全文获取类型
收费全文 | 77708篇 |
免费 | 318篇 |
国内免费 | 374篇 |
专业分类
化学 | 23924篇 |
晶体学 | 794篇 |
力学 | 6720篇 |
数学 | 31924篇 |
物理学 | 15038篇 |
出版年
2018年 | 10430篇 |
2017年 | 10257篇 |
2016年 | 6051篇 |
2015年 | 833篇 |
2014年 | 281篇 |
2013年 | 298篇 |
2012年 | 3753篇 |
2011年 | 10470篇 |
2010年 | 5614篇 |
2009年 | 6030篇 |
2008年 | 6566篇 |
2007年 | 8731篇 |
2006年 | 200篇 |
2005年 | 1289篇 |
2004年 | 1515篇 |
2003年 | 1957篇 |
2002年 | 999篇 |
2001年 | 241篇 |
2000年 | 287篇 |
1999年 | 150篇 |
1998年 | 189篇 |
1997年 | 142篇 |
1996年 | 195篇 |
1995年 | 114篇 |
1994年 | 78篇 |
1993年 | 93篇 |
1992年 | 54篇 |
1991年 | 65篇 |
1990年 | 52篇 |
1989年 | 60篇 |
1988年 | 61篇 |
1987年 | 58篇 |
1986年 | 58篇 |
1985年 | 48篇 |
1984年 | 46篇 |
1983年 | 38篇 |
1982年 | 42篇 |
1981年 | 42篇 |
1980年 | 49篇 |
1979年 | 44篇 |
1978年 | 34篇 |
1973年 | 25篇 |
1914年 | 45篇 |
1913年 | 40篇 |
1912年 | 40篇 |
1910年 | 24篇 |
1909年 | 41篇 |
1908年 | 40篇 |
1907年 | 32篇 |
1904年 | 28篇 |
排序方式: 共有10000条查询结果,搜索用时 0 毫秒
281.
Kalnina I Klimkane L Kirilova E Toma MM Kizane G Meirovics I 《Journal of fluorescence》2007,17(6):619-625
The fluorescent probe-aminoderivative of benzanthrone, ABM (developed at Riga Technical University, Riga, Latvia) was used
to characterize the membranes of lymphocytes of cancer patients: 46 patients with gastrointestinal diseases, 13 patients having
different primary localizations with massive metastases and intoxication. Patients were divided into three groups: (1) with
decreased fluorescence intensity, (2) normal fluorescence intensity, (3) increased fluorescence intensity. The lymphocytes
distribution among subsets differed between groups, in correspondence to the level of florescence intensity. Surgical treatment
affected the main immunological parameters and elevated the functional activity of lymphocytes. In the advanced tumors group,
fluorescence intensity correlates with the survival rate. Results suggest that determination of lymphocytes functional activity
by ABM can aid evaluation of the immune status in cancer patients. 相似文献
282.
The value of intrinsic chlorophyll fluorescence polarization, and the intensity in emission spectrum were investigated in
leaf segments of Alocasia macrorrhiza under several stress conditions including different temperatures (25–50°C), various concentrations of NaCl (0–250 mM), methyl
viologen (MV, 0–25 μM), SDS (0–1.0%) and NaHSO3 (0–80 μM). Fluorescence emission spectrum of leaves at wavelength regions of 500–800 nm was monitored by excitation at 436 nm.
The value of fluorescence polarization (P value), as result of energy transfer and mutual orientation between chlorophyll molecules, was determined by excitation at
436 nm and emission at 685 nm. The results showed that elevated temperature and concentrations of salt (NaCl), photooxidant
(MV), surfactant (SDS) and simulated SO2 (NaHSO3) treatments all induced a reduction of fluorescence polarization to various degrees. However, alteration of the fluorescence
spectrum and emission intensity of F685 and F731 depended on the individual treatment. Increase in temperature and concentration of NaHSO3 enhanced fluorescence intensity mainly at F685, while an increase in MV concentration led to a decrease at both F685 and F731. On the contrary, NaCl and SDS did not cause remarkable change in fluorescence spectrum. Among different treatments, the
negative correlation between polarization and fluorescence intensity was found with NaHSO3 treatments only. We concluded that P value being measured with intrinsic chlorophyll fluorescence as probe in leaves is a susceptible indicator responding to
changes in environmental conditions. The alteration of P value and fluorescence intensity might not always be shown a functional relation pattern. The possible reasons of differed
response to various treatments were discussed. 相似文献
283.
