全文获取类型
收费全文 | 4397篇 |
免费 | 295篇 |
专业分类
4692篇 |
出版年
2023年 | 31篇 |
2022年 | 55篇 |
2021年 | 101篇 |
2020年 | 75篇 |
2019年 | 82篇 |
2018年 | 141篇 |
2017年 | 111篇 |
2016年 | 174篇 |
2015年 | 231篇 |
2014年 | 241篇 |
2013年 | 328篇 |
2012年 | 367篇 |
2011年 | 338篇 |
2010年 | 212篇 |
2009年 | 213篇 |
2008年 | 254篇 |
2007年 | 244篇 |
2006年 | 197篇 |
2005年 | 209篇 |
2004年 | 187篇 |
2003年 | 171篇 |
2002年 | 165篇 |
2001年 | 44篇 |
2000年 | 43篇 |
1999年 | 50篇 |
1998年 | 28篇 |
1997年 | 37篇 |
1996年 | 35篇 |
1995年 | 27篇 |
1994年 | 32篇 |
1993年 | 26篇 |
1992年 | 20篇 |
1991年 | 18篇 |
1990年 | 11篇 |
1989年 | 15篇 |
1988年 | 12篇 |
1987年 | 13篇 |
1986年 | 12篇 |
1985年 | 13篇 |
1984年 | 14篇 |
1983年 | 6篇 |
1982年 | 8篇 |
1980年 | 11篇 |
1979年 | 6篇 |
1978年 | 6篇 |
1976年 | 9篇 |
1973年 | 11篇 |
1971年 | 5篇 |
1968年 | 5篇 |
1946年 | 5篇 |
排序方式: 共有4692条查询结果,搜索用时 15 毫秒
1.
Lucia Di Giambattista P. Grimaldi S. Gaudenzi D. Pozzi M. Grandi S. Morrone I. Silvestri A. Congiu Castellano 《European biophysics journal : EBJ》2010,39(6):929-934
We have made a preliminary analysis of the results about the effects on tumoral cell line (lymphoid T cell line Jurkat) induced
by UVB radiation (dose of 310 mJ/cm2) with and without a vegetable mixture. In the present study, we have used two techniques: Fourier transform infrared spectroscopy
(FTIR) and flow cytometry. FTIR spectroscopy has the potential to provide the identification of the vibrational modes of some
of the major compounds (lipid, proteins and nucleic acids) without being invasive in the biomaterials. The second technique
has allowed us to perform measurements of cytotoxicity and to assess the percentage of apoptosis. We already studied the induction
of apoptotic process in the same cell line by UVB radiation; in particular, we looked for correspondences and correlations
between FTIR spetroscopy and flow cytometry data finding three highly probable spectroscopic markers of apoptosis (Pozzi et
al. in Radiat Res 168:698–705, 2007). In the present work, the results have shown significant changes in the absorbance and
spectral pattern in the wavenumber protein and nucleic acids regions after the treatments. 相似文献
2.
The assembly of a large physical map of genomes requires simultaneous analysis of many cosmid clones for overlapping regions. The search for overlapping regions may be achieved by various means. High-performance liquid chromatography (HPLC) provides an alternative to gel electrophoresis since microgram amounts of each DNA fragment may be collected into individual test tubes for further analysis. HPLC has been used to identify overlapping cosmid clones from a pool of cosmid DNA containing the terminal portion of the long arm of the human X chromosome (Xq24-qter). Among 400 cosmids analyzed, 3 were shown to overlap. 相似文献
3.
4.
Lucia Lioi 《Biologia Plantarum》1987,29(1):49-53
Relationships among storage proteins in seeds from cultivars and primitive accessions of the four economically most important
species ofPhaseolus — P. vulgaris, P. coccineus, P. acutifolius andP. lunatus — were studied.
Analysis of SDS-polyacrylamide gel electrophoretic patterns of storage seed proteins revealed common characteristics in the
major groups of polypeptides forP. vulgaris, P. coccineus andP. acutifolius, while clear differences existed between thesePhaseolus species and P.lunatus. 相似文献
5.
Bruna Tedeschi Patrizia Vernole M.Lucia Sanna Benedetto Nicoletti 《Human genetics》1992,89(5):543-547
Summary Chromosome fragile sites are inducible by aphidicolin in cultured human lymphocytes. To assess the frequency and distribution of these common fragile sites in the general population, a cytogenetic survey was performed on 126 subjects, 59 males and 67 females, whose age ranged from 1 day to 72 years. Common fragile sites, induced by aphidicolin, were widespread and showed a remarkably different sensitivity among individuals; age influenced the overall frequency of fragile sites. Moreover, both age and sex seemed to modulate the expression of specific fragile sites. In our population, the most common fragile sites were: 3p14, 16q23, Xp22, 6q26, 1p31, 4q31, 1p22, 7q22, 2q33, 3q27, 2q31, 7q32, 14q24, 10q22, 5q31, 2q37, 6p21. 相似文献
6.
