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Research 151–180 of 1000+
- Integrative transcriptomic and metabolomic analyses reveal the role of melatonin in promoting secondary hair follicle development in cashmere goats
- Spatial and Single-Cell Transcriptional Profiling Identifies Functionally Distinct Human Dermal Fibroblast Subpopulations
- Topobiology of Human Pigmentation: P-Cadherin Selectively Stimulates Hair Follicle Melanogenesis
- Stabilization of epithelial β-catenin compromises mammary cell fate acquisition and branching morphogenesis
- Exploring Differentially Expressed Genes by RNA-Seq in Cashmere Goat (Capra hircus) Skin during Hair Follicle Development and Cycling
- Desmosomes in Developing Human Epidermis
- Pentacyclic Triterpenoid Maslinic Acid Promotes Hair Growth Comparable to Minoxidil: A New Insight on the Potential Involvement of Cilia Activity
- The Genetics of Acne
- Association between PITX2 polymorphism and androgenetic alopecia in the Indian population
- Orchestrated Role of microRNAs in Skin Development and Regeneration
- The Role of ATP-dependent Chromatin Remodeling in the Control of Epidermal Differentiation and Skin Stem Cell Activity
- Sustainability of functional hair follicle activity: Impact of spatially anchored multifunctional tetrahedral framework nucleic acids
- Construction of transcriptome atlas of white yak hair follicle during anagen and catagen using single-cell RNA sequencing
- Single-Cell Transcriptomics Reveals the Molecular Anatomy of Sheep Hair Follicle Heterogeneity and Wool Curvature
- Temporal Dynamics of Endothelium After Radiation Injury Reveal a Transient Pro-Angiogenic Capillary Subpopulation Associated with Skin Repair
- Application of multi-omics techniques to androgenetic alopecia: Current status and perspectives
- Case report of Schöpf–Schulz–Passarge syndrome resulting from a missense mutation, p.Arg104Cys, in <i>WNT10A</i>
- Mutations in SNRPE, which Encodes a Core Protein of the Spliceosome, Cause Autosomal-Dominant Hypotrichosis Simplex
- Roles of Wnt7a in embryo development, tissue homeostasis, and human diseases
- Conditional Knockout in Mice Reveals the Critical Roles of Ppp2ca in Epidermis Development
- Human ClinicalPhenotype Associated with FOXN1 Mutations
- Differentiation genes were governed by DNA methylation during hair follicle morphogenesis in Cashmere goat
- Genome Wide Differential Expression Profiles in Nevus Sebaceous Uncovered Low Expression of CDKN2AIP and Construction of a ceRNA Network
- Multiple cell types guided by neurocytes orchestrate horn bud initiation in dairy goats
- AP-2α/AP-2β transcription factors are key regulators of epidermal homeostasis
- Signaling pathways and targeted therapeutic strategies for polycystic ovary syndrome
- Whole-genome SNP genotyping mapped a novel locus for hereditary hypotrichosis on chromosome 2q31.1–q32.2
- The idiosyncratic genome of Korean long-tailed chicken as a valuable genetic resource
- Position effect on <i>FGF13</i> associated with X-linked congenital generalized hypertrichosis
- miR-370-3p Inhibited the Proliferation of Sheep Dermal Papilla Cells by Inhibiting the Expression of SMAD4