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Research 31–60 of 113
- A Mixture of Tocopherol Acetate and L-Menthol Synergistically Promotes Hair Growth in C57BL/6 Mice
- CD201+ fascia progenitors choreograph injury repair
- Differences in cell subsets between sun-exposed and unexposed skin: preliminary single-cell sequencing and biological analysis from a single case
- Deep phenotyping of skin tissue remodeling in patients with systemic sclerosis treated with CD19-CAR T cells
- Hoxc13 polyglycine repeat gain-of-function drives mammalian integument evolution by altering targeted genes and interactions
- A multi-omic single-cell landscape of perinatal mouse skin maps lineage specification and reveals shared dynamics in human fetal skin
- Precision therapeutics in non-scarring alopecia: a systemic genomic and pathway-based framework for targeted interventions
- Farmácia Sanches - Leiria e nos Serviços Farmacêuticos do Hospital Lusíadas - Porto
- Wasabi leaf extract changes the expression levels of cytokine related genes in dermal papilla cells, which identified by the whole transcriptome
- Nouvelles thérapeutiques dans la prise en charge de l’alopécie androgénétique
- Fibroblast heterogeneity and functions: insights from single-cell sequencing in wound healing, breast cancer, ovarian cancer and melanoma
- <i>DSG4</i> Gene Variants as a Cause of Hypotrichosis in the Child with Severe Atopic Dermatitis: Clinical Case
- TNC+ fibroblasts involve in skin inflammation via neuro-immune and interacting with T cells
- Two females with hair loss
- A systematic review of randomized controlled trials assessing phytochemicals and natural ingredients for skin and hair care
- SPT6 maintains epidermal homeostasis by inhibiting an NF-κB-positive feedback loop to prevent excessive inflammation
- Geriatric Dermatologic Therapy
- Multi-ancestry tandem repeat association study of hair colour using exome-wide sequencing
- Therapies
- Alopezien und Hypotrichosen im Kindesalter
- Impaired metabolic effects of metformin in men with early-onset androgenic alopecia
- Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles
- Mutations in SNRPE, which Encodes a Core Protein of the Spliceosome, Cause Autosomal-Dominant Hypotrichosis Simplex
- A systematic simulation-based meta-analytical framework for prediction of physiological biomarkers in alopecia
- Expression of Signaling Components in Embryonic Eyelid Epithelium
- Development of Woolly Hair and Hairlessness in a CRISPR−Engineered Mutant Mouse Model with KRT71 Mutations
- Genome-wide detection of RNA editing events during the hair follicles cycle of Tianzhu white yak
- Interaction of the AKT and β-catenin signalling pathways and the influence of photobiomodulation on cellular signalling proteins in diabetic wound healing
- Role of Aire and Notch4 Allelic Mutations in Alopecia Areata in C3H/HeJ Mice
- Fibroblasts: Origins, definitions, and functions in health and disease