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Research 181–210 of 1000+
- The Enrichment of Specific Hair Follicle-Associated Cell Populations in Plucked Hairs Offers an Opportunity to Study Gene Expression Underlying Hair Traits
- Epidermal Dysplasia and Abnormal Hair Follicles in Transgenic Mice Overexpressing Homeobox Gene MSX-2
- Seasonal Variability in Transcript Expression of Type I and Type II Keratins in Wool Follicles of Lustrous Fleece-Producing Magra Sheep
- Impaired Hair Follicle Morphogenesis and Cycling with Abnormal Epidermal Differentiation in nackt Mice, a Cathepsin L-Deficient Mutation
- The nude gene and the skin
- Significance of stress keratin expression in normal and diseased epithelia
- Characterization of the Promoter Regions of Two Sheep Keratin-Associated Protein Genes for Hair Cortex-Specific Expression
- Structure and expression of the ovine Hoxc-13 gene
- Spatiotemporal Expression and Haplotypes Identification of KRT84 Gene and Their Association with Wool Traits in Gansu Alpine Fine-Wool Sheep
- Bullous Congenital Ichthyosiform Erythroderma with Tinea Capitis in Half-Siblings: Rare Phenomenon in Ichthyosis with Co-Existing Trichophyton rubrum Infection and Blocker Displacement Amplification for Mosaic Mutation Detection
- Skin transcriptome profiling of Changthangi goats highlights the relevance of genes involved in Pashmina production
- Hairless controls hair fate decision via Wnt/β–catenin signaling
- 314 Molecular genetic dissection of ILVEN leads to successful targeted therapy
- <i>Hoxc13</i> mutant mice lack external hair
- Cloning of wrinkle-free, a previously uncharacterized mouse mutation, reveals crucial roles for fatty acid transport protein 4 in skin and hair development
- Gene expression profiling gets to the root of human hair follicle stem cells
- Mammalian keratin associated proteins (KRTAPs) subgenomes: disentangling hair diversity and adaptation to terrestrial and aquatic environments
- Hair Follicle Disruption Facilitates Pathogenesis to UVB-Induced Cutaneous Inflammation and Basal Cell Carcinoma Development in Ptch+/− Mice
- Discreet monilethrix: De novo mutation on the example of polish families
- Differential expression of keratin and keratin associated proteins are linked with hair loss condition in spontaneously mutated inbred mice
- The naked truth: Sphynx and Devon Rex cat breed mutations in KRT71
- Diagnosis and treatment of isolated autosomal recessive woolly hair/hypotrichosis
- The Catalog of Human Hair Keratins
- APCDD1 is a novel Wnt inhibitor mutated in hereditary hypotrichosis simplex
- Ichthyosis, Follicular Atrophoderma, and Hypotrichosis Caused by Mutations in ST14 Is Associated with Impaired Profilaggrin Processing
- p53 Is a Direct Transcriptional Repressor of Keratin 17: Lessons from a Rat Model of Radiation Dermatitis
- Skin-specific regulation of SREBP processing and lipid biosynthesis by glycerol kinase 5
- Sequencing KRT71 as a candidate gene for hair shape variation in dromedary camels
- Relationship of a Novel c.429delC Deletion in Hairless Gene HR with Alopecia in Two Families from Southern Punjab, Pakistan
- Hutchinson-Gilford Progeria Syndrome—Current Status and Prospects for Gene Therapy Treatment