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91.
本文合成了苯甲酰三氟丙酮(L)和三苯基氧膦(TPPO)、联吡啶(Bipy)、邻菲罗啉(phen)、四甲基氢化铵(NMe4OH)与稀土Y、La、Eu、Tb离子的混合型配合物。测定配合物的H1NMR谱及质谱,并对测定结果进行了分析。 相似文献
92.
室温,氮气氛下,铜(Ⅱ)盐和双二苯基膦戊烷(dppp5)在溶液中通过还原取代反应合成了8种铜(Ⅰ)配合物(1.[Cu(dppp5)]2(BF4)2,2.[Cu2(dppp5)2(C8H3O2SF3)2],3.[Cu2(dppp5)3](CCl3COO)2,4.[CuBr(dppp5)]2,5.[Cu2(dppp5)Cl2],6.[Cu2(dppp5)3](CH3COO)2,7.[Cu(dppp5)(NO3)],8.[Cu2(dppp5)3](ClO4)2)。通过元素分析、红外光谱、热重、摩尔电导测定对其进行表征,表明这是一种行之有效的有机膦配合物的合成方法。 相似文献
93.
以满江红鱼腥藻(Aac)提取总DNA为模板,通过PCR技术,扩增得到其谷氨酰胺合成酶基因(glnA)上游区.经酶切得到409bp的片段,并将其连接到pBluescriptⅡks+上测序.将测序结果与Anabaena7120调控序列比较,有982%的同源性.在上游调控中也具有niflike和E.colilike启动子,值得注意的是,调节蛋白VF1的结合位点正好位于niflike启动子上.所克隆的片段不但对蓝藻固氮、泌氨的基因调控研究具有意义,也对表达载体的构建具有实用价值. 相似文献
94.
阳离子交换树脂催化合成1—萘乙酸甲酯的研究 总被引:6,自引:0,他引:6
本文研究了用强酸性阳离子交换树脂作催化剂,1—萘乙酸和甲醇直接酯化合成1—萘乙酸甲酯的反应。考察了催化剂用量,反应物料配比,反应时间等因素对产率的影响,通过正交实验,找到了较佳反应条件:当催化剂用量为反应液的3%,醇酸摩尔比为20~30,在回流温度下反应4小时,酯的收率>92%,纯度>99%。该法工艺简单,操作方便,无三废污染,适合工业化生产。 相似文献
95.
1,6—二磷酸果糖制备研究:Ⅰ.菌种的筛选及培养条件 总被引:3,自引:2,他引:1
介绍了1,6-二磷酸果糖产生菌的筛选和最佳培养条件的确定,在所筛选的菌种中9518、9519号菌株均具较高的产1,6-二磷酸果糖酶系活力。其最佳培养条件为:培养温度28℃,pH6.5。 相似文献
96.
Semiconductor(ZnxCd1−x
S) doped silica glasses were prepared by Sol-Gel process andin situ growth technique. The structure of the materials was characterized by X-ray diffraction technique, the particle size of semiconductor
crystallites from X-ray patterns was estimated less than 10 nm. From absorption spectra, it is obtained that the absorption
edges shifted to short wavelength direction when Zn contents increased, and the absorption edge can be adjusted from 2.46
eV to 2.96 eV by controlling Zn contents. The third-order nonlinear optical susceptibility was studied at 532 nm with 8 ns
pulse laser by degenerate four wave mixing (DFWM) technique. 相似文献
97.
Cytosine deaminase gene ofEscherichia coli strain H-30 was cloned, and its initiation codon of ‘GTG’ was mutated to ‘ATG’ by PCR. Prokaryotic recombinant expression
vector pBV220-CD was constructed. Clone with high enzyme activity were selected by detecting their specific activity of cytosine
deaminase. 5-FC(5-FC, 5-fluorocytosine) could induce the lethal toxicity to cells containing active CD gene. DNA sequence
analysis indicated that there were 16 altered bases and 5 of them resulted in the alteration of amino acids in predicted peptide
by comparing DNA sequence of the clone H-30-CD-11 with high enzyme activity with CD gene reported in Gene Bank. 相似文献
98.
Colony-stimulating factor-1 (CSF-1), which is necessary for cell proliferation and differentiation, regulates both immediate
and delayed early responses throughout G1 phase. The binding of CSF-1 to its receptor (CSF-1R) triggers phosphorylation of
the receptor and its intrinsic tyrosine kinase. The activated receptor binds directly to cytoplasmic effector proteins, which
induce multiple-signal transduction pathways. CSF-1 can induce the c-myc gene expression via Ras and Ets-related proteins.
The expression of c-fos/jun family genes is also targeted following the activation of Ras. CSF-1R activates STAT1 and STAT3
to participate in signaling, but JAKs do not appear to contribute to signaling by CSF-1R. CSF-1R activates PI3-kinase, and
PI3-ki can interact with downstream proteins by the MAPKK-related pathway independent of Ras/Raf. PC-PLC can enforce signaling
in response to CSF-1. Furthermore, the turnover and dephosphorylation by the phosphatase SHPTP1 of CSF-1R are the major mechanism
in the negative regulation of signaling by CSF-1R 相似文献
99.
《科学通报(英文版)》1998,43(5):363-363
During the long period of time when people have been seeking for an effective therapeutic method for PD, the gene therapy has shown greater and greater advantages over other methods. It can be performed mainly in two ways: ex vivo and in vivo. With the former, TH gene as well as some neurotrophic factor genes (such as GDNF, BNDF genes) can be invited to some cell lines or primary cells thus forming engineered cells and then implanting them into brain. While with the latter, viral vectors including HSV-1, Ad, AAV that can be utilized to construct recombinant viruses, or non-virus vectors can be used to delived DNA into brain directly. The present review summarizes the recent research advances in the gene therapy for PD, and it is reasonable for us to predict a notable progress in prevention and treatment for PD in the next decade. 相似文献
100.