Search
for
Sort by
Research 121–150 of 1000+
- Epidermal abnormalities and increased malignancy of skin tumors in human epidermal keratin 8‐expressing transgenic mice
- Mutant laboratory mice with abnormalities in hair follicle morphogenesis, cycling, and/or structure: An update
- Involvement of the Edar Signaling in the Control of Hair Follicle Involution (Catagen)
- Hereditary Hypotrichosis and Localized Morphea: A New Clinical Entity
- People’s experiences of eyebrow transplantation: A qualitative study
- Case report: A novel splice-site mutation of MTX2 gene caused mandibuloacral dysplasia progeroid syndrome: the first report from China and literature review
- Analysis of 72,469 UK Biobank exomes links rare variants to male-pattern hair loss
- Molecular Mechanisms Regulating Hair Follicle Development
- Comparative genome analyses reveal the unique genetic composition and selection signals underlying the phenotypic characteristics of three Chinese domestic goat breeds
- Hair of the Dog: Identification of a Cis-Regulatory Module Predicted to Influence Canine Coat Composition
- The mouse hairy ears mutation exhibits an extended growth (anagen) phase in hair follicles and altered <i>Hoxc</i> gene expression in the ears
- A Comprehensive Review of GWASs of Human Hair Traits
- The Genomic Variation in Textured Hair: Implications in Developing a Holistic Hair Care Routine
- Molecular Genetic Characteristics of the Hoxc13 Gene and Association Analysis of Wool Traits
- 092 Novel biallelic RIPK4 mutations cause ectodermal dysplasia with cutaneous syndactyly
- Cicatricial (Scarring) Alopecias
- Genome-wide meta-analysis implicates mediators of hair follicle development and morphogenesis in risk for severe acne
- Discrimination of Dysplastic Nevi from Common Melanocytic Nevi by Cellular and Molecular Criteria
- Madarosis
- Gata6 promotes hair follicle progenitor cell renewal by genome maintenance during proliferation
- The Genetics of Human Skin Disease
- Alopecia in Epidermolysis Bullosa
- Tooth, hair and claw: Comparing epithelial stem cell niches of ectodermal appendages
- A rare LMNA missense mutation causing a severe phenotype of mandibuloacral dysplasia type A: a case report
- Alopecia and Its homoeopathic treatment
- Androgenetic Alopecia in Men: An Update On Genetics
- Biology of the wool follicle: an excursion into a unique tissue interaction system waiting to be re‐discovered
- The Female Pattern Hair Loss: Review of Etiopathogenesis and Diagnosis
- Lifestyle and Physiological Factors Associated with Facial Wrinkling in Men and Women
- WNT10A mutation causes ectodermal dysplasia by impairing progenitor cell proliferation and KLF4-mediated differentiation