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Research 661–690 of 1000+
- Regulation of masculinization: androgen signalling for external genitalia development
- NUDT15 R139C-related thiopurine leukocytopenia is mediated by 6-thioguanine nucleotide-independent mechanism in Japanese patients with inflammatory bowel disease
- A locus on distal chromosome 10 (ahl4) affecting age-related hearing loss in A/J mice
- Exploring the possibility of predicting human head hair greying from DNA using whole-exome and targeted NGS data
- Silk Fibroin and Its Nanocomposites for Wound Care: A Comprehensive Review
- Exomic Sequencing of Immune-Related Genes Reveals Novel Candidate Variants Associated with Alopecia Universalis
- Exome-wide age-of-onset analysis reveals exonic variants in ERN1 and SPPL2C associated with Alzheimer’s disease
- Type 1 Diabetes Mellitus and Autoimmune Diseases: A Critical Review of the Association and the Application of Personalized Medicine
- Novel mutations of the ABCA12, KRT1 and ST14 genes in three unrelated newborns showing congenital ichthyosis
- Genome-Wide Association Study of Alopecia Areata in Taiwan: The Conflict Between Individuals and Hair Follicles
- Two-Stage Machine Learning-Based GWAS for Wool Traits in Central Anatolian Merino Sheep
- Atrichia congenita with papular lesions: A rare cause of pediatric alopecia
- 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
- IRF2BP2 genes provide new insights into coat type and fiber composition variation in sheep
- 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
- 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
- Hair and cord blood element levels and their relationship with air pollution, dietary intake, gestational diabetes mellitus, and infant neurodevelopment
- 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
- Clouston syndrome: A complete genotype–Phenotype correlation after four decades and six generations