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Research 271–300 of 553
- Suprabasal Desmoglein 3 Expression in the Epidermis of Transgenic Mice Results in Hyperproliferation and Abnormal Differentiation
- 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
- Desmogleins: Hair perspective
- A new mutation Rim3 resembling Re den is mapped close to retinoic acid receptor alpha (Rara) gene on mouse Chromosome 11
- Differential structural properties and expression patterns suggest functional significance for multiple mouse desmoglein 1 isoforms
- Focal palmoplantar callosities in non-Herlitz junctional epidermolysis bullosa
- 010 Development of a Desmocollin-3 Active Mouse Model Recapitulating Human Atypical Pemphigus
- DEVELOPMENT OF A DESMOCOLLIN-3 ACTIVE MOUSE MODEL RECAPITULATING HUMAN ATYPICAL PEMPHIGUS
- Mutations in the Desmoglein 4 Gene Underlie Localized Autosomal Recessive Hypotrichosis with Monilethrix Hairs and Congenital Scalp Erosions
- Keratins and skin disease
- Desmoglein 4 is regulated by transcription factors implicated in hair shaft differentiation
- A Missense Mutation in the Cadherin Interaction Site of The Desmoglein 4 Gene Underlies Localized Autosomal Recessive Hypotrichosis
- Identification of Differentially Expressed Genes During a Wool Follicle Growth Cycle Induced by Prolactin
- 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
- Faculty Opinions recommendation of Loss of desmocollin 3 in mice leads to epidermal blistering.
- 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
- Expression of Plectin-1 and Trichohyalin in Human Tongue Cancer Cells
- Conjoint analysis of methylation, transcriptomic, and proteomic profiles in pemphigus vulgaris
- Treatment of hypotrichosis simplex of the scalp with the combination of botanic extracts and minoxidil: a case report
- The epidermis: rising to the surface
- 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