Search
for
Sort by
Research 751–780 of 1000+
- Epidermolysis bullosa simplex: a paradigm for disorders of tissue fragility
- An Overview of Biopolymeric Electrospun Nanofibers Based on Polysaccharides for Wound Healing Management
- Fibroblast growth factors: key players in regeneration and tissue repair
- WNT Signaling in Disease
- FGF5 is a crucial regulator of hair length in humans
- Integrated analysis of coding genes and non-coding RNAs during hair follicle cycle of cashmere goat (Capra hircus)
- Cell death in the skin
- Integument pattern formation involves genetic and epigenetic controls: feather arrays simulated by digital hormone models.
- Concise Review: Wnt Signaling Pathways in Skin Development and Epidermal Stem Cells
- Human Eccrine Sweat Gland Cells Can Reconstitute a Stratified Epidermis
- Hox in hair growth and development
- Potential Use of Human Periapical Cyst-Mesenchymal Stem Cells (hPCy-MSCs) as a Novel Stem Cell Source for Regenerative Medicine Applications
- The Proteins of Hair and Other Hard α-Keratins
- Recent progress in the manipulation of biochemical and biophysical cues for engineering functional tissues
- The molecular basis of human keratin disorders
- Diseases associated with hidranitis suppurativa: part 2 of a series on hidradenitis
- Fibroblasts – the cellular choreographers of wound healing
- The biology and genetics of curly hair
- Mammalian keratin associated proteins (KRTAPs) subgenomes: disentangling hair diversity and adaptation to terrestrial and aquatic environments
- WNT10A promotes an invasive and self-renewing phenotype in esophageal squamous cell carcinoma
- p63: a crucial player in epithelial stemness regulation
- Heterozygous FOXN1 Variants Cause Low TRECs and Severe T Cell Lymphopenia, Revealing a Crucial Role of FOXN1 in Supporting Early Thymopoiesis
- Overexpression of Sonic Hedgehog suppresses embryonic hair follicle morphogenesis
- Defolliculated (Dfl): A Dominant Mouse Mutation Leading to Poor Sebaceous Gland Differentiation and Total Elimination of Pelage Follicles
- Loss of epidermal Evi/Wls results in a phenotype resembling psoriasiform dermatitis
- Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles
- Integrated single-cell chromatin and transcriptomic analyses of human scalp identify gene-regulatory programs and critical cell types for hair and skin diseases
- Transcriptional Characteristics Showed That miR-144-y/FOXO3 Participates in Embryonic Skin and Feather Follicle Development in Zhedong White Goose
- Plasma Dermatology: Skin Therapy Using Cold Atmospheric Plasma
- Overexpression of the calcium sensing receptor accelerates epidermal differentiation and permeability barrier formation in vivo