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- Intracorneal vacuoles in skin diseases with parakeratotic hyperkeratosis in the dog: a retrospective light‐microscopy study of 111 cases (1973–2000)
- Activation of Nrf2 in keratinocytes causes chloracne (MADISH)‐like skin disease in mice
- Cutaneous Ultrastructural Features of the Flaky Skin (<i>fsn</i>) Mouse Mutation
- Respective Treatment Modalities with the Use of Combined Ingredients to Address Acne Prone Skin
- The Link Between Obesity and the Skin
- Lesions in the skin, intestine, and central nervous system induced by an antimetabolite of niacin.
- 738 Cryo-EM and molecular dynamics of TRPV3 channel in activated state reveal structural features implicated in severe itch and hyperkeratosis
- RASopathic Skin Eruptions during Vemurafenib Therapy
- Reversing wrinkled skin and hair loss in mice by restoring mitochondrial function
- Skin barrier, phenotypic and genotypic characterisation of autosomal recessive ichthyosis in TGM1‐deficient Jack Russell Terriers and response to topical ceramide
- Cyclic Alopecia and Abnormal Epidermal Cornification in Zdhhc13 -Deficient Mice Reveal the Importance of Palmitoylation in Hair and Skin Differentiation
- Obesity and the skin
- Gsdma3 Mutation Causes Bulge Stem Cell Depletion and Alopecia Mediated by Skin Inflammation
- Skin manifestations of obesity: a comparative study
- Murine Epidermal Ceramide Synthase 4 Is a Key Regulator of Skin Barrier Homeostasis
- Correction: RASopathic Skin Eruptions during Vemurafenib Therapy
- Immunohistochemical Expression of Keratins in Normal Ovine Skin and in Chronic Dermatitis due to Sarcoptes scabiei
- Skin Lesions in a Daclizumab-treated Patient with Multiple Sclerosis
- Epidermis-specific ablation of claudin-1 in adult mice demonstrates the essential role of a tight junction barrier in skin homeostasis
- Ligand-Independent Vitamin D Receptor Actions Essential for Keratinocyte Homeostasis in the Skin
- Ligand-Independent Vitamin D Receptor Actions Essential for Keratinocyte Homeostasis in the Skin
- 393 Skin manifestations and biophysical properties in patients with morbid obesity and changes after weight loss: A two-year prospective study
- Case Report: Bi-allelic missense variant in the desmocollin 3 gene causes hypotrichosis and recurrent skin vesicles
- Skin, Genetic Defects, and Aging
- The Roles of Smad2 and Smad3 in Mouse Skin Development
- Biotinidase deficiency characterized by skin and hair findings
- Unilateral nevoid hyperkeratosis of the nipple and areola in a Saudi female
- Skin Disorders in Overweight and Obese Patients and Their Relationship With Insulin
- Vitamin D receptor ablation alters skin architecture and homeostasis of dendritic epidermal T cells
- A Scandinavian case of skin fragility, alopecia and cardiomyopathy caused by<i>DSP</i>mutations