The difference in time-resolved fluorescence spectrum between the cortical sarcoma and the adjacent normal tissue was studied
in both experimental and theoretical ways. The Clinical data were obtained in vivo using a time-resolved fluorescence spectrometer employing a single fiber-optic probe for excitation and detection. Tissue
was modeled as s-180 sarcoma tumor surrounded with normal muscle and was mediated by the Palladium-porphyrin photosensitizer
(Pd-TCPP). The emitted fluorescence was considered as arising from the tumor tissue or the normal muscle, due to the presence
of the photosensitizer. A computational code which could simulating time-resolved fluorescence emission was presented and
applied to comparing fluorescence decay of photosensitizer in different stages of tumor growth. In this code the different
stages of the tumor was modeled through changing the time τ, the delay of the fluorescence photon emission and z
max, the thickness of the tumor. It was found in the in vivo experiment that the fluorescence from tumor tissue decayed more quickly than from the adjacent normal muscle. For the ten
rats in the first experiment day, the mean decay constant of tumor T
s and normal tissue T
n were 554 and 526 μs, respectively. And T
s increased with the tumor growth, from 554 μs in the first day to 634 μs in the eighth day while T
s kept steady. It was believed that the more adequate oxygen supplied by the normal tissue can more effectively quench the
fluorescence and in the normal tissue the photosensitizer lifetime is smaller. As a result the simulated time-resolved fluorescence
spectrum of normal tissue showed more quickly decay. And the thickness of the tumor can also delay the fluorescence decay.
Both the experimental and simulated results indicated that the germination of the tumor would increase the decay constant
of the time-resolved fluorescence spectrum. So decay constant of the tumor tissue spectrum should be larger than that of adjacent
normal tissue for the reason of hypoxia and overgrouth. This fact could be of use in the tumor diagnoses. 相似文献
284.
Poly(ethylene glycol) (PEG) hydrogels have been used to encapsulate fluorescently labeled molecules in order to detect a variety
of analytes. The hydrogels are designed with a mesh size that will retain the sensing elements while allowing for efficient
diffusion of small analytes. Some sensing assays, however, require a conformational change or binding of large macromolecules,
which may be sterically prohibited in a dense polymer matrix. A process of hydrogel microporation has been developed to create
cavities within PEG microspheres to contain the assay components in solution. This arrangement provides improved motility
for large sensing elements, while limiting leaching and increasing sensor lifetime. Three hydrogel compositions, 100% PEG,
50% PEG, and microporated 100% PEG, were used to create pH-sensitive microspheres that were tested for response time and stability.
In order to assess motility, a second, more complex sensor, namely a FITC-dextran/TRITC-Con A glucose-specific assay was encapsulated
within the microspheres. 相似文献
285.
Agkisacutacin isolated from the venom of Agkistrodon acutus is a coagulation factor IX / coagulation factor X-binding protein with marked anticoagulant- and platelet-modulating activities.
Ca2+ ion-induced stabilization and refolding of Agkisacutacin have been studied by following fluorescent measurements. Ca2+ ions not only increase the structural stability of agkisacutacin against GdnHCl denaturation, but also induce its refolding.
The GdnHCl-induced unfolding of the apo-agkisacutacin and the purified agkisacutacin is a single-step process with no detectable
intermediate state. Ca2+ ions play an important role in the stabilization of the structure of agkisacutacin. Ca2+-stabilized agkisacutacin exhibits higher resistance to GdnHCl denaturation than the apo-agkisacutacin. It is possible to
induce refolding of the unfolded apo-agkisacutacin merely by adding 1 mM Ca2+ ions without changing the concentration of the denaturant. The kinetic result of Ca2+-induced refolding provides evidences for that agkisacutacin consists of at least two refolding phases and the first phase
of Ca2+-induced refolding should involve the formation of the compact Ca2+-binding site regions, and subsequently, the protein undergoes further conformational rearrangements to form the native structure. 相似文献
286.
