Search
for
Sort by
Research 30 of 1000+
- A Mouse Model for the Basal Transcription/DNA Repair Syndrome Trichothiodystrophy
- Prognosis and Management of Congenital Hair Shaft Disorders with Fragility—Part I
- Office Diagnosis of Hair Shaft Defects
- Muir-torre syndrome in two families in Leicestershire, United Kingdom
- 312 CRISPR/Cas9-based targeted genome editing for correction of recessive dystrophic epidermolysis bullosa using iPS cells
- Skin precancer.
- Photosensitive Trichothiodystrophy with Complex Cerebral Abnormalities
- 924 Efficient genome editing using CRISPR/Cas9 ribonucleoprotein approach in iPS cells for recessive dystrophic epidermolysis bullosa
- Trichothiodystrophy hair shafts display distinct ultrastructural features
- 461 Identification of a Novel Pathogenic XPC:c.2420+1G>C Variant in a Patient with Xeroderma Pigmentosum
- Strategies for High-Efficiency Mutation Using the CRISPR/Cas System
- The Editor's Choice
- Deficiency in Nucleotide Excision Repair Family Gene Activity, Especially ERCC3, Is Associated with Non-Pigmented Hair Fiber Growth
- The mutational analysis of mitochondrial DNA in maternal inheritance of polycystic ovarian syndrome
- Genome Array on Differentially Expressed Genes of Skin Tissue in Cashmere Goat at Early Anagen of Cashmere Growth Cycle Using DNA Microarray
- Nucleocytoplasmic Communication in Progeria
- Progeroide Syndrome
- Multiple basal cell carcinomas in a patient with myotonic dystrophy type 1
- Milestones in Photocarcinogenesis
- Contribution of Environmental Constituents in the Genomic Disruption of Cytokeratins
- Human and animal cells under influence of different lighting and stimulus
- Deletion of the Developmentally Essential Gene ATR in Adult Mice Leads to Age-Related Phenotypes and Stem Cell Loss
- High-confidence cancer patient stratification through multiomics investigation of DNA repair disorders
- PNKP is required for maintaining the integrity of progenitor cell populations in adult mice
- Spectrum of Phenotypes Associated with Human MC1R Variations
- Identification of a novel homozygous LAMB3 mutation in a Chinese male with junctional epidermolysis bullosa and severe urethra stenosis: A case report
- Myotonic Dystrophy—A Progeroid Disease?
- New clinico‐genetic classification of trichothiodystrophy
- Do Changes in Chromosomes Cause Aging?
- The 1,25-dihydroxyvitamin D3-independent actions of the vitamin D receptor in skin