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  • Search Condition : Filter (MeSH = Epidermis / metabolism*)
Species Resource
Silkworms EST database Catalogue of epidermal genes: genes expressed in the epidermis during larval molt of the silkworm Bombyx mori.
C.intestinalis / (O.japonicus) Wild C.int Transcriptional regulation of the retinoic acid receptor in the dorsal midline epidermis in the Ciona intestinalis embryo.
Silkworms ? Melanin-synthesis enzymes coregulate stage-specific larval cuticular markings in the swallowtail butterfly, Papilio xuthus.
Zebrafish Epidermal regulation of bone morphogenesis through the development and regeneration of osteoblasts in the zebrafish scale.
C.elegans tm773 , tm1984 , tm5924 , tm2373 , tm520 , tm2337 Cuticle integrity and biogenic amine synthesis in Caenorhabditis elegans require the cofactor tetrahydrobiopterin (BH4).
C.elegans tm1463 , tm776 , tm760 , tm1146 , tm3036 C. elegans epidermal wounding induces a mitochondrial ROS burst that promotes wound repair.
Drosophila 5988R-3 , 5680R-1 Spatiotemporal regulation of cell fusion by JNK and JAK/STAT signaling during Drosophila wound healing.
Mice C57BL/6-Tg(CAG-EGFP)C14-Y01-FM131Osb Two distinct types of mouse melanocyte: differential signaling requirement for the maintenance of non-cutaneous and dermal versus epidermal melanocytes.
C.elegans tm1945 The conserved zinc finger protein VAB-23 is an essential regulator of epidermal morphogenesis in Caenorhabditis elegans.
Human and Animal Cells Mechanical Stretch on Human Skin Equivalents Increases the Epidermal Thickness and Develops the Basement Membrane.
Human and Animal Cells CACO-2(RCB0988) H(+)/peptide transporter (PEPT2) is expressed in human epidermal keratinocytes and is involved in skin oligopeptide transport.
Human and Animal Cells Electric stimulus opens intercellular spaces in skin.
Human and Animal Cells BSCC-93 (RCB1202) Expression of REIC/Dkk-3 in normal and hyperproliferative epidermis.
Human and Animal Cells Jyg-MC(B) (RCB0527) Characterization and expression analysis of the Spink5 gene, the mouse ortholog of the defective gene in Netherton syndrome.