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Research 631–660 of 1000+
- Case report of Schöpf–Schulz–Passarge syndrome resulting from a missense mutation, p.Arg104Cys, in <i>WNT10A</i>
- S100A6 Protein—Expression and Function in Norm and Pathology
- Evolution of Trichocyte Keratins
- Case report: Two individuals with AEBP1-related classical-like EDS: Further clinical characterisation and description of novel AEBP1 variants
- Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis
- The Genetics of Acne
- Orchestrated Role of microRNAs in Skin Development and Regeneration
- Stabilization of epithelial β-catenin compromises mammary cell fate acquisition and branching morphogenesis
- Spatial and Single-Cell Transcriptional Profiling Identifies Functionally Distinct Human Dermal Fibroblast Subpopulations
- Exploring Differentially Expressed Genes by RNA-Seq in Cashmere Goat (Capra hircus) Skin during Hair Follicle Development and Cycling
- Roles of Wnt7a in embryo development, tissue homeostasis, and human diseases
- Whole-genome SNP genotyping mapped a novel locus for hereditary hypotrichosis on chromosome 2q31.1–q32.2
- Skin Development and Disease: A Molecular Perspective
- Adaptive 3D Self‐Assembly of Colorectal Cancer Cells With Unchanged Tumor Phenotype and Drug Sensitivity
- Mechanisms of Impaired Skeletal Muscle Regeneration and Therapeutic Approaches in Aging and Chronic Disease
- WNT10B (wingless-type MMTV integration site family)
- Epidermal Wnt/beta-catenin signalling promotes dermal adipocyte differentiation during hair follicle morphogenesis and regeneration
- Molecular evolution of HR, a gene that regulates the postnatal cycle of the hair follicle
- TGF-β Family Signaling in Epithelial Differentiation and Epithelial–Mesenchymal Transition
- Hair follicle development and related gene and protein expression of skins in Rex rabbits during the first 8 weeks of life
- Role of the Wnt signaling pathway in keratoacanthoma
- Identifying novel strategies for treating human hair loss disorders: Cyclosporine A suppresses the Wnt inhibitor, SFRP1, in the dermal papilla of human scalp hair follicles
- Perspectives of Alopecia behind the Regulation of Foxn1 Gene Exposes the Human Nude Phenotype
- Effect of Adenovirus-Mediated Expression of Sonic Hedgehog Gene on Hair Regrowth in Mice With Chemotherapy-Induced Alopecia
- Seasonal Gene Expression Profile Responsible For Hair Follicle Development In Angora Goats
- Seasonal Gene Expression Profile Responsible for Hair Follicle Development in Angora Goats
- Gene Expression During Drosophila Wing Morphogenesis and Differentiation
- Molecular Cloning and Expression Analysis of Prostaglandin E Receptor 2 Gene in Cashmere Goat (<i>Capra hircus</i>) Skin during Hair Follicle Development
- Differential activity of 2-methylene-19-nor vitamin D analogs on growth factor gene expression in rhino mouse skin and comparison to all-trans retinoic acid
- Exosome-based Therapies for Androgenetic Alopecia: Mechanisms, MicroRNAs, and Clinical Prospects