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排序方式: 共有110条查询结果,搜索用时 281 毫秒
81.
C Van Broeckhoven H Backhovens M Cruts G De Winter M Bruyland P Cras J J Martin 《Nature genetics》1992,2(4):335-339
Genetic linkage studies with chromosome 21 DNA markers and mutation analysis of the beta-amyloid protein precursor gene located in 21q21.3 have indicated that early-onset Alzheimer's disease (EOAD) is a heterogeneous disorder for which at least one other chromosomal locus exists. We examined two extended histopathologically confirmed EOAD pedigrees, AD/A and AD/B, with highly informative short tandem repeat (STR) polymorphisms and found complete linkage of the disease to a (CA)n dinucleotide repeat polymorphism at locus D14S43 in 14q24.3 (Zmax = 13.25 at theta = 0.0). Using additional chromosome 14 STR polymorphisms we were able to delineate the region containing the EOAD gene to an area of, at most, 8.9 centiMorgans between D14S42 and D14S53, flanking D14S43 on both sides. 相似文献
82.
Farima Zahedi Maliheh Nazari-Jahantigh Zhe Zhou Pallavi Subramanian Yuanyuan Wei Jochen Grommes Stefan Offermanns Sabine Steffens Christian Weber Andreas Schober 《Cellular and molecular life sciences : CMLS》2017,74(2):359-372
MicroRNAs (miRNAs) coordinate vascular repair by regulating injury-induced gene expression in vascular smooth muscle cells (SMCs) and promote the transition of SMCs from a contractile to a proliferating phenotype. However, the effect of miRNA expression in SMCs on neointima formation is unclear. Therefore, we studied the role of miRNA biogenesis by Dicer in SMCs in vascular repair. Following wire-induced injury to carotid arteries of Apolipoprotein E knockout (Apoe ?/?) mice, miRNA microarray analysis revealed that the most significantly regulated miRNAs, such as miR-222 and miR-21-3p, were upregulated. Conditional deletion of Dicer in SMCs increased neointima formation by reducing SMC proliferation in Apoe ?/? mice, and decreased mainly the expression of miRNAs, such as miR-147 and miR-100, which were not upregulated following vascular injury. SMC-specific deletion of Dicer promoted growth factor and inflammatory signaling and regulated a miRNA–target interaction network in injured arteries that was enriched in anti-proliferative miRNAs. The most connected miRNA in this network was miR-27a-3p [e.g., with Rho guanine nucleotide exchange factor 26 (ARHGEF26)], which was expressed in medial and neointimal SMCs in a Dicer-dependent manner. In vitro, miR-27a-3p suppresses ARHGEF26 expression and inhibits SMC proliferation by interacting with a conserved binding site in the 3′ untranslated region of ARHGEF26 mRNA. We propose that Dicer expression in SMCs plays an essential role in vascular repair by generating anti-proliferative miRNAs, such as miR-27a-3p, to prevent vessel stenosis due to exaggerated neointima formation. 相似文献
83.
During cardiogenesis, the epicardium grows from the proepicardial organ to form the outermost layer of the early heart. Part of the epicardium undergoes epithelial-mesenchymal transformation, and migrates into the myocardium. These epicardium-derived cells differentiate into interstitial fibroblasts, coronary smooth muscle cells, and perivascular fibroblasts. Moreover, epicardium-derived cells are important regulators of formation of the compact myocardium, the coronary vasculature, and the Purkinje fiber network, thus being essential for proper cardiac development. The fibrous structures of the heart such as the fibrous heart skeleton and the semilunar and atrioventricular valves also depend on a contribution of these cells during development. We hypothesise that the essential properties of epicardium-derived cells can be recapitulated in adult diseased myocardium. These cells can therefore be considered as a novel source of adult stem cells useful in clinical cardiac regeneration therapy. 相似文献
84.
A genome-wide association scan of nonsynonymous SNPs identifies a susceptibility variant for Crohn disease in ATG16L1 总被引:16,自引:0,他引:16
Hampe J Franke A Rosenstiel P Till A Teuber M Huse K Albrecht M Mayr G De La Vega FM Briggs J Günther S Prescott NJ Onnie CM Häsler R Sipos B Fölsch UR Lengauer T Platzer M Mathew CG Krawczak M Schreiber S 《Nature genetics》2007,39(2):207-211
We performed a genome-wide association study of 19,779 nonsynonymous SNPs in 735 individuals with Crohn disease and 368 controls. A total of 7,159 of these SNPs were informative. We followed up on all 72 SNPs with P 0.4), these data suggest that the underlying biological process may be specific to Crohn disease. 相似文献
85.
