全文获取类型
收费全文 | 18009篇 |
免费 | 1710篇 |
国内免费 | 3篇 |
专业分类
19722篇 |
出版年
2023年 | 67篇 |
2022年 | 167篇 |
2021年 | 335篇 |
2020年 | 196篇 |
2019年 | 222篇 |
2018年 | 305篇 |
2017年 | 248篇 |
2016年 | 419篇 |
2015年 | 731篇 |
2014年 | 771篇 |
2013年 | 972篇 |
2012年 | 1346篇 |
2011年 | 1314篇 |
2010年 | 824篇 |
2009年 | 719篇 |
2008年 | 1087篇 |
2007年 | 1104篇 |
2006年 | 983篇 |
2005年 | 917篇 |
2004年 | 972篇 |
2003年 | 816篇 |
2002年 | 826篇 |
2001年 | 288篇 |
2000年 | 252篇 |
1999年 | 264篇 |
1998年 | 237篇 |
1997年 | 185篇 |
1996年 | 168篇 |
1995年 | 158篇 |
1994年 | 150篇 |
1993年 | 119篇 |
1992年 | 184篇 |
1991年 | 165篇 |
1990年 | 136篇 |
1989年 | 139篇 |
1988年 | 135篇 |
1987年 | 127篇 |
1986年 | 145篇 |
1985年 | 107篇 |
1984年 | 105篇 |
1983年 | 101篇 |
1982年 | 107篇 |
1981年 | 88篇 |
1980年 | 70篇 |
1979年 | 89篇 |
1978年 | 91篇 |
1977年 | 65篇 |
1976年 | 75篇 |
1975年 | 71篇 |
1974年 | 82篇 |
排序方式: 共有10000条查询结果,搜索用时 15 毫秒
921.
David Wragg Elizabeth A. J. Cook Perle Latr de Lat Tatjana Sitt Johanneke D. Hemmink Maurine C. Chepkwony Regina Njeru E. Jane Poole Jessica Powell Edith A. Paxton Rebecca Callaby Andrea Talenti Antoinette A. Miyunga Gideon Ndambuki Stephen Mwaura Harriet Auty Oswald Matika Musa Hassan Karen Marshall Timothy Connelley Liam J. Morrison B. Mark deC. Bronsvoort W. Ivan Morrison Philip G. Toye James G. D. Prendergast 《PLoS genetics》2022,18(4)
East Coast fever, a tick-borne cattle disease caused by the Theileria parva parasite, is among the biggest natural killers of cattle in East Africa, leading to over 1 million deaths annually. Here we report on the genetic analysis of a cohort of Bos indicus (Boran) cattle demonstrating heritable tolerance to infection with T. parva (h2 = 0.65, s.e. 0.57). Through a linkage analysis we identify a 6 Mb genomic region on bovine chromosome 15 that is significantly associated with survival outcome following T. parva exposure. Testing this locus in an independent cohort of animals replicates this association with survival following T. parva infection. A stop gained variant in a paralogue of the FAF1 gene in this region was found to be highly associated with survival across both related and unrelated animals, with only one of the 20 homozygote carriers (T/T) of this change succumbing to the disease in contrast to 44 out of 97 animals homozygote for the reference allele (C/C). Consequently, we present a genetic locus linked to tolerance of one of Africa’s most important cattle diseases, raising the promise of marker-assisted selection for cattle that are less susceptible to infection by T. parva. 相似文献
922.
Plant and Soil - In this opinion paper we review recent methodological developments underpinning the study of roots, the rhizosphere and interactions affecting soil functions, and explore new... 相似文献
923.
924.
Kan Xiong Douglas Shea Justin Rhoades Timothy Blewett Ruolin Liu Jin
H Bae Erica Nguyen G Mike Makrigiorgos Todd R Golub Viktor
A Adalsteinsson 《Nucleic acids research》2022,50(1):e1
Accurate DNA sequencing is crucial in biomedicine. Underlying the most accurate methods is the assumption that a mutation is true if altered bases are present on both strands of the DNA duplex. We now show that this assumption can be wrong. We establish that current methods to prepare DNA for sequencing, via ‘End Repair/dA-Tailing,’ may substantially resynthesize strands, leading amplifiable lesions or alterations on one strand to become indiscernible from true mutations on both strands. Indeed, we discovered that 7–17% and 32–57% of interior ‘duplex base pairs’ from cell-free DNA and formalin-fixed tumor biopsies, respectively, could be resynthesized in vitro and potentially introduce false mutations. To address this, we present Duplex-Repair, and show that it limits interior duplex base pair resynthesis by 8- to 464-fold, rescues the impact of induced DNA damage, and affords up to 8.9-fold more accurate duplex sequencing. Our study uncovers a major Achilles’ heel in sequencing and offers a solution to restore high accuracy. 相似文献
925.
