全文获取类型
收费全文 | 19756篇 |
免费 | 1590篇 |
国内免费 | 140篇 |
专业分类
21486篇 |
出版年
2024年 | 33篇 |
2023年 | 199篇 |
2022年 | 237篇 |
2021年 | 460篇 |
2020年 | 359篇 |
2019年 | 417篇 |
2018年 | 756篇 |
2017年 | 608篇 |
2016年 | 739篇 |
2015年 | 816篇 |
2014年 | 838篇 |
2013年 | 1285篇 |
2012年 | 1615篇 |
2011年 | 1693篇 |
2010年 | 940篇 |
2009年 | 674篇 |
2008年 | 1203篇 |
2007年 | 1119篇 |
2006年 | 1099篇 |
2005年 | 843篇 |
2004年 | 868篇 |
2003年 | 775篇 |
2002年 | 690篇 |
2001年 | 484篇 |
2000年 | 564篇 |
1999年 | 321篇 |
1998年 | 197篇 |
1997年 | 150篇 |
1996年 | 127篇 |
1995年 | 112篇 |
1994年 | 112篇 |
1993年 | 103篇 |
1992年 | 120篇 |
1991年 | 118篇 |
1990年 | 85篇 |
1989年 | 73篇 |
1988年 | 56篇 |
1987年 | 56篇 |
1986年 | 35篇 |
1985年 | 58篇 |
1984年 | 45篇 |
1983年 | 44篇 |
1982年 | 39篇 |
1981年 | 31篇 |
1980年 | 25篇 |
1979年 | 30篇 |
1978年 | 24篇 |
1977年 | 24篇 |
1974年 | 26篇 |
1973年 | 30篇 |
排序方式: 共有10000条查询结果,搜索用时 0 毫秒
101.
Our understanding of the evolution of the insulin signaling pathway (ISP) is still incomplete. One intriguing unanswered question is the explanation of the emergence of the glucostatic role of insulin in mammals. To find out whether this is due to the development of new sets of signaling transduction elements in these organisms, or to the establishment of new interactions between pre-existing proteins, we rebuilt putative orthologous ISPs in 17 eukaryotic organisms. Then, we computed the conservation of orthologous ISPs at different levels, from sequence similarity of orthologous proteins to co-evolution of interacting domains. We found that the emergence of glucostatic role in mammals can neither be explained by the development of new sets of signaling elements, nor by the establishment of new interactions between pre-existing proteins. The comparison of orthologous IRS molecules indicates that only in mammals have they acquired their complete functionality as efficient recruiters of effector sub-pathways. 相似文献
102.
A method for the in vitro pollination of chicory (Cichorium intybus L.) ovules was developed. The purpose was to avoid self-incompatibility after in vitro self-pollination of ovules isolated
from flower buds before anthesis and from open flower heads. Seedlings were obtained at a low percentage (0.76%), and the
results were explained in terms of pollen viability, pollen germination on the ovule, embryogenesis studies and ploidy analysis.
Received: 9 April 1997 / Revision received: 23 July 1997 / Accepted: 6 September 1999 相似文献
103.
Tao Tan Jun Wu Chenyang Si Shaoxing Dai Youyue Zhang Nianqin Sun E Zhang Honglian Shao Wei Si Pengpeng Yang Hong Wang Zhenzhen Chen Ran Zhu Yu Kang Reyna Hernandez-Benitez Llanos Martinez Martinez Estrella Nuñez Delicado W. Travis Berggren Juan Carlos Izpisua Belmonte 《Cell》2021,184(8):2020-2032.e14
104.
A Garcia-Muñoz MA Rodriguez R Bologna-Molina FE Cazares-Raga FC Hernandez-Hernandez JE Farfan-Morales JJ Trujillo C Liceaga-Escalera G Mendoza-Hernandez 《Proteome science》2012,10(1):49
ABSTRACT: BACKGROUND: Odontogenic myxoma (OM) is a benign, but locally invasive, neoplasm occurring in the jaws. However, the molecules implicated in its development are unknown. OM as well as Dental Follicle (DF), an odontogenic tissue surrounding the enamel organ, is derived from ectomesenchymal/mesencyhmal elements. To identify some protein that could participate in the development of this neoplasm, total proteins from OM were separated by two-dimensional electrophoresis and the profiles were compared with those obtained from DF, used as a control. RESULTS: We identified eight proteins with differential expression; two of them were downregulated and six upregulated in OM. A spot consistently overexpressed in odontogenic myxoma, with a molecular weight of 44-kDa and a pI of 3.5 was identified as the orosomucoid 1 protein. Western blot experiments confirmed the overexpression of this protein in odontogenic myxoma and immunohistochemical assays showed that this protein was mainly located in the cytoplasm of stellate and spindle-shaped cells of this neoplasm. CONCLUSION: Orosomucoid 1, which belongs to a group of acute-phase proteins, may play a role in the modulation of the immune system and possibly it influences the development of OM. 相似文献
105.
