全文获取类型
收费全文 | 6798篇 |
免费 | 670篇 |
国内免费 | 1篇 |
专业分类
7469篇 |
出版年
2023年 | 25篇 |
2022年 | 63篇 |
2021年 | 109篇 |
2020年 | 79篇 |
2019年 | 85篇 |
2018年 | 96篇 |
2017年 | 91篇 |
2016年 | 194篇 |
2015年 | 319篇 |
2014年 | 336篇 |
2013年 | 439篇 |
2012年 | 567篇 |
2011年 | 511篇 |
2010年 | 360篇 |
2009年 | 299篇 |
2008年 | 406篇 |
2007年 | 421篇 |
2006年 | 410篇 |
2005年 | 376篇 |
2004年 | 370篇 |
2003年 | 322篇 |
2002年 | 346篇 |
2001年 | 96篇 |
2000年 | 102篇 |
1999年 | 104篇 |
1998年 | 93篇 |
1997年 | 58篇 |
1996年 | 51篇 |
1995年 | 49篇 |
1994年 | 38篇 |
1993年 | 50篇 |
1992年 | 47篇 |
1991年 | 39篇 |
1990年 | 39篇 |
1989年 | 28篇 |
1988年 | 28篇 |
1987年 | 21篇 |
1986年 | 21篇 |
1985年 | 19篇 |
1984年 | 24篇 |
1983年 | 24篇 |
1982年 | 20篇 |
1981年 | 19篇 |
1979年 | 16篇 |
1977年 | 19篇 |
1974年 | 20篇 |
1973年 | 21篇 |
1972年 | 19篇 |
1971年 | 15篇 |
1969年 | 23篇 |
排序方式: 共有7469条查询结果,搜索用时 15 毫秒
61.
Isabelle?Grosdemouge Anne?Bachelot Aurélie?Lucas Nathalie?Baran Paul?A?Kelly Nadine?BinartEmail author 《Reproductive biology and endocrinology : RB&E》2003,1(1):12
Prolactin (PRL) exerts pleiotropic physiological effects in various cells and tissues, and is mainly considered as a regulator
of reproduction and cell growth. Null mutation of the PRL receptor (R) gene leads to female sterility due to a complete failure
of embryo implantation. Pre-implantatory egg development, implantation and decidualization in the mouse appear to be dependent
on ovarian rather than uterine PRLR expression, since progesterone replacement permits the rescue of normal implantation and
early pregnancy. To better understand PRL receptor deficiency, we analyzed in detail ovarian and corpora lutea development
of PRLR-/- females. The present study demonstrates that the ovulation rate is not different between PRLR+/+ and PRLR-/- mice.
The corpus luteum is formed but an elevated level of apoptosis and extensive inhibition of angiogenesis occur during the luteal
transition in the absence of prolactin signaling. These modifications lead to the decrease of LH receptor expression and consequently
to a loss of the enzymatic cascades necessary to produce adequate levels of progesterone which are required for the maintenance
of pregnancy. 相似文献
62.
63.
Sébastien Besseau Franziska Kellner Arnaud Lanoue Antje M.K. Thamm Vonny Salim Bernd Schneider Fernando Geu-Flores René H?fer Grégory Guirimand Anthony Guihur Audrey Oudin Ga?lle Glevarec Emilien Foureau Nicolas Papon Marc Clastre Nathalie Giglioli-Guivarc’h Benoit St-Pierre Danièle Werck-Reichhart Vincent Burlat Vincenzo De Luca Sarah E. O’Connor Vincent Courdavault 《Plant physiology》2013,163(4):1792-1803
64.
Melisa Gualdrón-López Nathalie Chevalier Patrick Van Der Smissen Pierre J. Courtoy Daniel J. Rigden Paul A.M. Michels 《Biochimica et Biophysica Acta (BBA)/Molecular Cell Research》2013,1833(12):3076-3092
Trypanosomatids contain peroxisome-like organelles called glycosomes. Peroxisomal biogenesis involves a cytosolic receptor, PEX5, which, after its insertion into the organellar membrane, delivers proteins to the matrix. In yeasts and mammalian cells, transient PEX5 monoubiquitination at the membrane serves as the signal for its retrieval from the organelle for re-use. When its recycling is impaired, PEX5 is polyubiquitinated for proteasomal degradation. Stably monoubiquitinated TbPEX5 was detected in cytosolic fractions of Trypanosoma brucei, indicative for its role as physiological intermediate in receptor recycling. This modification's resistance to dithiothreitol suggests ubiquitin conjugation of a lysine residue. T. brucei PEX4, the functional homologue of the ubiquitin-conjugating (UBC) enzyme responsible for PEX5 monoubiquitination in yeast, was identified. It is associated with the cytosolic face of the glycosomal membrane, probably anchored by an identified putative TbPEX22. The involvement of TbPEX4 in TbPEX5 ubiquitination was demonstrated using procyclic ?PEX4 trypanosomes. Surprisingly, glycosomal matrix protein import was only mildly affected in this mutant. Since other UBC homologues were upregulated, it might be possible that these have partially rescued PEX4's function in PEX5 ubiquitination. In addition, the altered expression of UBCs, notably of candidates involved in cell-cycle control, could be responsible for observed morphological and motility defects of the ?PEX4 mutant. 相似文献
65.
