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Research 31–60 of 1000+
- Cell wall-associated ROOT HAIR SPECIFIC 10, a proline-rich receptor-like kinase, is a negative modulator of Arabidopsis root hair growth
- Clomiphene Citrate versus Letrozole for Ovulation Induction in PCOS: A Comparative Study
- Short anagen hair syndrome
- A Single-Scar Technique for Donor Harvesting in Hair Transplantation Surgery
- A Missense Mutation within the Helix Initiation Motif of the Keratin K71 Gene Underlies Autosomal Dominant Woolly Hair/Hypotrichosis
- Regulatory T cells in dominant immunologic tolerance
- Inherited Disorders of the Hair
- 218 Chemokine receptor CCR5 is the novel target for the treatment of alopecia areata
- 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
- 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