排序方式: 共有102条查询结果,搜索用时 31 毫秒
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Jijun Yuan Jessica C. Zweers Jan Maarten van Dijl Ross E. Dalbey 《Cellular and molecular life sciences : CMLS》2010,67(2):179-199
In the three domains of life, the Sec, YidC/Oxa1, and Tat translocases play important roles in protein translocation across
membranes and membrane protein insertion. While extensive studies have been performed on the endoplasmic reticular and Escherichia coli systems, far fewer studies have been done on archaea, other Gram-negative bacteria, and Gram-positive bacteria. Interestingly,
work carried out to date has shown that there are differences in the protein transport systems in terms of the number of translocase
components and, in some cases, the translocation mechanisms and energy sources that drive translocation. In this review, we
will describe the different systems employed to translocate and insert proteins across or into the cytoplasmic membrane of
archaea and bacteria. 相似文献
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Garnett MJ Edelman EJ Heidorn SJ Greenman CD Dastur A Lau KW Greninger P Thompson IR Luo X Soares J Liu Q Iorio F Surdez D Chen L Milano RJ Bignell GR Tam AT Davies H Stevenson JA Barthorpe S Lutz SR Kogera F Lawrence K McLaren-Douglas A Mitropoulos X Mironenko T Thi H Richardson L Zhou W Jewitt F Zhang T O'Brien P Boisvert JL Price S Hur W Yang W Deng X Butler A Choi HG Chang JW Baselga J Stamenkovic I Engelman JA Sharma SV Delattre O Saez-Rodriguez J Gray NS Settleman J Futreal PA Haber DA 《Nature》2012,483(7391):570-575
Clinical responses to anticancer therapies are often restricted to a subset of patients. In some cases, mutated cancer genes are potent biomarkers for responses to targeted agents. Here, to uncover new biomarkers of sensitivity and resistance to cancer therapeutics, we screened a panel of several hundred cancer cell lines--which represent much of the tissue-type and genetic diversity of human cancers--with 130 drugs under clinical and preclinical investigation. In aggregate, we found that mutated cancer genes were associated with cellular response to most currently available cancer drugs. Classic oncogene addiction paradigms were modified by additional tissue-specific or expression biomarkers, and some frequently mutated genes were associated with sensitivity to a broad range of therapeutic agents. Unexpected relationships were revealed, including the marked sensitivity of Ewing's sarcoma cells harbouring the EWS (also known as EWSR1)-FLI1 gene translocation to poly(ADP-ribose) polymerase (PARP) inhibitors. By linking drug activity to the functional complexity of cancer genomes, systematic pharmacogenomic profiling in cancer cell lines provides a powerful biomarker discovery platform to guide rational cancer therapeutic strategies. 相似文献
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BA Peters BG Kermani AB Sparks O Alferov P Hong A Alexeev Y Jiang F Dahl YT Tang J Haas K Robasky AW Zaranek JH Lee MP Ball JE Peterson H Perazich G Yeung J Liu L Chen MI Kennemer K Pothuraju K Konvicka M Tsoupko-Sitnikov KP Pant JC Ebert GB Nilsen J Baccash AL Halpern GM Church R Drmanac 《Nature》2012,487(7406):190-195
Recent advances in whole-genome sequencing have brought the vision of personal genomics and genomic medicine closer to reality. However, current methods lack clinical accuracy and the ability to describe the context (haplotypes) in which genome variants co-occur in a cost-effective manner. Here we describe a low-cost DNA sequencing and haplotyping process, long fragment read (LFR) technology, which is similar to sequencing long single DNA molecules without cloning or separation of metaphase chromosomes. In this study, ten LFR libraries were made using only ~100?picograms of human DNA per sample. Up to 97% of the heterozygous single nucleotide variants were assembled into long haplotype contigs. Removal of false positive single nucleotide variants not phased by multiple LFR haplotypes resulted in a final genome error rate of 1 in 10?megabases. Cost-effective and accurate genome sequencing and haplotyping from 10-20 human cells, as demonstrated here, will enable comprehensive genetic studies and diverse clinical applications. 相似文献
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Most inner main-belt asteroids are primitive rock and metal bodies in orbit about the Sun between Mars and Jupiter. Disruption, through high-velocity collisions or rotational spin-up, is believed to be the primary mechanism for the production and destruction of small asteroids and a contributor to dust in the Sun's zodiacal cloud, while analogous collisions around other stars feed dust to their debris disks. Unfortunately, direct evidence about the mechanism or rate of disruption is lacking, owing to the rarity of the events. Here we report observations of P/2010?A2, a previously unknown inner-belt asteroid with a peculiar, comet-like morphology. The data reveal a nucleus of diameter approximately 120?metres with an associated tail of millimetre-sized dust particles. We conclude that it is most probably the remnant of a recent asteroidal disruption in February/March 2009, evolving slowly under the action of solar radiation pressure, in agreement with independent work. 相似文献
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Replacement fertility is a term commonly used by demographers when referring to levels of childbearing and yet is rarely explained. It is normally presented as being around 2.1 children per woman. Continued below replacement fertility in developed countries and fertility falling in developing countries has given the concept of replacement fertility a higher profile. This article explains how replacement level is calculated and explores the concept further. Past replacement fertility levels are calculated for England and Wales. A possible alternative definition of replacement is also presented. Simple projection scenarios are used to show the effect on population of below replacement fertility, and also of postponement of fertility. The importance and implications of below replacement fertility are discussed. 相似文献
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Harte J Ostling A Green JL Kinzig A 《Nature》2004,430(6995):3 p following 33; discussion following 33
Thomas et al. have carried out a useful analysis of the extinction risk from climate warming. Their overall conclusion, that a large fraction of extant species could be driven to extinction by expected climate trends over the next 50 years, is compelling: it adds to the many other reasons why new energy policies are needed to reduce the pace of warming. 相似文献