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Research 271–300 of 401
- Faculty Opinions recommendation of Loss of desmocollin 3 in mice leads to epidermal blistering.
- The Transient Role for Calcium and Vitamin D during the Developmental Hair Follicle Cycle
- A pair of transmembrane receptors essential for the retention and pigmentation of hair
- Monilethrix – Case report of a rare disease
- Low‐level laser (light) therapy (LLLT) for treatment of hair loss
- Tyrosine Kinases in Autoimmune and Inflammatory Skin Diseases
- Environmental Air Pollutants Affecting Skin Functions with Systemic Implications
- A Comprehensive Review of Mammalian Pigmentation: Paving the Way for Innovative Hair Colour-Changing Cosmetics
- Pathological Mechanisms Involved in Epidermolysis Bullosa Simplex: Current Knowledge and Therapeutic Perspectives
- Key Factors in the Complex and Coordinated Network of Skin Keratinization: Their Significance and Involvement in Common Skin Conditions
- Znaczenie chorób pęcherzycowych w diagnostyce różnicowej estetycznych problemów twarzy
- Persistent pemphigus vulgaris and pemphigus foliaceus showing features of tufted hair folliculitis just on the scalp
- Corneodesmosin gene ablation induces lethal skin-barrier disruption and hair-follicle degeneration related to desmosome dysfunction
- The Nude Mutant Gene Foxn1 Is a HOXC13 Regulatory Target during Hair Follicle and Nail Differentiation
- Primary Follicular Dystrophy With Scarring Dermatitis in C57BL/6 Mouse Substrains Resembles Central Centrifugal Cicatricial Alopecia in Humans
- Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles
- Mutations in SNRPE, which Encodes a Core Protein of the Spliceosome, Cause Autosomal-Dominant Hypotrichosis Simplex
- Krtap11-1, a hair keratin-associated protein, as a possible crucial element for the physical properties of hair shafts
- Characterization and functional analysis of Krtap11-1 during hair follicle development in Angora rabbits (Oryctolagus cuniculus)
- Autosomal recessive monilethrix: Novel variants of the <i>DSG4</i> gene in three Chinese families
- Bald thigh syndrome in sighthounds—Revisiting the cause of a well-known disease
- Alopezien und Hypotrichosen im Kindesalter
- Value of dermoscopy for the diagnosis of monilethrix
- Rare Coexistence of Monilethrix and Trichorrhexis Nodosa in a Pediatric Patient: A Case Report
- Moniletrix of the scalp from almost normal aspect to total alopecia: variable intrafamilial expressiveness
- Mice lacking desmocollin 1 show epidermal fragility accompanied by barrier defects and abnormal differentiation
- Fundamental hair follicle biology and fine fibre production in animals
- Human Eccrine Sweat Gland Cells Can Reconstitute a Stratified Epidermis
- Ichthyosis, Follicular Atrophoderma, and Hypotrichosis Caused by Mutations in ST14 Is Associated with Impaired Profilaggrin Processing
- Netherton syndrome subtypes share IL-17/IL-36 signature with distinct IFN-α and allergic responses