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Research 391–420 of 1000+
- Compound glycyrrhizin promotes hair growth in C57BL/6 mice by regulating the Wnt/β-catenin pathway
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- Atypical Progeroid Syndrome due to Heterozygous Missense LMNA Mutations
- Emergence of the natural history of Myhre syndrome: 47 patients evaluated in the Massachusetts General Hospital Myhre Syndrome Clinic (2016–2023)
- Hair Growth Cycle Is Arrested in SCD1 Deficiency by Impaired Wnt3a-Palmitoleoylation and Retrieved by the Artificial Lipid Barrier
- Structural and epistatic regulatory variants cause hallmark white spotting in cattle
- Linear trichoepithelioma on the neck of a 15-year-old girl
- Female Androgenetic (?) Alopecia
- Congenital atrichia associated with situs inversus and mesocardia
- Causes and Management of Hypertrichosis
- Efficacy of Dupilumab in Treating Atopic Dermatitis With Recurrent Eczema Herpeticum in a Patient With DOCK8-Deficiency Hyper-IgE Syndrome: A Case Report
- Inducible expression of gasdermin A3 in the epidermis causes epidermal hyperplasia and skin inflammation
- Unraveling the complex role of MAPT-containing H1 and H2 haplotypes in neurodegenerative diseases
- A TP63 Mutation Causes Prominent Alopecia with Mild Ectodermal Dysplasia
- FGF5 is a crucial regulator of hair length in humans
- 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
- Three Streams for the Mechanism of Hair Graying
- Expanding phenotype of hereditary fibrosing poikiloderma with tendon contractures, myopathy, and pulmonary fibrosis caused by FAM111B mutations: Report of an additional family raising the question of cancer predisposition and a short review of early-onset poikiloderma
- The color of skin: white diseases of the skin, nails, and mucosa
- Botanical extract combined with minoxidil improve hidrotic ectodermal dysplasia caused by p.G11R mutations: a case report
- Ichthyosis Follicularis, Alopecia, and Photophobia Syndrome in a Saudi Child: A Case Report
- Genetic Prediction of Eye, Hair, and Skin Color: Forensic Applications and Challenges in Latin American Populations
- Genetic Analysis of Male Pattern Baldness and the 5α-Reductase Genes
- Birt–Hogg–Dubé syndrome: from gene discovery to molecularly targeted therapies
- Steatocystoma Multiplex
- A Case of Loose Anagen Hair Syndrome in a Southeast Asian Boy
- How to defeat male pattern alopecia in a trompeur de femmes, who loves to abuse of libido boosters?
- Heterozygous <i>COL5A1</i> deletion in a cat with classical Ehlers–Danlos syndrome
- Clouston’s syndrome: a rare case report
- Comparative Study of Some Potential Paracrine Factors Produced by Normal and Androgenetic Alopecia Hair Follicles