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Research 211–240 of 1000+
- Analysis of Copy Number Variation in the Whole Genome of Normal-Haired and Long-Haired Tianzhu White Yaks
- Genetic Variants and Protective Immunity against SARS-CoV-2
- Genomic and Transcriptomic Characterization of Atypical Recurrent Flank Alopecia in the Cesky Fousek
- Zebrafish Model of Hereditary Pigmentary Disorders
- Msx2 deficiency in mice causes pleiotropic defects in bone growth and ectodermal organ formation
- Polycystic ovary syndrome
- Wool Keratin-Associated Protein Genes in Sheep—A Review
- Targeted transgenic expression of the mutation causing Hutchinson-Gilford progeria syndrome leads to proliferative and degenerative epidermal disease
- Molecular Genetics of the PI3K-AKT-mTOR Pathway in Genodermatoses: Diagnostic Implications and Treatment Opportunities
- Effects of lifelong testosterone exposure on health and disease using Mendelian randomization
- The Genetic Architecture of Alopecia Areata
- Transglutaminase 3: The Involvement in Epithelial Differentiation and Cancer
- Hair Growth Effect of Emulsion Extracted Brevilin A, a JAK3 Inhibitor, from Centipeda minima
- The role of P-cadherin in skin biology and skin pathology: lessons from the hair follicle
- Telomere Dynamics and Telomerase in the Biology of Hair Follicles and their Stem Cells as a Model for Aging Research
- Evidence on Hidradenitis Suppurativa as an Autoinflammatory Skin Disease
- Mutational spectrum associated with oculocutaneous albinism and Hermansky-Pudlak syndrome in nine Pakistani families
- <i>IGF2BP2</i> and <i>IGFBP3</i> Genotypes, Haplotypes, and Genetic Models Studies in Polycystic Ovary Syndrome
- Wwox Deficiency Causes Downregulation of Prosurvival ERK Signaling and Abnormal Homeostatic Responses in Mouse Skin
- Bald thigh syndrome in sighthounds—Revisiting the cause of a well-known disease
- Fetal alpha 5-reductase Val89Leu mutation is associated with late miscarriage
- A rare LMNA missense mutation causing a severe phenotype of mandibuloacral dysplasia type A: a case report
- Polymorphisms of the genes ABCG2, SLC22A12 and XDH and their relation with hyperuricemia and hypercholesterolemia in Mexican young adults
- A Comprehensive Review of GWASs of Human Hair Traits
- The Role of MicroRNA, Long Non-Coding RNA and Circular RNA in the Pathogenesis of Polycystic Ovary Syndrome: A Literature Review
- Association between DNA Methylation in the Core Promoter Region of the CUT-like Homeobox 1 (CUX1) Gene and Lambskin Pattern in Hu Sheep
- Genetic association of wool quality characteristics in United States Rambouillet sheep
- 26-SNP Panel Aids Guiding Androgenetic Alopecia Therapy and Provides Insight into Mechanisms of Action
- Genetic architecture of thermotolerance traits in beef cattle: a novel integration of SNP and breed-of-origin effects
- Androgenetic Alopecia: A Review