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Research 871–900 of 1000+
- Recently Identified Forms of Epidermolysis Bullosa
- GRHL3 binding and enhancers rearrange as epidermal keratinocytes transition between functional states
- Preliminary study on microR-148a and microR-10a in dermal papilla cells of Hu sheep
- Genetically separable determinants of hair keratin gene expression
- Unraveling the complex role of MAPT-containing H1 and H2 haplotypes in neurodegenerative diseases
- The Genetics of Human Skin Disease
- Mutations in the vitamin D receptor gene in four patients with hereditary 1,25-dihydroxyvitamin D-resistant rickets
- New CDH3 mutation in the first Spanish case of hypotrichosis with juvenile macular dystrophy, a case report
- Association Between Interleukin 18 Polymorphisms and Alopecia Areata in Koreans
- Developmental genetics of color pattern establishment in cats
- miR-150 regulates endothelial progenitor cell differentiation via Akt and promotes thrombus resolution
- The molecular pathogenesis of Trichilemmal carcinoma
- Small RNAs Loom Large During Reprogramming
- The secret identities of TMPRSS2: Fertility factor, virus trafficker, inflammation moderator, prostate protector and tumor suppressor
- Congenital Zinc Deficiency from Mutations of the<i>SLC39A4</i>Gene as the Genetic Background of Acrodermatitis Enteropathica
- Interplay of MicroRNA-21 and SATB1 in Epidermal Keratinocytes during Skin Aging
- Skin transcriptome reveals the periodic changes in genes underlying cashmere (ground hair) follicle transition in cashmere goats
- Multiomics global landscape of stemness-related gene clusters in adipose-derived mesenchymal stem cells
- An epistatic effect of KRT25 on SP6 is involved in curly coat in horses
- Syntaxin 9 is Enriched in Skin Hair Follicle Epithelium and Interacts With the Epidermal Growth Factor Receptor
- [Implication of VEGF, steroid hormones and neuropeptides in hair follicle cell responses].
- A novel mutation in ST14 at a functionally significant amino acid residue expands the spectrum of ichthyosis-hypotrichosis syndrome
- Wound Healing Impairment in Type 2 Diabetes Model of Leptin-Deficient Mice—A Mechanistic Systematic Review
- Molecular Basis for Hair Loss in Mice Carrying a Novel Nonsense Mutation (<i>Hr<sup>rh-R</sup></i>) in the Hairless Gene (<i>Hr</i>)
- Epidermal PPARγ Is a Key Homeostatic Regulator of Cutaneous Inflammation and Barrier Function in Mouse Skin
- Melatonin Regulates the Periodic Growth of Cashmere by Upregulating the Expression of Wnt10b and β-catenin in Inner Mongolia Cashmere Goats
- RETRACTED ARTICLE: Up-regulated lncRNA5322 elevates MAPK1 to enhance proliferation of hair follicle stem cells as a ceRNA of microRNA-19b-3p
- CDH3 gene related hypotrichosis and juvenile macular dystrophy – A case with a novel mutation
- The retarded hair growth ( rhg ) mutation in mice is an allele of ornithine aminotransferase ( Oat )
- Identification of functional circRNAs regulating ovarian follicle development in goats