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Research 31–60 of 42
- A Kaleidoscope of Keratin Gene Expression and the Mosaic of Its Regulatory Mechanisms
- Gene expression profile of human follicle dermal papilla cells in response to <i>Camellia japonica</i> phytoplacenta extract
- Particulate matter exposure induces maternal scalp hair loss after birth in C57/B6 mouse via alteration of inflammatory and apoptotic pathways
- Keratin 15 promotes a progenitor cell state in basal keratinocytes of skin epidermis
- 568 Novel synthetic melanin nanoparticles improve skin wound healing
- SOX9 in organogenesis: shared and unique transcriptional functions
- Implication of microRNA regulation in para-phenylenediamine-induced cell death and senescence in normal human hair dermal papilla cells
- Adipose Tissue-Derived Therapies for Osteoarthritis: Multifaceted Mechanisms and Clinical Prospects
- Acetyl-CoA synthesis in the skin is a key determinant of systemic lipid homeostasis
- A comprehensive genome-wide analysis for signatures of selection in goat (genus Capra) revealed new candidate genes for environmental adaptation and productive traits
- Vitamins and their derivatives synergistically promote hair shaft elongation ex vivo via PlGF/VEGFR-1 signalling activation
- Table_1_Bioinformatics and Network Pharmacology Identify the Therapeutic Role and Potential Mechanism of Melatonin in AD and Rosacea.xlsx
- Mutations in KLHL24 Add to the Molecular Heterogeneity of Epidermolysis Bullosa Simplex
- KLHL24-Mediated Hair Follicle Stem Cells Structural Disruption Causes Alopecia
- Syndromic epidermolysis bullosa simplex subtype due to mutations in the KLHL24 gene: series of case reports in Russian families
- 474 Stabilizing mutations of KLHL24 ubiquitin ligase cause loss of keratin 14 and human skin fragility
- 454 Modeling epidermolysis bullosa simplex with cardiomyopathy using KLHL24-mutant pluripotent stem cells.
- Novel insights into cardiocutaneous syndromes
- Pathogenesis and clinical features of alopecia in epidermolysis bullosa: A systematic review
- De Novo-Designed Bifunctional Proteins for Targeted Protein Degradation
- De novo designed bifunctional proteins for targeted protein degradation
- <i>De novo</i> designed bifunctional proteins for targeted protein degradation
- 475 Paraoxonase 1 (PON1) L55M and Q192R polymorphisms, lipid profiles and psoriasis
- 476 Development of an intrinsic skin sensor for blood glucose level with CRISPR-mediated genome editing in epidermal stem cells
- Transcriptome sequencing reveals the expression profiles of lncRNAs and mRNAs in goat skin tissues with different types of wool coats
- Inherited Epidermolysis Bullosa: A Clinical Case
- SOX11 and SOX4 drive the reactivation of an embryonic gene program during murine wound repair
- Peripheral blood gene expression in alopecia areata reveals molecular pathways distinguishing heritability, disease and severity
- Detecting the Mechanism behind the Transition from Fixed Two-Dimensional Patterned Sika Deer (Cervus nippon) Dermal Papilla Cells to Three-Dimensional Pattern
- Hair Dermal papilla maintain its hair inducing characteristics via autocrine exosomal miR-23a-3p