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Research 421–450 of 1000+
- Regulation of Keratin 9 in Nonpalmoplantar Keratinocytes by Palmoplantar Fibroblasts Through Epithelial–Mesenchymal Interactions
- Mutations in the hair cortex keratin hHb6 cause the inherited hair disease monilethrix
- The HOXC13-controlled expression of early hair keratin genes in the human hair follicle does not involve TALE proteins MEIS and PREP as cofactors
- Ultrastructural localization of hair keratins, high sulfur keratin-associated proteins and sulfhydryl oxidase in the human hair
- The molecular basis of human keratin disorders
- Atrichia Caused by Mutations in the Vitamin D Receptor Gene is a Phenocopy of Generalized Atrichia Caused by Mutations in the Hairless Gene
- Keratin 6A promotes skin inflammation through JAK1-STAT3 activation in keratinocytes
- Ancient lineages of the keratin-associated protein (KRTAP) genes and their co-option in the evolution of the hair follicle
- The Role of the Slc39a Family of Zinc Transporters in Zinc Homeostasis in Skin
- <i>De Novo</i>Transcriptome Assembly and Differential Gene Expression Profiling of Three<i>Capra hircus</i>Skin Types during Anagen of the Hair Growth Cycle
- The expanding significance of keratin intermediate filaments in normal and diseased epithelia
- Keratin 15 promotes a progenitor cell state in basal keratinocytes of skin epidermis
- Genomic Organization, Transcriptomic Analysis, and Functional Characterization of Avian α- and β-Keratins in Diverse Feather Forms
- Human keratin hydrogels support fibroblast attachment and proliferation in vitro
- Crosslinking Between Trichocyte Keratins and Keratin Associated Proteins
- Structural Transition of Trichocyte Keratin Intermediate Filaments During Development in the Hair Follicle
- Conditional Activin Receptor Type 1B (Acvr1b) Knockout Mice Reveal Hair Loss Abnormality
- Hereditary 1,25‐Dihydroxyvitamin D‐Resistant Rickets in a Pomeranian Dog Caused by a Novel Mutation in the Vitamin D Receptor Gene
- Effect of the FA2H Gene on cashmere fineness of Jiangnan cashmere goats based on transcriptome sequencing
- Using WGCNA (weighted gene co-expression network analysis) to identify the hub genes of skin hair follicle development in fetus stage of Inner Mongolia cashmere goat
- Investigating the role of keratin proteins and microbial associations in hereditary and pathogenic alopecia
- FOXN1: A Master Regulator Gene of Thymic Epithelial Development Program
- The nude gene and the skin
- Gene therapy to enhance angiogenesis in chronic wounds
- The Immunological Impact of IL-1 Family Cytokines on the Epidermal Barrier
- Targeting the Janus Kinase Family in Autoimmune Skin Diseases
- Integrated multiple machine learning and Mendelian randomization reveal LTF gene as a prognostic biomarker for nonspecific orbital inflammation
- Gene-knockout mice with abnormal epidermal and hair follicular development
- Polygenic control of the wavy coat of the NCT mouse: involvement of an intracisternal A particle insertional mutation of the protease, serine 53 (Prss53) gene, and a modifier gene
- p63 Regulates Human Keratinocyte Proliferation via MYC-regulated Gene Network and Differentiation Commitment through Cell Adhesion-related Gene Network