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Research 121–150 of 1000+
- Genome-wide meta-analysis implicates mediators of hair follicle development and morphogenesis in risk for severe acne
- HR Gene Variants Identified in Mexican Patients with Alopecia Areata
- Uncovering the genetic architecture and evolutionary roots of androgenetic alopecia in African men
- https://researchopenworld.com/genetics-of-hidradenitis-suppurativa/#
- Genetics of Diabetes in Childhood
- Six novel susceptibility Loci for early-onset androgenetic alopecia and their unexpected association with common diseases
- HSD3B1 gene polymorphism and female pattern hair loss in women with polycystic ovary syndrome
- Uncovering the genetic architecture and evolutionary roots of androgenetic alopecia in African men
- Role of bulge epidermal stem cells and TSLP signaling in psoriasis
- Identification of the Keratin-Associated Protein 22-2 Gene in the Capra hircus and Association of Its Variation with Cashmere Traits
- Association between PITX2 polymorphism and androgenetic alopecia in the Indian population
- Autoimmunity: Alopecia Areata
- Activator Protein-1 Activity Regulates Epithelial Tumor Cell Identity
- Do Changes in Chromosomes Cause Aging?
- BLIMP1 Is Required for Postnatal Epidermal Homeostasis but Does Not Define a Sebaceous Gland Progenitor under Steady-State Conditions
- Major Histocompatibility Complex Class I Chain-Related Gene A Polymorphisms and Extended Haplotypes Are Associated with Familial Alopecia Areata
- The Hairless Phenotype of the Hirosaki Hairless Rat Is Due to the Deletion of an 80-kb Genomic DNA Containing Five Basic Keratin Genes
- IL-36γ drives skin toxicity induced by EGFR/MEK inhibition and commensal Cutibacterium acnes
- Genetically separable determinants of hair keratin gene expression
- Case Series: Gene Expression Analysis in Canine Vogt-Koyanagi-Harada/Uveodermatologic Syndrome and Vitiligo Reveals Conserved Immunopathogenesis Pathways Between Dog and Human Autoimmune Pigmentary Disorders
- Methylenetetrahydrofolate reductase C677T mutation in patients with alopecia areata in Turkish population
- Causal relationship between inflammatory cytokines and polycystic ovary syndrome: a bidirectional mendelian randomization study
- Skin morphology of the mutant hairless USP mouse
- A polymorphism in the matrix metalloproteinase-1 gene promoter is associated with the presence of polycystic ovary syndrome in Caucasian women
- Granulocyte colony stimulating factor promotes scarless tissue regeneration
- Author response: Effects of lifelong testosterone exposure on health and disease using Mendelian randomization
- rs4541843 G > A variant near miR-182 is associated with susceptibility, severity, and increased hsa-miR-182-5p expression in alopecia areata
- Tru9I Variant as a Novel Genetic Marker for Vitamin D Deficiency in Alopecia Areata
- Mult-trait analysis of GWAS - Perceived youtfulness - UKBB
- Mult-trait analysis of GWAS - Perceived youtfulness - UKBB