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Research 451–480 of 1000+
- Hair Biology and Nutritional Influences
- Non-Neoplastic Disorders of Hair
- Tratamento da alopecia areata com corticóide tópico: estudo prospectivo randomizado duplo cego em crianças * Therapy of alopecia areata with topical corticosteroid: prospective double-blind controlled assay in children *
- Allergens and Irritants
- Differential Diagnosis of Male and Female Pattern Hair Loss
- Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles
- Acrodermatitis Enteropathica: A Case Report Involving a Delayed Diagnosis
- Analysis of the abnormal human hair keratins by two-dimensional polyacrylamide gel electrophoresis
- Delayed epidermal permeability barrier formation and hair follicle aberrations in Inv-Cldn6 mice
- Sebaceous gland abnormalities in fatty acyl CoA reductase 2 (Far2) null mice result in primary cicatricial alopecia
- De novo variation in ARID1B gene causes Coffin-Siris syndrome 1 in a Chinese family with excessive early-onset high myopia
- British Association of Dermatologists living guideline for managing people with alopecia areata 2025
- Monilethrix: a typical case report with microscopic and dermatoscopic findings
- Congenital atrichia associated with situs inversus and mesocardia
- Subcutaneous Injection of Large Volumes of Polidocanol
- A Combination Flap for Repair of Eclabium
- A Variable Monilethrix Phenotype Associated With a Novel Mutation, Glu402Lys, in the Helix Termination Motif of the Type II Hair Keratin hHb1
- Apoptosis resistance in peripheral blood lymphocytes of alopecia areata patients
- More than One Gene Involved in Monilethrix: Intracellular but also Extracellular Players
- Krt6a-Cre Transgenic Mice Direct LoxP-Mediated Recombination to the Companion Cell Layer of the Hair Follicle and Following Induction by Retinoic Acid to the Interfollicular Epidermis
- [Loss of hair due to vitamin A].
- Inducible deletion of epidermal <i>Dicer</i> and <i>Drosha</i> reveals multiple functions for miRNAs in postnatal skin
- The RAIG Family Member, GPRC5D, Is Associated with Hard-Keratinized Structures
- Novel Mutations in X-Linked Dominant Chondrodysplasia Punctata (CDPX2)
- Identification of an Intronic Regulatory Element Necessary for Tissue-Specific Expression of <i>Foxn1</i> in Thymic Epithelial Cells
- Molecular Targeted Agents and Biologic Therapies for Non-small Cell Lung Cancer
- Pili Torti: A Feature of Numerous Congenital and Acquired Conditions
- RSPO1-mutated keratinocytes from palmoplantar keratoderma display impaired differentiation, alteration of cell–cell adhesion, EMT-like phenotype and invasiveness properties: implications for squamous cell carcinoma susceptibility in patients with 46XX disorder of sexual development
- Read-Through for Nonsense Mutations in Type XVII Collagen‒Deficient Junctional Epidermolysis Bullosa
- Treatment of Alopecia in Children