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81.
中华金叶榆子代苗光合特性及叶片呈色机制探讨 总被引:1,自引:0,他引:1
中华金叶榆是普通白榆的天然黄叶突变体,黄叶性状在子代中可稳定遗传,自由授粉子一代出现黄绿性状分离。该研究以中华金叶榆子代黄叶苗和绿叶苗为试验材料,从生长速率、叶片色素含量、光合特性、叶绿素荧光及叶绿体超微结构等方面对黄叶苗的光合特性和叶片呈色机制进行了探讨。结果显示:(1)黄叶苗生长缓慢,净光合速率(12.5μmol·m-2·s-1)显著低于绿叶苗(17.5μmol·m-2·s-1),而蒸腾速率、气孔导度和叶片温度显著高于绿叶苗。(2)黄叶苗和绿叶苗叶片的光合色素种类基本相同,但黄叶苗的叶绿素a、叶绿素b、类胡萝卜素和花青素4种主要色素含量始终低于绿叶苗且相对稳定,各种色素含量在生育期内不同月份略有变化,类胡萝卜素含量始终低于叶绿素含量。(3)黄叶苗叶片光系统Ⅱ(PSⅡ)发育不完全,电子传递效率低。(4)黄叶苗叶绿体内膜系统发育紊乱,基粒垛叠失败。研究表明,中华金叶榆子代黄叶苗叶绿体内膜系统发育缺陷,基粒片层垛叠失败,进而多种色素含量大幅下降,光合系统发育不完全,致使其叶片呈现黄色、光合性能下降、植株生长缓慢。 相似文献
82.
为研究不同生理环境对蛛丝蛋白组装及成丝的影响,首次以MiSp序列为对象,研究其NTR1SR2CT重组模块在不同种类(浓度)盐离子条件下的聚集和成纤维特性及其在成纤维过程中二级结构的变化。基于大腹园蛛MiSp全长序列构建NTR1SR2CT模块,并在大肠杆菌Escherichia coli BL21中成功表达。借助8 mol/L尿素裂解包涵体进行变性纯化得到NTR1SR2CT重组蛋白。NTR1SR2CT重组蛋白二级结构主要为无规则卷曲(Random coil)或α螺旋(Helix),在自然成丝及冻干过程中部分random coil或helix转变为β折叠(β-sheet),甲醇能促进该转变过程。另外,钾离子和磷酸根离子有利于NTR1SR2CT重组蛋白聚集从而促进丝纤维的形成。研究结果为成丝机理研究奠定了基础,同时也为工业化生产高品质的蛛丝纤维提供了条件。 相似文献
83.
84.
《DNA Repair》2014
Cancer risk and radiation sensitivity are often associated with alterations in DNA repair, cell cycle, or apoptotic pathways. Interindividual variability in mutagen or radiation sensitivity and in cancer susceptibility may also be traced back to polymorphisms of genes affecting e.g. DNA repair capacity. We studied possible associations between 70 polymorphisms of 12 DNA repair genes with basal and initial DNA damage and with repair thereof. We investigated DNA damage induced by ionizing radiation in lymphocytes isolated from 177 young lung cancer patients and 169 cancer-free controls. We also sought replication of our findings in an independent sample of 175 families (in total 798 individuals). DNA damage was assessed by the Olive tail moment (OTM) of the comet assay. DNA repair capacity (DRC) was determined for 10, 30 and, 60 min of repair.Genes involved in the single-strand-repair pathway (SSR; like XRCC1 and MSH2) as well as genes involved in the double-strand-repair pathway (DSR; like RAD50, XRCC4, MRE11 and ATM) were found to be associated with DNA damage. The most significant association was observed for marker rs3213334 (p = 0.005) of XRCC1 with basal DNA damage (B), in both cases and controls. A clear additive effect on the logarithm of OTM was identified for the marker rs1001581 of the same LD-block (p = 0.039): BCC = −1.06 (95%-CI: −1.16 to −0.96), BCT = −1.02 (95%-CI: −1.11 to −0.93) and BTT = −0.85 (95%-CI: −1.01 to −0.68). In both cases and controls, we observed significantly higher DNA basal damage (p = 0.007) for carriers of the genotype AA of marker rs2237060 of RAD50 (involved in DSR). However, this could not be replicated in the sample of families (p = 0.781). An alteration to DRC after 30 min of repair with respect to cases was observed as borderline significant for marker rs611646 of ATM (involved in DSR; p = 0.055), but was the most significant finding in the sample of families (p = 0.009).Our data indicate that gene variation impacts measurably on DNA damage and repair, suggesting at least a partial contribution to radiation sensitivity and lung cancer susceptibility. 相似文献
85.
86.