B P Griffith S R McCormick C K Fong J T Lavallee H L Lucia E Goff 《Journal of virology》1985,55(2):402-409
The development of cytomegalovirus (CMV) infection in the placenta was studied in Hartley guinea pigs inoculated at midgestation, and its role in determining the outcome of fetal CMV infection was assessed. A hematogenous spread of CMV from the mother to the placenta occurred early during the course of the infection. However, the virus remained present in placental tissues long after CMV had been cleared from maternal blood (i.e., 3 and 4 weeks postinoculation). At that time, the virus was able to replicate in placental tissues in the presence of specific maternal antibodies. Viral nucleocapsids were seen within nuclei of trophoblastic cells, and virions were present surrounding infected cells. In addition, typical CMV-induced histopathological lesions bearing CMV antigens were consistently localized at the transitional zone between the capillarized labyrinth and the noncapillarized interlobium. Whenever CMV infection of the fetus occurred, virus was isolated from the associated placenta. Among placental-fetal units with CMV-infected placentas, only 27% of the fetuses were found to be infected. In addition, there was a delay in the establishment of the infection in the fetus in relation to the placenta, although frequencies of virus isolation in placental and fetal tissues peaked at 3 weeks after CMV inoculation. These results suggest that during primary CMV infection of pregnant guinea pigs, the placenta not only serves as a reservoir for CMV but also acts to limit transmission of the virus to the fetus. 相似文献
7.
8.
S. Liechti-Gallati M. Koenig L. M. Kunkel D. Frey E. Boltshauser V. Schneider S. Braga H. Moser 《Human genetics》1989,82(4):343-348
Summary DNA from 80 Duchenne (DMD) and 15 Becker (BMD) index patients was analyzed with 12 genomic probes and the total cDNA. Deletions
were detected in 24 DMD (30%) and 10 BMD patients (67%) by genomic probes alone, mostly p20, pXJ, and/or pERT87. All deletions
were confirmed by cDNA probes, and an additional 29 DMD deletions were detected, resulting in a total of 63/95 deletions (66%).
The majority of the deletions are localized between kb 6.7 and 9.7 of the cDNA; a smaller group, between kb 0.5 and 3.5. Of
the deletions, 90% are detected by the three cDNA probes 1–2a, 7, and 8. This can be applied to strategies for carrier detection
and prenatal diagnosis. The order of 13 exon-containing HindIII fragments in the region between probes 7 and 9–10, where most of the deletions are found, could be defined. The deletion
patterns in DMD and BMD patients are different and well in accordance with the “reading frame theory” of Monaco and coworkers.
Thus our findings indicate that a DMD or BMD phenotype may be predicted according to the breakpoint position and the number
of deleted exons. 相似文献
9.
Actions of Excitatory Amino Acids on Somatostatin Release from Cortical Neurons in Primary Cultures 总被引:1,自引:1,他引:0
L-Glutamate, N-methyl-D-aspartic acid (NMDA), quisqualate, and kainate were found to increase endogenous somatostatin release from primary cultures of rat cortical neurons in a dose-dependent manner. The rank order of potency calculated from the dose-response curves was quisqualate greater than glutamate = NMDA greater than kainate, with EC50 values of 0.4, 20, and 40 microM, respectively. Alanine, glutamine, and glycine did not modify the release of somatostatin. The stimulation of somatostatin release elicited by L-glutamate was Ca2+ dependent, was decreased by Mg2+, and was blocked by DL-amino-5-phosphonovaleric acid (APV) and thienylphencyclidine (TCP), two specific antagonists of NMDA receptors. The NMDA stimulatory effect was strongly inhibited by APV in a competitive manner (IC50 = 50 microM) and by TCP in a noncompetitive manner (IC50 = 90 nM). The release of somatostatin induced by the excitatory amino acid agonists was not blocked by tetrodotoxin (1 microM), a result suggesting that tetrodotoxin-sensitive, sodium-dependent action potentials are not involved in the effect. Somatostatin release in response to NMDA was potentiated by glycine, but the inhibitory strychnine-sensitive glycine receptor did not appear to be involved. Our data suggest that glutamate exerts its stimulatory action on somatostatin release essentially through an NMDA receptor subtype. 相似文献
10.
Heterotrimeric guanine nucleotide-binding regulatory proteins (G proteins) serve to transduce information from agonist-bound receptors to effector enzymes or ion channels. Current models of G protein activation-deactivation indicate that the oligomeric GDP-bound form must undergo release of GDP, bind GTP and undergo subunit dissociation, in order to be in active form (GTP bound subunits and free dimers) and to regulate effectors. The effect of receptor occupation by an agonist is generally accepted to be promotion of guanine nucleotide exchange thus allowing activation of the G protein. Recent studies indicate that transphosphorylation leading to the formation of GTP from GDP and ATP in the close vicinity, or even at the G protein, catalysed by membrane-associated nucleoside diphosphate kinase, may further activate G proteins. This activation is demonstrated by a decreased affinity of G protein-coupled receptors for agonists and an increased response of G protein coupled effectors. In addition, a phosphorylation of G protein subunits and consequent phosphate transfer reaction resulting in G protein activation has also been demonstrated. Finally, endogenously formed GTP was preferentially effective in activating some G proteins compared to exogenous GTR The aim of this report is to present an overview of the evidence to date for a transphosphorylation as a means of G protein activation (see also refs [1 and 2] for reviews). (Mol Cell Biochem 157: 593, 1996)Recipient of Servier Investigator Award 相似文献