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Research 331–360 of 1000+
- Congenital hair loss disorders: Rare, but not too rare
- No Evidence that 2D:4D is Related to the Number of CAG Repeats in the Androgen Receptor Gene
- Fluoroquinolone-induced serious, persistent, multisymptom adverse effects
- Desferrioxamine treatment of aceruloplasminemia: Long‐term follow‐up
- Polarity signaling ensures epidermal homeostasis by coupling cellular mechanics and genomic integrity
- Adrenal Disorders and the Paediatric Brain: Pathophysiological Considerations and Clinical Implications
- Platelet-derived growth factor signaling modulates adult hair follicle dermal stem cell maintenance and self-renewal
- Identification of potential key genes and pathways associated with the Pashmina fiber initiation using RNA-Seq and integrated bioinformatics analysis
- De novo single-nucleotide and copy number variation in discordant monozygotic twins reveals disease-related genes
- Trichoscopy in Hair Shaft Disorders
- Label Retaining Cells (LRCs) with Myoepithelial Characteristic from the Proximal Acinar Region Define Stem Cells in the Sweat Gland
- MOUSE MODELS FOR THE STUDY OF HUMAN HAIR LOSS
- A distinct gene close to the hairless locus on chromosome 8p underlies hereditary Marie Unna type hypotrichosis in a German family
- Fibromodulin reduces scar formation in adult cutaneous wounds by eliciting a fetal-like phenotype
- Hydrogen peroxide and monoethanolamine are the key causative ingredients for hair dye-induced dermatitis and hair loss
- Regulation of VDR by ΔNp63α is associated with inhibition of cell invasion
- Planar cell polarity-dependent and independent functions in the emergence of tissue-scale hair follicle patterns
- Fibromodulin-Deficiency Alters Temporospatial Expression Patterns of Transforming Growth Factor-β Ligands and Receptors during Adult Mouse Skin Wound Healing
- A Clinical Approach to Severe Insulin Resistance
- Smad1 and 5 but Not Smad8 Establish Stem Cell Quiescence Which Is Critical to Transform the Premature Hair Follicle During Morphogenesis Toward the Postnatal State
- Histopathological and Ultrastructural Study of Ectodermal Dysplasia/Skin Fragility Syndrome
- Glucocorticoid Receptor Mutants Demonstrate Increased Motility Inside the Nucleus of Living Cells: Time of Fluorescence Recovery After Photobleaching (FRAP) Is an Integrated Measure of Receptor Function
- Steroidogenic Isoenzymes in Human Hair and Their Potential Role in Androgenetic Alopecia
- Dermatological symptoms and sexual abuse: a review and case reports
- Expanding the Nude SCID/CID Phenotype Associated with FOXN1 Homozygous, Compound Heterozygous, or Heterozygous Mutations
- Inhibition of glycosphingolipid synthesis reverses skin inflammation and hair loss in ApoE−/− mice fed western diet
- Hairless is a nuclear receptor corepressor essential for skin function
- Differential diagnosis of hair loss in children. Differentialdiagnose des Haarausfalls bei Kindern
- Variation in the caprine keratin-associated protein 15-1 (KAP15-1) gene affects cashmere fibre diameter
- An Ovol2‐Zeb1 transcriptional circuit regulates epithelial directional migration and proliferation