全文获取类型
收费全文 | 13904篇 |
免费 | 1204篇 |
国内免费 | 1篇 |
专业分类
15109篇 |
出版年
2024年 | 20篇 |
2023年 | 146篇 |
2022年 | 95篇 |
2021年 | 216篇 |
2020年 | 208篇 |
2019年 | 211篇 |
2018年 | 570篇 |
2017年 | 466篇 |
2016年 | 503篇 |
2015年 | 402篇 |
2014年 | 424篇 |
2013年 | 785篇 |
2012年 | 1120篇 |
2011年 | 1281篇 |
2010年 | 663篇 |
2009年 | 436篇 |
2008年 | 948篇 |
2007年 | 855篇 |
2006年 | 844篇 |
2005年 | 649篇 |
2004年 | 674篇 |
2003年 | 621篇 |
2002年 | 562篇 |
2001年 | 418篇 |
2000年 | 525篇 |
1999年 | 258篇 |
1998年 | 133篇 |
1997年 | 101篇 |
1996年 | 95篇 |
1995年 | 80篇 |
1994年 | 80篇 |
1993年 | 77篇 |
1992年 | 71篇 |
1991年 | 64篇 |
1990年 | 39篇 |
1989年 | 33篇 |
1988年 | 32篇 |
1987年 | 35篇 |
1986年 | 18篇 |
1985年 | 42篇 |
1984年 | 29篇 |
1983年 | 25篇 |
1982年 | 31篇 |
1981年 | 23篇 |
1980年 | 22篇 |
1979年 | 23篇 |
1978年 | 21篇 |
1977年 | 19篇 |
1974年 | 17篇 |
1973年 | 18篇 |
排序方式: 共有10000条查询结果,搜索用时 0 毫秒
31.
G. Egea J. M. Ureña X. Graña J. Marsal J. Carreras F. Climent 《Histochemistry and cell biology》1992,97(3):269-275
Summary We have previously reported (Ureña et al. Eur. J. Cell Biol. 1990) that in skeletal muscle, type MM phosphoglycerate mutase isozyme is present in the nucleus as well as in the cytosol. To determine whether type BB phosphoglycerate mutase isozyme is also present in nucleus, the subcellular location of this isozyme was studied in different rat tissues by cell fractionation and immunogold techniques. With the aid of high affinity-purified anti-phosphoglycerate mutase BB isozyme antibodies, the isozyme was located in the nucleus of neuronal, astroglial and liver cells but not in the nucleus of oligodendroglial and endothelial cells. Biochemical studies on purified nuclear fractions also demonstrated the presence of phosphoglycerate mutase activity in the nucleus. Both immunocytochemical and biochemical techniques showed that nuclear phosphoglycerate mutase-specific activity depended on the type of cell.Abbreviations PGAM
phosphoglycerate mutase
- PGAM-M(M)
muscle specific subunit (isozyme) of PGAM
- PGAM-B(B)
brain type subunit (isozyme) of PGAM
- ssDNA
single stranded DNA
- PBS
0.001 M phosphate buffer, pH 7.4, containing 0.15 M NaCl
- kDa
kilodalton 相似文献
32.
Rita Maria Ulloa Hector Norberto Torres Claudia M. Ochatt Maria Teresa Téllez-Iñón 《Molecular and cellular biochemistry》1991,102(2):155-163
DEAE-cellulose column chromatography of Neurospora crassa soluble mycelial extracts leads to the resolution of three major protein kinase activity peaks designated PKI, PKII, and PKIII.PKII activity is stimulated by Ca2+ and Neurospora or brain calmodulin. Maximal stimulation was observed at 2 µM-free Ca2+ and 1 µg/ml of the modulator. The stimulatory effect of the Ca2+-calmodulin complex was blocked by EGTA and by some calmodulin antagonists such as phenothiazine drugs or compound 48/80.PKII phosphorylates different proteins, among which histone II-A at a low concentration and CDPKS, the synthetic peptide specific for Ca2+-calmodulin dependent protein kinases, are the best substrates. Some phosphorylation can be detected in the absence of any exogenous acceptor. PKII activity assayed in the presence of histone II-A or in the absence of exogenous phosphate acceptor (autophosphorylation) co-elute in a DEAE-cellulose column at 0.28 M NaCl. As result of the autophosphorylation reaction of the purified enzyme a main phosphorylated component of 70 kDa was resolved by SDS-polyacrylamide gel electrophoresis. It is possible that this component is an active part of this enzyme. 相似文献
33.
