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Research 91–120 of 1000+
- Embryologic layers in dermatology: Developmental checkpoint disorders, diagnostic insight, and regenerative futures
- <i>DSG4</i> Gene Variants as a Cause of Hypotrichosis in the Child with Severe Atopic Dermatitis: Clinical Case
- Neuroendocrine Controls of Keratin Expression in Human Skin
- A Case of Hair Structure Abnormality Associated with Iron Deficiency Anaemia
- Single and repeated dose of finasteride topical solution in subjects with androgenetic alopecia: A pharmacokinetic and pharmacodynamic study
- Role of trichoscopy in diagnosis of different hair and scalp disorders in pediatrics
- Morphological Approach to Hair Disorders
- Clinical Approach to the Patient With Alopecia
- Farmácia Padrão da Légua, Custóias e nos Serviços Farmacêuticos da Klinicka Bolnica Dubrava, Croácia
- Alopecia in a Novel Mouse Model RCO3 Is Caused by mK6irs1 Deficiency
- Botanical extract combined with minoxidil improve hidrotic ectodermal dysplasia caused by p.G11R mutations: a case report
- Investigating the role of keratin proteins and microbial associations in hereditary and pathogenic alopecia
- Independent DSG4 frameshift variants in cats with hair shaft dystrophy
- Molecular Genetics of Human Hair Diseases
- A novel mutation in ST14 at a functionally significant amino acid residue expands the spectrum of ichthyosis-hypotrichosis syndrome
- Mast cell hyperplasia in the skin of Dsg4-deficient hypotrichosis mice, which are long-living mutants of lupus-prone mice
- Heterozygous Arrhythmogenic Cardiomyopathy-desmoplakin Mutation Carriers Exhibit a Subclinical Cutaneous Phenotype with Cell Membrane Disruption and Lack of Intercellular Adhesion
- Spontaneous Quick Resolution of Uncombable Hair Syndrome-Like Disease
- Immunostaining study of cytokeratins in human hair follicle development
- Circ 0020938 inhibits hair follicle stem cells proliferation via the miR-142-5p/DSG4 axis in cashmere goats
- The molecular basis of human keratin disorders
- Pili Torti: A Feature of Numerous Congenital and Acquired Conditions
- Hair microscopy: an easy adjunct to diagnosis of systemic diseases in children
- Morphologic and molecular characterization of two novel Krt71 (Krt2-6g) mutations: Krt71 rco12 and Krt71 rco13
- Madarosis: A marker of many Maladies
- The Hairless Phenotype of the Hirosaki Hairless Rat Is Due to the Deletion of an 80-kb Genomic DNA Containing Five Basic Keratin Genes
- A Spontaneous Deletion within the Desmoglein 3 Extracellular Domain of Mice Results in Hypomorphic Protein Expression, Immunodeficiency, and a Wasting Disease Phenotype
- Bald thigh syndrome in sighthounds—Revisiting the cause of a well-known disease
- Diseases of Hair
- <i>De novo</i> filament formation by human hair keratins K85 and K35 follows a filament development pattern distinct from cytokeratin filament networks