Chathurika Henpita Rajesh Vyas Chastity L. Healy Tra L. Kieu Aditi U. Gurkar Matthew J. Yousefzadeh Yuxiang Cui Aiping Lu Luise A. Angelini Ryan D. O'Kelly Sara J. McGowan Sanjay Chandrasekhar Rebecca R. Vanderpool Danielle Hennessy-Wack Mark A. Ross Timothy N. Bachman Charles McTiernan Smitha P. S. Pillai Warren Ladiges Mitra Lavasani Johnny Huard Donna Beer-Stolz Claudette M. St. Croix Simon C. Watkins Paul D. Robbins Ana L. Mora Eric E. Kelley Yinsheng Wang Timothy D. O'Connell Laura J. Niedernhofer 《Aging cell》2023,22(4):e13782
Cardiomyopathy is a progressive disease of the myocardium leading to impaired contractility. Genotoxic cancer therapies are known to be potent drivers of cardiomyopathy, whereas causes of spontaneous disease remain unclear. To test the hypothesis that endogenous genotoxic stress contributes to cardiomyopathy, we deleted the DNA repair gene Ercc1 specifically in striated muscle using a floxed allele of Ercc1 and mice expressing Cre under control of the muscle-specific creatinine kinase (Ckmm) promoter or depleted systemically (Ercc1−/D mice). Ckmm-Cre+/−;Ercc1−/fl mice expired suddenly of heart disease by 7 months of age. As young adults, the hearts of Ckmm-Cre+/−;Ercc1−/fl mice were structurally and functionally normal, but by 6-months-of-age, there was significant ventricular dilation, wall thinning, interstitial fibrosis, and systolic dysfunction indicative of dilated cardiomyopathy. Cardiac tissue from the tissue-specific or systemic model showed increased apoptosis and cardiac myocytes from Ckmm-Cre+/-;Ercc1−/fl mice were hypersensitive to genotoxins, resulting in apoptosis. p53 levels and target gene expression, including several antioxidants, were increased in cardiac tissue from Ckmm-Cre+/−;Ercc1−/fl and Ercc1−/D mice. Despite this, cardiac tissue from older mutant mice showed evidence of increased oxidative stress. Genetic or pharmacologic inhibition of p53 attenuated apoptosis and improved disease markers. Similarly, overexpression of mitochondrial-targeted catalase improved disease markers. Together, these data support the conclusion that DNA damage produced endogenously can drive cardiac disease and does so mechanistically via chronic activation of p53 and increased oxidative stress, driving cardiac myocyte apoptosis, dilated cardiomyopathy, and sudden death. 相似文献
926.
Dorothee Hodapp Irene T. Roca Dario Fiorentino Cristina Garilao Kristin Kaschner Kathleen Kesner-Reyes Birgit Schneider Joachim Segschneider Ádám T. Kocsis Wolfgang Kiessling Thomas Brey Rainer Froese 《Global Change Biology》2023,29(12):3304-3317
Driven by climate change, marine biodiversity is undergoing a phase of rapid change that has proven to be even faster than changes observed in terrestrial ecosystems. Understanding how these changes in species composition will affect future marine life is crucial for conservation management, especially due to increasing demands for marine natural resources. Here, we analyse predictions of a multiparameter habitat suitability model covering the global projected ranges of >33,500 marine species from climate model projections under three CO2 emission scenarios (RCP2.6, RCP4.5, RCP8.5) up to the year 2100. Our results show that the core habitat area will decline for many species, resulting in a net loss of 50% of the core habitat area for almost half of all marine species in 2100 under the high-emission scenario RCP8.5. As an additional consequence of the continuing distributional reorganization of marine life, gaps around the equator will appear for 8% (RCP2.6), 24% (RCP4.5), and 88% (RCP8.5) of marine species with cross-equatorial ranges. For many more species, continuous distributional ranges will be disrupted, thus reducing effective population size. In addition, high invasion rates in higher latitudes and polar regions will lead to substantial changes in the ecosystem and food web structure, particularly regarding the introduction of new predators. Overall, our study highlights that the degree of spatial and structural reorganization of marine life with ensued consequences for ecosystem functionality and conservation efforts will critically depend on the realized greenhouse gas emission pathway. 相似文献
927.
928.
Laura N. L. Johnson Brenna A. McLeod Lynne E. Burns Krista Arseneault Timothy R. Frasier Hugh G. Broders 《PloS one》2015,10(5)
During late summer and early autumn, temperate bats migrate from their summering sites to swarming sites, where mating likely occurs. However, the extent to which individuals of a single summering site migrate to the same swarming site, and vice versa, is not known. We examined the migratory connectivity between summering and swarming sites in two temperate, North American, bat species, the little brown bat (Myotis lucifugus) and the northern long-eared bat (Myotis septentrionalis). Using mitochondrial and microsatellite DNA markers, we examined population structuring within and among summering and swarming sites. Both species exhibited moderate degrees of mitochondrial DNA differentiation (little brown bat: FST(SWARMING)= 0.093, FST(SWARMING)= 0.052; northern long-eared bat: FST(SWARMING)= 0.117, FST(SWARMING)= 0.043) and little microsatellite DNA differentiation among summering and among swarming sites. Haplotype diversity was significantly higher at swarming sites than summering sites, supporting the idea that swarming sites are comprised of individuals from various summering sites. Further, pairwise analyses suggest that swarming sites are not necessarily comprised of only individuals from the most proximal summering colonies. 相似文献
929.