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Research 481–510 of 1000+
- Constitutive activation of Stat3 in mouse epidermis is linked to hair deficiency and cytoskeletal network damage
- Keratosis Follicularis Squamosa in Unilateral Buttock: A Case Report and Review of Literature in China
- A missense mutation in Lama3 causes androgen alopecia
- Testosterone: The Male Sex Hormone
- Cells to Surgery Quiz: April 2020
- Dunnigan-Type Familial Partial Lipodystrophy: Understanding and Treating the Syndrome
- Acrodermatitis Enteropathica in an adult: a case report
- The role of mutations on gene AR, in androgenetic alopecia syndrome
- An early diagnosis of trichorhinophalangeal syndrome type 1: a case report and a review of literature
- Eph Receptors and Ephrins: Therapeutic Opportunities
- Cloning of wrinkle-free, a previously uncharacterized mouse mutation, reveals crucial roles for fatty acid transport protein 4 in skin and hair development
- Pathology of Mouse Models of Accelerated Aging
- Peroxisome proliferator-activated receptors (PPARs) and PPAR agonists: the ‘future’ in dermatology therapeutics?
- Impaired Hair Follicle Morphogenesis and Cycling with Abnormal Epidermal Differentiation in nackt Mice, a Cathepsin L-Deficient Mutation
- Immune mechanisms associated with sex-based differences in severe COVID-19 clinical outcomes
- Genomewide analysis of copy number variants in alopecia areata in a Central European cohort reveals association with <i>MCHR2</i>
- Systematic analysis of somatic mutations driving cancer: uncovering functional protein regions in disease development
- From structural resilience to cell specification — Intermediate filaments as regulators of cell fate
- A study on efficacy of oral zinc therapy for treatment of acrodermatitis enteropathica
- Types of Human Stem Cells and Their Therapeutic Applications
- Fetal alpha 5-reductase Val89Leu mutation is associated with late miscarriage
- Polycystic Ovary Syndrome Phenotypes and Infertility Treatment
- Exploring lncRNA-Mediated Mechanisms in Muscle Regulation and Their Implications for Duchenne Muscular Dystrophy
- Genome-Wide Associations with Body and Fleece Weight in United States Sheep
- EDA Missense Variant in a Cat with X-Linked Hypohidrotic Ectodermal Dysplasia
- E-Poster
- A Brazilian case of IFAP syndrome with severe congenital ichthyosis and limb malformations caused by a rare variant in MBTPS2
- Occurrence of Klinefelter Syndrome Mosaic 45,X/46,XY/47,XXY/48,XXYY/48,XXXY and Primary Hyperparathyroidism
- Cytochrome P450: A Target for Drug Development for Skin Diseases
- Androgen Regulation of the Human Hair Follicle: The Type I Hair Keratin hHa7 Is a Direct Target Gene in Trichocytes