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Embryo development

Anthrahydroquinones have been patented in Japan as bird repeUents (73), and anthraquinone [84-65-1] (qv) is used widely in Europe as a spray to protect growing crops and as a wood dressing. The synthetic pyrethroid deltamethrin [52918-63-5] (27) was evaluated (74), as were other materials, including bendiocarb (20) (75) and 20,25-dia2ocholesterol dihydrochloride [1249-84-9] (Omitrol) (28), a steroid that inhibits embryo development when adsorbed or ingested as a seed treatment of bait com (55,76). [Pg.121]

Puromycin. Puromycin (19), elaborated by S. alboniger (1—4), inhibits protein synthesis by replacing aminoacyl-tRNA at the A-site of peptidyltransferase (48,49). Photosensitive analogues of (19) have been used to label the A-site proteins of peptidyltransferase and tRNA (30). Compound (19), and its carbocycHc analogue have been used to study the accumulation of glycoprotein-derived free sialooligosaccharides, accumulation of mRNA, methylase activity, enzyme transport, rat embryo development, the acceptor site of human placental 80S ribosomes, and gene expression in mammalian cells (51—60). [Pg.121]

Hahnel, A.C., Gifford, D.J., Heikkila, J.J., Schultz, G.A. (1986). Expression of the major heat shock protein hsp70 family during early mouse embryo development Teratogen. Carcinog. Mutagen. 6, 493-510. [Pg.454]

Choi, T., Aoki, E, Mori, M., Yamashita, M., Nagahama, Y., and Kohmoto, K. (1991). Activation of p34nfc2 protein kinase activity in meiotic and mitotic cell cycles in mouse oocytes and embryos. Development 113 789-795. [Pg.37]

Dalby, B., and Glover, D. M. (1992). 3 non-translated sequences in Drosophila cyclin B transcripts direct posterior pole accumulation late in oogenesis and perinuclear association in syncitial embryos. Development 115 989-997. [Pg.38]

McConnell, J., and Lee, M. (1989). Presence of cdc2+-like proteins in the preimplantation mouse embryo. Development 107 481-487. [Pg.45]

Raff, J. W Whitfield, W. G. F, and Glover, D. M. (1990). Two distinct mechanisms localise cyclin B transcripts in syncitial Drosophila embryos. Development 110 1249-1261. [Pg.49]

Candia, A. F., Hu, J Crosby, J Lalley, R A., Noclen, D Nadeau, J., and Wright, C. V. E (1992). Mox-1 and Mox-2 define a novel homeobox gene subfamily and are differentially expressed during early mesodermal patterning in mouse embryos. Development 116 1123-1136. [Pg.119]

Serbedzija, G. N., Bronner-Fraser, M., and Fraser, S. E. (1992). Vital dye analysis of cranial neural crest cell migration in the mouse embryo. Development 116 297-307. [Pg.176]

Foe VE 1989 Mitotic domains reveal early commitment of cells in Drosophila embryos. Development 107 1—22... [Pg.12]

Boyd L, Guo S, Levitan D, Stinchcomb DT, Kemphues KJ 1996 PAR-2 is asymmetrically distributed and promotes association of P granules and PAR-1 with the cortex in C. elegant embryos. Development 122 3075-3084... [Pg.175]

Hung TJ, Kemphues KJ 1999 PAR-6 is a conserved PDZ domain-containing protein that colocalizes with PAR-3 in Caenorhabditit elegant embryos. Development 126 127—135 Izumi Y, Hirose T, Tamai Y et al 1998 An atypical PKC directly associates and colocalizes at the epithelial tight junction with ASIP, a mammalian homologue of Caenorhabditit elegant polarity protein PAR-3. J Cell Biol 143 95-106... [Pg.175]

Cheng NN, Kirby CM, Kemphues KJ 1995 Control of cleavage spindle orientation in Caenorhabditis elegans-. the role of the genes par-2 and par-3. Genetics 139 549-559 Edgar LG, Wolf N, Wood WB 1994 Early transcription in Caenorhabditis elegans embryos. Development 120 443—451... [Pg.180]

