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941.
942.
Meenakshi Gaur Carissa Ritner Rich Sievers Anissa Pedersen Megha Prasad Harold S. Bernstein Yerem Yeghiazarians 《Cytotherapy》2010,12(6):807-817
Background aimsHeart failure therapy with human embryonic stem cell (hESC)-derived cardiomyocytes (hCM) has been limited by the low rate of spontaneous hCM differentiation. As others have shown that p38 mitogen-activated protein kinase (p38MAPK) directs neurogenesis from mouse embryonic stem cells, we investigated whether the p38MAPK inhibitor, SB203580, might influence hCM differentiation.MethodsWe treated differentiating hESC with SB203580 at specific time-points, and used flow cytometry, immunocytochemistry, quantitative real-time (RT)–polymerase chain reaction (PCR), teratoma formation and transmission electron microscopy to evaluate cardiomyocyte formation.ResultsWe observed that the addition of inhibitor resulted in 2.1-fold enrichment of spontaneously beating human embryoid bodies (hEB) at 21 days of differentiation, and that 25% of treated cells expressed cardiac-specific α-myosin heavy chain. This effect was dependent on the stage of differentiation at which the inhibitor was introduced. Immunostaining and teratoma formation assays demonstrated that the inhibitor did not affect hESC pluripotency; however, treated hESC gave rise to hCM exhibiting increased expression of sarcomeric proteins, including cardiac troponin T, myosin light chain and α-myosin heavy chain. This was consistent with significantly increased numbers of myofibrillar bundles and the appearance of nascent Z-bodies at earlier time-points in treated hCM. Treated hEB also demonstrated a normal karyotype by array comparative genomic hybridization and viability in vivo following injection into mouse myocardium.ConclusionsThese studies demonstrate that p38MAPK inhibition accelerates directed hCM differentiation from hESC, and that this effect is developmental stage-specific. The use of this inhibitor should improve our ability to generate hESC-derived hCM for cell-based therapy. 相似文献
943.
944.
NT Krarup N Grarup K Banasik M Friedrichsen K Færch CH Sandholt T Jørgensen P Poulsen DR Witte A Vaag T Sørensen O Pedersen T Hansen 《PloS one》2012,7(7):e40376
Background and Aim
Non-alcoholic fatty liver disease (NAFLD) is a common condition, associated with hepatic insulin resistance and the metabolic syndrome including hyperglycaemia and dyslipidemia. We aimed at studying the potential impact of the NAFLD-associated PNPLA3 rs738409 G-allele on NAFLD-related metabolic traits in hyperglycaemic individuals.Methods
The rs738409 variant was genotyped in the population-based Inter99 cohort examined by an oral glucose-tolerance test, and a combined study-sample consisting of 192 twins (96 twin pairs) and a sub-set of the Inter99 population (n = 63) examined by a hyperinsulinemic euglycemic clamp (n total = 255). In Inter99, we analyzed associations of rs738409 with components of the WHO-defined metabolic syndrome (n = 5,847) and traits related to metabolic disease (n = 5,663). In the combined study sample we elucidated whether the rs738409 G-allele altered hepatic or peripheral insulin sensitivity. Study populations were divided into individuals with normal glucose-tolerance (NGT) and with impaired glucose regulation (IGR).Results
The case-control study showed no associations with components of the metabolic syndrome or the metabolic syndrome. Among 1,357 IGR individuals, the rs738409 G-allele associated with decreased fasting serum triglyceride levels (per allele effect(β) = −9.9% [−14.4%;−4.0% (95% CI)], p = 5.1×10−5) and fasting total cholesterol (β = −0.2 mmol/l [−0.3;−0.01 mmol/l(95% CI)], p = 1.5×10−4). Meta-analyses showed no impact on hepatic or peripheral insulin resistance in carriers of the rs738409 G-allele.Conclusion
Our findings suggest that the G-allele of PNPLA3 rs738409 associates with reduced fasting levels of cholesterol and triglyceride in individuals with IGR. 相似文献945.
An important role of endothelial hairy‐related transcription factors in mouse vascular development 下载免费PDF全文
946.