106.
Alfredo Saldaña Christopher H. Lusk Wilfredo L. Gonzáles Ernesto Gianoli 《Evolutionary ecology》2007,21(5):651-662
Unlike other species of the genus Blechnum, the fern Blechnum chilense occurs in a wide range of habitats in Chilean temperate rainforest, from shaded forest understories to abandoned clearings
and large gaps. We asked if contrasting light environments can exert differential selection on ecophysiological traits of
B. chilense. We measured phenotypic selection on functional traits related to carbon gain: photosynthetic capacity (A
max), dark respiration rate (R
d), water use efficiency (WUE), leaf size and leaf thickness in populations growing in gaps and understorey environments. We
assessed survival until reproductive stage and fecundity (sporangia production) as fitness components. In order to determine
the potential evolutionary response of traits under selection, we estimated the genetic variation of these traits from clonally
propagated individuals in common garden experiments. In gaps, survival of B. chilense was positively correlated with WUE and negatively correlated with leaf size. In contrast, survival in shaded understories
was positively correlated with leaf size. We found positive directional fecundity selection on WUE in gaps population. In
understories, ferns of lower R
d and greater leaf size showed greater fecundity. Thus, whereas control of water loss was optimized in gaps, light capture
and net carbon balance were optimized in shaded understories. We found a significant genetic component of variation in WUE,
R
d and leaf size. This study shows the potential for evolutionary responses to heterogeneous light environments in functional
traits of B. chilense, a unique fern species able to occupy a broad successional niche in Chilean temperate rainforest. 相似文献
107.
Hemizygosity at the NCF1 gene in patients with Williams-Beuren syndrome decreases their risk of hypertension 下载免费PDF全文
Del Campo M Antonell A Magano LF Muñoz FJ Flores R Bayés M Pérez Jurado LA 《American journal of human genetics》2006,78(4):533-542
Williams-Beuren syndrome (WBS), caused by a heterozygous deletion at 7q11.23, represents a model for studying hypertension, the leading risk factor for mortality worldwide, in a genetically determined disorder. Haploinsufficiency at the elastin gene is known to lead to the vascular stenoses in WBS and is also thought to predispose to hypertension, present in approximately 50% of patients. Detailed clinical and molecular characterization of 96 patients with WBS was performed to explore clinical-molecular correlations. Deletion breakpoints were precisely defined and were found to result in variability at two genes, NCF1 and GTF2IRD2. Hypertension was significantly less prevalent in patients with WBS who had the deletion that included NCF1 (P=.02), a gene coding for the p47(phox) subunit of the NADPH oxidase. Decreased p47(phox) protein levels, decreased superoxide anion production, and lower protein nitrotyrosination were all observed in cell lines from patients hemizygous at NCF1. Our results indicate that the loss of a functional copy of NCF1 protects a proportion of patients with WBS against hypertension, likely through a lifelong reduced angiotensin II-mediated oxidative stress. Therefore, antioxidant therapy that reduces NADPH oxidase activity might have a potential benefit in identifiable patients with WBS in whom serious complications related to hypertension have been reported, as well as in forms of essential hypertension mediated by a similar pathogenic mechanism. 相似文献
108.
109.
110.
Barrionuevo P Delpino MV Velásquez LN García Samartino C Coria LM Ibañez AE Rodríguez ME Cassataro J Giambartolomei GH 《Microbes and infection / Institut Pasteur》2011,13(3):239-250
The strategies that allow Brucella abortus to persist for years inside macrophages subverting host immune responses are not completely understood. Immunity against this bacterium relies on the capacity of IFN-γ to activate macrophages, endowing them with the ability to destroy intracellular bacteria. We report here that infection with B. abortus down-modulates the expression of the type I receptor for the Fc portion of IgG (FcγRI, CD64) and FcγRI-restricted phagocytosis regulated by IFN-γ in human monocytes/macrophages. Both phenomena were not dependent on bacterial viability, since they were also induced by heat-killed B. abortus (HKBA), suggesting that they were elicited by a structural bacterial component. Accordingly, a prototypical B. abortus lipoprotein (L-Omp19), but not its unlipidated form, inhibited both CD64 expression and FcγRI-restricted phagocytosis regulated by IFN-γ. Moreover, a synthetic lipohexapeptide that mimics the structure of the protein lipid moiety also inhibited CD64 expression, indicating that any Brucella lipoprotein could down-modulate CD64 expression and FcγRI-restricted phagocytosis. Pre-incubation of monocytes/macrophages with anti-TLR2 mAb blocked the inhibition of the CD64 expression mediated by HKBA and L-Omp19. These results, together with our previous observations establish that B. abortus utilizes its lipoproteins to inhibit the monocytes/macrophages activation mediated by IFN-γ and to subvert host immunonological responses. 相似文献