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Research 901–930 of 1000+
- Zinc transporter ZIP13 G289R variant from Spondylocheirodysplastic Ehlers-Danlos syndrome (SCD-EDS) is associated with abnormal hair quality
- Identification of a Rare Variant in the <i>SRD5A2</i> Gene in Siblings With 46,XY Disorders of Sexual Development
- Genome-Wide Association Studies of Hair Whorl in Pigs
- Association study reveals a susceptibility locus with male pattern baldness in the Han Chinese population
- Causal links between 13 autoimmune diseases and graft dysfunction: A Mendelian randomization study
- Genetic Differences between Male and Female Pattern Hair Loss in a Korean Population
- EDA Missense Variant in a Cat with X-Linked Hypohidrotic Ectodermal Dysplasia
- Elucidating causal relationships of diet-derived circulating antioxidants and the risk of non-scarring alopecia: A Mendelian randomization study
- Resequencing Analyses Revealed Genetic Diversity and Selection Signatures during Rabbit Breeding and Improvement
- Twins with psychiatric features and a nonsense HRAS variant affecting transcript processing
- Whole-Genome Resequencing Reveals Selection Signal Related to Sheep Wool Fineness
- Female Pattern Hair Loss: An Overview with Focus on the Genetics
- Effects of Androgen Treatment on Growth in Patients with 5-α-Reductase Type 2 Deficiency
- Clinical Findings, Response to Steroid Treatment, and Recurrence Rate in Alopecia Areata Patients with or without a Nonsynonymous Variant of Coiled-Coil Alpha-Helical Rod Protein 1
- Forensic DNA Phenotyping
- The influence of ESR1 polymorphisms on selected hormonal, metabolic and mineral balance markers in women with hyperandrogenism
- Correlation analysis of four KRTAP gene polymorphisms and cashmere fiber diameters in two cashmere goat breeds
- Rare and Underappreciated Causes of Polycystic Ovarian Syndrome
- Decision letter: Effects of lifelong testosterone exposure on health and disease using Mendelian randomization
- Male-pattern hair loss: Comprehensive identification of the associated genes as a basis for understanding pathophysiology
- Genetic Polymorphisms of Immunity Regulatory Genes and Alopecia Areata Susceptibility in Jordanian Patients
- Serum levels of interleukin-1 (IL-1α, IL-1β) in patients with alopecia areata
- The JAK/STAT signaling pathway: from bench to clinic
- A Ca <sup>2+</sup> /calmodulin-dependent protein kinase required for symbiotic nodule development: Gene identification by transcript-based cloning
- Nerve-Derived Sonic Hedgehog Defines a Niche for Hair Follicle Stem Cells Capable of Becoming Epidermal Stem Cells
- Wnt Signaling, Lgr5, and Stem Cells in the Intestine and Skin
- Wnt/β-catenin signalling: function, biological mechanisms, and therapeutic opportunities
- TRPA1 Modulates Mechanotransduction in Cutaneous Sensory Neurons
- Integrin signalling regulates YAP/TAZ to control skin homeostasis
- The resistance mechanisms of bacteria against ciprofloxacin and new approaches for enhancing the efficacy of this antibiotic