Wang HQ Huang ZL Liu TC Wang JH Cao YC Hua XF Li XQ Zhao YD 《Journal of fluorescence》2007,17(2):133-138
Multicolor encoded beads were achieved by incorporating two color core-shell quantum dots (QDs) (CdSe/ZnS) to commercial polystyrene
(PS) beads. By controlling the concentration ratios of the two quantum dots (QDs) in doping solutions, a series of codes with
different intensity ratios were obtained. Based on the multiple encoded carboxylic modified polystyrene beads, fluorescent
dyes labeled antibodies were distinguished successfully on the beads’ surface. It suggests that the encoded beads from this
method have the practicability in biological applications and chemical analysis.
Hai-Qiao Wang and Zhen-Li Huang authors contribute equally to this work 相似文献
287.
A new anthracene-based fluorescent PET sensor 1 with a tridentate ionophore of amide/β-amino alcohol displays very good selectivity and sensitivity for Fe3+ (K
a = 1.6 × 103 M−1) and Hg2+ (K
a = 2.1 × 103 M−1) in CH3CN–H2O (3:7, v/v) with detection limit of 1 μM. More fluorescence enhancement was observed when 1 selectively detected Fe3+ or Hg2+ in CH3CN and its detection limit was up to 0.03 μM. 相似文献
288.
In this short letter, we describe the effects of low temperature on the Metal-Enhanced Fluorescence (MEF) phenomenon. Fluorophores
close to Silver Island Films (SiFs) show on average two- to ten-fold enhancements in their fluorescence signatures at room
temperature. However, at 77 K, we have observed that MEF is even more pronounced as compared to an identical glass control
sample. We also demonstrate that the further enhancements in MEF occur at low temperature over a range of visible wavelengths
for different fluorophores, for both SiFs and 20 nm surface deposited gold colloids. 相似文献
289.
Proteoliposomes carrying reconstituted yeast plasma membrane H+-ATPase in their lipid membrane or plasma membrane vesicles are model systems convenient for studying basic electrochemical
processes involved in formation of the proton electrochemical gradient (ΔμH
+) across the microbial or plant cell membrane. Δψ- and pH-sensitive fluorescent probes were used to monitor the gradients
formed between inner and outer volume of the reconstituted vesicles. The Δψ-sensitive fluorescent ratiometric probe oxonol
VI is suitable for quantitative measurements of inside-positive Δψ generated by the reconstituted H+-ATPase. Its Δψ response can be calibrated by the K+/valinomycin method and ratiometric mode of fluorescence measurements reduces undesirable artefacts. In situ pH-sensitive fluorescent probe pyranine was used for quantitative measurements of pH inside the proteoliposomes. Calibration
of pH-sensitive fluorescence response of pyranine entrapped inside proteoliposomes was performed with several ionophores combined
in order to deplete the gradients passively formed across the membrane. Presented model system offers a suitable tool for
simultaneous monitoring of both components of the proton electrochemical gradient, Δψ and ΔpH. This approach should help in
further understanding how their formation is interconnected on biomembranes and even how transport of other ions is combined
to it. 相似文献
290.
Carbon nanostructures (CNS) with high electrical conductivity and unique branched structure of carbon nanotubes combined with NiO nanofibers (NFs) were used as anode for lithium-ion batteries. CNS works as a framework substrate for the anodic conversion reaction of nickel oxide (NiO). Electrochemical performance and behavior of CNS/NiO anodes is compared with the conventional carbon (C)/NiO anodes. CNS/NiO NF-based anode retains high specific capacity under different current densities compared to C/NiO anode. Moreover, specific capacity as high as 450 mAh/g for CNS/NiO NF anode is observed compared to only 90 mAh/g for C/NiO NFs using a current density of 500 mA/g after 500 cycles. This improved performance is attributed to the highly conductive network of CNS leading to efficient charge transfer. The high porosity, electrical conductivity as well as the branched and networked nature of CNS reveal to be of critical importance to allow the electrochemical conversion reactions. 相似文献