全文获取类型
收费全文 | 12928篇 |
免费 | 884篇 |
国内免费 | 512篇 |
出版年
2023年 | 216篇 |
2022年 | 260篇 |
2021年 | 448篇 |
2020年 | 435篇 |
2019年 | 604篇 |
2018年 | 563篇 |
2017年 | 350篇 |
2016年 | 354篇 |
2015年 | 406篇 |
2014年 | 835篇 |
2013年 | 971篇 |
2012年 | 612篇 |
2011年 | 750篇 |
2010年 | 526篇 |
2009年 | 603篇 |
2008年 | 596篇 |
2007年 | 636篇 |
2006年 | 539篇 |
2005年 | 481篇 |
2004年 | 447篇 |
2003年 | 379篇 |
2002年 | 338篇 |
2001年 | 211篇 |
2000年 | 169篇 |
1999年 | 173篇 |
1998年 | 174篇 |
1997年 | 170篇 |
1996年 | 136篇 |
1995年 | 121篇 |
1994年 | 110篇 |
1993年 | 97篇 |
1992年 | 96篇 |
1991年 | 99篇 |
1990年 | 77篇 |
1989年 | 68篇 |
1988年 | 51篇 |
1987年 | 50篇 |
1985年 | 82篇 |
1984年 | 142篇 |
1983年 | 104篇 |
1982年 | 147篇 |
1981年 | 114篇 |
1980年 | 91篇 |
1979年 | 97篇 |
1978年 | 66篇 |
1977年 | 70篇 |
1976年 | 54篇 |
1975年 | 42篇 |
1974年 | 40篇 |
1973年 | 46篇 |
排序方式: 共有10000条查询结果,搜索用时 15 毫秒
41.
Summary Dissociated single cells from chicken retina or tectum kept in rotation-mediated cell culture aggregate, proliferate and establish a certain degree of histotypical cellto-cell relationships (sorting out), but these systems never form highly laminated aggregates (nonstratified R- and T-aggregates). In contrast, a mixture of retinal plus pigment epithelial cells forms highly stratified aggregates (RPE-aggregates, see Vollmer et al. 1984). The present comparative study of stratified and nonstratified aggregates enables us to investigate the process of cell proliferation uncoupled from that of tissue stratification. Here we try to relate these two basic neurogenetic processes with patterns of expression of cholinesterases (AChE, BChE) during formation of both types of aggregates.During early aggregate formation, in both stratified and nonstratified aggregates an increased butyrylcholinesterase activity is observed close to mitotically active cells. Quantitatively both phenomena show their maxima after 2–3 days in culture. In contrast, AChE-expression in all systems increases with incubation time. In nonproliferative areas, in the center of RPE-aggregates, the formation of plexiform layers is characterized initially by weak BChE and then strong AChE-activity. These areas correspond with the inner (IPL) and outer (OPL) plexiform layers of the retina in vivo. Although by sucrose gradient centrifugation we find that the 6S- and the fiber-associated 11S-molecules of AChE are present in all types of aggregates, during the culture period the ratio of 11S/6S-forms increases only in RPE-aggregates, which again indicates the advanced degree of differentiation within these aggregates.It is thus demonstrated that cholinesterases first correlate with neuronal cell proliferation and later with stratification, which indicates functions of both enzymes during both developmental periods.Abbreviations
AChE
acetylcholinesterase
-
BChE
butyrylcholinesterase
-
iso-OMPA
specific inhibitor of BChE
-
BW 284C51
specific inhibitor of AChE
-
IPL
inner plexiform layer
-
OPL
outer plexiform layer 相似文献
42.
T. de la Rubia J. Gonzalez-Lopez J. Moreno M. V. Martinez-Toledo A. Ramos-Cormenzana 《Archives of microbiology》1987,147(4):354-357
The effect of a low phosphate concentration on intracellular adenine nucleotide content, oxygen consumption and poly--hydroxybutyrate deposition was investigated with N-free and NH
4
+
batch cultures of Azotobacter vinelandii. When the microorganisms were cultured under low-phosphate concentrations the cells contained much larger amounts of poly--hydroxybutyrate, but displayed lower oxygen consumption activities and energy charge values than did control cells. Also, the ratio ATP to ADP was much higher in control cells and the intracellular levels of ATP were lower in low-phosphate cells. 相似文献
43.