Rafael Balaña Fouce Maria I. Escribano Jose M. Alunda 《Molecular and cellular biochemistry》1991,107(2):127-133
Summary The putrescine uptake/efflux regulation and their regulatory role on intracellular polyamine pools have been studied in the parasitic protozoa Leishmania infantum. Putrescine uptake was age-dependent with maximal values in logarithmic phase promastigotes and minimal in stationary phase. Moreover, putrescine uptake was activated in response to depletion of intracellular polyamines by alpha-difluoromethylornithine (DFMO) — a well known irreversible enzyme-activated inhibitor of ornithine decarboxylase. Kinetic studies of putrescine uptake induction showed a notable rise in Vmax without Km changes, suggesting a de novo synthesis of putrescine carriers. Putrescine uptake was able to replenish polyamine content and also to recover the proliferative rate in cells treated during 24 hours with DFMO. 相似文献
34.
Palmar flexion creases have been studied in schizophrenics with a family history of schizophrenia or other psychiatric disorders
and without such a background, and compared to a control population. Palmar flexion creases have been analyzed according to
the method suggested byBali & Chaube (1971). When compared to controls, differences in the DRBC and TRBC frequencies are significant in the subgroup with no family
history, supporting the existence of biological heterogeneity in schizophrenia, and of congenital factors when there is no
known genetic background. 相似文献
35.
36.
General recombination mechanisms in extracts of meiotic cells 总被引:9,自引:0,他引:9
Yasuo Hotta Satoshi Tabata Robert A. Bouchard Ramon Piñon Herbert Stern 《Chromosoma》1985,93(2):140-151
RecA-like proteins have been purified from somatic and meiotic cells of mouse and lily. The rec proteins have been designated s-rec and m-rec to indicate their respective tissues of origin. The two proteins differ in molecular weight and in their response to temperature, the latter being consistent with the optimal temperature for physiological function of their tissues of origin. There is a major increase in m-rec protein with the entry of cells into meiosis, the peak of activity being early pachytene. Extracts of the cells and also those of yeast (Saccharomyces cerevisiae) have been prepared that have the capacity to catalyze homologous recombination. These extracts behave similarly to the m-rec proteins upon entry of cells into meiosis. Yeast transferred to sporulation medium displays a 100-fold increase in the recombination activity of the extract at about the time of entry into meiosis. The occurrence of peak levels of m-rec and recombination activity in extracts from cells in early pachytene points strongly to that stage as the time at which the enzymatic phase of recombination occurs. 相似文献
37.
Summary Studies on intercalary regeneration in several organisms have shown that a regenerate is formed when surfaces of different positional value along the proximo-distal axis are opposed. One of the main problems posed by this phenomenon is to know which piece contributes to the building of the regenerate. In the present work we have studied this problem in planarians using chimaeras made between pieces of different body levels, irradiated or not, of the sexual and asexual races ofDugesia(S)mediterranea that differ in a chromosomal marker.The results found show very clearly that intercalary regenerates in planarians are formed by cells coming from both pieces (stumps), and that irradiated pieces keep the positional values and interact with non-irradiated pieces to restore the missing parts. This means that distal and proximal transformation do actually occur at the same time during intercalary regeneration in planarians. The implications of these results as regards to the origin of cells in the regenerate and to present models of intercalary regeneration are discussed. 相似文献
38.
Dr. Manuel Megias Miguel A. Caviedes Francisco Rodriguez-Quiñones Antonio J. Palomares Francisco Ruiz-Berraquero 《Current microbiology》1985,12(6):325-328
Rhizobium trifolii was highly resistant to the lethal effect ofN-methyl-N-nitro-N-nitrosoguanidine (MNNG), but it was sensitive to the mutagenic action of this chemical. A concentration of 500g/ml yields a survival of between 1% and 10%, which allows us to obtain a higher number of mutants than lower concentrations that yield higher survival rates. Lethal damage produced by nitrosoguanidine was repaired, and repair is inhibited by acriflavine. 相似文献
39.
J. Fernandez-Piqueras A. Rodriguez Campos C. Sentis Castaño E. Rojo Garcis 《Genetica》1983,61(1):9-12
The chromosomal location of the active NORs has been analyzed by a silver impregnation procedure in theSteropleurus martorelli complex. A primary NOR, which is always present at the first meiotic prophase, has been found in each of the four described races. In addition to this, all races possess one or two secondary NORs which are less active than the former and can be occasionally shown. Usually only one of the two homologous chromosomes has been found to be involved with nucleolus organisation.These results are discussed in relation to hypotheses on the chromosome differentiation of this species complex. 相似文献
40.