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Research 271–300 of 1000+
- Exome-wide age-of-onset analysis reveals exonic variants in ERN1 and SPPL2C associated with Alzheimer’s disease
- The relationship among androgens, insulin resistanceand ghrelin polymorphisms in post-adolescent malepatients with severe acne vulgaris
- Genomic and transcriptomic landscape to decipher the genetic basis of hyperpigmentation in Lanping black-boned sheep (Ovis aries)
- No genetic support for a contribution of prostaglandins to the aetiology of androgenetic alopecia
- Transcriptomics analysis reveals molecular alterations underpinning spaceflight dermatology
- The pioneer factor SOX9 competes for epigenetic factors to switch stem cell fates
- Advances in Hair Diseases
- Glycolytic Dysfunction in Granulosa Cells and Its Contribution to Metabolic Dysfunction in Polycystic Ovary Syndrome
- Aberrant inflammasome activation as a driving force of human autoimmune skin disease
- Analysis of the function of ADAM17 in iRhom2 curly-bare and tylosis with esophageal cancer mutant mice
- The PER3 rs772027021 SNP induces pigmentation phenotypes of dyschromatosis universalis hereditaria
- Minoxidil Cannot Be Used To Target Lysyl Hydroxylases during Postnatal Mouse Lung Development: A Cautionary Note
- Premature Greying of Hair (Premature Canities): A Concern for Parent and Child
- Inherited Disorders of the Hair
- Six SNPs and a TTG indel in sheep desmoglein 4 gene are in complete linkage disequilibrium
- Transcriptome sequencing reveals the expression profiles of lncRNAs and mRNAs in goat skin tissues with different types of wool coats
- Genome-Wide Association Study of Alopecia Areata in Taiwan: The Conflict Between Individuals and Hair Follicles
- Skin transcriptome reveals the Periodic changes in genes underlying hair follicle cycling in Cashmere goats
- The Role of Histone Demethylases in Disease
- From basic biology to engineered therapies: the keratinocyte stem cell playbook
- Ca <sup>2+</sup> -mediated protein citrullination regulates proliferation in the regenerating and malignant CNS
- CLINICAL PROFILE AND OUTCOMES OF PATIENTS WITH POLYCYSTIC OVARIAN SYNDROME
- Association of Cyp11a Gene with Polycystic Ovarian Syndrome Patients in Lahore, Pakistan
- Understanding Polycystic Ovary Syndrome
- Immunoglobulin E and Serum Interleukin-13 and Bacteria in Patients with Alopecia Areata
- Identifying causal genes in alopecia areata using integrative analysis of differential expression and Mendelian randomization
- Woodhouse-Sakati syndrome: genotype–phenotype review and case of intra-familial heterogeneity
- The evaluation of IL-4 intron 3 VNTR and TNF-α (rs1799964) gene polymorphisms in Egyptian patients with Alopecia Areata: a case-control study
- Molecular heterogeneity of quiescent melanocyte stem cells revealed by single-cell RNA-sequencing
- Polikistik Over Sendromu ve Obezite: FTO ve MC4R Gen Polimorfizmlerinin Rolü