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Research 901–930 of 1000+
- A replication study confirmed the EDAR gene to be a major contributor to population differentiation regarding head hair thickness in Asia
- Autoimmunity and autoimmune co-morbidities in psoriasis
- Detection of circular RNA expression and related quantitative trait loci in the human dorsolateral prefrontal cortex
- Goat Genomic Resources: The Search for Genes Associated with Its Economic Traits
- Recent positive selection of a human androgen receptor/ectodysplasin A2 receptor haplotype and its relationship to male pattern baldness
- Hidradenitis Suppurativa as a Potential Subtype of Autoinflammatory Keratinization Disease
- Chronic overlapping pain conditions and nociplastic pain
- Expanding on the phenotypic spectrum of Woodhouse‐Sakati syndrome due to founder pathogenic variant in <i>DCAF17</i>: Report of 58 additional patients from Qatar and literature review
- Presentation, diagnosis, and management options of lipedematous alopecia
- Evaluation of loci to predict ear morphology using two SNaPshot assays
- Single nucleotide polymorphisms in the KRT82 promoter region modulate irregular thickening and patchiness in the dorsal skin of New Zealand rabbits
- Association Between Retinoid X Receptor Gene Variants and Dyslipidemia Risk in an Iranian Population
- Formulation & Evaluation of Herbal Hair Serum containing Rosemary oil
- Identification of a Rare Variant in the <i>SRD5A2</i> Gene in Siblings With 46,XY Disorders of Sexual Development
- [Androgenetic alopecia].
- Common Variants in the Trichohyalin Gene Are Associated with Straight Hair in Europeans
- Mutations in Three Genes Encoding Proteins Involved in Hair Shaft Formation Cause Uncombable Hair Syndrome
- Ichthyosis, Follicular Atrophoderma, and Hypotrichosis Caused by Mutations in ST14 Is Associated with Impaired Profilaggrin Processing
- Differentiation of frontal fibrosing alopecia and Lichen planopilaris on trichoscopy: A comprehensive review
- Gut instinct: Using tofacitinib to treat alopecia areata in the context of comorbid inflammatory bowel disease
- Coloration in Equine: Overview of Candidate Genes Associated with Coat Color Phenotypes
- Emergence of the natural history of Myhre syndrome: 47 patients evaluated in the Massachusetts General Hospital Myhre Syndrome Clinic (2016–2023)
- Lymphocytes, neuropeptides, and genes involved in alopecia areata
- GABRA2 Alleles Moderate the Subjective Effects of Alcohol, Which are Attenuated by Finasteride
- Metformin therapy for the reproductive and metabolic consequences of polycystic ovary syndrome
- Regulation of masculinization: androgen signalling for external genitalia development
- A Humanized Mouse Model of Hereditary 1,25-Dihydroxyvitamin D–Resistant Rickets Without Alopecia
- Cronkhite–Canada syndrome: from clinical features to treatment
- The molecular pathogenesis of Trichilemmal carcinoma
- Clinical characterization of men with long QT syndrome and torsades de pointes associated with hypogonadism: A review and pharmacovigilance study