Search
for
Sort by
Research 211–240 of 1000+
- Post-transcriptional Regulation of Keratinocyte Progenitor Cell Expansion, Differentiation and Hair Follicle Regression by miR-22
- Disorders of Keratinization
- Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome
- <i>Msx2</i> Prevents Stratified Squamous Epithelium Formation in the Enamel Organ
- Pathological Mechanisms Involved in Epidermolysis Bullosa Simplex: Current Knowledge and Therapeutic Perspectives
- Focal palmoplantar callosities in non-Herlitz junctional epidermolysis bullosa
- The Mechanisms of Fur Development and Color Formation in American Mink Revealed Using Comparative Transcriptomics
- Effect of Oral Minoxidil on Monilethrix
- The formulation and in‐vitro evaluation of WS Biotin, a novel encapsulated form of D‐Biotin with improved water solubility for hair and skin treatment applications
- Evidence for Novel Functions of the Keratin Tail Emerging from a Mutation Causing Ichthyosis Hystrix
- Skin Appendage Proteins of Tetrapods: Building Blocks of Claws, Feathers, Hair and Other Cornified Epithelial Structures
- Dermal papilla-induced hair differentiation of adult epithelial stem cells from human skin
- Multi-omics analysis of functional substances and expression verification in cashmere fineness
- Human Female Hair Follicles Are a Direct, Nonclassical Target for Thyroid-Stimulating Hormone
- Fundamental hair follicle biology and fine fibre production in animals
- Characterization of Hair Follicle Antigens Targeted by the Anti-Hair Follicle Immune Response
- Multi-potentiality of a new immortalized epithelial stem cell line derived from human hair follicles
- The Effects of Spermidine on Functional and Transcriptomic Markers in Human Primary Keratinocytes
- Cylindroma as Tumor of Hair Follicle Origin
- Characterisation of Four New Genes in the Ovine KAP19 Family
- The human keratins: biology and pathology
- Autosomal Recessive Transmission of a Rare KRT74 Variant Causes Hair and Nail Ectodermal Dysplasia: Allelism with Dominant Woolly Hair/Hypotrichosis
- <i>De novo</i> filament formation by human hair keratins K85 and K35 follows a filament development pattern distinct from cytokeratin filament networks
- Keratins: the hair shaft's backbone revealed
- Characterisation of the Ovine KRTAP36-1 Gene in Chinese Tan Lambs and Its Impact on Selected Wool Traits
- Identification and characterization of genes for skin and hair disorders
- Keratin 17 null mice exhibit age- and strain-dependent alopecia
- A new look into an old problem: keratins as tools to investigate determination, morphogenesis, and differentiation in skin.
- Keratin 17 modulates hair follicle cycling in a TN<i>Fα</i>-dependent fashion
- A Missense Mutation within the Helix Termination Motif of KRT25 Causes Autosomal Dominant Woolly Hair/Hypotrichosis