diffuse plate-like sheets of desquamation
- Contribution of Environmental Constituents in the Genomic Disruption of Cytokeratins
- Porokeratotic adnexal ostial nevus: a paradigm of cutaneous mosaicism
- Circle Hairs in a Patient with Multiple Myeloma
- Ichthyosiform Erythroderma, a Multifaceted Syndromic Entity
- Dynamics of Hair Follicle Morphogenesis and Skin Homeostasis
- British Society for Paediatric Dermatology Annual Meeting, Sheffield, 18-19 November 2016
- A polarizing light microscopy can be an easy and reliable diagnostic tool of congenital keratinizing disorders including Netherton syndrome
- Skin, Genetic Defects, and Aging
- Clinical Snippets
- Steroid Sulfatase: Molecular Biology, Regulation, and Inhibition
- Human stratum corneum proteomics reveals cross‐linking of a broad spectrum of proteins in cornified envelopes
- Roles of steroid sulfatase in brain and other tissues
- Genetic Mapping Of Hereditary Ectodermal Dysplasias And Hair Loss Genes
- Case Report of Wound Treatment with Hyiodine Gel in an Occasional KID Syndrome Patient
- Novel Mutations in X-Linked Dominant Chondrodysplasia Punctata (CDPX2)
- From molecular biology to therapeutics