Search
for
Sort by
Research 301–330 of 1000+
- The stem cell niche
- ATP-dependent chromatin remodeling during mammalian development
- A keratin scaffold regulates epidermal barrier formation, mitochondrial lipid composition, and activity
- Complete Structure of an Epithelial Keratin Dimer: Implications for Intermediate Filament Assembly
- Lactoferrin promotes hair growth in mice and increases dermal papilla cell proliferation through Erk/Akt and Wnt signaling pathways
- Skin regeneration with conical and hair follicle structure of deep second-degree scalding injuries via combined expression of the EPO receptor and beta common receptor by local subcutaneous injection of nanosized rhEPO
- The Necessity to Investigate In Vivo Fate of Nanoparticle-Loaded Dissolving Microneedles
- Integrin β1 Establishes Liver Microstructure and Modulates Transforming Growth Factor β during Liver Development and Regeneration
- Are fingernails a key to unlocking the puzzle of mammalian limb regeneration?
- <i>Pseudomonas aeruginosa</i> heme metabolites biliverdin IXβ and IXδ are integral to lifestyle adaptations associated with chronic infection
- Beneficial uses of Breadfruit (Artocarpus altilis)
- Epithelial loss of mitochondrial oxidative phosphorylation leads to disturbed enamel and impaired dentin matrix formation in postnatal developed mouse incisor
- Testosterone up-regulates vacuolar ATPase expression and functional activities in vas deferens of orchidectomized rats
- NIGELLA SATIVA L.: AN OVERVIEW
- 877 Small T antigen from a folliculotropic polyomavirus activates canonical Wnt/β-catenin signaling in vivo
- Leucaena Leucocephala a Nutrition Profile
- The ZIP7 Gene (Slc39a7) Encodes a Zinc Transporter Involved in Zinc Homeostasis of the Golgi Apparatus
- Severe Zinc Deficiency in Male and Female Rats
- A Homozygous Nonsense Mutation in the Zinc-Finger Domain of the Human Hairless Gene Underlies Congenital Atrichia
- A Homozygous Frameshift Mutation in the<i>HOXC13</i>Gene Underlies Pure Hair and Nail Ectodermal Dysplasia in a Syrian Family
- A new mutation resulting in the truncation of the TRAF6-interacting domain of XEDAR: a possible novel cause of hypohidrotic ectodermal dysplasia: Figure 1
- Identification of Beta-Sitosterol and Stigmasterol as Possible Inhibitors of 5 Alpha-Reductase 1: An In-Silico Study
- Trace element status of the patients with alopecia areata
- Nutritional composition and consumer acceptability study of different preparations of edamame soy beans.
- Roles for Msx and Dlx homeoproteins in vertebrate development
- Quantitative Single-Cell Approaches to Stem Cell Research
- Significance of the S100A4 Protein in Psoriasis
- 973 Dipeptidyl-peptidase 4 (DPP4)-positive fibroblasts are responsible for secretion of pro-fibrotic matrix proteins in the human skin
- Significance of the Synthesis of Essential Fatty Acids in Swine
- Localization of varicella-zoster virus nucleic acids and proteins in human skin