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Research 511–540 of 823
- Regulation of Receptor Binding Specificity of FGF9 by an Autoinhibitory Homodimerization
- SWEET SYNDROME: AN UNUSUAL PRESENTATION OF CHRONIC GRANULOMATOUS DISEASE IN A CHILD
- Stem Cell Therapies for Epidermolysis Bullosa Treatment
- p53 Is a Direct Transcriptional Repressor of Keratin 17: Lessons from a Rat Model of Radiation Dermatitis
- KATP Channel Openers Inhibit Lymphatic Contractions and Lymph Flow as a Possible Mechanism of Peripheral Edema
- Skin-specific regulation of SREBP processing and lipid biosynthesis by glycerol kinase 5
- Novel insights into the molecular mechanisms underlying generalized glucocorticoid resistance and hypersensitivity syndromes
- Skin Development and Disease: A Molecular Perspective
- Directed Expression of a Chimeric Type II Keratin Partially Rescues Keratin 5-null Mice
- The Study on Biological Function of Keratin 26, a Novel Member of Liaoning Cashmere Goat Keratin Gene Family
- Gene network analysis reveals candidate genes related with the hair follicle development in sheep
- Hair shaft disorders in children – An update
- Hair Loss Caused by Gain-of-Function Mutant TRPV3 Is Associated with Premature Differentiation of Follicular Keratinocytes
- A novel mutation in ST14 at a functionally significant amino acid residue expands the spectrum of ichthyosis-hypotrichosis syndrome
- Developing Patient-Derived 3D-Bioprinting models of pancreatic cancer
- Single-Cell Transcriptomics Reveals the Molecular Anatomy of Sheep Hair Follicle Heterogeneity and Wool Curvature
- The protease corin regulates electrolyte homeostasis in eccrine sweat glands
- Pili Torti: A Feature of Numerous Congenital and Acquired Conditions
- From structural resilience to cell specification — Intermediate filaments as regulators of cell fate
- The association between rs2476601 polymorphism in PTPN22 gene and risk of alopecia areata
- An overview of current strategies and future prospects in drug repurposing in tuberculosis
- Evolution, classification, structure, and functional diversification of steroid 5α-reductase family in eukaryotes
- Novel mutations of the ABCA12, KRT1 and ST14 genes in three unrelated newborns showing congenital ichthyosis
- Testicular Steroidogenesis
- Expression and localization of Artemis serine 516 phosphorylation in human scalp skin
- Cutaneous, Cranial, and Skeletal Defects in Children and Adults with Focal Dermal Hypoplasia
- Association between Mesenchymal Stem Cells and COVID-19 Therapy: Systematic Review and Current Trends
- Molecular Regulatory Mechanisms in Chicken Feather Follicle Morphogenesis
- Immunological and Metabolic Causes of Infertility in Polycystic Ovary Syndrome
- A Kaleidoscope of Keratin Gene Expression and the Mosaic of Its Regulatory Mechanisms