全文获取类型
收费全文 | 17986篇 |
免费 | 97篇 |
国内免费 | 227篇 |
专业分类
系统科学 | 383篇 |
丛书文集 | 382篇 |
教育与普及 | 72篇 |
理论与方法论 | 60篇 |
现状及发展 | 6248篇 |
研究方法 | 776篇 |
综合类 | 9868篇 |
自然研究 | 521篇 |
出版年
2014年 | 140篇 |
2013年 | 278篇 |
2012年 | 480篇 |
2011年 | 1013篇 |
2010年 | 360篇 |
2009年 | 343篇 |
2008年 | 528篇 |
2007年 | 612篇 |
2006年 | 607篇 |
2005年 | 543篇 |
2004年 | 399篇 |
2003年 | 308篇 |
2002年 | 317篇 |
2001年 | 507篇 |
2000年 | 559篇 |
1999年 | 411篇 |
1992年 | 288篇 |
1991年 | 252篇 |
1990年 | 250篇 |
1989年 | 229篇 |
1988年 | 209篇 |
1987年 | 226篇 |
1986年 | 203篇 |
1985年 | 245篇 |
1984年 | 235篇 |
1983年 | 159篇 |
1982年 | 172篇 |
1981年 | 157篇 |
1980年 | 199篇 |
1979年 | 445篇 |
1978年 | 340篇 |
1977年 | 367篇 |
1976年 | 264篇 |
1975年 | 322篇 |
1974年 | 446篇 |
1973年 | 379篇 |
1972年 | 360篇 |
1971年 | 421篇 |
1970年 | 484篇 |
1969年 | 425篇 |
1968年 | 407篇 |
1967年 | 442篇 |
1966年 | 384篇 |
1965年 | 301篇 |
1959年 | 155篇 |
1958年 | 231篇 |
1957年 | 179篇 |
1956年 | 138篇 |
1955年 | 154篇 |
1954年 | 132篇 |
排序方式: 共有10000条查询结果,搜索用时 15 毫秒
371.
Large intergenic non-coding RNA-RoR modulates reprogramming of human induced pluripotent stem cells 总被引:1,自引:0,他引:1
372.
373.
374.
José M. Bravo-San Pedro Mireia Niso-Santano Rubén Gómez-Sánchez Elisa Pizarro-Estrella Ana Aiastui-Pujana Ana Gorostidi Vicente Climent Rakel López de Maturana Rosario Sanchez-Pernaute Adolfo López de Munain José M. Fuentes Rosa A. González-Polo 《Cellular and molecular life sciences : CMLS》2013,70(1):121-136
Mutations in leucine-rich repeat kinase 2 (LRRK2) are a major cause of familial Parkinsonism, and the G2019S mutation of LRRK2 is one of the most prevalent mutations. The deregulation of autophagic processes in nerve cells is thought to be a possible cause of Parkinson’s disease (PD). In this study, we observed that G2019S mutant fibroblasts exhibited higher autophagic activity levels than control fibroblasts. Elevated levels of autophagic activity can trigger cell death, and in our study, G2019S mutant cells exhibited increased apoptosis hallmarks compared to control cells. LRRK2 is able to induce the phosphorylation of MAPK/ERK kinases (MEK). The use of 1,4-diamino-2,3-dicyano-1,4-bis[2-aminophenylthio]butadiene (U0126), a highly selective inhibitor of MEK1/2, reduced the enhanced autophagy and sensibility observed in G2019S LRRK2 mutation cells. These data suggest that the G2019S mutation induces autophagy via MEK/ERK pathway and that the inhibition of this exacerbated autophagy reduces the sensitivity observed in G2019S mutant cells. 相似文献
375.
376.
377.
A. Venerando L. Cesaro O. Marin A. Donella-Deana L. A. Pinna 《Cellular and molecular life sciences : CMLS》2014,71(12):2193-2196
The motif “SYDE”, incorporating the protein kinase CK2 consensus sequence (S-x-x-E) has been found to be phosphorylated at both its serine and tyrosine residues in several proteins. Of special interest is the case of cystic fibrosis Transmembrane-conductance Regulator (CFTR), where this motif is close to the residue (F508), whose deletion is the by far commonest cause of cystic fibrosis. Intriguingly, however, CFTR S511 cannot be phosphorylated by CK2 to any appreciable extent. Using a number of peptide substrates encompassing the CFTR “SYDE” site we have recently shown that: (1) failure of CK2 to phosphorylate the S511YDE motif is due to the presence of Y512; (2) CK2 readily phosphorylates S511 if Y512 is replaced by a phospho-tyrosine; (3) the Src family protein tyrosine kinase Lyn phosphorylates Y512 in a manner that is enhanced by the deletion of F508. These data, in conjunction with the recent observation that by inhibiting CK2 the degradation of F508delCFTR is reduced, lead us to hypothesize that the hierarchical phosphorylation of the motif SYDE by the concerted action of protein tyrosine kinases and CK2 is one of the mechanisms that cooperate to the premature degradation of F508delCFTR. 相似文献
378.
379.
Fatma Berri Vuong Ba Lê Martine Jandrot-Perrus Bruno Lina Béatrice Riteau 《Cellular and molecular life sciences : CMLS》2014,71(5):885-898
Influenza viruses cause acute respiratory infections, which are highly contagious and occur as seasonal epidemic and sporadic pandemic outbreaks. Innate immune response is activated shortly after infection with influenza A viruses (IAV), affording effective protection of the host. However, this response should be tightly regulated, as insufficient inflammation may result in virus escape from immunosurveillance. In contrast, excessive inflammation may result in bystander lung tissue damage, loss of respiratory capacity, and deterioration of the clinical outcome of IAV infections. In this review, we give a comprehensive overview of the innate immune response to IAV infection and summarize the most important findings on how the host can inappropriately respond to influenza. 相似文献
380.
Jiyong Wang Stephanie T. Lawry Allison L. Cohen Songtao Jia 《Cellular and molecular life sciences : CMLS》2014,71(24):4841-4852
Chromatin is generally classified as euchromatin or heterochromatin, each with distinct histone modifications, compaction levels, and gene expression patterns. Although the proper formation of heterochromatin is essential for maintaining genome integrity and regulating gene expression, heterochromatin can also spread into neighboring regions in a sequence-independent manner, leading to the inactivation of genes. Because the distance of heterochromatin spreading is stochastic, the formation of boundaries, which block the spreading of heterochromatin, is critical for maintaining stable gene expression patterns. Here we review the current understanding of the mechanisms underlying heterochromatin spreading and boundary formation. 相似文献