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- Defects in mitochondrial DNA replication and oxidative damage in muscle of mtDNA mutator mice
- Hair Defects and Pup Loss in Mice with Targeted Deletion of the First Cut Repeat Domain of theCux/CDPHomeoprotein Gene
- 244 Defective maintenance of hair follicle stem cells through COL17A1 loss orchestrates the hair follicle aging program
- Genetic Ablation of the <i>CDP/Cux</i> Protein C Terminus Results in Hair Cycle Defects and Reduced Male Fertility
- Office Diagnosis of Hair Shaft Defects
- Comprehensive Administrative and Engineering Strategies for Radiation Protection and Occupational Health Safety
- Scraggly, a new hair loss mutation on mouse Chromosome 19
- Stem cells and aberrant signaling of molecular systems in skin aging
- Photosensitive Trichothiodystrophy with Complex Cerebral Abnormalities
- A Mouse Model for the Basal Transcription/DNA Repair Syndrome Trichothiodystrophy
- Recommended Articles
- Signaling pathways in hair aging
- RBPJ Mutations Identified in Two Families Affected by Adams-Oliver Syndrome
- The mutational analysis of mitochondrial DNA in maternal inheritance of polycystic ovarian syndrome
- Mitochondrial DNA Damage, Oxidative Stress, and Atherosclerosis
- The Hairless Phenotype of the Hirosaki Hairless Rat Is Due to the Deletion of an 80-kb Genomic DNA Containing Five Basic Keratin Genes
- The pharmacology of methotrexate
- Inactivation of the Vitamin D Receptor Enhances Susceptibility of Murine Skin to UV-Induced Tumorigenesis
- Tissue regenerative delays and synthetic lethality in adult mice after combined deletion of Atr and Trp53
- EGFR Controls Hair Shaft Differentiation in a p53-Independent Manner
- New clinico‐genetic classification of trichothiodystrophy
- Forkhead/winged-helix transcription factor whn regulates hair keratin gene expression: Molecular analysis of theNude skin phenotype
- Polarity signaling ensures epidermal homeostasis by coupling cellular mechanics and genomic integrity
- Intermittent treatment with farnesyltransferase inhibitor and sulforaphane improves cellular homeostasis in Hutchinson-Gilford progeria fibroblasts
- The 1,25-dihydroxyvitamin D3-independent actions of the vitamin D receptor in skin
- Facial preservation following extreme mummification: Shrunken heads
- Epithelial loss of mitochondrial oxidative phosphorylation leads to disturbed enamel and impaired dentin matrix formation in postnatal developed mouse incisor
- Skin-specific transgenic overexpression of ovine β-catenin in mice
- Redox-directed interventions targeting skin photodamage
- Muir-torre syndrome in two families in Leicestershire, United Kingdom