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Research 121–150 of 1000+
- Acupuncture in Polycystic Ovary Syndrome: Potential and Challenge
- Genetic Defects in Human Pericentrin Are Associated With Severe Insulin Resistance and Diabetes
- Mutant laboratory mice with abnormalities in hair follicle morphogenesis, cycling, and/or structure: An update
- Hairless-knockout piglets generated using the clustered regularly interspaced short palindromic repeat/CRISPR-associated-9 exhibit abnormalities in the skin and thymus
- Atypical Juvenile Pityriasis Rubra Pilaris: A Case Report of Early Onset With Late Diagnosis
- 034 Characterization of novel TMEM173 mutation causing a lupus- and SAVI-like phenotype, modified by polymorphisms in TMEM173 and IFIH1
- RBPJ Mutations Identified in Two Families Affected by Adams-Oliver Syndrome
- Systematic analysis of somatic mutations driving cancer: uncovering functional protein regions in disease development
- Case report: Novel p.Val306Met missense mutation in TRPV3 in a case of Olmsted syndrome accompanied by squamous cell carcinoma
- WNT10A mutation causes ectodermal dysplasia by impairing progenitor cell proliferation and KLF4-mediated differentiation
- The retarded hair growth ( rhg ) mutation in mice is an allele of ornithine aminotransferase ( Oat )
- The role of mutations on gene AR, in androgenetic alopecia syndrome
- TCF/Lef1-Mediated Control of Lipid Metabolism Regulates Skin Barrier Function
- 892 Behavior of the two circulating androgens testosterone and DHEA and their main intracellular metabolites in an androgen-sensitive sebocyte cell line
- A homozygous missense mutation in the fibroblast growth factor 5 gene is associated with the long-hair trait in Angora rabbits
- Two mutations at KRT74 and EDAR synergistically drive the fine-wool production in Chinese sheep
- The Multifaceted Functions of TRPV4 and Calcium Oscillations in Tissue Repair
- Gene Variant in Amish a Clue to Better Aging
- The acyl-CoA binding protein is required for normal epidermal barrier function in mice
- <i>AXR3</i>and<i>SHY2</i>interact to regulate root hair development
- Basal cell carcinomas acquire secondary mutations to overcome dormancy and progress from microscopic to macroscopic disease
- Clinical and Immunological Phenotype of Patients With Primary Immunodeficiency Due to Damaging Mutations in NFKB2
- Mitochondrial Function in Murine Skin Epithelium Is Crucial for Hair Follicle Morphogenesis and Epithelial–Mesenchymal Interactions
- Hair Follicular Expression and Function of Group X Secreted Phospholipase A2 in Mouse Skin
- ABCD1 Gene Mutations: Mechanisms and Management of Adrenomyeloneuropathy
- Clinical, biochemical and mutational findings in biotinidase deficiency among Malaysian population
- A TP63 Mutation Causes Prominent Alopecia with Mild Ectodermal Dysplasia
- Targeting of Smoothened for therapeutic gain
- Somatic Mutations in Normal Tissues: New Perspectives on Early Carcinogenesis
- The mutational analysis of mitochondrial DNA in maternal inheritance of polycystic ovarian syndrome