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Research 151–180 of 458
- Controversies in plastic surgery: Suction-assisted lipectomy (SAL) and the hCG (human chorionic gonadotropin) protocol for obesity treatment
- ERG induces androgen receptor-mediated regulation of SOX9 in prostate cancer
- Biotin and biotinidase deficiency
- Transcriptomic landscape of early hair follicle and epidermal development
- Inherited ichthyoses/generalized Mendelian disorders of cornification
- STUB1 mutations in autosomal recessive ataxias – evidence for mutation-specific clinical heterogeneity
- Myotonic Dystrophy—A Progeroid Disease?
- The role of WNT10B in physiology and disease: A 10-year update
- Betaine supplementation is less effective than methionine restriction in correcting phenotypes of CBS deficient mice
- Toward Elucidating Epigenetic and Metabolic Regulation of Stem Cell Lineage Plasticity in Skin Aging
- Decay of Skin-Specific Gene Modules in Pangolins
- Epithelial loss of mitochondrial oxidative phosphorylation leads to disturbed enamel and impaired dentin matrix formation in postnatal developed mouse incisor
- Risk of ovarian hyperstimulation syndrome in infertile patients with PCOS treated by HP HMG
- Infertility in Polycystic Ovary Syndrome: Focus on Low-Dose Gonadotropin Treatment
- Molecular cloning and characterization analysis of LEF-1 gene from Inner Mongolia Cashmere Goat
- Bioprinting of hair follicle germs for hair regenerative medicine
- Genome-wide association study identifies a new locus JMJD1C at 10q21 that may influence serum androgen levels in men
- A null mutation in the cystatin M/E gene of ichq mice causes juvenile lethality and defects in epidermal cornification
- A position effect on TRPS1 is associated with Ambras syndrome in humans and the Koala phenotype in mice
- Epidermal expression of the truncated prelamin A causing Hutchinson-Gilford progeria syndrome: effects on keratinocytes, hair and skin
- Genetic studies on the functional relevance of the protein prenyltransferases in skin keratinocytes
- Transgenic mouse models support HCR as an effector gene in the PSORS1 locus
- Skin and hair: models for exploring organ regeneration
- Analysis of hidradenitis suppurativa–linked mutations in four genes and the effects of PSEN1-P242LfsX11 on cytokine and chemokine expression in macrophages
- Lymphotoxin-β regulates periderm differentiation during embryonic skin development
- A gene for monilethrix is closely linked to the type II keratin gene cluster at 12q13
- Folliculin interacts with p0071 (plakophilin-4) and deficiency is associated with disordered RhoA signalling, epithelial polarization and cytokinesis
- Hair follicle stem cells: A new arena
- Tcf3 and Lef1 regulate lineage differentiation of multipotent stem cells in skin
- Expression and localization of Sox10 during hair follicle morphogenesis and induced hair cycle