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Research 541–570 of 1000+
- The Roles of EDA2R in Ageing and Disease
- Male-pattern hair loss: Comprehensive identification of the associated genes as a basis for understanding pathophysiology
- Antiandrogens as Therapies for COVID-19: A Systematic Review
- Genome-Wide Association Study for Udder Conformation Traits in Chinese Holstein Cattle
- Hair follicle–derived IL-7 and IL-15 mediate skin-resident memory T cell homeostasis and lymphoma
- PandaOmics: An AI-Driven Platform for Therapeutic Target and Biomarker Discovery
- Primary Follicular Dystrophy With Scarring Dermatitis in C57BL/6 Mouse Substrains Resembles Central Centrifugal Cicatricial Alopecia in Humans
- Identification of Candidate Genes for Min Pig Villi Hair Traits by Genome-Wide Association of Copy Number Variation
- Tissue Regeneration, Stem Cells, and Wound Healing
- Whole-genome resequencing to investigate the genetic diversity and the molecular basis underlying key economic traits in indigenous sheep breeds adapted to hypoxic environments
- Hirsutism Beyond PCOS: Genome-wide Evidence for Genetic Factors
- Androgens and Hirsutism in a Large Cohort of Portuguese Women
- Rare and Underappreciated Causes of Polycystic Ovarian Syndrome
- Frizzled Receptors in Development and Disease
- Keratins and disease at a glance
- Hidradenitis Suppurativa as a Potential Subtype of Autoinflammatory Keratinization Disease
- Ichthyosis with confetti: clinics, molecular genetics and management
- Large Intragenic KRT1 Deletion Underlying Atypical Autosomal Dominant Keratinopathic Ichthyosis
- Challenges in treatment of patients with non-classic congenital adrenal hyperplasia
- E-Poster
- Endocrine abnormalities in ring chromosome 11: a case report and review of the literature
- Ichthyosis follicularis, alopecia, and photophobia (IFAP) syndrome
- Genetic screening of non-classic CAH females with hyperandrogenemia identifies a novel CYP11B1 gene mutation
- Birt–Hogg–Dubé syndrome: from gene discovery to molecularly targeted therapies
- Elucidating causal relationships of diet-derived circulating antioxidants and the risk of non-scarring alopecia: A Mendelian randomization study
- Morphologic and molecular characterization of two novel Krt71 (Krt2-6g) mutations: Krt71 rco12 and Krt71 rco13
- Transcriptomic regulation of seasonal coat color change in hares
- Structural and epistatic regulatory variants cause hallmark white spotting in cattle
- Forensic DNA Phenotyping
- Cutaneous and Mucosal Lichen Planus: A Comprehensive Review of Clinical Subtypes, Risk Factors, Diagnosis, and Prognosis