David Fong Martine Bisson Gino Laberge Stephen McManus Guillaume Grenier Nathalie Faucheux Sophie Roux 《Cellular signalling》2013,25(4):717-728
BMP-9 is a potent osteogenic factor; however, its effects on osteoclasts, the bone-resorbing cells, remain unknown. To determine the effects of BMP-9 on osteoclast formation, activity and survival, we used human cord blood monocytes as osteoclast precursors that form multinucleated osteoclasts in the presence of RANKL and M-CSF in long-term cultures. BMP-9 did not affect osteoclast formation, but adding BMP-9 at the end of the culture period significantly increased bone resorption compared to untreated cultures, and reduced both the rate of apoptosis and caspase-9 activity. BMP-9 also significantly downregulated the expression of pro-apoptotic Bid, but only after RANKL and M-CSF, which are both osteoclast survival factors, had been eliminated from the culture medium. To investigate the mechanisms involved in the effects of BMP-9, we first showed that osteoclasts expressed some BMP receptors, including BMPR-IA, BMPR-IB, ALK1, and BMPR-II. We also found that BMP-9 was able to induce the phosphorylation of Smad-1/5/8 and ERK 1/2 proteins, but did not induce p38 phosphorylation. Finally, knocking down the BMPR-II receptor abrogated the BMP-9-induced ERK-signaling, as well as the increase in bone resorption. In conclusion, these results show for the first time that BMP-9 directly affects human osteoclasts, enhancing bone resorption and protecting osteoclasts against apoptosis. BMP-9 signaling in human osteoclasts involves the canonical Smad-1/5/8 pathway, and the ERK pathway. 相似文献
66.
67.
Beno?t de Chassey Anne Aublin-Gex Alessia Ruggieri Laurène Meyniel-Schicklin Fabrine Pradezynski Nathalie Davoust Thibault Chantier Lionel Tafforeau Philippe-Emmanuel Mangeot Claire Ciancia Laure Perrin-Cocon Ralf Bartenschlager Patrice André Vincent Lotteau 《PLoS pathogens》2013,9(7)
Influenza A NS1 and NS2 proteins are encoded by the RNA segment 8 of the viral genome. NS1 is a multifunctional protein and a virulence factor while NS2 is involved in nuclear export of viral ribonucleoprotein complexes. A yeast two-hybrid screening strategy was used to identify host factors supporting NS1 and NS2 functions. More than 560 interactions between 79 cellular proteins and NS1 and NS2 proteins from 9 different influenza virus strains have been identified. These interacting proteins are potentially involved in each step of the infectious process and their contribution to viral replication was tested by RNA interference. Validation of the relevance of these host cell proteins for the viral replication cycle revealed that 7 of the 79 NS1 and/or NS2-interacting proteins positively or negatively controlled virus replication. One of the main factors targeted by NS1 of all virus strains was double-stranded RNA binding domain protein family. In particular, adenosine deaminase acting on RNA 1 (ADAR1) appeared as a pro-viral host factor whose expression is necessary for optimal viral protein synthesis and replication. Surprisingly, ADAR1 also appeared as a pro-viral host factor for dengue virus replication and directly interacted with the viral NS3 protein. ADAR1 editing activity was enhanced by both viruses through dengue virus NS3 and influenza virus NS1 proteins, suggesting a similar virus-host co-evolution. 相似文献
68.
