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  • Therapeutic microRNA Delivery Suppresses Tumorigenesis in a Murine Liver Cancer Model
    [作者:Kota, J; Chivukula, RR; O'Donnell, KA; Wentzel, EA; Montgomery, CL; Hwang, HW; Chang, TC; Vivekanandan, P; Torbenson, M; Clark, KR; Mendell, JR; Mendell, JT,期刊:Cell, 页码:1005-1017 , 文章类型: Article,,卷期:2009年137-6]
  • Therapeutic strategies based on modulation of microRNA (miRNA) activity hold great promise due to the ability of these small RNAs to potently influence cellular behavior. In this study, we investigated the efficacy of a ...
  • A Pleiotropically Acting MicroRNA, miR-31, Inhibits Breast Cancer Metastasis
    [作者:Valastyan, S; Reinhardt, F; Benaich, N; Calogrias, D; Szasz, AM; Wang, ZGC; Brock, JE; Richardson, AL; Weinberg, RA,期刊:Cell, 页码:1032-1046 , 文章类型: Article,,卷期:2009年137-6]
  • MicroRNAs are well suited to regulate tumor metastasis because of their capacity to coordinately repress numerous target genes, thereby potentially enabling their intervention at multiple steps of the invasion-metastasis...
  • Cyfip1 Is a Putative Invasion Suppressor in Epithelial Cancers
    [作者:Silva, JM; Ezhkova, E; Silva, J; Heart, S; Castillo, M; Campos, Y; Castro, V; Bonilla, F; Cordon-Cardo, C; Muthuswamy, SK; Powers, S; Fuchs, E; Hannon, GJ,期刊:Cell, 页码:1047-1061 , 文章类型: Article,,卷期:2009年137-6]
  • Identification of bona fide tumor suppressors is often challenging because of the large number of genetic alterations present in most human cancers. To evaluate candidate genes present within chromosomal regions recurren...
  • Autophagy Suppresses Tumorigenesis through Elimination of p62
    [作者:Mathew, R; Karp, CM; Beaudoin, B; Vuong, N; Chen, GH; Chen, HY; Bray, K; Reddy, A; Bhanot, G; Gelinas, C; DiPaola, RS; Karantza-Wadsworth, V; White, E,期刊:Cell, 页码:1062-1075 , 文章类型: Article,,卷期:2009年137-6]
  • Allelic loss of the essential autophagy gene beclin1 occurs in human cancers and renders mice tumor-prone suggesting that autophagy is a tumor-suppression mechanism. While tumor cells utilize autophagy to survive metabol...
  • Evolutionary Divergence of Enzymatic Mechanisms for Posttranslational Polyglycylation
    [作者:Rogowski, K; Juge, F; van Dijk, J; Wloga, D; Strub, JM; Levilliers, N; Thomas, D; Bre, MH; Van Dorsselaer, A; Gaertig, J; Janke, C,期刊:Cell, 页码:1076-1087 , 文章类型: Article,,卷期:2009年137-6]
  • Polyglycylation is a posttranslational modification that generates glycine side chains on proteins. Here we identify a family of evolutionarily conserved glycine ligases that modify tubulin using different enzymatic m...

  • The Notch Ligands Dll4 and Jagged1 Have Opposing Effects on Angiogenesis
    [作者:Benedito, R; Roca, C; Sorensen, I; Adams, S; Gossler, A; Fruttiger, M; Adams, RH,期刊:Cell, 页码:1124-1135 , 文章类型: Article,,卷期:2009年137-6]
  • The Notch pathway is a highly conserved signaling system that controls a diversity of growth, differentiation, and patterning processes. In growing blood vessels, sprouting of endothelial tip cells is inhibited by Notch ...
  • Dissociation of the Opioid Receptor Mechanisms that Control Mechanical and Heat Pain
    [作者:Scherrer, G; Imamachi, N; Cao, YQ; Contet, C; Mennicken, F; O'Donnell, D; Kieffer, BL; Basbaum, AI,期刊:Cell, 页码:1148-1159 , 文章类型: Article,,卷期:2009年137-6]
  • Delta and mu opioid receptors (DORs and MORs) are inhibitory G protein-coupled receptors that reportedly cooperatively regulate the transmission of pain messages by substance P and TRPV1-expressing pain fibers. Using a D...