Registro:

Referencias:

• Martin, P., Parkhurst, S.M., Parallels between tissue repair and embryo morphogenesis (2004) Development, 131, pp. 3021-3034
• Harden, N., Signaling pathways directing the movement and fusion of epithelial sheets: lessons from dorsal closure in Drosophila (2002) Differentiation, 70, pp. 181-203
• Wood, W., Jacinto, A., Grose, R., Woolner, S., Gale, J., Wound healing recapitulates morphogenesis in Drosophila embryos (2002) Nature Cell Biology, 4, pp. 907-912
• Martin, P., Wound healing--aiming for perfect skin regeneration (1997) Science, 276, pp. 75-81
• McCluskey, J., Martin, P., Analysis of the tissue movements of embryonic wound healing--DiI studies in the limb bud stage mouse embryo (1995) Developmental Biology, 170, pp. 102-114
• Martin, P., Lewis, J., Actin cables and epidermal movement in embryonic wound healing (1992) Nature, 360, pp. 179-183
• Martin-Blanco, E., Pastor-Pareja, J.C., Garcia-Bellido, A., JNK and decapentaplegic signaling control adhesiveness and cytoskeleton dynamics during thorax closure in Drosophila (2000) Proc Natl Acad Sci U S A, 97, pp. 7888-7893
• Li, G., Gustafson-Brown, C., Hanks, S.K., Nason, K., Arbeit, J.M., c-Jun is essential for organization of the epidermal leading edge (2003) Developmental Cell, 4, pp. 865-877
• Zenz, R., Scheuch, H., Martin, P., Frank, C., Eferl, R., c-Jun regulates eyelid closure and skin tumor development through EGFR signaling (2003) Developmental Cell, 4, pp. 879-889
• Mace, K.A., Pearson, J.C., McGinnis, W., An epidermal barrier wound repair pathway in Drosophila is mediated by grainy head (2005) Science, 308, pp. 381-385
• Galko, M.J., Krasnow, M.A., Cellular and genetic analysis of wound healing in Drosophila larvae (2004) PLoS biology, 2, p. 239
• Ramet, M., Lanot, R., Zachary, D., Manfruelli, P., JNK signaling pathway is required for efficient wound healing in Drosophila (2002) Developmental Biology, 241, pp. 145-156
• Bosch, M., Serras, F., Martin-Blanco, E., Baguna, J., JNK signaling pathway required for wound healing in regenerating Drosophila wing imaginal discs (2005) Developmental Biology, 280, pp. 73-86
• Bergantinos, C., Corominas, M., Serras, F., Cell death-induced regeneration in wing imaginal discs requires JNK signalling (2010) Development, 137, pp. 1169-1179
• Nishimura, M., Kumsta, C., Kaushik, G., Diop, S.B., Ding, Y., A dual role for integrin-linked kinase and beta1-integrin in modulating cardiac aging (2014) Aging Cell, 13, pp. 431-440
• Patel, U., Myat, M.M., Receptor guanylyl cyclase Gyc76C is required for invagination, collective migration and lumen shape in the Drosophila embryonic salivary gland (2013) Biol Open, 2, pp. 711-717
• Agnes, F., Suzanne, M., Noselli, S., The Drosophila JNK pathway controls the morphogenesis of imaginal discs during metamorphosis (1999) Development, 126, pp. 5453-5462
• Pastor-Pareja, J.C., Grawe, F., Martin-Blanco, E., Garcia-Bellido, A., Invasive cell behavior during Drosophila imaginal disc eversion is mediated by the JNK signaling cascade (2004) Developmental Cell, 7, pp. 387-399
• Calleja, M., Moreno, E., Pelaz, S., Morata, G., Visualization of gene expression in living adult Drosophila (1996) Science, 274, pp. 252-255
• Bryant, P.J., Fraser, S.E., Wound healing, cell communication, and DNA synthesis during imaginal disc regeneration in Drosophila (1988) Developmental Biology, 127, pp. 197-208
• Schubiger, G., Regeneration, duplication and transdetermination in fragments of the leg disc of Drosophila melanogaster (1971) Developmental Biology, 26, pp. 277-295
• Frydman, J., Nimmesgern, E., Ohtsuka, K., Hartl, F.U., Folding of nascent polypeptide chains in a high molecular mass assembly with molecular chaperones (1994) Nature, 370, pp. 111-117
• Brackley, K.I., Grantham, J., Activities of the chaperonin containing TCP-1 (CCT): implications for cell cycle progression and cytoskeletal organisation (2009) Cell Stress Chaperones, 14, pp. 23-31
