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Research 91–120 of 1000+
- 036 Expanded T cells under lymphopenic condition exhibit memory phenotype and infiltrate around hair follicle
- Clonal Growth of Dermal Papilla Cells in Hydrogels Reveals Intrinsic Differences between Sox2-Positive and -Negative Cells In Vitro and In Vivo
- Skin Organoids for Disease Modelling, Drug Screening and Regenerative Medicine: Recent Advances and Future Perspectives
- Rotterdam criteria–based diagnostic subtype is not a strong predictor of cutaneous phenotype in patients with polycystic ovary syndrome: A cross-sectional study
- Mechanism of Vitamin D Receptor Action
- Natural killer cells in atopic and autoimmune diseases of the skin
- Inflammatory memory-activated biomimetic nanovesicles regulate neutrophil plasticity and metabolic reprogramming for rapid diabetic wound healing via targeting miR-193a-5p/TLR4/JNK/P38 MAPK pathways
- Site of beige (<i>bg</i>) and leaden (<i>ln</i>) pigment gene expression determined by recombinant embryonic skin grafts and aggregation mouse chimaeras employing sash (<i>W</i><sup><i>sh</i></sup>) homozygotes
- Ox40-Cre–mediated deletion of BRD4 reveals an unexpected phenotype of hair follicle stem cells in alopecia
- Imbalanced redox dynamics induce fibroblast senescence leading to impaired stem cell pools and skin aging
- Alkaline ceramidase 1 is essential for mammalian skin homeostasis and regulating whole‐body energy expenditure
- Microskin‐Inspired Injectable MSC‐Laden Hydrogels for Scarless Wound Healing with Hair Follicles
- A Genome-Wide Association Study and Machine-Learning Algorithm Analysis on the Prediction of Facial Phenotypes by Genotypes in Korean Women
- The human cysteine protease cathepsin V can compensate for murine cathepsin L in mouse epidermis and hair follicles
- Morpho-Regulation of Ectodermal Organs
- Deficiency of kinase suppressor of Ras1 prevents oncogenic ras signaling in mice.
- Ornithine decarboxylase transgenic mice as a model for human atrichia with papular lesions
- THE EXPRESSION AND INTERACTION OF HEREDITARY FACTORS PRODUCING HYPOTRICHOSIS IN THE MOUSE: HISTOLOGY AND EXPERIMENTAL RESULTS
- Adam10 haploinsufficiency causes freckle-like macules in Hairless mice
- 9. Immunology and Genetics
- Novel skin phenotypes revealed by a genome-wide mouse reverse genetic screen
- Ottawa, Ontario, Canada, February 13–16, 2013
- CuATSM Enhances Wound Repair Without Scarring via Hippo/YAP Signalling Pathway to Reduce Ferroptosis and Macrophage Polarisation
- 266 Myristoylphorbol Acetate (MPA) Enhances Metastasis Via Up-regulation of Eph A2 Transcription Activity
- Modulation of the differentiated phenotype of keratinocytes of the hair follicle and from epidermis
- Genotype-phenotype correlation in boys with X-linked hypohidrotic ectodermal dysplasia
- Characterization of Bsk mice: I. The Bsk mutation does not involve a recombination of cornea-specific keratin 12 and skin-specific hair keratin genes.
- Stem Cell Secretome for Skincare: Of Cell Types, Exosomes, Extracellular Vesicles, and Soluble Fractions
- Trichoscopy of aplasia cutis congenita of the scalp in skin of color
- ADM Scaffolds Generate a Pro-regenerative Microenvironment During Full-Thickness Cutaneous Wound Healing Through M2 Macrophage Polarization via Lamtor1