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Research 841–870 of 1000+
- Montagna Symposium 2013—Light and Skin: How Light Sustains, Damages, Treats, Images and Modifies Skin Biology
- Screening of circRNAs Associated with Secondary Wool Follicle Development in Fine-Wool Sheep and Construction of Their ceRNA Network
- Identification and single-cell analysis of prognostic genes related to mitochondrial and neutrophil extracellular traps in bladder cancer
- The role of hsa‐miR‐193a‐5p as an important factor for control of inositol in alopecia areata
- Recent Updates of the CRISPR/Cas9 Genome Editing System: Novel Approaches to Regulate Its Spatiotemporal Control by Genetic and Physicochemical Strategies
- Resequencing Analyses Revealed Genetic Diversity and Selection Signatures during Rabbit Breeding and Improvement
- Bioinspired engineering ADSC nanovesicles thermosensitive hydrogel enhance autophagy of dermal papilla cells for androgenetic alopecia treatment
- Apoptotic dysregulation mediates stem cell competition and tissue regeneration
- Bioinformatic analysis of gene expression data reveals Src family protein tyrosine kinases as key players in androgenetic alopecia
- Genome Wide Differential Expression Profiles in Nevus Sebaceous Uncovered Low Expression of CDKN2AIP and Construction of a ceRNA Network
- <i>OsPHR2</i> Is Involved in Phosphate-Starvation Signaling and Excessive Phosphate Accumulation in Shoots of Plants
- Genome-wide Maps of Histone Modifications Unwind In Vivo Chromatin States of the Hair Follicle Lineage
- The Two Functional Keratin 6 Genes of Mouse Are Differentially Regulated and Evolved Independently from Their Human Orthologs
- Concerted gene duplications in the two keratin gene families
- Mutations in SNRPE, which Encodes a Core Protein of the Spliceosome, Cause Autosomal-Dominant Hypotrichosis Simplex
- Epidermal PPARγ Is a Key Homeostatic Regulator of Cutaneous Inflammation and Barrier Function in Mouse Skin
- CDH3 gene related hypotrichosis and juvenile macular dystrophy – A case with a novel mutation
- The retarded hair growth ( rhg ) mutation in mice is an allele of ornithine aminotransferase ( Oat )
- The potential role of hsa_circ_0001079 in androgenetic alopecia via sponging hsa‐miR‐136‐5p
- A TP63 Mutation Causes Prominent Alopecia with Mild Ectodermal Dysplasia
- Catecholaminergic neurons boost fibroblast osteogenic activity in keloid
- Unraveling Evolutionary Insights into AVT Peptide Conservation and Antimicrobial Motif Prediction Across Taxa
- Generating detailed intercellular communication patterns in psoriasis at the single-cell level using social networking, pattern recognition, and manifold learning methods to optimize treatment strategies
- Gene variants associated with acne vulgaris presentation and severity: a systematic review and meta-analysis
- Genome-Wide Association Study of Alopecia Areata in Taiwan: The Conflict Between Individuals and Hair Follicles
- A complete guide to human microbiomes: Body niches, transmission, development, dysbiosis, and restoration
- Topical delivery of nanoemulsions for skin cancer treatment
- Neutrophil extracellular traps impair regeneration
- Autosomal recessive woolly hair/hypotrichosis caused by LIPH mutations: a case report
- Dermal β-Catenin Is Required for Hedgehog-Driven Hair Follicle Neogenesis.