• Reinhardt, C.A., Hodgkin, N.M., Bryant, P.J., Wound healing in the imaginal discs of Drosophila (1977) I. Scanning electron microscopy of normal and healing wing discs. Developmental Biology, 60, pp. 238-257
• Pavlidis, P., Noble, W.S., Analysis of strain and regional variation in gene expression in mouse brain (2001) Genome biology, 2
• Stevens, L.J., Page-McCaw, A., A secreted MMP is required for reepithelialization during wound healing (2012) Molecular Biology of the Cell, 23, pp. 1068-1079
• Abreu-Blanco, M.T., Verboon, J.M., Parkhurst, S.M., Cell wound repair in Drosophila occurs through three distinct phases of membrane and cytoskeletal remodeling (2011) Journal of Cell Biology, 193, pp. 455-464
• Brown, N.H., Gregory, S.L., Rickoll, W.L., Fessler, L.I., Prout, M., Talin is essential for integrin function in Drosophila (2002) Dev Cell, 3, pp. 569-579
• Yagi, R., Ishimaru, S., Yano, H., Gaul, U., Hanafusa, H., A novel muscle LIM-only protein is generated from the paxillin gene locus in Drosophila (2001) EMBO Rep, 2, pp. 814-820
• Sokol, N.S., Cooley, L., Drosophila filamin encoded by the cheerio locus is a component of ovarian ring canals (1999) Curr Biol, 9, pp. 1221-1230
• Konsolaki, M., Schupbach, T., windbeutel, a gene required for dorsoventral patterning in Drosophila, encodes a protein that has homologies to vertebrate proteins of the endoplasmic reticulum (1998) Genes Dev, 12, pp. 120-131
• Ashburner, M., Ball, C.A., Blake, J.A., Botstein, D., Butler, H., Gene ontology: tool for the unification of biology (2000) The Gene Ontology Consortium. Nature genetics, 25, pp. 25-29
• Aza-Blanc, P., Ramirez-Weber, F.A., Laget, M.P., Schwartz, C., Kornberg, T.B., Proteolysis that is inhibited by hedgehog targets Cubitus interruptus protein to the nucleus and converts it to a repressor (1997) Cell, 89, pp. 1043-1053
• Grantham, J., Brackley, K.I., Willison, K.R., Substantial CCT activity is required for cell cycle progression and cytoskeletal organization in mammalian cells (2006) Exp Cell Res, 312, pp. 2309-2324
• Coue, M., Brenner, S.L., Spector, I., Korn, E.D., Inhibition of actin polymerization by latrunculin A (1987) FEBS Lett, 213, pp. 316-318
• Stramer, B., Winfield, M., Shaw, T., Millard, T.H., Woolner, S., Gene induction following wounding of wild-type versus macrophage-deficient Drosophila embryos (2008) EMBO Reports, 9, pp. 465-471
• Blanco, E., Ruiz-Romero, M., Beltran, S., Bosch, M., Punset, A., Gene expression following induction of regeneration in Drosophila wing imaginal discs (2010) Expression profile of regenerating wing discs. BMC Dev Biol, 10, p. 94
• Bosch, M., Baguna, J., Serras, F., Origin and proliferation of blastema cells during regeneration of Drosophila wing imaginal discs (2008) Int J Dev Biol, 52, pp. 1043-1050
• Lee, N., Maurange, C., Ringrose, L., Paro, R., Suppression of Polycomb group proteins by JNK signalling induces transdetermination in Drosophila imaginal discs (2005) Nature, 438, pp. 234-237
• Mattila, J., Omelyanchuk, L., Kyttala, S., Turunen, H., Nokkala, S., Role of Jun N-terminal Kinase (JNK) signaling in the wound healing and regeneration of a Drosophila melanogaster wing imaginal disc (2005) Int J Dev Biol, 49, pp. 391-399
• Bergantinos, C., Vilana, X., Corominas, M., Serras, F., Imaginal discs: Renaissance of a model for regenerative biology (2010) Bioessays, 32, pp. 207-217
• McCawley, L.J., Matrisian, L.M., Matrix metalloproteinases: they’re not just for matrix anymore! (2001) Curr Opin Cell Biol, 13, pp. 534-540
• Werner, S., Grose, R., Regulation of wound healing by growth factors and cytokines (2003) Physiol Rev, 83, pp. 835-870
• Singer, A., Clark, R., Cutaneous Wound Healing (1999) New England Journal of Medicine, 341, pp. 738-746
• Braddock, M., The transcription factor Egr-1: a potential drug in wound healing and tissue repair (2001) Annals of Medicine, 33, pp. 313-318
• Brock, J., Midwinter, K., Lewis, J., Martin, P., Healing of incisional wounds in the embryonic chick wing bud: characterization of the actin purse-string and demonstration of a requirement for Rho activation (1996) Journal of Cell Biology, 135, pp. 1097-1107
