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Research 241–270 of 1000+
- A novel missense mutation in the mouse hairless gene causes irreversible hair loss: Genetic and molecular analyses of Hrm1Enu
- Molecular Analysis of the ABCA4 Gene Mutations in Patients with Stargardt Disease Using Human Hair Follicles
- Evolution, classification, structure, and functional diversification of steroid 5α-reductase family in eukaryotes
- Heterogeneity in the genetic alterations and in the clinical presentation of acrodermatitis enteropathic: Case report and review of the literature
- Phenotyping mice with skin, hair, or nail abnormalities: A systematic approach and methodologies from simple to complex
- Folate receptor β performs an immune checkpoint function in activated macrophages
- Genetic association of wool quality characteristics in United States Rambouillet sheep
- Genetic analysis does not confirm non-classical congenital adrenal hyperplasia in more than a third of the women followed with this diagnosis
- Mutations in the helix termination motif of mouse type I IRS keratin genes impair the assembly of keratin intermediate filament
- Genotype Triad for HOTAIR rs10783618, LINC-ROR rs1942347, and MALAT1 rs3200401 as Molecular Markers in Systemic Lupus Erythematous
- Cell-Free Fat Extract (Ceffe) Combined with GelMA Hydrogel to Improve the Survival Rate of Random Skin Flaps in Mice
- A recently characterized, underdiagnosed cause of female androgenetic alopecia and polycystic ovarian syndrome: non-classical 21 hydroxylase deficiency
- A Brazilian case of IFAP syndrome with severe congenital ichthyosis and limb malformations caused by a rare variant in MBTPS2
- A Rare Case of Keratosis Follicularis Spinulosa Decalvans Affecting a Female Child
- Nanoscale microenvironment engineering for expanding human hair follicle stem cell and revealing their plasticity
- A novel calmodulin‐interacting Domain of Unknown Function 506 protein represses root hair elongation in <i>Arabidopsis</i>
- COVID-19: The question of genetic diversity and therapeutic intervention approaches
- Human Hair Keratin Modification Enhances the Biocompatibility, Bioactivity, and Osteogenic Property of BCP/PMMA Bone Cement
- SARS-CoV-2 Infection and COVID-19 Vaccination Associated with Post-Acute Alopecia: Prevalence, Clinical Patterns, and Determinants Among Saudi Adults
- New aspects of vitamin D metabolism and action — addressing the skin as source and target
- Genetic Disorders and Defects in Vitamin D Action
- Intracrine androgen biosynthesis, metabolism and action revisited
- Mutations in the vitamin D receptor and hereditary vitamin D-resistant rickets
- WNT10A mutation causes ectodermal dysplasia by impairing progenitor cell proliferation and KLF4-mediated differentiation
- A Missense Mutation in the Zinc-Finger Domain of the Human Hairless Gene Underlies Congenital Atrichia in a Family of Irish Travellers
- Four Independent Mutations in the Feline Fibroblast Growth Factor 5 Gene Determine the Long-Haired Phenotype in Domestic Cats
- Novel Hairless Mutations in Two Kindreds with Autosomal Recessive Papular Atrichia
- Recently Identified Forms of Epidermolysis Bullosa
- A Missense Mutation in the Cadherin Interaction Site of The Desmoglein 4 Gene Underlies Localized Autosomal Recessive Hypotrichosis
- FOXN1 deficient nude severe combined immunodeficiency