R. G. Ovodova V. V. Golovchenko A. S. Shashkov S. V. Popov Yu. S. Ovodov 《Russian Journal of Bioorganic Chemistry》2000,26(10):669-676
A pectic polysaccharide, lemnan, was isolated from freshly collected duckweedLemna minor L. Its sugar chain was shown to be mainly composed of the residues ofD-galacturonic acid (64%), galactose, arabinose, xylose, andD-apiose, a branched chain sugar. The high content ofD-apiose (25%) indicated that lemnan is an apiogalacturonan type pectin similar to zosteran, a pectic polysaccharide from a
sea phanerogam of the Zosteraceae family. The results of partial acidic hydrolysis, pectinase digestion, and NMR studies of
lemnan demonstrated that its macromolecule contains regions of the linear α-1,4-D-galacturonan and branched apiogalacturonan. The side chains of apiogalacturonan were found to be formed of single and 1,5-linked
residues ofD-apiofuranose attached to 2- and 3-positions of theD-galacturonic acid residues of the apiogalacturonan backbone. Lemnan was shown to exhibit an immunomodulatory effect activating
the system of phagocytosis. 相似文献
87.
不同育苗方式对移栽后侧柏和白榆幼苗根系生长的影响 总被引:1,自引:0,他引:1
不同类型苗木,具有不同的根系结构特征,其根系结构也将影响林木的生长和恢复生态系统的稳定性。以侧柏和白榆为研究对象,对移栽18个月后的种基盘苗与营养钵苗根系的生长进行了调查。结果表明:侧柏种基盘苗的总根长和平均直径比营养钵苗分别增加了316.20 cm和0.05mm,白榆苗则分别增加了651.54 cm和0.88mm。侧柏和白榆种基盘苗的根系表面积比营养钵苗分别增加了40.05%和73.04%。侧柏种基盘苗的根系总体积与营养钵苗的差异不显著,而白榆种基盘苗的根系总体积则比营养钵苗增加了54.70%。侧柏和白榆营养钵苗的一级侧根数量大于种基盘苗,增幅分别为42.31%和30.65%。对于侧柏来说,营养钵苗的根尖总数比种基盘苗的增加324个,但白榆苗差异不显著。各种处理的幼苗总根长与根系表面积都有显著相关性,但与根体积不具有显著相关性。营养钵苗的根系平均直径和根尖数量具有相对独立性,而种基盘的根系平均直径与总根长以及根体积均表现为显著相关。种基盘苗能提高侧柏、白榆幼苗的根冠比,促进幼苗株高、地径和主根的生长。采用种基盘苗进行植被恢复,由于其具有较大的根表面积和根长度,林木便具有了较大的吸收水分和营养的能力,以及较高的固结表层土壤能力。 相似文献
88.
89.
长序榆是我国二级重点保护的濒危植物,对研究榆属、榆科植物的系统发生有重要意义,并且具有潜在的经济价值。研究长序榆的生境特点,对该种的引种、科学保护有重大意义,通过对分布在我国的长序榆近两年的踏查发现,长序榆主要集中在我国的安徽、浙江、江西和福建等省,长序榆生境已经严重片段化,自然干扰和人为干扰是造成其濒临灭绝的主要原因。长序榆多分布在海拔600—900 m的阳坡或半阳坡上,其中最大的种群分布在浙江开化和遂昌,分布区的特殊地势使其成为长序榆的冰期避难所。对18项生物学、生态学指标的主成分分析结果表明,影响长序榆生存的主要环境因子是:光照、土壤养分、坡向和海拔。对浙江松阳、江西武宁和福建南平数量极少的种群需优先进行迁地保护,积极引种栽培;而对于安徽歙县、浙江临安、开化和遂昌等大种群分布区,应该扩大核心保护区面积,避免人为破坏。 相似文献
90.
Raitis Peculis Ilze Konrade Elina Skapare Davids Fridmanis Liene Nikitina-Zake Aivars Lejnieks Valdis Pirags Maija Dambrova Janis Klovins 《Gene》2013
The glyoxalase system and its main enzyme, glyoxalase 1 (GLO1), protect cells from advanced glycation end products (AGEs), such as methylglyoxal (MG) and other reactive dicarbonyls, the formation of which is increased in diabetes patients as a result of excessive glycolysis. MG is partly responsible for harmful protein alterations in living cells, notably in neurons, leading to their dysfunction, and recent studies have shown a negative correlation between GLO1 expression and tissue damage. Neuronal dysfunction is a common diabetes complication due to elevated blood sugar levels, leading to high levels of AGEs. The aim of our study was to determine whether single nucleotide polymorphisms (SNPs) in the GLO1 gene influence activity of the enzyme. In total, 125 healthy controls, 101 type 1 diabetes, and 100 type 2 diabetes patients were genotyped for three common SNPs, rs2736654 (A111E), rs1130534 (G124G), and rs1049346 (5′-UTR), in GLO1. GLO1 activity was determined in whole blood lysates for all participants of the study. 相似文献