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Research 361–390 of 555
- Hair Loss in Children
- Influence of donor sources and culture media on the histo-morphological quality of human artificial skin models
- Untersuchungen der Fremdstoffbindung in permanenten Keratinozyten- und Melanozyten-Zelllinien sowie die Eignung von Primärkulturen aus humanen Haarfollikeln zur In-vitro-Messung der Fremdstoffaufnahme im Haar
- LITERATURE REVIEW
- Localization of Merkel cells at hairless and hairy human skin sites using keratin 18
- Histological and molecular restoration of type VII collagen in Recessive dystrophic epidermolysis bullosa mouse skin by topical injection of keratinocyte-like cells differentiated from human adipose-derived mesenchymal stromal cells
- Keratins and skin disease
- Morphological analysis of in vitro human hair growth
- Ultrastructural characteristics of trichilemmal cysts: report of two cases
- DSP c.6310delA p.(Thr2104Glnfs*12) associates with arrhythmogenic cardiomyopathy, increased trabeculation, curly hair, and palmoplantar keratoderma
- Corneodesmosomes and corneodesmosin: from the stratum corneum cohesion to the pathophysiology of genodermatoses
- Ichthyosis follicularis, alopecia, and photophobia (IFAP) syndrome
- Dermatopathy in juvenile Angus cattle due to vitamin A deficiency
- Treatment of hypotrichosis simplex of the scalp with the combination of botanic extracts and minoxidil: a case report
- The complement of native α-keratin polypeptides of hair-forming cells: A subset of eight polypeptides that differ from epithelial cytokeratins
- Basal cell carcinoma — molecular biology and potential new therapies
- Regulation of Involucrin Gene Expression
- K6irs1, K6irs2, K6irs3, and K6irs4 Represent the Inner-Root-Sheath-Specific Type II Epithelial Keratins of the Human Hair Follicle1
- Evidence for Novel Functions of the Keratin Tail Emerging from a Mutation Causing Ichthyosis Hystrix
- Delineation of Matriptase Protein Expression by Enzymatic Gene Trapping Suggests Diverging Roles in Barrier Function, Hair Formation, and Squamous Cell Carcinogenesis
- Increased acetylcholine levels in skin biopsies of patients with atopic dermatitis
- Selective Expression of Calcium-Binding Proteins S100A8 and S100A9 at Distinct Sites of Hair Follicles
- Transcriptional profiling of putative human epithelial stem cells
- Store-operated calcium channels in skin
- Heterozygous Arrhythmogenic Cardiomyopathy-desmoplakin Mutation Carriers Exhibit a Subclinical Cutaneous Phenotype with Cell Membrane Disruption and Lack of Intercellular Adhesion
- Impact of constant light exposure during pregnancy on skin of neonatal New Zealand rabbits: structural and ultrastructural study
- A case of pemphigus vulgaris developing after platelet-rich plasma treatment
- A Novel Model System to Identify Cellular and Molecular Defects Underlying Rare Genetic Disorders
- Autosomal recessive woolly hair syndrome: a series of eight patients in an Indian population
- Microarray Gene Expression Analysis of Lesional Skin in Canine Pemphigus Foliaceus