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Research 541–570 of 684
- TCF/Lef1-Mediated Control of Lipid Metabolism Regulates Skin Barrier Function
- Alopecia Areata: Pathogenesis, Diagnosis, and Therapies
- Emergence of the natural history of Myhre syndrome: 47 patients evaluated in the Massachusetts General Hospital Myhre Syndrome Clinic (2016–2023)
- Human scalp hair as a thermoregulatory adaptation
- A Monoallelic Two-Hit Mechanism in PLCD1 Explains the Genetic Pathogenesis of Hereditary Trichilemmal Cyst Formation
- Developmental genetics of color pattern establishment in cats
- Alkaline Ceramidase 1 Protects Mice from Premature Hair Loss by Maintaining the Homeostasis of Hair Follicle Stem Cells
- Skin-specific regulation of SREBP processing and lipid biosynthesis by glycerol kinase 5
- Exomic Sequencing of Immune-Related Genes Reveals Novel Candidate Variants Associated with Alopecia Universalis
- Epidermal Deletion of Rac1 Causes Stem Cell Depletion, Irrespective of whether Deletion Occurs during Embryogenesis or Adulthood
- Identification of an Intronic Regulatory Element Necessary for Tissue-Specific Expression of <i>Foxn1</i> in Thymic Epithelial Cells
- Tissue Regeneration: Hair Follicle as a Model
- Chronic overlapping pain conditions and nociplastic pain
- Mice lacking the epidermal retinol dehydrogenases SDR16C5 and SDR16C6 display accelerated hair growth and enlarged meibomian glands
- The common regulatory pathway of COVID-19 and multiple inflammatory diseases and the molecular mechanism of cepharanthine in the treatment of COVID-19
- Fibrotic enzymes modulate wound‐induced skin tumorigenesis
- Hair Growth Effect of Emulsion Extracted Brevilin A, a JAK3 Inhibitor, from Centipeda minima
- The effect of dietary modulation of sulfur amino acids on cystathionine β synthase–deficient mice
- Variant 1859G→A (Arg620Gln) of the “Hairless” Gene: Absence of Association with Papular Atrichia or Androgenetic Alopecia
- Proopiomelanocortin (POMC) and Psychodermatology
- Hair Loss Caused by Gain-of-Function Mutant TRPV3 Is Associated with Premature Differentiation of Follicular Keratinocytes
- A Spontaneous Deletion within the Desmoglein 3 Extracellular Domain of Mice Results in Hypomorphic Protein Expression, Immunodeficiency, and a Wasting Disease Phenotype
- Enriching Proteolysis Targeting Chimeras with a Second Modality: When Two Are Better Than One
- Developmental and evolutionary comparative analysis of a regulatory landscape in mouse and chicken
- Hair follicles modulate skin barrier function
- Pili Torti: A Feature of Numerous Congenital and Acquired Conditions
- The retarded hair growth ( rhg ) mutation in mice is an allele of ornithine aminotransferase ( Oat )
- Past, Present and Future Perspectives of Forensic Genetics
- A review of genotrichoses and hair pathology associated with inherited skin diseases
- A weighted non-negative matrix factorization approach to predict potential associations between drug and disease