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  • Genomics in Africa: Avoiding Past Pitfalls
    [作者:Kaplan, M,期刊:Cell, 页码:11-13 , 文章类型: Editorial Material,,卷期:2011年147-1]
  • A landmark genomics project is taking shape in Africa that shifts the power and prominence to local scientists. If successful, the program will offer valuable insights into the inheritance of common diseases and reshape ...
  • An Alternative Splicing Switch Regulates Embryonic Stem Cell Pluripotency and Reprogramming
    [作者:Gabut, M; Samavarchi-Tehrani, P; Wang, XC; Slobodeniuc, V; O'Hanlon, D; Sung, HK; Alvarez, M; Talukder, S; Pan, Q; Mazzoni, EO; Nedelec, S; Wichterle, H; Woltjen, K; Hughes, TR; Zandstra, PW; Nagy, A; Wrana, JL; Blencowe, BJ,期刊:Cell, 页码:132-146 , 文章类型: Article,,卷期:2011年147-1]
  • Alternative splicing (AS) is a key process underlying the expansion of proteomic diversity and the regulation of gene expression. Here, we identify an evolutionarily conserved embryonic stem cell (ESC)-specific AS event ...
  • Genetics and Genomics to the Clinic: A Long Road ahead
    [作者:Ginsburg, D,期刊:Cell, 页码:17-19 , 文章类型: Editorial Material,,卷期:2011年147-1]
  • Advances in genomic technology have produced an explosion of new information about the genetic basis for human disease, fueling extraordinarily high expectations for improved treatments. This perspective will take brief ...
  • Translocation Mapping Exposes the Risky Lifestyle of B Cells
    [作者:McCord, RP; Dekker, J,期刊:Cell, 页码:20-22 , 文章类型: Editorial Material,,卷期:2011年147-1]
  • Recurrent chromosomal translocations can drive oncogenesis, but how they form has remained elusive. Now, Chiarle et al. (2011) and Klein et al. (2011) characterize the genome-wide spectrum of translocations that form fro...
  • Splicing up Pluripotency
    [作者:Graveley, BR,期刊:Cell, 页码:22-24 , 文章类型: Editorial Material,,卷期:2011年147-1]
  • In this issue of Cell, Gabut and colleagues (2011) identify a new splice variant of FOXP1 that directly regulates the expression of pluripotency genes. It endows human embryonic stem cells with their pluripotent nature a...
  • Beclin1 Controls the Levels of p53 by Regulating the Deubiquitination Activity of USP10 and USP13
    [作者:Liu, JL; Xia, HG; Kim, M; Xu, LH; Li, Y; Zhang, LH; Cai, Y; Norberg, HV; Zhang, T; Furuya, T; Jin, MZ; Zhu, ZM; Wang, HC; Yu, J; Li, YX; Hao, Y; Choi, A; Ke, HM; Ma, DW; Yuan, JY,期刊:Cell, 页码:223-234 , 文章类型: Article,,卷期:2011年147-1]
  • Autophagy is an important intracellular catabolic mechanism that mediates the degradation of cytoplasmic proteins and organelles. We report a potent small molecule inhibitor of autophagy named "spautin-1" for specific an...
  • Absence of CNTNAP2 Leads to Epilepsy, Neuronal Migration Abnormalities, and Core Autism-Related Deficits
    [作者:Penagarikano, O; Abrahams, BS; Herman, EI; Winden, KD; Gdalyahu, A; Dong, HM; Sonnenblick, LI; Gruver, R; Almajano, J; Bragin, A; Golshani, P; Trachtenberg, JT; Peles, E; Geschwind, DH,期刊:Cell, 页码:235-246 , 文章类型: Article,,卷期:2011年147-1]
  • Although many genes predisposing to autism spectrum disorders (ASD) have been identified, the biological mechanism(s) remain unclear. Mouse models based on human disease-causing mutations provide the potential for unders...