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Research 301–330 of 391
- Hair Shaft Abnormalities – Clues to Diagnosis and Treatment
- A Recurrent Intragenic Deletion in the Desmoglein 4 Gene Underlies Localized Autosomal Recessive Hypotrichosis
- Female pattern alopecia: current perspectives
- The investigation of insulin resistance and metabolic syndrome in male patients with early-onset androgenetic alopecia
- Alopecia in a Novel Mouse Model RCO3 Is Caused by mK6irs1 Deficiency
- Novel mutations in the keratin-74 (KRT74) gene underlie autosomal dominant woolly hair/hypotrichosis in Pakistani families
- Alopecias in lupus erythematosus
- Relevance of trichoscopy in the differential diagnosis of alopecia: A cross-sectional study from North India
- 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
- Recent Findings with Computerized Methods for Scalp Hair Growth Measurements
- In vivo reflectance confocal microscopy: usefulness for diagnosing hair diseases
- Wanted, dead and alive: Why a multidisciplinary approach is needed to unlock hair treatment potential
- Differences between ultrastructure and protein composition in straight hair fibres
- A novel mutation in ST14 at a functionally significant amino acid residue expands the spectrum of ichthyosis-hypotrichosis syndrome
- A Spontaneous Deletion within the Desmoglein 3 Extracellular Domain of Mice Results in Hypomorphic Protein Expression, Immunodeficiency, and a Wasting Disease Phenotype
- Hague (<i>Hag</i>): A New Mouse Hair Mutation With an Unstable Semidominant Allele
- Genetics of Wool and Cashmere Fibre: Progress, Challenges, and Future Research
- Trichoscopy of Alopecia Areata: Hair Loss Feature Extraction and Computation Using Grid Line Selection and Eigenvalue
- Semidominant Inheritance in Epidermolytic Ichthyosis
- Nodules on the hair: A rare case of mixed piedra
- Optical coherent tomography: promising in vivo measurement of hair shaft cross section
- Whole exome sequencing in Alopecia Areata identifies rare variants in KRT82
- Pili Torti: A Feature of Numerous Congenital and Acquired Conditions
- A review of genotrichoses and hair pathology associated with inherited skin diseases
- Transcription Regulation and Protein Subcellular Localization of the Truncated Basic Hair Keratin hHb1-ΔN in Human Breast Cancer Cells
- Autophagy-Mediated Cellular Remodeling during Terminal Differentiation of Keratinocytes in the Epidermis and Skin Appendages
- Management of hair loss after severe acute respiratory syndrome coronavirus 2 infection: Insight into the pathophysiology with implication for better management
- Mast cell hyperplasia in the skin of Dsg4-deficient hypotrichosis mice, which are long-living mutants of lupus-prone mice
- Safety and efficacy of ALRV5XR in women with androgenetic alopecia or telogen effluvium: A randomised, double-blinded, placebo-controlled clinical trial