排序方式: 共有9条查询结果,搜索用时 15 毫秒
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Marine iguanas shrink to survive El Niño 总被引:3,自引:0,他引:3
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I. Ember J. Szöllösi V. Thomázy I. Arany P. Rády P. Kertai 《Cellular and molecular life sciences : CMLS》1982,38(10):1234-1235
Summary Transplantation of virus and chemically induced leukemias from C3H/He-mgxAKR/F1 hybrid mice into C3H/He-mg males induced leukemias in the latter, which was followed by a spontaneous regression of the disease within a few days. The regression of leukemia could easily be followed by measuring the changes in the pyruvate kinase activity of para-aortic lymph node cells. 相似文献
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Rahn T Eiler JM Boering KA Wennberg PO McCarthy MC Tyler S Schauffler S Donnelly S Atlas E 《Nature》2003,424(6951):918-921
Molecular hydrogen (H2) is the second most abundant trace gas in the atmosphere after methane (CH4). In the troposphere, the D/H ratio of H2 is enriched by 120 per thousand relative to the world's oceans. This cannot be explained by the sources of H2 for which the D/H ratio has been measured to date (for example, fossil fuels and biomass burning). But the isotopic composition of H2 from its single largest source--the photochemical oxidation of methane--has yet to be determined. Here we show that the D/H ratio of stratospheric H2 develops enrichments greater than 440 per thousand, the most extreme D/H enrichment observed in a terrestrial material. We estimate the D/H ratio of H2 produced from CH4 in the stratosphere, where production is isolated from the influences of non-photochemical sources and sinks, showing that the chain of reactions producing H2 from CH4 concentrates D in the product H2. This enrichment, which we estimate is similar on a global average in the troposphere, contributes substantially to the D/H ratio of tropospheric H2. 相似文献
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Quantum annealing with manufactured spins 总被引:1,自引:0,他引:1
Johnson MW Amin MH Gildert S Lanting T Hamze F Dickson N Harris R Berkley AJ Johansson J Bunyk P Chapple EM Enderud C Hilton JP Karimi K Ladizinsky E Ladizinsky N Oh T Perminov I Rich C Thom MC Tolkacheva E Truncik CJ Uchaikin S Wang J Wilson B Rose G 《Nature》2011,473(7346):194-198
Many interesting but practically intractable problems can be reduced to that of finding the ground state of a system of interacting spins; however, finding such a ground state remains computationally difficult. It is believed that the ground state of some naturally occurring spin systems can be effectively attained through a process called quantum annealing. If it could be harnessed, quantum annealing might improve on known methods for solving certain types of problem. However, physical investigation of quantum annealing has been largely confined to microscopic spins in condensed-matter systems. Here we use quantum annealing to find the ground state of an artificial Ising spin system comprising an array of eight superconducting flux quantum bits with programmable spin-spin couplings. We observe a clear signature of quantum annealing, distinguishable from classical thermal annealing through the temperature dependence of the time at which the system dynamics freezes. Our implementation can be configured in situ to realize a wide variety of different spin networks, each of which can be monitored as it moves towards a low-energy configuration. This programmable artificial spin network bridges the gap between the theoretical study of ideal isolated spin networks and the experimental investigation of bulk magnetic samples. Moreover, with an increased number of spins, such a system may provide a practical physical means to implement a quantum algorithm, possibly allowing more-effective approaches to solving certain classes of hard combinatorial optimization problems. 相似文献
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In the embryo and in the adult, skeletal muscle growth is dependent on the proliferation and the differentiation of muscle progenitors present within muscle masses. Despite the importance of these progenitors, their embryonic origin is unclear. Here we use electroporation of green fluorescent protein in chick somites, video confocal microscopy analysis of cell movements, and quail-chick grafting experiments to show that the dorsal compartment of the somite, the dermomyotome, is the origin of a population of muscle progenitors that contribute to the growth of trunk muscles during embryonic and fetal life. Furthermore, long-term lineage analyses indicate that satellite cells, which are known progenitors of adult skeletal muscles, derive from the same dermomyotome cell population. We conclude that embryonic muscle progenitors and satellite cells share a common origin that can be traced back to the dermomyotome. 相似文献
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Control of grip and stick in cell adhesion through lateral relationships of membrane glycoproteins 总被引:12,自引:0,他引:12
Although cell adhesion to substrate must ultimately depend on 'sticking' by physical forces at the outer surface, we suggest that control is exercised through the 'grip' of the cytoskeleton. Our experiments indicate that grip can be relaxed by agents which release surface glycoproteins from some form of side-to-side organisation, and can be consolidated by suitable cross-linking to augment this organisation. 相似文献
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Scheper GC van der Klok T van Andel RJ van Berkel CG Sissler M Smet J Muravina TI Serkov SV Uziel G Bugiani M Schiffmann R Krägeloh-Mann I Smeitink JA Florentz C Van Coster R Pronk JC van der Knaap MS 《Nature genetics》2007,39(4):534-539
Leukoencephalopathy with brain stem and spinal cord involvement and lactate elevation (LBSL) has recently been defined based on a highly characteristic constellation of abnormalities observed by magnetic resonance imaging and spectroscopy. LBSL is an autosomal recessive disease, most often manifesting in early childhood. Affected individuals develop slowly progressive cerebellar ataxia, spasticity and dorsal column dysfunction, sometimes with a mild cognitive deficit or decline. We performed linkage mapping with microsatellite markers in LBSL families and found a candidate region on chromosome 1, which we narrowed by means of shared haplotypes. Sequencing of genes in this candidate region uncovered mutations in DARS2, which encodes mitochondrial aspartyl-tRNA synthetase, in affected individuals from all 30 families. Enzyme activities of mutant proteins were decreased. We were surprised to find that activities of mitochondrial complexes from fibroblasts and lymphoblasts derived from affected individuals were normal, as determined by different assays. 相似文献
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