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Research 181–210 of 398
- Kaposi Varicelliform Eruption in a Patient with Pemphigus Vulgaris: A Case Report and Review of the Literature
- Independent DSG4 frameshift variants in cats with hair shaft dystrophy
- 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
- A Missense Mutation within the Helix Initiation Motif of the Keratin K71 Gene Underlies Autosomal Dominant Woolly Hair/Hypotrichosis
- Dermatoscopy of hair shaft disorders
- Bidirectional binding property of high glycine–tyrosine keratin-associated protein contributes to the mechanical strength and shape of hair
- 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
- Diverse Role of OX40 on T Cells as a Therapeutic Target for Skin Diseases
- Polymorphisms of FST gene and their association with wool quality traits in Chinese Merino sheep
- Heparanase 1: a key participant of inner root sheath differentiation program and hair follicle homeostasis
- Monilethrix: a typical case report with microscopic and dermatoscopic findings
- The Transient Role for Calcium and Vitamin D during the Developmental Hair Follicle Cycle
- Crosslinking Between Trichocyte Keratins and Keratin Associated Proteins
- Monilethrix: A rare hereditary condition
- Keratinization of outer root sheath cells is prevented by contact with inner root sheath of rat hair follicles
- 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
- More is not always better in hair growth factors. epidermal growth factor: hair growth factor involved in alopecia areata pathogenesis
- Monilethrix, a rare inherited hair shaft disorder in siblings
- Eleven pairs of Japanese male twins suggest the role of epigenetic differences in androgenetic alopecia
- Monilethrix
- Value of dermoscopy for the diagnosis of monilethrix
- Case report: Dermatosis neglecta mimicking pemphigus foliaceus in association with obsessive–compulsive disorder
- 3D organotypic skin models recapitulate autoantibody-driven pemphigus pathomechanisms and targeted therapeutic response
- Co-occurrence of monilethrix and Type 1 diabetes mellitus
- Discreet monilethrix: De novo mutation on the example of polish families