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Research 241–270 of 1000+
- Clinical Snippets
- Beyond Expectations
- Mutations in KLHL24 Add to the Molecular Heterogeneity of Epidermolysis Bullosa Simplex
- EBS in Children with De Novo Pathogenic Variants Disturbing Krt14
- The epidermis: rising to the surface
- Epidermolysis bullosa simplex: a paradigm for disorders of tissue fragility
- Keratinization and its Disorders
- Post-transcriptional Regulation of Keratinocyte Progenitor Cell Expansion, Differentiation and Hair Follicle Regression by miR-22
- Prolactin: an emerging force along the cutaneous–endocrine axis
- Epidermal Dysplasia and Abnormal Hair Follicles in Transgenic Mice Overexpressing Homeobox Gene MSX-2
- Embryonic keratinization in vertebrates in relation to land colonization
- Disorders of Keratinization
- Vitamin D<sub>3</sub>Analogs Stimulate Hair Growth in Nude Mice
- Epidermal keratinocytes initiate wound healing and pro-inflammatory immune responses following percutaneous schistosome infection
- Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome
- Multi-potentiality of a new immortalized epithelial stem cell line derived from human hair follicles
- Disrupted Ectodermal Organ Morphogenesis in Mice with a Conditional Histone Deacetylase 1, 2 Deletion in the Epidermis
- Retinoids and Keratinization
- The Hair Follicle: An Underutilized Source of Cells and Materials for Regenerative Medicine
- Harlequin ichthyosis (ichq): a juvenile lethal mouse mutation with ichthyosiform dermatitis.
- Expression Profiling Reveals Genes Involved in the Regulation of Wool Follicle Bulb Regression and Regeneration in Sheep
- Integrated miRNA-mRNA analysis reveals regulatory pathways underlying the curly fleece trait in Chinese tan sheep
- Structural and biochemical changes underlying a keratoderma-like phenotype in mice lacking suprabasal AP1 transcription factor function
- Fine structure and immunocytochemistry of monotreme hairs, with emphasis on the inner root sheath and trichohyalin‐based cornification during hair evolution
- Laminin 332 Is Indispensable for Homeostatic Epidermal Differentiation Programs
- 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
- A newborn presenting with congenital blistering
- Equine Hoof Stem Progenitor Cells (HPC) CD29 + /Nestin + /K15 + – a Novel Dermal/epidermal Stem Cell Population With a Potential Critical Role for Laminitis Treatment