Eriksson O Friis EM Pedersen KR Crane PR 《International journal of plant sciences》2000,161(2):319-329
Seeds and fruits of Early Cretaceous (Barremian-Aptian) angiosperms from the Famalic?o locality in Portugal were analyzed to establish seed and fruit size (volume) distributions and to infer the proportion of animal-dispersed fruits. On the basis of a sample of 106 angiosperm fruit and seed taxa, the average seed size was 0.78 mm3 (range 0.02-6.86 mm3), whereas the average fruit size was 2.06 mm3 (range 0.12-8.34 mm3). Variation in seed size among taxa is smaller than in modern plant communities, but within-taxon variation is similar to that known for extant plants. No significant difference in the size of "fleshy" versus other fruits was observed. The proportion of fleshy fruits was 24.5%. This high figure was surprising and indicates that the significance of animal dispersal during an early stage in angiosperm evolution has been underestimated. We suggest that reptiles and multituberculates, and perhaps other mammals and birds as well, were the likely seed dispersers and that the early angiosperms from Famalic?o probably were herbs or small shrubs that inhabited a semiopen coniferous woodland. 相似文献
947.
Karen Koefoed Iben R?nn Veland Lotte Bang Pedersen Lars Allan Larsen S?ren Tvorup Christensen 《Organogenesis》2014,10(1):108-125
Primary cilia are unique sensory organelles that coordinate a wide variety of different signaling pathways to control cellular processes during development and in tissue homeostasis. Defects in function or assembly of these antenna-like structures are therefore associated with a broad range of developmental disorders and diseases called ciliopathies. Recent studies have indicated a major role of different populations of cilia, including nodal and cardiac primary cilia, in coordinating heart development, and defects in these cilia are associated with congenital heart disease. Here, we present an overview of the role of nodal and cardiac primary cilia in heart development. 相似文献
948.
Dahl SW Slaughter C Lauritzen C Bateman RC Connerton I Pedersen J 《Protein expression and purification》2000,20(1):27-36
A full-length cDNA encoding Carica papaya glutamine cyclotransferase was cloned by RT-PCR on the basis of results from amino acid sequencing of tryptic fragments of the native enzyme. The cDNA of 1036 nucleotides encodes a typical 22-residue signal peptide and a mature protein of 266 residues with a calculated molecular mass of 30,923 Da. Five plant ESTs encoding putative QCs highly homologous to PQC were identified and the numbers and locations of cysteines and N-glycosylation sites are conserved. The plant QC amino acid sequences are very different from the known mammalian QC sequences and no clear homology was observed. The PQC cDNA was expressed in Escherichia coli as either His-tagged PQC, with three different signal peptides and in fusions with thioredoxin, glutathione S-transferase, and (pre-) maltose-binding protein. In all cases, the expressed protein was either undetectable or insoluble. Expression in Pichia pastoris of PQC fused to the alpha-factor leader resulted in low levels of PQC activity. Extracellular expression of PQC in the insect cell/baculovirus system was successful and 15-50 mg/liter of active PQCs with three different secretion signals was expressed and purified. Further, PQC N-terminally fused to a combined secretion signal/His-tag peptide was correctly processed by the host signal peptidase and the His-tag could subsequently be removed with dipeptidyl peptidase I. The expressed products were characterized by activity assays, SDS-PAGE, N-terminal amino acid sequencing, MALDI-TOF mass spectroscopy, and peptide mass fingerprint analysis. 相似文献
949.
Land cover change and management implications for the conservation of a seabird in an urban coastal zone under climate change 下载免费PDF全文
Amin Rastandeh Maibritt Pedersen Zari Daniel K. Brown 《Ecological Management & Restoration》2018,19(2):147-155
Little Penguin (Eudyptula minor) is one of the most ecologically important seabirds in New Zealand and depends strongly on terrestrial ecosystems for nesting, moulting and breeding. Wellington, New Zealand, is one of the world's most important biodiversity hot spots for this species, mostly in confluence with human urban settlements. This species is currently suffering from the local impacts of climate change associated with urbanisation. Two suburbs of Wellington, New Zealand, that are used seasonally by Little Penguin as terrestrial habitat were selected as the study area to address two issues: (i) how local impacts of climate change may affect the population and habitat structure of species in urban coastal zones where land cover change occurs; and (ii) how landscape management practices may help to mitigate the impacts imposed by climate change on the species in such a context. Remote Sensing and Geographical Information Systems techniques were applied to quantify and measure the extent of the prehuman forests and current land cover classes in the study area to reveal the degree to which land cover has changed from predevelopment to the present time. The research shows that land cover change in the study area has been widespread and partly irreversible, particularly in areas covered by the class Built‐up Area. Results reveal that there are still spatial opportunities to safeguard this vulnerable species against the ill effects of climate change through landscape management practices. 相似文献
950.
L. Ringoir J. W. Widdershoven S. S. Pedersen J. M. Keyzer V. J. Pop 《Netherlands heart journal》2014,22(5):234-239