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81.
草鱼出血病病毒多肽的免疫原性 总被引:10,自引:1,他引:9
采用中和试验比较了草鱼出血病病毒GCHV873的11个多肽的免疫原性,确定了主要中和抗原。纯化的单个病毒多肽免疫家兔获得抗血清,多太VP1、VP5、VP6和VP9的抗血清具有中和效价,而VP2、VP3、VP4、VP8、VP10和VP11则不能诱生中和抗体。其中VP5的抗血清中和效价最高,因此,VP6极可能是病毒多肽中的主要中和抗原。 相似文献
82.
本文设计一种由胶原和高分子聚合物组成的新型生物一人工复合血管。其研制过程是将包绕有聚酯网的硅胶棒埋入羊的皮下组织,再将形成的经聚酯网为支架的胶原管经醛化处理。作者通过肉眼和SEM观察提出了研制生物——人工复合血管的要点:聚酯网网孔要合适,其与硅胶棒的间隙要恰当,理化处理方法更要选择好。 相似文献
83.
蛋白激酶C在血小板聚集中的作用 总被引:3,自引:0,他引:3
利用 ̄(32)P-NaH2PO4标记猪血小板,以蛋白激酶C的40kD底物为蛋白激活的标志.用血小板激动剂在聚集浓度范围内处理血小板,结果表明,除了不能使猪血小板聚集的肾上腺素外,凝血酶等激动剂都使血小板40kD底物蛋白磷酸化明显增加,同时38kD,26kD蛋白质磷酸化也明显增加,且40kD底物磷酸化与血小板聚集有平行增加关系.蛋白激酶C在血小板聚集中可能起着重要的调节作用。 相似文献
84.
将编码人单核细胞趋化蛋白-1(MCP-1)的基因亚克隆到大肠杆菌表达载体pEX31A中,在大肠杆菌中表达出MS2/MCP-1融合蛋0白,该表达产物约占菌体总蛋白的15%左右,Westernblot检测表明,表达产物可与MCP-1抗体特异反应。采用琼脂糖平板法进行活性测定表明,表达产物具有明显的单核细胞趋化活性,说明N端融合一段细菌蛋白对MCP-1有无趋化活性可能没有影响。 相似文献
85.
We determined the nucleotide sequence of a DNA fragment which contains the replication region of pMSC262, a Mycobacterium scrofulaceum plasmid used to construct the Mycobacterium-Escherichia coli shuttle vector. The complete sequence of the fragment contained 2,504 bp with an overall G+C content of 69.8%. By deletion analysis, we found that the minimum length required for plasmid replication in M. bovis BCG was about 1.6 kb. Within this region, several open reading frames (ORFs) and a putative replication origin (ori) were identified by computer analysis. One of the ORFs, ORF2, which encodes a putative 28.9-kDa basic protein with characteristics of DNA-binding proteins, appeared to be involved in replication of the plasmid in BCG. By separation of ORF2 and the putative ori region, it was revealed that the relative locations of ORF2 and the putative ori region are likely important for replication in BCG. No DNA or amino acid homologies were found between this replication region and that of pAL5000, another mycobacterial plasmid used for vector plasmid construction. In addition, we found that this replicon did not lead to replication in E. coli and was compatible in BCG with pAL5000-derived vector plasmid pYUB75 (R. G. Barletta, D. D. Kim, S. B. Snapper, B. R. Bloom, and W. R. Jacobs, J., J. Gen. Microbiol. 138:23-30, 1992). 相似文献
86.
