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Research 691–720 of 1000+
- Polycystic ovary syndrome and insulin-resistant hyperinsulinemia
- Deficient Plakophilin-1 Expression Due to a Mutation in PKP1 Causes Ectodermal Dysplasia-Skin Fragility Syndrome in Chesapeake Bay Retriever Dogs
- An Autosomal Recessive Form of Monilethrix Is Caused by Mutations in DSG4: Clinical Overlap with Localized Autosomal Recessive Hypotrichosis
- An LRH-RSL4 feedback regulatory loop controls the determinate growth of root hairs in Arabidopsis
- Genomewide Scan for Linkage Reveals Evidence of Several Susceptibility Loci for Alopecia Areata
- Finasteride and Dutasteride in the Treatment of Androgenetic Alopecia: Risk or Benefit?
- Ichthyosis, Follicular Atrophoderma, and Hypotrichosis Caused by Mutations in ST14 Is Associated with Impaired Profilaggrin Processing
- PA33 When bones speak through nails: insights from a paediatric case series
- Primary Follicular Dystrophy With Scarring Dermatitis in C57BL/6 Mouse Substrains Resembles Central Centrifugal Cicatricial Alopecia in Humans
- Escobar syndrome (multiple pterygium syndrome) associated with osteogenesis imperfecta: a case report
- Chemotherapy-Induced Alopecia by Docetaxel: Prevalence, Treatment and Prevention
- The role of reactive oxygen species in cell growth: lessons from root hairs
- Androgenetic alopecia: An update
- 17 beta-hydroxysteroid dehydrogenase 3 deficiency in the Mediterranean population.
- Novel Mutations in X-Linked Dominant Chondrodysplasia Punctata (CDPX2)
- Novel insights into the molecular mechanisms underlying generalized glucocorticoid resistance and hypersensitivity syndromes
- Case report: Acrodermatitis enteropathica result from a novel SLC39A4 gene mutation
- T Cell Immunodeficiency, Congenital Alopecia, and Nail Dystrophy
- A novel mutation in ST14 at a functionally significant amino acid residue expands the spectrum of ichthyosis-hypotrichosis syndrome
- Cell Type-specific Functions of the Lysosomal Protease Cathepsin L in the Heart
- Expanding the Phenotypic Spectrum of APMR4 Syndrome Caused by a Novel Variant in LSS Gene
- Ichthyosis Follicularis, Alopecia, and Photophobia Syndrome in a Saudi Child: A Case Report
- Author response: Plant Trans-Golgi Network/Early Endosome pH regulation requires Cation Chloride Cotransporter (CCC1)
- Genomic Characterization of Quality Wool Traits in Spanish Merino Sheep
- LB1076 Using the frog embryonic epidermis as a model to study desmosome function during development
- Genomic prediction and genome-wide association studies of morphological traits and distraction index in Korean Sapsaree dogs
- K <sub>ATP</sub> Channels and Cardiovascular Disease
- Central centrifugal cicatricial alopecia: challenges and solutions
- Urinary steroids in women with androgenic alopecia
- Mutations in Homocysteine Metabolism Genes Increase Keratin <i>N</i>-Homocysteinylation and Damage in Mice