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Research 31–60 of 1000+
- Regulatory T cells in dominant immunologic tolerance
- Inherited Disorders of the Hair
- Loose Anagen Hair as a Cause of Hereditary Hair Loss in Children
- Acquired Uncombable Hair
- Hereditary Hypotrichosis and Localized Morphea: A New Clinical Entity
- Genetic correlation by pedigree analysis in patients diagnosed with PCOS as per Rotterdam’s criteria
- A Case Report of Kaphaja Granthi w.s.r. to Trichilemmal Cyst
- Early Skin Biopsy in Conradi‐Hünermann‐Happle Syndrome (X‐Linked Dominant Chondrodysplasia Punctata)
- The Chicken Frizzle Feather Is Due to an α-Keratin (KRT75) Mutation That Causes a Defective Rachis
- Defolliculated (Dfl): A Dominant Mouse Mutation Leading to Poor Sebaceous Gland Differentiation and Total Elimination of Pelage Follicles
- Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome
- Bacteria Display Differential Growth and Adhesion Characteristics on Human Hair Shafts
- Alopecia Diffusa while Using Interleukin-17 Inhibitors against Psoriasis Vulgaris
- Tracing selection signatures in the pig genome gives evidence for selective pressures on a unique curly hair phenotype in Mangalitza
- Monilethrix
- Acquired non-scarring vertex alopecia in three women revealing trichotillomania: Diagnostic accuracy of trichoscopy
- Hair Shaft Defect in a Teenage Girl: Trichoscopy Saves the Day!
- The nocebo effect: A clinicians guide
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- A Splice Site Mutation in the Gene of the Human Type I Hair Keratin hHa1 Results in the Expression of a Tailless Keratin Isoform
- Effect of gelatin nanoparticles’ size and charge on iontophoretic targeted deposition to the hair follicles
- Novel Combination Scalp Therapy for Androgenetic Alopecia: A Preliminary Retrospective Case Series with an Illustrative Four-Year Case
- Fibroblast Lineage Switching as the Developmental Origin of Scarring and Target for Regenerative Healing
- Genetic Variant of the Canine FGF5 Gene for the Hair Length Trait in the Akita: Utility for Hair Coat Variations and Welfare in Conservation Breeding
- Regenerative potential of CD200- subpopulations of hair follicle bulge
- IMPACT OF POLY CYSTIC OVARIAN SYNDROME ON THE QUALITY OF LIFE OF MARRIED FEMALES: A CROSS-SECTIONAL STUDY
- Interrelation of immunity and tissue repair or regeneration
- Variation in the caprine keratin-associated protein 15-1 (KAP15-1) gene affects cashmere fibre diameter
- The inconsistent regulation of HOXC13 on different keratins and the regulation mechanism on HOXC13 in cashmere goat (Capra hircus)
- Upregulation of interfollicular epidermal and hair infundibulum β-catenin expression in Gsdma3 mutant mice