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Research 391–420 of 403
- Moniletrix of the scalp from almost normal aspect to total alopecia: variable intrafamilial expressiveness
- Hair Anomalies in a 6-Year-Old Girl
- Resurgent Clinical Science (and it's all about Health)
- Monilethrix in pattern distribution in siblings: Diagnosis by trichoscopy
- An autopsy case of unicentric Castleman's disease associated with bronchiolitis obliterans
- Pathology and pathogenesis of cutaneous lesions in beef cattle associated with buffalo fly infestation
- IgG/IgA pemphigus with differing regional presentations
- Rare Coexistence of Monilethrix and Trichorrhexis Nodosa in a Pediatric Patient: A Case Report
- Minoxidil Promotes Hair Growth in a Mouse Model of Telogen Effluvium Induced by Lipopolysaccharide
- Znaczenie chorób pęcherzycowych w diagnostyce różnicowej estetycznych problemów twarzy
- Deflúvio Telogénico Crónico
- Monilethrix – Case report of a rare disease
- Over-, ectopic-expression of FoxN1 at early life adversely influences lymphopoiesis (HEM3P.280)
- A Spontaneous Deletion within the Desmoglein 3 Extracellular Domain of Mice Results in Hypomorphic Protein Expression, Immunodeficiency, and a Wasting Disease Phenotype
- Immunolocalization of junctional proteins in human hairs indicates that the membrane complex stabilizes the inner root sheath while desmosomes contact the companion layer through specific keratins
- 441 RPGRIP1L facilitates desmosomal adhesion through suppressing PKCβII-mediated desmoglein endocytosis: Implication in pemphigus
- Desmoglein 4 is regulated by transcription factors implicated in hair shaft differentiation
- 876 Imaging nanoscale changes in desmosome protein organization
- t-Flavanone Improves the Male Pattern of Hair Loss by Enhancing Hair-Anchoring Strength: A Randomized, Double-Blind, Placebo-Controlled Study
- Stem Cells and their Niches
- Molecular biology of hair morphogenesis: Development and cycling
- Genetics of Alopecia
- A case of monilethrix caused by novel compound heterozygous mutations in the desmoglein 4 (DSG4) gene
- A Recurrent Intragenic Deletion in the Desmoglein 4 Gene Underlies Localized Autosomal Recessive Hypotrichosis
- 0040 Machine learning algorithms as tools for identifying predictive autoantibody biomarkers in pemphigus vulgaris
- Pseudo Pemphigus Phenotypes in Mice with Inactivated Desmoglein 3
- Smad4-dependent desmoglein-4 expression contributes to hair follicle integrity
- 875 A novel animal model of Desmoglein 1 (Dsg1) deficiency reveals an essential role for Dsg1 in epidermal barrier formation
- Mutations in the Desmoglein 4 Gene Underlie Localized Autosomal Recessive Hypotrichosis with Monilethrix Hairs and Congenital Scalp Erosions
- The lanceolate hair rat phenotype results from a missense mutation in a calcium coordinating site of the desmoglein 4 gene