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Research 691–720 of 1000+
- Hair Loss in Autoimmune Cutaneous Bullous Disorders
- Scd1 ab-Xyk : a new asebia allele characterized by a CCC trinucleotide insertion in exon 5 of the stearoyl-CoA desaturase 1 gene in mouse
- Mesothelial Stem Cells and Stromal Vascular Fraction for Skin Rejuvenation
- Hairless Up‐Regulates <i>Tgf‐β2</i> Expression via Down‐Regulation of miR‐31 in the Skin of “Hairpoor” (<i>Hr</i><sup><i>Hp</i></sup>) Mice
- The possible implication of the S250C variant of the autoimmune regulator protein in a patient with autoimmunity and immunodeficiency: in silico analysis suggests a molecular pathogenic mechanism for the variant
- The β9 Loop Domain of PA-PLA1α Has a Crucial Role in Autosomal Recessive Woolly Hair/Hypotrichosis
- Human retinal secretome: A cross-link between mesenchymal and retinal cells
- Expression of E6 and E7 papillomavirus oncogenes in the outer root sheath of hair follicles extends the growth phase and bypasses resting at telogen.
- The myeloid mineralocorticoid receptor regulates dermal angiogenesis and inflammation in glucocorticoid‐induced impaired wound healing
- STIM1 R304W in mice causes subgingival hair growth and an increased fraction of trabecular bone
- A disease-causing novel missense mutation in the ST14 gene underlies autosomal recessive ichthyosis with hypotrichosis syndrome in a consanguineous family
- CDH3 gene related hypotrichosis and juvenile macular dystrophy – A case with a novel mutation
- TCDD-induced activation of aryl hydrocarbon receptor regulates the skin stem cell population
- CtBP1 Overexpression in Keratinocytes Perturbs Skin Homeostasis
- Solitary fixed drug eruption caused by finasteride
- Celsr1 and Celsr2 exhibit distinct adhesive interactions and contributions to planar cell polarity
- Overactive Wnt5a signaling disrupts hair follicle polarity during mouse skin development
- Harnessing the Biomimetic Effect of Macromolecular Crowding in the Cell-Derived Model of Clubfoot Fibrosis
- Store-operated calcium channels in skin
- Regulation and Role of GLI1 in Cutaneous Squamous Cell Carcinoma Pathogenesis
- Runx Family Genes in Tissue Stem Cell Dynamics
- The genetic evolution of skin squamous cell carcinoma: tumor suppressor identity matters
- Heterogeneity in the genetic alterations and in the clinical presentation of acrodermatitis enteropathic: Case report and review of the literature
- Correction of Hair Shaft Defects through Allele-Specific Silencing of Mutant Krt75
- Increased 25(OH)D3 level in redheaded people: Could redheadedness be an adaptation to temperate climate?
- A Comprehensive Approach in Diagnosing the Polycystic Ovary Syndrome
- Familial 1q22 microduplication associated with psychiatric disorders, intellectual disability and late-onset autoimmune inflammatory response
- Identification of novel mutation in the<i>HR</i>gene responsible for atrichia with papular lesions in a Pakistani family
- Mimicking Hair Disorders by Genetic Manipulation of Organ-Cultured Human Hair Follicles
- Anterior neck fat deposition in lipodystrophy syndrome; a new variant on a theme?