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Research 481–510 of 1000+
- Androgenetic alopecia: a review
- Coronavirus Infection and Cholesterol Metabolism
- The role of WNT10B in physiology and disease: A 10-year update
- Transglutaminase 3: The Involvement in Epithelial Differentiation and Cancer
- Palatogenesis and cutaneous repair: A two‐headed coin
- Silk Fibroin and Its Nanocomposites for Wound Care: A Comprehensive Review
- A “hair‐raising” history of alopecia areata
- Endoplasmic reticulum in health and disease: the 12th International Calreticulin Workshop, Delphi, Greece
- Mutations in Homocysteine Metabolism Genes Increase Keratin <i>N</i>-Homocysteinylation and Damage in Mice
- Single-Cell Omics Advances in Understanding Tissue Development and Complex Trait Formation in Sheep and Goats
- Signal Peptide-CUB-EGF-like Domain-Containing Protein 3 (SCUBE3): From Molecule to Therapy
- Association between PITX2 polymorphism and androgenetic alopecia in the Indian population
- Diseases of Honeybee (Apis mellifera)
- Inheritance-Specific Dysregulation of Th1- and Th17-Associated Cytokines in Alopecia Areata
- Scalp microbiome of healthy women wearing hijab compared to those not wearing hijab: a cross-sectional study
- Association of androgenetic alopecia with a more severe form of COVID-19 infection
- A conditional multi-trait sequence GWAS discovers pleiotropic candidate genes and variants for sheep wool, skin wrinkle and breech cover traits
- Studies on basal cell carcinoma with emphasis on the role of the human homologue of the Drosophila patched gene
- Role of Aire and Notch4 Allelic Mutations in Alopecia Areata in C3H/HeJ Mice
- Association of insulin-like growth factor 2 Apa1 A820G gene (rs680) polymorphism with polycystic ovarian syndrome
- The Roles of EDA2R in Ageing and Disease
- Signature selection analysis reveals candidate genes associated with production traits in Iranian sheep breeds
- The crest phenotype in domestic chicken is caused by a 195 bp duplication in the intron of <i>HOXC10</i>
- Decay of Skin-Specific Gene Modules in Pangolins
- Epidermolysis bullosa simplex: a paradigm for disorders of tissue fragility
- Development of Heritable Melanoma in Transgenic Mice
- HR Gene Variants Identified in Mexican Patients with Alopecia Areata
- Hyperandrogenism in polycystic ovarian syndrome and role of CYP gene variants: a review
- Polymorphisms of the genes ABCG2, SLC22A12 and XDH and their relation with hyperuricemia and hypercholesterolemia in Mexican young adults
- Polymorphisms of the genes ABCG2, SLC22A12 and XDH and their relation with hyperuricemia and hypercholesterolemia in Mexican young adults