A genome-wide association scan identifies the hepatic cholesterol transporter ABCG8 as a susceptibility factor for human gallstone disease 总被引:6,自引:0,他引:6
Buch S Schafmayer C Völzke H Becker C Franke A von Eller-Eberstein H Kluck C Bässmann I Brosch M Lammert F Miquel JF Nervi F Wittig M Rosskopf D Timm B Höll C Seeger M ElSharawy A Lu T Egberts J Fändrich F Fölsch UR Krawczak M Schreiber S Nürnberg P Tepel J Hampe J 《Nature genetics》2007,39(8):995-999
With an overall prevalence of 10-20%, gallstone disease (cholelithiasis) represents one of the most frequent and economically relevant health problems of industrialized countries. We performed an association scan of >500,000 SNPs in 280 individuals with gallstones and 360 controls. A follow-up study of the 235 most significant SNPs in 1,105 affected individuals and 873 controls replicated the disease association of SNP A-1791411 in ABCG8 (allelic P value P(CCA) = 4.1 x 10(-9)), which was subsequently attributed to coding variant rs11887534 (D19H). Additional replication was achieved in 728 German (P = 2.8 x 10(-7)) and 167 Chilean subjects (P = 0.02). The overall odds ratio for D19H carriership was 2.2 (95% confidence interval: 1.8-2.6, P = 1.4 x 10(-14)) in the full German sample. Association was stronger in subjects with cholesterol gallstones (odds ratio = 3.3), suggesting that His19 might be associated with a more efficient transport of cholesterol into the bile. 相似文献
86.
Structure of a human gammadelta T-cell antigen receptor. 总被引:4,自引:0,他引:4
T-cell antigen receptors composed of gamma and delta polypeptide chains (gammadelta TCRs) can directly recognize antigens in the form of intact proteins or non-peptide compounds, unlike alphabeta TCRs, which recognize antigens bound to major histocompatibility complex molecules (MHC). About 5% of peripheral blood T cells bear gammadelta TCRs, most of which recognize non-peptide phosphorylated antigens. Here we describe the 3.1 A resolution structure of a human gammadelta TCR from a T-cell clone that is phosphoantigen-reactive. The orientation of the variable (V) and constant (C) regions of the gammadelta TCR is unique when compared with alphabeta TCRs or antibodies, and results from an unusually small angle between the Vgamma and Cgamma domains. The complementarity-determining regions (CDRs) of the V domains exhibit a chemically reasonable binding site for phosphorylated antigens, providing a possible explanation for the canonical usage of the Vgamma9 and Vdelta2 gene segments by phosphoantigen-reactive receptors. Although the gammadelta TCR V domains are similar in overall structure to those of alphabeta TCRs, gammadelta TCR C domains are markedly different. Structural differences in Cgamma and Cdelta, and in the location of the disulphide bond between them, may enable gammadelta TCRs to form different recognition/signalling complexes than alphabeta TCRs. 相似文献
87.
In this paper, we adopt a panel vector autoregressive (PVAR) approach to estimating and forecasting inflation dynamics in four different sectors—industry, services, construction and agriculture—across the euro area and its four largest member states: France, Germany, Italy and Spain. By modelling inflation together with real activity, employment and wages at the sectoral level, we are able to disentangle the role of unit labour costs and profit margins as the fundamental determinants of price dynamics on the supply side. In out‐of‐sample forecast comparisons, the PVAR approach performs well against popular alternatives, especially at a short forecast horizon and relative to standard VAR forecasts based on aggregate economy‐wide data. Over longer forecast horizons, the accuracy of the PVAR model tends to decline relative to that of the univariate alternatives, while it remains high relative to the aggregate VAR forecasts. We show that these findings are driven by the event of the Great Recession. Our qualitative results carry over to a multi‐country extension of the PVAR approach. Copyright © 2016 John Wiley & Sons, Ltd. 相似文献
88.
Ramirez A Heimbach A Gründemann J Stiller B Hampshire D Cid LP Goebel I Mubaidin AF Wriekat AL Roeper J Al-Din A Hillmer AM Karsak M Liss B Woods CG Behrens MI Kubisch C 《Nature genetics》2006,38(10):1184-1191
Neurodegenerative disorders such as Parkinson and Alzheimer disease cause motor and cognitive dysfunction and belong to a heterogeneous group of common and disabling disorders. Although the complex molecular pathophysiology of neurodegeneration is largely unknown, major advances have been achieved by elucidating the genetic defects underlying mendelian forms of these diseases. This has led to the discovery of common pathophysiological pathways such as enhanced oxidative stress, protein misfolding and aggregation and dysfunction of the ubiquitin-proteasome system. Here, we describe loss-of-function mutations in a previously uncharacterized, predominantly neuronal P-type ATPase gene, ATP13A2, underlying an autosomal recessive form of early-onset parkinsonism with pyramidal degeneration and dementia (PARK9, Kufor-Rakeb syndrome). Whereas the wild-type protein was located in the lysosome of transiently transfected cells, the unstable truncated mutants were retained in the endoplasmic reticulum and degraded by the proteasome. Our findings link a class of proteins with unknown function and substrate specificity to the protein networks implicated in neurodegeneration and parkinsonism. 相似文献
89.
Jan De Winter 《Studies in history and philosophy of science》2011,42(4):602-609
A mechanistic artifact explanation is an explanation that accounts for an artifact behavior by describing the underlying mechanism. The article shows that there are different kinds of mechanistic artifact explanation: top-down and bottom-up explanation, and I also distinguish between less and more inclusive top-down explanations. To illustrate these different kinds of explanation, the behavior of a simple, fictional artifact is explained in different ways. I defend that which explanation is ideal, depends on pragmatic factors (e.g., the background knowledge of the explainee and the specific goal for which the explanation will be used). For each kind of explanation, the situations, goals and interests for which it is most appropriate are specified, resulting in a pragmatic theory of mechanistic artifact explanation. This theory is compared to Jeroen de Ridder’s account of the pragmatics of mechanistic artifact explanation. 相似文献
90.