• Su, Y.C., Treisman, J.E., Skolnik, E.Y., The Drosophila Ste20-related kinase misshapen is required for embryonic dorsal closure and acts through a JNK MAPK module on an evolutionarily conserved signaling pathway (1998) Genes & Development, 12, pp. 2371-2380
• Stronach, B., Perrimon, N., Activation of the JNK pathway during dorsal closure in Drosophila requires the mixed lineage kinase, slipper (2002) Genes & Development, 16, pp. 377-387
• Yin, J., Lu, J., Yu, F.S., Role of small GTPase Rho in regulating corneal epithelial wound healing (2008) Invest Ophthalmol Vis Sci, 49, pp. 900-909
• Baek, S.H., Kwon, Y.C., Lee, H., Choe, K.M., Rho-family small GTPases are required for cell polarization and directional sensing in Drosophila wound healing (2010) Biochem Biophys Res Commun, 394, pp. 488-492
• Zeidler, M.P., Bach, E.A., Perrimon, N., The roles of the Drosophila JAK/STAT pathway (2000) Oncogene, 19, pp. 2598-2606
• Pastor-Pareja, J.C., Wu, M., Xu, T., An innate immune response of blood cells to tumors and tissue damage in Drosophila (2008) Dis Model Mech, 1, pp. 144-154
• Wu, M., Pastor-Pareja, J.C., Xu, T., Interaction between Ras(V12) and scribbled clones induces tumour growth and invasion (2010) Nature, 463, pp. 545-548
• Adachi-Yamada, T., Fujimura-Kamada, K., Nishida, Y., Matsumoto, K., Distortion of proximodistal information causes JNK-dependent apoptosis in Drosophila wing (1999) Nature, 400, pp. 166-169
• Ryoo, H.D., Gorenc, T., Steller, H., Apoptotic cells can induce compensatory cell proliferation through the JNK and the Wingless signaling pathways (2004) Developmental Cell, 7, pp. 491-501
• Campos, I., Geiger, J.A., Santos, A.C., Carlos, V., Jacinto, A., Genetic Screen in Drosophila melanogaster Uncovers a Novel Set of Genes Required for Embryonic Epithelial Repair (2010) Genetics, 184, pp. 129-140
• Lesch, C., Jo, J., Wu, Y., Fish, G.S., Galko, M.J., A Targeted UAS-RNAi Screen in Drosophila Larvae Identifies Wound Closure Genes Regulating Distinct Cellular Processes (2010) Genetics, 186, pp. 943-957
• Juarez, M.T., Patterson, R.A., Sandoval-Guillen, E., McGinnis, W., Duox, Flotillin-2, and Src42A are required to activate or delimit the spread of the transcriptional response to epidermal wounds in Drosophila (2011) PLoS Genetics, 7
• Belacortu, Y., Paricio, N., Drosophila as a Model of Wound Healing and Tissue Regeneration in Vertebrates (2011) Developmental Dynamics, 240, pp. 2379-2404
• Schäfer, M., Werner, S., Transcriptional Control of Wound Repair (2007) Annu Rev Cell Dev Biol, 23, pp. 69-92
• Dean, M., Rzhetsky, A., Allikmets, R., The human ATP-binding cassette (ABC) transporter superfamily (2001) Genome Research, 11, pp. 1156-1166
• Andersen, C.B., Becker, T., Blau, M., Anand, M., Halic, M., Structure of eEF3 and the mechanism of transfer RNA release from the E-site (2006) Nature, 443, pp. 663-668
• Gomez-Skarmeta, J.L., Diez del Corral, R., de la Calle-Mustienes, E., Ferre-Marco, D., Modolell, J., Araucan and caupolican, two members of the novel iroquois complex, encode homeoproteins that control proneural and vein-forming genes (1996) Cell, 85, pp. 95-105
• Kankel, M.W., Hurlbut, G.D., Upadhyay, G., Yajnik, V., Yedvobnick, B., Investigating the genetic circuitry of mastermind in Drosophila, a notch signal effector (2007) Genetics, 177, pp. 2493-2505
• Rosin, D., Schejter, E., Volk, T., Shilo, B.Z., Apical accumulation of the Drosophila PDGF/VEGF receptor ligands provides a mechanism for triggering localized actin polymerization (2004) Development, 131, pp. 1939-1948
• Cho, N.K., Keyes, L., Johnson, E., Heller, J., Ryner, L., Developmental control of blood cell migration by the Drosophila VEGF pathway (2002) Cell, 108, pp. 865-876
• Ishimaru, S., Ueda, R., Hinohara, Y., Ohtani, M., Hanafusa, H., PVR plays a critical role via JNK activation in thorax closure during Drosophila metamorphosis (2004) EMBO Journal, 23, pp. 3984-3994
