首页 | 本学科首页   官方微博 | 高级检索  
文章检索
  按 检索   检索词:      
出版年份:   被引次数:   他引次数: 提示:输入*表示无穷大
  收费全文   20969篇
  免费   2067篇
  国内免费   2223篇
  2024年   56篇
  2023年   235篇
  2022年   486篇
  2021年   893篇
  2020年   697篇
  2019年   855篇
  2018年   893篇
  2017年   699篇
  2016年   911篇
  2015年   1302篇
  2014年   1565篇
  2013年   1709篇
  2012年   2001篇
  2011年   1778篇
  2010年   1245篇
  2009年   971篇
  2008年   1209篇
  2007年   1072篇
  2006年   903篇
  2005年   842篇
  2004年   789篇
  2003年   781篇
  2002年   719篇
  2001年   404篇
  2000年   329篇
  1999年   335篇
  1998年   209篇
  1997年   158篇
  1996年   129篇
  1995年   115篇
  1994年   119篇
  1993年   71篇
  1992年   84篇
  1991年   79篇
  1990年   62篇
  1989年   54篇
  1988年   51篇
  1987年   32篇
  1986年   46篇
  1985年   32篇
  1984年   35篇
  1983年   20篇
  1982年   24篇
  1981年   19篇
  1979年   13篇
  1975年   13篇
  1973年   21篇
  1972年   12篇
  1966年   12篇
  1958年   13篇
排序方式: 共有10000条查询结果,搜索用时 437 毫秒
81.
采用 52℃下加热 6 min,后经 DEAE- 52、Sephacryls S- 2 0 0和 Q- Sepharose等柱层析方法 ,分离纯化了棕色固氮菌 (Azotobacter vinelandii)缺失 nif Z基因突变种固氮酶 Mo Fe(Δnif Z Mo Fe)蛋白 ,其纯度达到电泳纯。Δnif Z Mo Fe蛋白的固氮活性为 2 83nmol C2 H2 还原 / (min·mg蛋白 ) ,远低于野生种 Mo Fe蛋白。Δnif Z Mo Fe蛋白对氧更敏感 ;热稳定性略低于野生种。Δnif Z Mo Fe蛋白的可见光吸收光谱与野生种 Mo Fe蛋白极为相似。其圆二色谱和磁圆二色谱在 450~ 550 nm与野生种 Mo Fe蛋白显著不同 ,表明其 P- cluster及其周围环境与野生种 Mo Fe蛋白有所差异。这亦可能是造成缺失 nif Z突变种 Mo Fe蛋白固氮活性低的原因。  相似文献   
82.
紫竹梅雄蕊毛细胞发育过程中胞间连丝超微结构的变化   总被引:6,自引:0,他引:6  
紫竹梅(Setcreasea purpurea)雄蕊毛细胞间的胞间连丝随着细胞的生长、发育、衰老而呈现动态变化的过程.花蕾和开放花的雄蕊毛细胞间的胞间连丝,具备胞间连丝的一般结构,直径约50 nm .衰老花雄蕊毛细胞间的胞间连丝拓宽,内部结构逐步降解、撤离,呈开放式通道,直径约100 nm . 在胞间连丝的动态开放过程中,细胞内的细胞器也发生相应变化. 对胞间连丝形成开放性通道及其机理进行了讨论  相似文献   
83.
从每公斤萌发24h的玉米胚丙酮粉中可提纯得63mg的钙调素(CaM),这是目前从每公斤植物材料中所提纯得CaM的最高记录。对其理化性质的研究表明,玉米胚CaM 有较高的生物学活性,能较好地激活磷酸二酯酶,其紫色吸收光谱,SDS-PAGE电泳行为及氨基酸组成与其它的植物CaM相似。上述结果表明玉米胚是1个提取植物CaM相似。上述结果表明玉米胚是1个提取植物CaM的适宜材料。  相似文献   
84.
Akr1p, which contains six ankyrin repeats, was identified during a screen for mutations that displayed synthetic lethality with a mutant allele of the bud emergence gene BEM1. Cells from which AKR1 had been deleted were alive but misshapen at 30 degrees C and inviable at 37 degrees C. During a screen for mutants that required one or more copies of wild-type AKR1 for survival at 30 degrees C, we isolated mutations in GPA1, which encodes the G alpha subunit of the pheromone receptor-coupled G protein. (The active subunit of this G protein is G beta gamma, and G alpha plays an inhibitory role in G beta gamma-mediated signal transduction.) AKR1 could serve as a multicopy suppressor of the lethality caused by either loss of GPA1 or overexpression of STE4, which encodes the G beta subunit of this G protein, suggesting that pheromone signaling is inhibited by overexpression of Akr1p. Mutations in AKR1 displayed synthetic lethality with a weak allele of GPA1 and led to increased expression of the pheromone-inducible gene FUS1, suggesting that Akr1p normally (and not just when overexpressed) inhibits signaling. In contrast, deletion of BEM1 resulted in decreased expression of FUS1, suggesting that Bem1p normally facilitates pheromone signaling. During a screen for proteins that displayed two-hybrid interactions with Akr1p, we identified Ste4p, raising the possibility that an interaction between Akr1p and Ste4p contributes to proper regulation of the pheromone response pathway.  相似文献   
85.
