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Research 511–540 of 1000+
- De novo single-nucleotide and copy number variation in discordant monozygotic twins reveals disease-related genes
- Comedonal and Cystic Fibrofolliculomas in Birt-Hogg-Dube Syndrome
- Male pattern baldness and prostate cancer risk in a population-based case–control study
- The pressing need for standardization in epidemiologic studies of PCOS across the globe
- SlPHL1, a MYB‐CC transcription factor identified from tomato, positively regulates the phosphate starvation response
- A novel mutation in ST14 at a functionally significant amino acid residue expands the spectrum of ichthyosis-hypotrichosis syndrome
- Association between <i>IL16</i> gene polymorphisms and susceptibility to alopecia areata in the Korean population
- White piedra caused by <i>Trichosporon inkin</i> : a report of two cases in a northern climate
- Dermal papilla cells and melanocytes response to physiological oxygen levels depends on their interactions
- Variation and Heritability in Hair Diameter and Curvature in an Australian Twin Sample
- Delayed-onset pachyonychia congenita caused by a novel mutation in the V2 domain of keratin 6b
- Genetic determinants of skin ageing: a systematic review and meta-analysis of genome-wide association studies and candidate genes
- Atrichia with Papular Lesions in a Chinese Family Caused by Novel Compound Heterozygous Mutations and Literature Review
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- Diagnosis and management of vascular Ehlers-Danlos syndrome: Experience of the UK national diagnostic service, Sheffield
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- Regenerative potential of CD200- subpopulations of hair follicle bulge
- Genetic syndromes in paediatric alopecia areata: a systematic review
- Prevalence and Metabolic Characterization of Polycystic Ovary Syndrome in a Cohort of Patients Diagnosed with Spina Bifida: Study Protocol
- Review on Tridax Procumbens
- 516 Functional annotation of genes underlying hair disorders
- Diagnostic Challenges and Treatment Strategies in Neutrophilic Cicatricial Alopecias: A Narrative Review from Conventional Therapies to New Therapeutic Targets
- Male-pattern hair loss: Comprehensive identification of the associated genes as a basis for understanding pathophysiology
- Weakly supervised learning of biomedical information extraction from curated data
- Curly bare (cub), a new mouse mutation on chromosome 11 causing skin and hair abnormalities, and a modifier gene (mcub) on chromosome 5
- Skin deep: dermatologic challenges in PCOS through the female lifespan
- Discovery of Four New<em> FGF5</em> Variants Causing Long Hair in the Dog
- Dermal Papilla Cells and Melanocytes Response to Physiological Oxygen Levels Depends on Their Interactions
- Australian Hair and Wool Research Society Cutaneous Biology and Endocrinology Workshop
- Age-Related Loss of Innate Immune Antimicrobial Function of Dermal Fat Is Mediated by Transforming Growth Factor Beta