• McDonald, J.A., Pinheiro, E.M., Montell, D.J., PVF1, a PDGF/VEGF homolog, is sufficient to guide border cells and interacts genetically with Taiman (2003) Development, 130, pp. 3469-3478
• Wu, Y., Brock, A.R., Wang, Y., Fujitani, K., Ueda, R., A blood-borne PDGF/VEGF-like ligand initiates wound-induced epidermal cell migration in Drosophila larvae (2009) Current Biology, 19, pp. 1473-1477
• Vaduva, G., Martin, N.C., Hopper, A.K., Actin-binding verprolin is a polarity development protein required for the morphogenesis and function of the yeast actin cytoskeleton (1997) J Cell Biol, 139, pp. 1821-1833
• Jiang, W.G., Ye, L., Patel, G., Harding, K.G., Expression of WAVEs, the WASP (Wiskott-Aldrich syndrome protein) family of verprolin homologous proteins in human wound tissues and the biological influence on human keratinocytes (2010) Wound Repair Regen, 18, pp. 594-604
• Schafer, D.A., Cooper, J.A., Control of actin assembly at filament ends (1995) Annu Rev Cell Dev Biol, 11, pp. 497-518
• Machesky, L.M., Cooper, J.A., Cell motility (1999) Bare bones of the cytoskeleton. Nature, 401, pp. 542-543
• Janody, F., Treisman, J.E., Actin capping protein alpha maintains vestigial-expressing cells within the Drosophila wing disc epithelium (2006) Development, 133, pp. 3349-3357
• Ogienko, A.A., Karagodin, D.A., Lashina, V.V., Baiborodin, S.I., Omelina, E.S., Capping protein beta is required for actin cytoskeleton organisation and cell migration during Drosophila oogenesis (2013) Cell Biol Int, 37, pp. 149-159
• Bretscher, A., Fimbrin is a cytoskeletal protein that crosslinks F-actin in vitro (1981) Proc Natl Acad Sci U S A, 78, pp. 6849-6853
• Wu, J.Q., Bahler, J., Pringle, J.R., Roles of a fimbrin and an alpha-actinin-like protein in fission yeast cell polarization and cytokinesis (2001) Mol Biol Cell, 12, pp. 1061-1077
• Dobie, K.W., Kennedy, C.D., Velasco, V.M., McGrath, T.L., Weko, J., Identification of chromosome inheritance modifiers in Drosophila melanogaster (2001) Genetics, 157, pp. 1623-1637
• Sternlicht, H., Farr, G.W., Sternlicht, M.L., Driscoll, J.K., Willison, K., The t-complex polypeptide 1 complex is a chaperonin for tubulin and actin in vivo (1993) Proc Natl Acad Sci U S A, 90, pp. 9422-9426
• Kubota, H., Hynes, G., Willison, K., The chaperonin containing t-complex polypeptide 1 (TCP-1) (1995) Multisubunit machinery assisting in protein folding and assembly in the eukaryotic cytosol. Eur J Biochem, 230, pp. 3-16
• Coghlin, C., Carpenter, B., Dundas, S.R., Lawrie, L.C., Telfer, C., Characterization and over-expression of chaperonin t-complex proteins in colorectal cancer (2006) J Pathol, 210, pp. 351-357
• Kitamura, A., Kubota, H., Pack, C.G., Matsumoto, G., Hirayama, S., Cytosolic chaperonin prevents polyglutamine toxicity with altering the aggregation state (2006) Nat Cell Biol, 8, pp. 1163-1170
• Spiess, C., Miller, E.J., McClellan, A.J., Frydman, J., Identification of the TRiC/CCT substrate binding sites uncovers the function of subunit diversity in eukaryotic chaperonins (2006) Mol Cell, 24, pp. 25-37
• Satish, L., Johnson, S., Wang, J.H., Post, J.C., Ehrlich, G.D., Chaperonin containing T-complex polypeptide subunit eta (CCT-eta) is a specific regulator of fibroblast motility and contractility (2010) PLoS One, 5
• Cole, J., Tsou, R., Wallace, K., Gibran, N., Isik, F., Early gene expression profile of human skin to injury using high-density cDNA microarrays (2001) Wound Repair & Regeneration, 9, pp. 360-370
• Cooper, L., Johnson, C., Burslem, F., Martin, P., Wound healing and inflammation genes revealed by array analysis of “macrophageless” PU.1 null mice (2005) Genome Biol, 6, p. 5
• Lin, G., Zhang, X., Ren, J., Pang, Z., Wang, C., Integrin signaling is required for maintenance and proliferation of intestinal stem cells in Drosophila (2013) Dev Biol, 377, pp. 177-187

Citas:

---------- APA ----------

---------- CHICAGO ----------

---------- MLA ----------

---------- VANCOUVER ----------