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Research 481–510 of 1000+
- Biallelic Variants in Lanosterol Synthase (LSS) Cause Palmoplantar Keratoderma-Congenital Alopecia Syndrome Type 2
- Trichothiodystrophy: Current Concepts
- Two-Stage Machine Learning-Based GWAS for Wool Traits in Central Anatolian Merino Sheep
- Glucocorticoid Resistance Syndrome in 2 Patients With Diverse Genotype
- Research advances of tissue-derived extracellular vesicles in cancers
- Curly : a new hair defect mutation in the SELH/bc mouse strain
- Hutchinson-Gilford syndrome: History, causes, phenotype and research advances
- Integrative analysis of rare copy number variants and gene expression data in alopecia areata implicates an aetiological role for autophagy
- What Ages Hair?
- Update on Melasma—Part I: Pathogenesis
- Reclassification of Botryococcus braunii chemical races into separate species based on a comparative genomics analysis
- Efficient Gene Editing for Heart Disease via ELIP-Based CRISPR Delivery System
- Two mutations at KRT74 and EDAR synergistically drive the fine-wool production in Chinese sheep
- Viewpoint 1
- Novel Androgen Receptor Gene Variant Containing a Premature Termination Codon in a Patient with Androgen Insensitivity Syndrome
- Profibrotic Molecules Are Reduced in CRISPR-Edited Emery–Dreifuss Muscular Dystrophy Fibroblasts
- Spectrum of Phenotypes Associated with Human MC1R Variations
- CCDC22 and CCDC93, two potential retriever-interacting proteins, are required for root and root hair growth in Arabidopsis
- A Nonredundant Human Protein Chip for Antibody Screening and Serum Profiling
- A comprehensive genome-wide analysis for signatures of selection in goat (genus Capra) revealed new candidate genes for environmental adaptation and productive traits
- An Update of Congenital Adrenal Hyperplasia
- Distinct Regulatory Programs Control the Latent Regenerative Potential of Dermal Fibroblasts during Wound Healing
- Mutations in the vitamin D receptor and hereditary vitamin D-resistant rickets
- Chemoprevention – History and general principles
- Haplotypes spanning centromeric regions reveal persistence of large blocks of archaic DNA
- Human epidermal neural crest stem cells as a source of Schwann cells
- A Splice Site Mutation in the Gene of the Human Type I Hair Keratin hHa1 Results in the Expression of a Tailless Keratin Isoform
- Unraveling the complex role of MAPT-containing H1 and H2 haplotypes in neurodegenerative diseases
- Hair and Nail Relationship
- Novel insights into the molecular mechanisms underlying generalized glucocorticoid resistance and hypersensitivity syndromes