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Research 661–690 of 1000+
- The diversity of sex development: What do conditions affecting sex development teach us about sexual diversity?
- DNMT3B -579G>T POLYMORPHİSM AND THE RİSK OF COLORECTAL CANCER IN AZERBAİJAN POPULATİON
- Atrichia congenita with papular lesions: A rare cause of pediatric alopecia
- Uveodermatological syndrome in dogs: A review of diagnosis, management, and ophthalmic patient needs
- The role of candidate pharmacogenetic variants in determining valproic acid efficacy, toxicity and concentrations in patients with epilepsy
- Chronic Overlapping Pain Conditions and Nociplastic Pain
- Localized Hypotrichosis Type 1 Due to Intragenic Deletion of Exons 5-8 in Desmoglein Gene in a Neonate from Indian Family
- Hyperandrogenism and insulin resistance modulate gravid uterine and placental ferroptosis in PCOS-like rats
- Primary Follicular Dystrophy With Scarring Dermatitis in C57BL/6 Mouse Substrains Resembles Central Centrifugal Cicatricial Alopecia in Humans
- 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
- Laminin 332 Is Indispensable for Homeostatic Epidermal Differentiation Programs
- Exploring Hirsutism: Epidemiology, Associated Endocrinal Abnormalities, and Societal Challenges in GCC—A Narrative Review
- Correlation of trichoscopic findings with clinico-epidemiological factors in male pattern&nbsp;<span style="font-size: 1rem;">hairloss: A cross-sectional study from a tertiary care center in Chengalpattu</span>
- Mendelian Randomization Identifies CD25+ CD4+ Tregs and Plasma Proteins in Androgenetic Alopecia Pathogenesis
- Clinical and molecular features in a cohort of Middle Eastern patients with epidermolysis bullosa
- Gene polymorphisms and serum levels of BDNF and CRH in vitiligo patients
- Hair and cord blood element levels and their relationship with air pollution, dietary intake, gestational diabetes mellitus, and infant neurodevelopment
- The methodology of developing dermato-cosmetic remedies for prevention and treatment of alopecia
- Clouston syndrome: A complete genotype–Phenotype correlation after four decades and six generations
- Human epidermal neural crest stem cells as a source of Schwann cells
- Association Between Interleukin 18 Polymorphisms and Alopecia Areata in Koreans
- Integrative analysis of rare copy number variants and gene expression data in alopecia areata implicates an aetiological role for autophagy
- Recent advancements in wound management: Tailoring superwettable bio-interfaces
- Distinct tooth regeneration systems deploy a conserved battery of genes
- Metabolic dysfunction in female mice with disruption of 5α-reductase 1
- Biallelic Variants in Lanosterol Synthase (LSS) Cause Palmoplantar Keratoderma-Congenital Alopecia Syndrome Type 2
- Discovery of genes and proteins possibly regulating mean wool fibre diameter using cDNA microarray and proteomic approaches
- Linking allergy to mercury to HLA and burning mouth syndrome
- Identification and Characterization of Two Se6OMTs from Stephania epigaea Offer Novel Insights into the Biosynthetic Pathway of Cepharanthine