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Research 241–270 of 1000+
- Learning from nudity: lessons from the nude phenotype
- What causes hidradenitis suppurativa ?—15 years after
- Neuronal plasticity of the “brain–skin connection”: stress-triggered up-regulation of neuropeptides in dorsal root ganglia and skin via nerve growth factor-dependent pathways
- Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles
- The nude gene and the skin
- A unique insertion/duplication in the VDR gene that truncates the VDR causing hereditary 1,25-dihydroxyvitamin D-resistant rickets without alopecia
- A cluster of 21 keratin-associated protein genes within introns of another gene on human chromosome 21q22.3
- Identification and dissection of an enhancer controlling epithelial gene expression in skin
- Structural features and sites of expression of a new murine 65 kD and 48 kD hair-related keratin pair, associated with a special type of parakeratotic epithelial differentiation
- Interaction between stem cell factor and endothelin-1: effects on melanogenesis in human skin xenografts
- Whole Genome Scan and Selection Signatures for Climate Adaption in Yanbian Cattle
- Harnessing neuroendocrine controls of keratin expression: A new therapeutic strategy for skin diseases?
- Suppression of Wnt/β-catenin signaling by EGF receptor is required for hair follicle development
- Increased Susceptibility to Skin Carcinogenesis Associated with a Spontaneous Mouse Mutation in the Palmitoyl Transferase Zdhhc13 Gene
- Expression of Hex during feather bud development
- Signal transducer and activator of transcription 5B deficiency due to a novel missense mutation in the coiled-coil domain
- Biotinidase deficiency characterized by skin and hair findings
- 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>)
- A disease-causing novel missense mutation in the ST14 gene underlies autosomal recessive ichthyosis with hypotrichosis syndrome in a consanguineous family
- Tetrahydroxystilbene Glucoside Effectively Prevents Apoptosis Induced Hair Loss
- Genetic Variants at 20p11 Confer Risk to Androgenetic Alopecia in the Chinese Han Population
- Variable expressivity of syndromic BMP4-related eye, brain, and digital anomalies: A review of the literature and description of three new cases
- A novel 22-bp InDel within <i>FGF7</i> gene is significantly associated with growth traits in goat
- Association between <i>VEGF</i> gene polymorphisms (11 sites) and polycystic ovary syndrome risk
- Le gène<i>hairless</i>de la souris
- SNP Markers: Analysis of Genetic Diversity and Identification of Genomic Regions in Pantaneiro Sheep and Texel Sheep Under Natural Selection
- The PER3 rs772027021 SNP induces pigmentation phenotypes of dyschromatosis universalis hereditaria
- Staphylococcus aureus accessory gene regulator quorum-sensing system inhibits keratinocyte lipid enzymes and delays wound repair
- Regulation of feather follicle development and Msx2 gene SNP degradation in Hungarian white goose
- A computationally inferred regulatory heart aging model including post-transcriptional regulations