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Research 571–600 of 1000+
- Pathogenic variants affecting peptidyl arginine deiminase 3 and its major substrates underlie central centrifugal cicatricial alopecia
- miR-200a Targets PITX2 to Mediate Goose Fibroblast Proliferation Through the Wnt Pathway
- Association study reveals a susceptibility locus with male pattern baldness in the Han Chinese population
- Genomic Markers and Personalized Medicine in Androgenetic Alopecia: A Comprehensive Review
- Integration Analysis of Hair Follicle Transcriptome and Proteome Reveals the Mechanisms Regulating Wool Fiber Diameter in Angora Rabbits
- Algorithms For Preventive Measures For Disease Prevention And Antioxidant Protection
- Lymphocytes, neuropeptides, and genes involved in alopecia areata
- NUDT15 R139C-related thiopurine leukocytopenia is mediated by 6-thioguanine nucleotide-independent mechanism in Japanese patients with inflammatory bowel disease
- Exploring the possibility of predicting human head hair greying from DNA using whole-exome and targeted NGS data
- Type 1 Diabetes Mellitus and Autoimmune Diseases: A Critical Review of the Association and the Application of Personalized Medicine
- Single-Cell Transcriptomics Reveals the Molecular Anatomy of Sheep Hair Follicle Heterogeneity and Wool Curvature
- The Associations of Androgen-Related Genes CYP21A2 and CYP19A1 with Severe Acne Vulgaris in Patients from Southwest China
- Recessive Mutation in FAM83G Associated with Palmoplantar Keratoderma and Exuberant Scalp Hair
- Drivers of plateau adaptability in cashmere goats revealed by genomic and transcriptomic analyses
- Novel mutations of the ABCA12, KRT1 and ST14 genes in three unrelated newborns showing congenital ichthyosis
- Alopecia Areata in Sub-Saharan Africa: A Scoping Review Protocol on Epidemiology, Clinical Presentation, Burden, Treatment, and Evidence Gaps.
- Atrichia congenita with papular lesions: A rare cause of pediatric alopecia
- The rare association of congenital glaucoma, giant melanocytic nevus, alopecia, and hypospadias in an Egyptian child with neurofibromatosis type 1: a case report
- The evaluation of IL-4 VNTR intron 3 and TNF-α (rs1799964) gene polymorphisms in Egyptian patients with alopecia areata: a case–control study
- Role of polymorphism of the androgen receptor gene andnon-random x chromosome inactivation in the pathogenesisof androgenic alopecia
- An epistatic effect of KRT25 on SP6 is involved in curly coat in horses
- Chromosomal localization of acidic and basic keratin genes of the domestic dog
- Primary Follicular Dystrophy With Scarring Dermatitis in C57BL/6 Mouse Substrains Resembles Central Centrifugal Cicatricial Alopecia in Humans
- Laminin 332 Is Indispensable for Homeostatic Epidermal Differentiation Programs
- Trichothiodystrophy: Current Concepts
- Exploring Hirsutism: Epidemiology, Associated Endocrinal Abnormalities, and Societal Challenges in GCC—A Narrative Review
- Two-Stage Machine Learning-Based GWAS for Wool Traits in Central Anatolian Merino Sheep
- Natural variation in trichome density and biochemistry in Antirrhinum
- Assessment of androgenic hormones and other risk factors in Egyptian males with early onset androgenetic alopecia: a case control study
- Gene-Environment Interaction Between <i>CYP1B1</i> and Oral Contraception on Frontal Fibrosing Alopecia