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Research 271–300 of 1000+
- Regulatory mutations in TBX3 disrupt asymmetric hair pigmentation that underlies Dun camouflage color in horses
- Haplotypes spanning centromeric regions reveal persistence of large blocks of archaic DNA
- Hydrogels Modulating the Microbiome: Therapies for Tissue Regeneration with Infection Control
- A Homozygous Missense Variant in K25 Underlying Overlapping Phenotype with Woolly Hair and Dental Anomalies
- Correlation Analysis of BLTP1 (KIAA1109) and KIF27 Gene Polymorphisms with Wool Traits in Subo Merino Sheep
- The Genetic Landscape of Androgenetic Alopecia: Current Knowledge and Future Perspectives
- Gene variants associated with acne vulgaris presentation and severity: a systematic review and meta-analysis
- Polymorphisms of FST gene and their association with wool quality traits in Chinese Merino sheep
- RETRACTED: Explore the genetic exposure to alopecia areata
- Unraveling the Molecular Mechanism of Bider Marking Formation in Dun Mongolian Horses Through Transcriptome Sequencing
- Dietary and Genetic Aspects of Polycystic Ovary Syndrome (PCOS) in Polish Women-Part II: Association of
- Does Androgenic Alopecia Aggravate the Risk of Prostate Cancer? Evidence from Mendelian Randomization
- Genomic Regions Associated with Wool, Growth and Reproduction Traits in Uruguayan Merino Sheep
- Longitudinal Assessment of the Prevalence of Actinic Keratosis and Extensive Risk Factor Evaluation: An Update from the Rotterdam Study
- Harnessing Microbiome, Bacterial Extracellular Vesicle, and Artificial Intelligence for Polycystic Ovary Syndrome Diagnosis and Management
- Large-Scale Plasma Proteomics and Genetic Integration Uncover Novel Biological Pathways in Male Pattern Baldness
- Male-pattern hair loss: Comprehensive identification of the associated genes as a basis for understanding pathophysiology
- Hunting the genes in male‐pattern alopecia: how important are they, how close are we and what will they tell us?
- An epistatic effect of KRT25 on SP6 is involved in curly coat in horses
- Clinical and genetic investigation of ichthyosis in familial and sporadic cases in south of Tunisia: genotype–phenotype correlation
- Identification of key pathways and genes that regulate cashmere development in cashmere goats mediated by exogenous melatonin
- Genomic and Transcriptomic Characterization of Atypical Recurrent Flank Alopecia in the Cesky Fousek
- C‐reactive protein as a novel biomarker for vitamin D deficiency in alopecia areata
- Expanding the Phenotypic Spectrum of APMR4 Syndrome Caused by a Novel Variant in LSS Gene
- Chronic overlapping pain conditions and nociplastic pain
- How Our Microbiome Influences the Pathogenesis of Alopecia Areata
- Multi-Walled Carbon Nanotubes Can Promote Brassica napus L. and Arabidopsis thaliana L. Root Hair Development through Nitric Oxide and Ethylene Pathways
- Recent Advances in the Pathogenesis of Autoimmune Hair Loss Disease Alopecia Areata
- WNT10A mutation causes ectodermal dysplasia by impairing progenitor cell proliferation and KLF4-mediated differentiation
- Therapeutic strategy for hair regeneration: hair cycle activation, niche environment modulation, wound-induced follicle neogenesis, and stem cell engineering