A. Kanamori K. Kitajima Y. Inoue S. Inoue Z. Xulei C. Zuber J. Roth J. Ye F. A. Troy II 《Histochemistry and cell biology》1994,101(5):333-340
Two particular types of sialoglycoproteins have been detected in fish: polysialoglycoproteins containing 28-linked polysialic acid (8Neu5Gc2)
n
present in unfertilized Salmonidae fish eggs, and glycoproteins bearing oligo/polymers of deaminated neuraminic acids (KDN) found in the vitelline envelope of the eggs and ovarian fluid. We report the preparation and characterization of a monoclonal antibody specifically recognizing oligo/polymers of KDN sequences in glycoproteins and its application in immunohistochemistry. Fusion of spleen cells from a BALB/c mouse immunized with a KDN-rich glycoprotein (KDN-gp) containing (8KDN2)
n
6(KDN23Gal13GlNAc13) GalNAc1 residues, with mouse myeloma cells yielded a hybrid cell line producing a monoclonal antibody that bound to KDN-gp, but not to KDN-gp depleted of KDN residues. The specificity of the monoclonal antibody, designated mAb.kdn8kdn, was determined by an enzyme-linked immunosorbent assay using KDN-gp samples that varied in KDN content. These antigens were prepared by the selective removal of KDN residues from the native KDN-gp. The mAb.kdn8kdn reacted most strongly with the intact KDN-gp and less strongly with KDN-gp samples containing decreased numbers of KDN residues. The mAb.kdn8kdn was shown specifically to recognize the 28-linked oligo/polyKDN sequences, (8KDN2)
n
, and to be able to distinguish specifically (8KDN2)
n
chains from (8Neu5Ac2)
n
and (8Neu5Gc2)
n
chains. The antibody was used successfully for the immunohistochemical detection of reactive KDN epitopes in sections of paraffin embedded rat pancreas. Several controls verified the specificity of the immunohistochemical staining, thus providing the first demonstration of (8KDN2)
n
sequences in a mammalian tissue. The mAb.kdn8kdn can now be used to search further for glycoconjugates containing (8KDN2)
n
chains and will facilitate studies on their biosynthesis, intracellular localization and function. 相似文献
87.
华中冬青化学成分的研究 总被引:11,自引:0,他引:11
从华中冬青(Ilex centrochinensis S.Y.Hu)的叶片分离到9 种黄酮类化合物:1 种新化合物鉴定为3,5,5,7-四羟基二氢黄酮,命名为华中冬青黄酮(Ⅰ);8 种化合物鉴定为柚皮素(Ⅱ)、橙皮素(Ⅲ)、异樱花素(Ⅳ)、枸柑甙(Ⅴ)、橙皮甙(Ⅵ)、洋芹素(Ⅶ)、紫云英甙(Ⅷ)和野漆树甙(Ⅸ)。它们皆首次从该植物分得 相似文献
88.
芦苇耐盐变异植株及其细胞学鉴定 总被引:5,自引:0,他引:5
用甲基磺酸乙酯(EMS)处理芦苇(Phragm itescom m unis Trin.)胚性愈伤组织。从处理后的愈伤组织诱导获得芦苇耐盐变异植株R5002-12。变异植株能在含有1% NaCl的MS培养基上生长。细胞学检查变异植株是混倍体,染色体数目变异范围在100至33 之间。分蘖植株具有相似的形态学及染色体变异特性 相似文献
89.
刺果番荔枝中的番荔枝内酯 总被引:4,自引:0,他引:4
从刺果番荔枝(Annona m uricata L.)的种子中分离到3 个单四氢呋喃型番荔枝内酯类化合物,用波谱方法鉴定为海南哥纳香甲素(how iicin A, S13)、乙素(how iicin B, S5)和新化合物4-去氧海南哥纳香乙素(4-desoxyhow iicin B, S2)。 相似文献
90.
A simple and efficient method for DNA extraction from grapevine cultivars andVitis species 总被引:3,自引:0,他引:3
Muhammad A. Lodhi Guang-Ning Ye Norman F. Weeden Bruce I. Reisch 《Plant Molecular Biology Reporter》1994,12(1):6-13
A quick, simple, and reliable method for the extraction of DNA from grapevine species, hybrids, andAmpelopsis brevipedunculata (Vitaceae) has been developed. This method, based on that of Doyle and Doyle (1990), is a CTBA-based extraction procedure
modified by the use of NaCl to remove polysaccharides and PVP to eliminate polyphenols during DNA purification. The method
has also been used successfully for extraction of total DNA from other fruit species such as apple (Malus domestica), apricot (Prunus armeniaca), cherry (Prunus avium), peach (Prunus persica), plum (Prunus domestica), and raspberry (Rubus idaeus). DNA yield from this procedure is high (up to 1 mg/g of leaf tissue). DNA is completely digestible with restriction endonucleases
and amplifiable in the polymerase chain reaction (PCR), indicating freedom from common contaminating compounds. 相似文献