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排序方式: 共有64条查询结果,搜索用时 46 毫秒
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Non-local correlations between spatially separated systems have been extensively discussed in the context of the Einstein, Podolsky and Rosen (EPR) paradox and Bell's inequalities. Many proposals and experiments designed to test hidden variable theories and the violation of Bell's inequalities have been reported; usually, these involve correlated photons, although recently an experiment was performed with (9)Be(+) ions. Nevertheless, it is of considerable interest to show that such correlations (arising from quantum mechanical entanglement) are not simply a peculiarity of photons. Here we measure correlations between two degrees of freedom (comprising spatial and spin components) of single neutrons; this removes the need for a source of entangled neutron pairs, which would present a considerable technical challenge. A Bell-like inequality is introduced to clarify the correlations that can arise between observables of otherwise independent degrees of freedom. We demonstrate the violation of this Bell-like inequality: our measured value is 2.051 +/- 0.019, clearly above the value of 2 predicted by classical hidden variable theories. 相似文献
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Substrate specificity of mycodextranase 总被引:3,自引:0,他引:3
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Ansamitocin, a group of novel maytansinoid antibiotics with antitumour properties from Nocardia 总被引:1,自引:0,他引:1
E Higashide M Asai K Ootsu S Tanida Y Kozai T Hasegawa T Kishi Y Sugino M Yoneda 《Nature》1977,270(5639):721-722
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Knowledge or experience is voluntarily recalled from memory by reactivation of the neural representations in the cerebral association cortex. In inferior temporal cortex, which serves as the storehouse of visual long-term memory, activation of mnemonic engrams through electric stimulation results in imagery recall in humans, and neurons can be dynamically activated by the necessity for memory recall in monkeys. Neuropsychological studies and previous split-brain experiments predicted that prefrontal cortex exerts executive control upon inferior temporal cortex in memory retrieval; however, no neuronal correlate of this process has ever been detected. Here we show evidence of the top-down signal from prefrontal cortex. In the absence of bottom-up visual inputs, single inferior temporal neurons were activated by the top-down signal, which conveyed information on semantic categorization imposed by visual stimulus-stimulus association. Behavioural performance was severely impaired with loss of the top-down signal. Control experiments confirmed that the signal was transmitted not through a subcortical but through a fronto-temporal cortical pathway. Thus, feedback projections from prefrontal cortex to the posterior association cortex appear to serve the executive control of voluntary recall. 相似文献
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Kornum BR Kawashima M Faraco J Lin L Rico TJ Hesselson S Axtell RC Kuipers H Weiner K Hamacher A Kassack MU Han F Knudsen S Li J Dong X Winkelmann J Plazzi G Nevsimalova S Hong SC Honda Y Honda M Högl B Ton TG Montplaisir J Bourgin P Kemlink D Huang YS Warby S Einen M Eshragh JL Miyagawa T Desautels A Ruppert E Hesla PE Poli F Pizza F Frauscher B Jeong JH Lee SP Strohl KP Longstreth WT Kvale M Dobrovolna M Ohayon MM Nepom GT Wichmann HE Rouleau GA Gieger C Levinson DF Gejman PV Meitinger T 《Nature genetics》2011,43(1):66-71
Growing evidence supports the hypothesis that narcolepsy with cataplexy is an autoimmune disease. We here report genome-wide association analyses for narcolepsy with replication and fine mapping across three ethnic groups (3,406 individuals of European ancestry, 2,414 Asians and 302 African Americans). We identify a SNP in the 3' untranslated region of P2RY11, the purinergic receptor subtype P2Y?? gene, which is associated with narcolepsy (rs2305795, combined P = 6.1 × 10?1?, odds ratio = 1.28, 95% CI 1.19-1.39, n = 5689). The disease-associated allele is correlated with reduced expression of P2RY11 in CD8(+) T lymphocytes (339% reduced, P = 0.003) and natural killer (NK) cells (P = 0.031), but not in other peripheral blood mononuclear cell types. The low expression variant is also associated with reduced P2RY11-mediated resistance to ATP-induced cell death in T lymphocytes (P = 0.0007) and natural killer cells (P = 0.001). These results identify P2RY11 as an important regulator of immune-cell survival, with possible implications in narcolepsy and other autoimmune diseases. 相似文献
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The yak genome and adaptation to life at high altitude 总被引:8,自引:0,他引:8
Qiu Q Zhang G Ma T Qian W Wang J Ye Z Cao C Hu Q Kim J Larkin DM Auvil L Capitanu B Ma J Lewin HA Qian X Lang Y Zhou R Wang L Wang K Xia J Liao S Pan S Lu X Hou H Wang Y Zang X Yin Y Ma H Zhang J Wang Z Zhang Y Zhang D Yonezawa T Hasegawa M Zhong Y Liu W Zhang Y Huang Z Zhang S Long R Yang H Wang J Lenstra JA Cooper DN Wu Y Wang J Shi P Wang J Liu J 《Nature genetics》2012,44(8):946-949
Domestic yaks (Bos grunniens) provide meat and other necessities for Tibetans living at high altitude on the Qinghai-Tibetan Plateau and in adjacent regions. Comparison between yak and the closely related low-altitude cattle (Bos taurus) is informative in studying animal adaptation to high altitude. Here, we present the draft genome sequence of a female domestic yak generated using Illumina-based technology at 65-fold coverage. Genomic comparisons between yak and cattle identify an expansion in yak of gene families related to sensory perception and energy metabolism, as well as an enrichment of protein domains involved in sensing the extracellular environment and hypoxic stress. Positively selected and rapidly evolving genes in the yak lineage are also found to be significantly enriched in functional categories and pathways related to hypoxia and nutrition metabolism. These findings may have important implications for understanding adaptation to high altitude in other animal species and for hypoxia-related diseases in humans. 相似文献
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Miyagawa T Kawashima M Nishida N Ohashi J Kimura R Fujimoto A Shimada M Morishita S Shigeta T Lin L Hong SC Faraco J Shin YK Jeong JH Okazaki Y Tsuji S Honda M Honda Y Mignot E Tokunaga K 《Nature genetics》2008,40(11):1324-1328
Narcolepsy (hypocretin deficiency), a sleep disorder characterized by sleepiness, cataplexy and rapid eye movement (REM) sleep abnormalities, is tightly associated with HLA-DRB1*1501 (M17378) and HLA-DQB1*0602 (M20432). Susceptibility genes other than those in the HLA region are also likely involved. We conducted a genome-wide association study using 500K SNP microarrays in 222 Japanese individuals with narcolepsy and 389 Japanese controls, with replication of top hits in 159 Japanese individuals with narcolepsy and 190 Japanese controls, followed by the testing of 424 Koreans, 785 individuals of European descent and 184 African Americans. rs5770917, a SNP located between CPT1B and CHKB, was associated with narcolepsy in Japanese (rs5770917[C], odds ratio (OR) = 1.79, combined P = 4.4 x 10(-7)) and other ancestry groups (OR = 1.40, P = 0.02). Real-time quantitative PCR assays in white blood cells indicated decreased CPT1B and CHKB expression in subjects with the C allele, suggesting that a genetic variant regulating CPT1B or CHKB expression is associated with narcolepsy. Either of these genes is a plausible candidate, as CPT1B regulates beta-oxidation, a pathway involved in regulating theta frequency during REM sleep, and CHKB is an enzyme involved in the metabolism of choline, a precursor of the REM- and wake-regulating neurotransmitter acetylcholine. 相似文献
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