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A new species of the calanoid copepod genus Paramisophria T. Scott, 1897 is described from the Egyptian sublittoral zone of the Red Sea. Paramisophria aegypti sp. nov. appears to be closely related to the species Paramisophria ammophila and Paramisophria platysoma. Paramisophria aegypti differs from P. ammophila in having two unequal lateral setae plus one long terminal process and two tiny equal lateral setae plus one long terminal process on the third exopodal segment on the male right and left fifth legs (vs three terminal processes increasing in size inward on both male fifth legs). Paramisophria aegypti can be distinguished from P. platysoma in the following characters: prosome symmetrical (vs extreme asymmetry); third exopod segment of the right leg completely separated from the second segment and bears two unequal lateral setae plus one long terminal process (vs partially fused to the second segment and bears four terminal processes increasing in size inward); third exopod segment of the left leg with two lateral setules and one long terminal process (vs two lateral setules, one short outer medial process and one long terminal process); endopodal lobes of the female legs 5 bear one long plumose seta (vs setae are lacking).http://www.zoobank.org/urn:lsid:zoobank.org:pub:C0A92BF9-2306-4A35-AA39-CE3B5865A396 相似文献
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Alessandra Govoni Francesca Magri Simona Brajkovic Chiara Zanetta Irene Faravelli Stefania Corti Nereo Bresolin Giacomo P. Comi 《Cellular and molecular life sciences : CMLS》2013,70(23):4585-4602
Muscular dystrophy is a heterogeneous group of genetic disorders characterised by progressive muscle tissue degeneration. No effective treatment has been discovered for these diseases. Preclinical and clinical studies aimed at the development of new therapeutic approaches have been carried out, primarily in subjects affected with dystrophinopathies (Duchenne and Becker muscular dystrophy). In this review, we outline the current therapeutic approaches and past and ongoing clinical trials, highlighting both the advantages and limits of each one. The experimental designs of these trials were based on different rationales, including immunomodulation, readthrough strategies, exon skipping, gene therapy, and cell therapy. We also provide an overview of available outcome measures, focusing on their reliability in estimating meaningful clinical improvement in order to aid in the design of future trials. This perspective is extremely relevant to the field considering the recent development of novel therapeutic approaches that will result in an increasing number of clinical studies over the next few years. 相似文献
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Giacomo Sbrana 《Journal of forecasting》2012,31(1):85-98
This paper focuses on the contemporaneous aggregation of moving average processes. It is shown that aggregating across second (or first)‐order (integrated) moving average processes leads to a macro process whose parameters are exact functions of the parameters of its generation process. Similar results are obtained at single equation level when a vector moving average framework is considered. In addition, the out‐of‐sample forecasting properties of aggregate and disaggregate procedures to forecast the aggregate variable are provided. Moreover, it is shown that the condition of equality of aggregate and disaggregate predictors is not necessary for the equality of their mean squared errors. Finally, an application to the euro area real interest rate is presented and discussed. Copyright © 2011 John Wiley & Sons, Ltd. 相似文献
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Vik JO Stenseth NC Tavecchia G Mysterud A Lingjaerde OC 《Nature》2004,427(6976):697-8; discussion 698
Theory indicates that correlated weather may synchronize populations, but the extent to which this holds for non-identical, nonlinear systems is uncertain. Post and Forchhammer claim to have shown climate-induced synchrony for musk oxen and caribou that are separated by the Greenland ice sheet. However, logical and mathematical errors undermine their finding. Whether or not large-scale weather can be a major synchronizing factor across species remains an open question. 相似文献
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Mutations in kelch-like 3 and cullin 3 cause hypertension and electrolyte abnormalities 总被引:2,自引:0,他引:2
Boyden LM Choi M Choate KA Nelson-Williams CJ Farhi A Toka HR Tikhonova IR Bjornson R Mane SM Colussi G Lebel M Gordon RD Semmekrot BA Poujol A Välimäki MJ De Ferrari ME Sanjad SA Gutkin M Karet FE Tucci JR Stockigt JR Keppler-Noreuil KM Porter CC Anand SK Whiteford ML Davis ID Dewar SB Bettinelli A Fadrowski JJ Belsha CW Hunley TE Nelson RD Trachtman H Cole TR Pinsk M Bockenhauer D Shenoy M Vaidyanathan P Foreman JW Rasoulpour M Thameem F Al-Shahrouri HZ Radhakrishnan J Gharavi AG Goilav B 《Nature》2012,482(7383):98-102