Kellogg, D.R., Michison, T.J., and Alberts, B.M. (1988) Behavior of microtubules and actin filaments in living Drosophila embryos. Development (Cambridge, UK) 103, 675. [Pg.1081]

Modified from Hoffman, D.J. and W.C. Eastin, Jr. 1981. Effects of malathion, diazinon, and parathion on mallard embryo development and cholinesterase activity. Environ. Res. 26 472-485. [Pg.970]

Pacific oyster, Crassostrea gigas 55 62% of exposed embryos developed abnormally in 48 h 1... [Pg.1208]

Growth and fertilization rate normal liver copper >70 mg/kg DW 63% of embryos developed normally (2)... [Pg.1565]

Reduced food intake and efficiency of food use, altered iron metabolism, clinical signs of copper deficiency. Onset of puberty delayed 10 weeks, decreased conception rate (fertility 12-33% vs. 57-80% in controls), disrupted estrus cycle (67% were anestrus vs. 7% in controls), and other signs consistent with decreased releases of luteinizing hormones associated with altered ovarian secretion (3, 4) Growth and fertilization normal liver copper 10 mg/kg DW only 16% of embryos developed normally (2)... [Pg.1565]

Malekinejad H, Schoevers EJ, Daemen IJ, Zijlstra C, Colenbrander B, Fink-Gremmels F, Roelen BAJ (2007) Exposure of oocytes to the Fusarium toxins zearalenone and deoxynivalenol causes aneuploidy and abnormal embryo development in pigs. Biol Reprod 77 840-847 Maragos CM, Appell MD (2007) Capillary electrophoresis of the mycotoxin zearalenone using cyclodextrin-enhanced fluorescence. J Chromatogr A 1143 252-257... [Pg.433]

In doses of 1.2 mg Ni/kg and up to 20 mg Ni/kg, nickel chloride caused increased resorption rates and a number of malformations in murine foetuses, specific to the foetal skeletal system, as shown by atomic absorption [425]. It was believed that nickel chloride might influence embryos during the passage through the oviduct, with subsequent effect on the development after implantation [426]. Preimplantation mouse embryos have also been used to investigate toxic effects of nickel chloride on early embryo development in vitro, and a dose-dependent effect has been found [427]. [Pg.219]

Schoenwaelder MEA (2002b) Physode distribution and the effects of Thallus Sunburn in Hormosira banksii (Fucales, Phaeophyceae). Bot Mar 45 262-266 Schoenwaelder MAE, Wiencke C, Clayton MN, Glombitza KW (2003) The effect of elevated UV radiation on Fucus spp. (Fucales, Phaeophyta) zygote and embryo development. Plant Biol 5 366-377... [Pg.295]

Vitamin A has a rich associated human physiology. It is associated with vision, regulation of gene expression, reproduction, embryo development, and immune function. We cannot manage all of this but let s get started with vision. [Pg.193]

Oberlin E, Tavian M, Blazsek I and Peault B (2002). Blood-forming potential of vascular endothelium in the human embryo. Development. 129(17) 4147-57. [Pg.146]

Tavian M, Hallais MF, Peault B (1999). Emergence of intraembryonic hematopoietic precursors in the pre liver human embryo. Development 126 793-803. [Pg.146]

Costanzi, C., Stein, P., Worrad, D.M., Schultz, R.M., and Pehrson, J.R. (2000) Histone macroH2Al is concentrated in the inactive X chromosome of female preimplantation embryos. Development 127, 2283-2289. [Pg.202]


See other pages where Embryo development is mentioned: [Pg.241]    [Pg.42]    [Pg.64]    [Pg.67]    [Pg.68]    [Pg.427]    [Pg.109]    [Pg.275]    [Pg.220]    [Pg.131]    [Pg.132]    [Pg.181]    [Pg.3]    [Pg.6]    [Pg.306]    [Pg.259]    [Pg.181]    [Pg.556]    [Pg.558]    [Pg.560]    [Pg.215]    [Pg.158]    [Pg.275]   
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