Takashi Yutsudo Hisao Kurazono Chihiro Sasakawa Masanosuke Yoshikawa Makoto Iwaya Tae Takeda Yoshifumi Takeda 《FEMS microbiology letters》1987,48(1-2):273-276
Abstract A Vero toxin (VT2 or Shiga-like toxin II)-converting phage was isolated from Escherichia coli 0157: H7 strain J-2. Nontoxigenic E. coli C600 produced VT2 when lysogenized with the toxin-converting phage. Eco RI fragments of the phage DNA were ligated with Eco RI-digested pBR322 or pUC118 and were transformed into E. coli MC1061 or MV1184. Transformants exhibiting VT2 production commonly contained a 4.6 kb Eco RI fragment. It was found that a 2.3 kb Kpn I- Sph I fragment coded VT2 production and that this fragment hybridized weakly with the 2.1 kb fragment encoding VT1. 相似文献
44.
Summary DNA sequence analysis of genetic deletions in bacteriophage T7 has shown that these chromosomal rearrangements frequently
occur between directly repeated DNA sequences. To study this type of spontaneous deletion in more quantitative detail synthetic
fragments of DNA, made by hybridizing two complementary oligonucleotides, were introduced into the non-essential T7 gene 1.3
which codes for T7 DNA ligase. This insert blocked synthesis of functional ligase and made the phage that carried an insert
unable to form plaques on a host strain deficient in bacterial ligase. The sequence of the insert was designed so that after
it is put into the T7 genome the insert is bracketed by direct repeats. Perfect deletion of the insert between the directly
repeated sequences results in a wild-type phage. It was found that these deletion events are highly sensitive to the length
of the direct repeats at their ends. In the case of 5 bp direct repeats excision from the genome occurred at a frequency of
less than 10−10, while this value for an almost identical insert bracketed by 10 bp direct repeats was approximately 10−6. The deletion events were independent of a hostrecA mutation. 相似文献
45.
46.
47.
Matilde Jose Isabelle Tratner Maryse Poiret Jean-Louis Nahon Jean-Louis Danan Jose Maria Sala-Trepat 《Molecular & general genetics : MGG》1989,215(2):225-230
Summary The distribution of middle repetitive sequences in the genic and extragenic regions of the rat albumin and -fetoprotein genes was analyzed. Their presence was determined by probing Southern blots of restriction fragments of albumin and -fetoprotein genomic subclones with 32P-labeled total rat DNA. Repetitive sequences were detected in both genes. They were classified as weak, moderate and intense hybridizing elements according to the intensity of hybridization. Weak repetitive sequences were characterized as dG·dT repeats by using 32P-labeled poly-(dG·dT)(dC·dA) oligomer probe. They occurred in 5 and 3 extragenic regions of the two genes and in introns 4 and 5 of the albumin gene. The moderate repetitive sequence present in intron 6 of the albumin gene was identified as the rat SINES element, 4D12. The intense repetitive sequence, localized in the 3 non-coding region of the albumin gene, corresponded to the terminal segment of a rat high repeat long interspersed DNA family, L1Rn. 4D12 and L1Rn sequences were also scattered throughout the -fetoprotein locus as moderate and intense repetitive elements, respectively, but their distribution was different from that of the albumin genomic region. These results indicate that repetitive sequences invaded the two loci in a non-conservative manner. 相似文献
48.
49.
50.
Diurnal oscillations of steady-state mRNA levels encoding the chlorophyll a/b-binding proteins were monitored inLycopersicon esculentum, Glycine max, Phaseolus vulgaris, P. aureus, P. coccineus, Pisum sativum, Sinapis alba, Hordeum vulgare,
Triticum aestivum andZea mays. In these plant speciescab mRNA accumulation increases and decreases periodically indicating i) that the expression of the genes for chlorophyll a/b-binding
proteins (cab genes) is controlled by a circadian rhythm, and ii) that the rhythm is widely distributed among monocotyledonous and dicotyledonous
plant species. A detailed characterization of the pattern ofcab mRNA expression in tomato leaves shows that the amplitude of the oscillation is dependent on i) the developmental stage of
the leaves, ii) the circadian phase and duration of light and iii) the circadian phase and duration of darkness. In addition
to the chlorophyll a/b-binding proteins, genes coding for other cellular functions were examined for cyclic variations of
their mRNA levels. The analysis includes genes involved in i) carbon metabolism (e.g. phosphoenolpyruvate carboxylase, pyruvate
orthophosphate dikinase, alpha amylase, fructose-1,6-bisphosphate aldolase, triosephosphate isomerase), ii) photosynthesis
(large and small subunit of ribulose-1,5-bisphosphate carboxylase/oxygenase, QB-binding protein, reaction-center protein of photosystem I) and iii) other physiological or morphological reactions (e.g.
ubiquitin, actin). However, no periodic fluctuation pattern was detected for the mRNA levels of these genes in tomato and
maize leaves. 相似文献