Hypertension affects one billion people and is a principal reversible risk factor for cardiovascular disease. Pseudohypoaldosteronism type II (PHAII), a rare Mendelian syndrome featuring hypertension, hyperkalaemia and metabolic acidosis, has revealed previously unrecognized physiology orchestrating the balance between renal salt reabsorption and K(+) and H(+) excretion. Here we used exome sequencing to identify mutations in kelch-like 3 (KLHL3) or cullin 3 (CUL3) in PHAII patients from 41 unrelated families. KLHL3 mutations are either recessive or dominant, whereas CUL3 mutations are dominant and predominantly de novo. CUL3 and BTB-domain-containing kelch proteins such as KLHL3 are components of cullin-RING E3 ligase complexes that ubiquitinate substrates bound to kelch propeller domains. Dominant KLHL3 mutations are clustered in short segments within the kelch propeller and BTB domains implicated in substrate and cullin binding, respectively. Diverse CUL3 mutations all result in skipping of exon 9, producing an in-frame deletion. Because dominant KLHL3 and CUL3 mutations both phenocopy recessive loss-of-function KLHL3 mutations, they may abrogate ubiquitination of KLHL3 substrates. Disease features are reversed by thiazide diuretics, which inhibit the Na-Cl cotransporter in the distal nephron of the kidney; KLHL3 and CUL3 are expressed in this location, suggesting a mechanistic link between KLHL3 and CUL3 mutations, increased Na-Cl reabsorption, and disease pathogenesis. These findings demonstrate the utility of exome sequencing in disease gene identification despite the combined complexities of locus heterogeneity, mixed models of transmission and frequent de novo mutation, and establish a fundamental role for KLHL3 and CUL3 in blood pressure, K(+) and pH homeostasis. 相似文献
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Roati G D'Errico C Fallani L Fattori M Fort C Zaccanti M Modugno G Modugno M Inguscio M 《Nature》2008,453(7197):895-898
Anderson localization of waves in disordered media was originally predicted fifty years ago, in the context of transport of electrons in crystals. The phenomenon is much more general and has been observed in a variety of systems, including light waves. However, Anderson localization has not been observed directly for matter waves. Owing to the high degree of control over most of the system parameters (in particular the interaction strength), ultracold atoms offer opportunities for the study of disorder-induced localization. Here we use a non-interacting Bose-Einstein condensate to study Anderson localization. The experiment is performed with a one-dimensional quasi-periodic lattice-a system that features a crossover between extended and exponentially localized states, as in the case of purely random disorder in higher dimensions. Localization is clearly demonstrated through investigations of the transport properties and spatial and momentum distributions. We characterize the crossover, finding that the critical disorder strength scales with the tunnelling energy of the atoms in the lattice. This controllable system may be used to investigate the interplay of disorder and interaction (ref. 7 and references therein), and to explore exotic quantum phases. 相似文献
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Venegas JG Winkler T Musch G Vidal Melo MF Layfield D Tgavalekos N Fischman AJ Callahan RJ Bellani G Harris RS 《Nature》2005,434(7034):777-782
Asthma is a common disease affecting an increasing number of children throughout the world. In asthma, pulmonary airways narrow in response to contraction of surrounding smooth muscle. The precise nature of functional changes during an acute asthma attack is unclear. The tree structure of the pulmonary airways has been linked to complex behaviour in sudden airway narrowing and avalanche-like reopening. Here we present experimental evidence that bronchoconstriction leads to patchiness in lung ventilation, as well as a computational model that provides interpretation of the experimental data. Using positron emission tomography, we observe that bronchoconstricted asthmatics develop regions of poorly ventilated lung. Using the computational model we show that, even for uniform smooth muscle activation of a symmetric bronchial tree, the presence of minimal heterogeneity breaks the symmetry and leads to large clusters of poorly ventilated lung units. These clusters are generated by interaction of short- and long-range feedback mechanisms, which lead to catastrophic shifts similar to those linked to self-organized patchiness in nature. This work might have implications for the treatment of asthma, and might provide a model for studying diseases of other distributed organs. 相似文献