Kobayashi M  Matoh T  Azuma J 《Plant physiology》1996,110(3):1017-1020
Polysaccharide moiety of the boron-polysaccharide complex (T. Matoh, K. Ishigaki, K. Ohno, J. Azuma [1993] Plant Cell Physiol 34: 639-642) isolated from radish (Raphanus sativus) roots has been shown to be rhamnogalacturonan II by glycosyl-linkage analysis and the presence of diagnostic monosaccharides, including apiose, aceric acid, 2-O-methylfucose, and 3-deoxy-D-manno-2-octulosonic acid. Removal of boron from the complex reduced the molecular weight by one-half without causing a significant increase in the number of reducing end groups, indicating that boron, as boric acid, links two rhamnogalacturonan II chains together to form the boron-polysaccharide complex.  相似文献   
86.
While antibiotics are broadly used in dental and medical therapy, little attention has been directed towards the potential toxic side effects of antibiotics on tissue regeneration. Here we examined the effect of a quinolone antibiotic, pefloxacin (Rhone Poulenc) on rat parotid gland responses to chronic isoproterenol treatment. Groups of rats received injections of isoproterenol to induce glandular growth, saline (controls), pefloxacin, or isoproterenol and pefloxacin in combination. Parotid gland weight decreased significantly after pefloxacin treatment for 7 days as well as inhibiting glandular enlargement provoked by isoproterenol. The same trend was observed for the rates of DNA synthesis, with the incorporation of [3H]-thymidine in isoproterenol/pefloxacin-treated rats reduced to 49% of isoproterenol treatment alone levels. Saline-treated animals were 42% of the rate of [3H]-thymidine incorporation into DNA observed in isoproterenol treated rats. While isoproterenol treatment increased steady-state mRNA levels for fos, jun, myc, src, c-erbB-2, ras and topo II, inclusion of pefloxacin with the isoproterenol regimen blocked these increases. Pefloxacin treatment by itself did not alter proto-oncogene mRNA levels in the parotid gland. Glandular amylase activity was decreased in the pefloxacin treated group, while the combination of isoproterenol with pefloxacin did not decrease glandular amylase levels to the extent of that observed with -agonist treatment alone. In acute experiments, pefloxacin significantly decreased the volume of saliva secreted by the parotid gland. These results suggest that quinolone-based antibiotics disturb the secretory function of the parotid gland and can inhibit cell proliferation and regeneration. (Mol Cell Biochem 165: 55–63, 1996)  相似文献   
87.
部分酶解酵母高效电击转化研究   总被引:2,自引:0,他引:2  
以酵母质粒YCp50为外源DNA,电击转化部分酶解酵母宿主菌AB1380,转化效率稳定在10~6转化子/μg质粒DNA左右,比不酶解酵母或酵母原生质球作受体的电击转化效率高一个数量级以上,也比PEG介导的酵母原生质球转化高3~5倍,而且适合于大片段DNA如水稻YAC分子的转化。达最佳转化时的有关技术参数为:新接菌种通气培养至细胞密度1×10~8~1.5×10~8个/ml;转化时细胞密度控制在1×10~9~1.5×10~9个/ml;每毫升酶解缓冲液加15u溶菌酶(lyticase),30℃下处理酵母5min进行部分酶解;电击时,电场设置在6.25kV/cm、电容25μF,电击后直接铺板。  相似文献   
88.
89.
We have examined the structure and chromatin organization of telomeres in Nicotiana tabacum. In tobacco the blocks of simple telomeric repeats (TTTAGGG)n are many times larger than in other plants, e.g., Arabidopsis thatiana or tomato. They are resolved as multiple fragments 60–160 kb in size (in most cases 90–130 kb) on pulsed-field gel electrophoresis (PFGE) of restriction endonuclease-digested DNA. The major subtelomeric repeat of the HRS60 family forms large homogeneous blocks of a basic 180 by motif having comparable lengths. Micrococcal nuclease (MNase) cleaves tobacco telomeric chromatin into subunits with a short repeat length of 157±5 bp; the subtelomeric heterochromatin characterized by tandemly repeated sequences of the HRS60 family is cut by MNase with a 180 by periodicity. The monomeric and dimeric particles of telomeric and subtelomeric chromatin differ in sensitivity to MNase treatment: the telomeric particles are readily digested, producing ladders with a periodicity of 7 bp, while the subtelomeric particles appear to be rather resistant to intranucleosomal cleavage. The results presented show apparent similarities in the organization of telomeric chromatin in higher plants and mammals.  相似文献   
90.
猪精子凝集素的纯化,性质及其作用   总被引:3,自引:1,他引:2  
用胎球蛋白-Sepharose亲和层析和凝胶过滤层析从精子和精浆中分离纯化了猪精子凝集素(简称BSL)。BSL的血凝活性只被若干糖蛋白和聚糖所抑制。BSL的分子量为56kd,由分子量分别为13.6kd(β)和16.0kd(α)的两个不同的亚基以α1β3所组成。BSL为糖蛋白,含中性糖3.2%,不含唾液酸。用ELISA法测定猪精子中BSL的含量及分布,表明70%嵌入在精子膜中,25%结合在精子表面,  相似文献   
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号