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Research 271–300 of 1000+
- Emerging interactions between skin stem cells and their niches
- ICP5249 Promotes Hair Growth by Activating the AMPK-Autophagy Signaling Pathway
- Oral Retinoids in Dermatology
- A Missense Mutation within the Helix Termination Motif of KRT25 Causes Autosomal Dominant Woolly Hair/Hypotrichosis
- Recent Advances in the Pathogenesis of Autoimmune Hair Loss Disease Alopecia Areata
- Epidemiology and burden of alopecia areata: a systematic review
- Transforming growth factor-β in stem cells and tissue homeostasis
- Deficient Plakophilin-1 Expression Due to a Mutation in PKP1 Causes Ectodermal Dysplasia-Skin Fragility Syndrome in Chesapeake Bay Retriever Dogs
- Hair shaft structures in EDAR induced ectodermal dysplasia
- Alopecia Areata: Pathogenesis, Diagnosis, and Therapies
- More than One Gene Involved in Monilethrix: Intracellular but also Extracellular Players
- Ichthyosis, Follicular Atrophoderma, and Hypotrichosis Caused by Mutations in ST14 Is Associated with Impaired Profilaggrin Processing
- Novel potential therapeutic targets of alopecia areata
- An Autosomal Recessive Form of Monilethrix Is Caused by Mutations in DSG4: Clinical Overlap with Localized Autosomal Recessive Hypotrichosis
- Autosomal recessive hereditary hypotrichosis simplex: A case report
- Twins with psychiatric features and a nonsense HRAS variant affecting transcript processing
- A novel pathogenic variant of NECTIN4 gene in a child with ectodermal dysplasia-syndactyly syndrome
- APCDD1 is a novel Wnt inhibitor mutated in hereditary hypotrichosis simplex
- Role of Trichoscopy in diagnosing Genotrichosis—A Report of Two Cases
- Alopecia areata: current concepts
- Trichotillomania
- Conditional Knockout in Mice Reveals the Critical Roles of Ppp2ca in Epidermis Development
- Complex X chromosome rearrangement associated with multiorgan autoimmunity
- Collagen Involvement in Health, Disease, and Medicine
- Why Do Not All Chemotherapy Patients Lose Their Hair? Answering an Intriguing Question
- A Comprehensive Review on Alopecia: Mechanisms, Classification, and Therapeutic Strategies
- Diagnosis of hyperandrogenism: clinical criteria
- Mutations in Homocysteine Metabolism Genes Increase Keratin <i>N</i>-Homocysteinylation and Damage in Mice
- Marie Unna hereditary hypotrichosis: A Turkish family with loss of eyebrows and a <i>U2HR</i> mutation
- Hair and scalp disorders in ethnic populations