Anna G. Himler Eric J. Caldera Boris C. Baer Hermógenes Fernández-Marín Ulrich G. Mueller 《Proceedings. Biological sciences / The Royal Society》2009,276(1667):2611-2616
Asexual reproduction imposes evolutionary handicaps on asexual species, rendering them prone to extinction, because asexual reproduction generates novel genotypes and purges deleterious mutations at lower rates than sexual reproduction. Here, we report the first case of complete asexuality in ants, the fungus-growing ant Mycocepurus smithii, where queens reproduce asexually but workers are sterile, which is doubly enigmatic because the clonal colonies of M. smithii also depend on clonal fungi for food. Degenerate female mating anatomy, extensive field and laboratory surveys, and DNA fingerprinting implicate complete asexuality in this widespread ant species. Maternally inherited bacteria (e.g. Wolbachia, Cardinium) and the fungal cultivars can be ruled out as agents inducing asexuality. M. smithii societies of clonal females provide a unique system to test theories of parent–offspring conflict and reproductive policing in social insects. Asexuality of both ant farmer and fungal crop challenges traditional views proposing that sexual farmer ants outpace coevolving sexual crop pathogens, and thus compensate for vulnerabilities of their asexual crops. Either the double asexuality of both farmer and crop may permit the host to fully exploit advantages of asexuality for unknown reasons or frequent switching between crops (symbiont reassociation) generates novel ant–fungus combinations, which may compensate for any evolutionary handicaps of asexuality in M. smithii. 相似文献
69.
Sylvie Rodrigues-Ferreira Anne Di Tommaso Ariane Dimitrov Sylvie Cazaubon Nadège Gruel Hélène Colasson André Nicolas Nathalie Chaverot Vincent Molinié Fabien Reyal Brigitte Sigal-Zafrani Benoit Terris Olivier Delattre Fran?ois Radvanyi Franck Perez Anne Vincent-Salomon Clara Nahmias 《PloS one》2009,4(10)
Background
Breast cancer is a heterogeneous disease that is not totally eradicated by current therapies. The classification of breast tumors into distinct molecular subtypes by gene profiling and immunodetection of surrogate markers has proven useful for tumor prognosis and prediction of effective targeted treatments. The challenge now is to identify molecular biomarkers that may be of functional relevance for personalized therapy of breast tumors with poor outcome that do not respond to available treatments. The Mitochondrial Tumor Suppressor (MTUS1) gene is an interesting candidate whose expression is reduced in colon, pancreas, ovary and oral cancers. The present study investigates the expression and functional effects of MTUS1 gene products in breast cancer.Methods and Findings
By means of gene array analysis, real-time RT-PCR and immunohistochemistry, we show here that MTUS1/ATIP3 is significantly down-regulated in a series of 151 infiltrating breast cancer carcinomas as compared to normal breast tissue. Low levels of ATIP3 correlate with high grade of the tumor and the occurrence of distant metastasis. ATIP3 levels are also significantly reduced in triple negative (ER- PR- HER2-) breast carcinomas, a subgroup of highly proliferative tumors with poor outcome and no available targeted therapy. Functional studies indicate that silencing ATIP3 expression by siRNA increases breast cancer cell proliferation. Conversely, restoring endogenous levels of ATIP3 expression leads to reduced cancer cell proliferation, clonogenicity, anchorage-independent growth, and reduces the incidence and size of xenografts grown in vivo. We provide evidence that ATIP3 associates with the microtubule cytoskeleton and localizes at the centrosomes, mitotic spindle and intercellular bridge during cell division. Accordingly, live cell imaging indicates that ATIP3 expression alters the progression of cell division by promoting prolonged metaphase, thereby leading to a reduced number of cells ungergoing active mitosis.Conclusions
Our results identify for the first time ATIP3 as a novel microtubule-associated protein whose expression is significantly reduced in highly proliferative breast carcinomas of poor clinical outcome. ATIP3 re-expression limits tumor cell proliferation in vitro and in vivo, suggesting that this protein may represent a novel useful biomarker and an interesting candidate for future targeted therapies of aggressive breast cancer. 相似文献70.
Kazumi Funane Nathalie Libessart Douglas Stewart Toru Michishita Jack Preiss 《The protein journal》1998,17(7):579-590
Incubation of maize branching enzyme, mBEI and mBEII, with 100 μM diethylpyrocarbonate (DEPC) rapidly inactivated the enzymes.
Treatment of the DEPC-inactivated enzymes with 100–500 mM hydroxylamine restored the enzyme activities. Spectroscopic data
indicated that the inactivation of BE with DEPC was the result of histidine modification. The addition of the substrate amylose
or amylopectin retarded the enzyme inactivation by DEPC, suggesting that the histidine residues are important for substrate
binding. In maize BEII, conserved histidine residues are in catalytic regions 1 (His320) and 4 (His508). His320 and His508
were individually replaced by Ala via site-directed mutagenesis to probe their role in catalysis. Expression of these mutants
inE. coli showed a significant decrease of the activity and the mutant enzymes hadK
m values 10 times higher than the wild type. Therefore, residues His320 and His508 do play an important role in substrate binding. 相似文献