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Research 211–240 of 1000+
- A Founder Mutation in the <i>POMC</i> 5′-UTR Causes Proopiomelanocortin Deficiency Through Splicing-Mediated Decrease of mRNA
- Impacts of iron on phosphate starvation-induced root hair growth in Arabidopsis
- Comparison of Calcium and Barium Microcapsules as Scaffolds in the Development of Artificial Dermal Papillae
- Analgesic Effect of Human Placenta Hydrolysate on CFA-Induced Inflammatory Pain in Mice
- Hydrogel-mediated extracellular vesicles for enhanced wound healing: the latest progress, and their prospects for 3D bioprinting
- Research advances in smart responsive-hydrogel dressings with potential clinical diabetic wound healing properties
- A comparative study of skin transcriptomes and histological observations for black and white hair colors of giant panda
- Potential of Natural Products in Hangeshashinto Water Extract on the Direct Suppression of Stomatitis Induced by Intra-/Extracellular Advanced Glycation End-Products
- Advanced Applications of Vitamin B Complex in Plastic and Cosmetic Surgery: Mechanisms and Therapeutic Benefits
- Dynamics and Epigenetics of the Epidermal Differentiation Complex
- Metabolic Engineering of Microorganisms to Produce L-Aspartate and Its Derivatives
- Targeted transgenic expression of the mutation causing Hutchinson-Gilford progeria syndrome leads to proliferative and degenerative epidermal disease
- The potential application of natural products in cutaneous wound healing: A review of preclinical evidence
- Effects of Microwave-Assisted Opuntia humifusa Extract in Inhibiting the Impacts of Particulate Matter on Human Keratinocyte Skin Cell
- Catecholaminergic neurons boost fibroblast osteogenic activity in keloid
- Genetically Induced Cell Death in Bulge Stem Cells Reveals Their Redundancy for Hair and Epidermal Regeneration
- ENZYMES
- Coexisting trichorrhexis nodosa and pili annulati: a case report of hair shaft abnormalities in a syrian family
- Inflammatory perifollicular fibrosis and alopecia
- A new mutation in the type II hair cortex keratin hHb1 involved in the inherited hair disorder monilethrix
- A Variable Monilethrix Phenotype Associated With a Novel Mutation, Glu402Lys, in the Helix Termination Motif of the Type II Hair Keratin hHb1
- The Fate of Trichohyalin
- Increased dipicolinic acid production with an enhanced <i>spoVF</i> operon in <i>Bacillus subtilis</i> and medium optimization
- Follikelhormone
- In Human Skin, UVB Initiates Early Induction of IL-10 Over IL-12 Preferentially in the Expanding Dermal Monocytic/Macrophagic Population
- Partial Purification and Characterization of Two Distinct Types of Caspases from Human Epidermis
- A Splice Site Mutation in the Gene of the Human Type I Hair Keratin hHa1 Results in the Expression of a Tailless Keratin Isoform
- Isolation and Characterization of a Putative Keratin-Associated Protein Gene Expressed in Embryonic Skin of Mice
- Rat steroid 5α-reductase kinetic characteristics: Extreme pH-dependency of the type II isozyme in prostate and epididymis homogenates
- Cutaneous signals of immune system disease