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Research 691–720 of 1000+
- A case of <i>MBTPS1</i>‐related disorder due to compound heterozygous variants in <i>MBTPS1</i> gene: Genotype–phenotype expansion and the emergence of a novel syndrome
- Regulatory pathways implicated in male androgenetic alopecia pathogenesis
- Exploring the possibility of predicting human head hair greying from DNA using whole-exome and targeted NGS data
- A Genetically Defined Male Counterpart of Polycystic Ovary Syndrome: Evidence for Ovarian-Independent Pathogenesis
- Lymphocytes, neuropeptides, and genes involved in alopecia areata
- From gene to therapy in spinal and bulbar muscular atrophy: Are we there yet?
- Keratins: the hair shaft's backbone revealed
- Type 1 Diabetes Mellitus and Autoimmune Diseases: A Critical Review of the Association and the Application of Personalized Medicine
- Laminin 332 Is Indispensable for Homeostatic Epidermal Differentiation Programs
- Hidradenitis suppurativa and Mediterranean fever gene mutations
- The rare association of congenital glaucoma, giant melanocytic nevus, alopecia, and hypospadias in an Egyptian child with neurofibromatosis type 1: a case report
- Atrichia congenita with papular lesions: A rare cause of pediatric alopecia
- Recent trends in nanocarrier formulations of actives beyond minoxidil and 5-α reductase inhibitors in androgenetic alopecia management: A systematic review
- Cyberspace Chat
- Human stratum corneum proteomics reveals cross‐linking of a broad spectrum of proteins in cornified envelopes
- Tracing the cellular origin of cancer
- Update on Melasma—Part I: Pathogenesis
- Exploring Hirsutism: Epidemiology, Associated Endocrinal Abnormalities, and Societal Challenges in GCC—A Narrative Review
- Hardwiring Stem Cell Communication through Tissue Structure
- Primary Follicular Dystrophy With Scarring Dermatitis in C57BL/6 Mouse Substrains Resembles Central Centrifugal Cicatricial Alopecia in Humans
- Low-sulfur hair syndrome associated with UVB photosensitivity and testicular failure
- Homozygous ALOXE3 Nonsense Variant Identified in a Patient with Non-Bullous Congenital Ichthyosiform Erythroderma Complicated by Superimposed Bullous Majocchi’s Granuloma: The Consequences of Skin Barrier Dysfunction
- An epistatic effect of KRT25 on SP6 is involved in curly coat in horses
- Evidence on Hidradenitis Suppurativa as an Autoinflammatory Skin Disease
- Drivers of plateau adaptability in cashmere goats revealed by genomic and transcriptomic analyses
- Premature Graying of Hair: A Comprehensive Review and Recent Insights
- Two-Stage Machine Learning-Based GWAS for Wool Traits in Central Anatolian Merino Sheep
- Hutchinson-Gilford syndrome: History, causes, phenotype and research advances
- A Case Report and a Review of TRAPPC4‐Related TRAPPopathy
- Uveodermatological syndrome in dogs: A review of diagnosis, management, and ophthalmic patient needs