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Research 331–360 of 1000+
- A second <i>KRT</i>71 allele in curly coated dogs
- Evolution and genetic architecture of sex-limited polymorphism in cuckoos
- The post-terminal differentiation fate of RNAs revealed by next-generation sequencing
- EBS in Children with De Novo Pathogenic Variants Disturbing Krt14
- An Autosomal Recessive Form of Monilethrix Is Caused by Mutations in DSG4: Clinical Overlap with Localized Autosomal Recessive Hypotrichosis
- WNT10A mutation causes ectodermal dysplasia by impairing progenitor cell proliferation and KLF4-mediated differentiation
- Ichthyosis follicularis, alopecia, and photophobia (IFAP) syndrome
- Spermidine Promotes Human Hair Growth and Is a Novel Modulator of Human Epithelial Stem Cell Functions
- Impaired Hair Follicle Morphogenesis and Cycling with Abnormal Epidermal Differentiation in nackt Mice, a Cathepsin L-Deficient Mutation
- Comparative Anatomy of Mouse and Human Nail Units
- Post-transcriptional Regulation of Keratinocyte Progenitor Cell Expansion, Differentiation and Hair Follicle Regression by miR-22
- Gsdma3 is required for hair follicle differentiation in mice
- Comparative proteomic analyses using iTRAQ-labeling provides insights into fiber diversity in sheep and goats
- The Parathyroid Hormone Second Receptor PTH2R and its Ligand Tuberoinfundibular Peptide of 39 Residues TIP39 Regulate Intracellular Calcium and Influence Keratinocyte Differentiation
- Telomere dysfunction impairs epidermal stem cell specification and differentiation by disrupting BMP/pSmad/P63 signaling
- Identification of novel glucocorticoid receptor-regulated genes involved in epidermal homeostasis and hair follicle differentiation
- A comparison of transcriptomic patterns measured in the skin of Chinese fine and coarse wool sheep breeds
- Complementary evolution of coding and noncoding sequence underlies mammalian hairlessness
- Regulatory pathway analysis of coat color genes in Mongolian horses
- Breast cancer resistance protein identifies clonogenic keratinocytes in human interfollicular epidermis
- The mineralocorticoid receptor plays a transient role in mouse skin development
- Structure and expression of the ovine Hoxc-13 gene
- A Heritable Keratinization Defect of the Superficial Epidermis in Norfolk Terriers
- Hague (<i>Hag</i>): A New Mouse Hair Mutation With an Unstable Semidominant Allele
- Semidominant Inheritance in Epidermolytic Ichthyosis
- The human promyelocytic leukemia protein is a tumor suppressor for murine skin carcinogenesis
- From structural resilience to cell specification — Intermediate filaments as regulators of cell fate
- Integration Analysis of Transcriptome and Proteome Reveal the Mechanisms of Goat Wool Bending
- Autosomal recessive monilethrix: Novel variants of the <i>DSG4</i> gene in three Chinese families
- KLHL24-Mediated Hair Follicle Stem Cells Structural Disruption Causes Alopecia