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9篇 您的检索式:作者名="David Baltimore"
    题名 作者 年代 出处 被引量
1Microarray,SAGE and their applications to cardiovascular diseases显示文摘The wealth of DNA data generated by the human genome project coupling with recently invented high-throughput gene expression profiling techniques has dramatically sped up the process for biomedical researchers on elucidating the role of genes in human diseases. One powerful method to reveal insight into gene functions is the systematic analysis of gene expression. Two popular high-throughput gene expression technologies, microarray and Serial Analysis of Gene Expression (SAGE) are capable of producing large amounts of gene expression data with the potential of providing novel insights into fundamental disease processes, especially complex syndromes such as cardiovascular disease, whose etiologies are due to multiple genetic factors and their interplay with the environment. Microarray and SAGE have already been used to examine gene expression patterns of cell-culture, animal and human tissues models of cardiovascular diseases. In this review, we will first give a brief introduction of microarray and SAGE technologies and point out their limitations. We will then discuss the major discoveries and the new biological insightsthat have emerged from their applications to cardiovascular diseases. Finally we will touch upon potential challenges and future developments in this area.SHUI QING YE, TERA LAVOIE, DAVID C USHER, LI Q. ZHANG1 Division of Pulmonary and Critical Care Medicine, Johns Hopkins University, School of Medicine, Baltimore, MD 21224, USA2Department of Biological Science, University of Delaware, Newark, DE 19716, USA 2002Cell Research2002,12,2:5
2MicroRNA-155 Promotes Autoimmune Inflammation by Enhancing Inflammatory T Cell Development显示文摘Ryan M. O’Connell Daniel Kahn William S.J. Gibson June L. Round Rebecca L. Scholz Aadel A. Chaudhuri Melissa E. Kahn Dinesh S. Rao David Baltimore 2010Immunity2010,,4:3
3Function of miR-146a in Controlling Treg Cell-Mediated Regulation of Th1 Responses显示文摘Li-Fan Lu Mark P. Boldin Ashutosh Chaudhry Ling-Li Lin Konstantin D. Taganov Toshikatsu Hanada Akihiko Yoshimura David Baltimore Alexander Y. Rudensky 2010Cell2010,,6:2
4NF-κB: Ten Years After显示文摘Patrick A Baeuerle David Baltimore 1996Cell1996,,1:2
5Conversion of Danger Signals into Cytokine Signals by Hematopoietic Stem and Progenitor Cells for Regulation of Stress-Induced Hematopoiesis显示文摘Jimmy L. Zhao Chao Ma Ryan M. O’Connell Arnav Mehta Race DiLoreto James R. Heath David Baltimore 2014Cell Stem Cell2014,,:1
6Molecular evolution of the vertebrate immune system显示文摘Simona Bartl David Baltimore Irving L Weissman 1994Proceedings of the National Academy of Sciences of the United States of America1994,91,10:1
7NF-κB:ten years after显示文摘Patrick AB David Baltimore 0,,:1
8A prudent path forward for genom- ie engineering and germline gene modification 显示文摘David Baltimore Paul Berg 2015Science2015,,03:1
9细胞内免疫显示文摘Ⅰ.黑尔斯考兹(Ira Herskowitz)在去年出版的《自然》杂志上发表的一篇文章中指出。研究克隆基因功能的最好途径是刨制那些能够提供一种显性负表型的突变体,当能表达这种突变基因的质粒在细胞内稳定下来时,它的产物就能显性地干扰宿主基因产物所表现的功能。这将有助于阐明野生型等位基因的功能。在本期《自然》杂志上,A·弗里德曼等(Alan Friedman)David Baltimore 许仁林 1990世界科学1990,,3:0
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