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Research 151–180 of 1000+
- Geographic Influence and Metabolomics-Driven Discovery of 5-Alpha Reductase Inhibitors in Tectona grandis L.f. (Teak) Leaves
- Rare and misdiagnosed entity fibrosing alopecia in a pattern distribution: A case report
- Ethnopharmacology and hair: Indian perspectives
- Interventions for nail psoriasis
- Glutamine Metabolism Controls Stem Cell Fate Reversibility and Long-Term Maintenance in the Hair Follicle
- Updates in the understanding and treatments of skin & hair disorders in women of color
- Hair Histology as a Tool for Forensic Identification of Various Animals
- An Insightful Analysis of Trichological Principles in Ayurveda: A Systematic Review
- The Effect of Finasteride in Men with Benign Prostatic Hyperplasia
- Large-scale genome-wide meta-analysis of polycystic ovary syndrome suggests shared genetic architecture for different diagnosis criteria
- Genetic Variation in the Human Androgen Receptor Gene Is the Major Determinant of Common Early-Onset Androgenetic Alopecia
- Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis
- Susceptibility variants for male-pattern baldness on chromosome 20p11
- Addressing continuous data for participants excluded from trial analysis: a guide for systematic reviewers
- Skin Adipocyte Stem Cell Self-Renewal Is Regulated by a PDGFA/AKT-Signaling Axis
- Cryptic Patterning of Avian Skin Confers a Developmental Facility for Loss of Neck Feathering
- Variant <i>PADI3</i> in Central Centrifugal Cicatricial Alopecia
- Stimulation of Hair Growth by Small Molecules that Activate Autophagy
- Loss-of-Function Mutations in HOXC13 Cause Pure Hair and Nail Ectodermal Dysplasia
- Amino acid–derived defense metabolites from plants: A potential source to facilitate novel antimicrobial development
- Trans‐species hair growth induction by human hair follicle dermal papillae
- Genome-wide Scan and Fine-Mapping Linkage Study of Androgenetic Alopecia Reveals a Locus on Chromosome 3q26
- Netherton syndrome subtypes share IL-17/IL-36 signature with distinct IFN-α and allergic responses
- Bi-allelic Mutations in LSS, Encoding Lanosterol Synthase, Cause Autosomal-Recessive Hypotrichosis Simplex
- Progenitor Cell Dysfunctions Underlie Some Diabetic Complications
- Overview of Caffeine Effects on Human Health and Emerging Delivery Strategies
- Mutations in SNRPE, which Encodes a Core Protein of the Spliceosome, Cause Autosomal-Dominant Hypotrichosis Simplex
- Long‐term safety and efficacy of bimatoprost solution 0·03% application to the eyelid margin for the treatment of idiopathic and chemotherapy‐induced eyelash hypotrichosis: a randomized controlled trial
- Gene therapy to enhance angiogenesis in chronic wounds
- Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome