全文获取类型
收费全文 | 2946篇 |
免费 | 153篇 |
国内免费 | 2篇 |
出版年
2023年 | 14篇 |
2022年 | 36篇 |
2021年 | 61篇 |
2020年 | 51篇 |
2019年 | 47篇 |
2018年 | 61篇 |
2017年 | 83篇 |
2016年 | 89篇 |
2015年 | 111篇 |
2014年 | 130篇 |
2013年 | 215篇 |
2012年 | 252篇 |
2011年 | 221篇 |
2010年 | 170篇 |
2009年 | 152篇 |
2008年 | 190篇 |
2007年 | 160篇 |
2006年 | 162篇 |
2005年 | 155篇 |
2004年 | 126篇 |
2003年 | 131篇 |
2002年 | 101篇 |
2001年 | 39篇 |
2000年 | 32篇 |
1999年 | 22篇 |
1998年 | 22篇 |
1997年 | 16篇 |
1996年 | 11篇 |
1995年 | 15篇 |
1994年 | 17篇 |
1993年 | 11篇 |
1992年 | 13篇 |
1991年 | 22篇 |
1990年 | 10篇 |
1989年 | 14篇 |
1988年 | 11篇 |
1987年 | 13篇 |
1986年 | 7篇 |
1985年 | 16篇 |
1984年 | 15篇 |
1983年 | 5篇 |
1982年 | 16篇 |
1980年 | 9篇 |
1979年 | 8篇 |
1978年 | 4篇 |
1974年 | 3篇 |
1973年 | 3篇 |
1971年 | 5篇 |
1970年 | 3篇 |
1965年 | 3篇 |
排序方式: 共有3101条查询结果,搜索用时 15 毫秒
1.
Samaiya Puneet K. Krishnamurthy Sairam Kumar Ashok 《Molecular and cellular biochemistry》2021,476(12):4421-4434
Molecular and Cellular Biochemistry - Perinatal asphyxia (PA)-induced brain injury may present as hypoxic-ischemic encephalopathy in the neonatal period, and long-term sequelae such as spastic... 相似文献
2.
Molecular and Cellular Biochemistry - 相似文献
3.
Gerald R.V. Hammond Matthias P. Machner Tamas Balla 《The Journal of cell biology》2014,205(1):113-126
Polyphosphoinositides are an important class of lipid that recruit specific effector proteins to organelle membranes. One member, phosphatidylinositol 4-phosphate (PtdIns4P) has been localized to Golgi membranes based on the distribution of lipid binding modules from PtdIns4P effector proteins. However, these probes may be biased by additional interactions with other Golgi-specific determinants. In this paper, we derive a new PtdIns4P biosensor using the PtdIns4P binding of SidM (P4M) domain of the secreted effector protein SidM from the bacterial pathogen Legionella pneumophila. PtdIns4P was necessary and sufficient for localization of P4M, which revealed pools of the lipid associated not only with the Golgi but also with the plasma membrane and Rab7-positive late endosomes/lysosomes. PtdIns4P distribution was determined by the localization and activities of both its anabolic and catabolic enzymes. Therefore, P4M reports a wider cellular distribution of PtdIns4P than previous probes and therefore will be valuable for dissecting the biological functions of PtdIns4P in its assorted membrane compartments. 相似文献
4.
5.
6.
Effect of orally-administered epidermal growth factor on intestinal iron absorption and mucosal permeability 总被引:1,自引:0,他引:1
A progressive increase in intestinal 59Fe3+ absorption was observed on oral feeding of mice with physiological doses of EGF/UGO. Maximal changes were apparent after 3d and appeared to be dose-dependent. In addition to a small increase in intestinal cell proliferation, as reflected by increased ornithine decarboxylase activity, EGF/UGO-feeding increased mucosal permeability (evaluated with [51Cr]-EDTA): the latter could account for the increase in iron absorption. Sialoadenectomy, to remove the major source of endogenous EGF/UGO, had no appreciable effect on the intestinal absorption of iron. 相似文献
7.
8.
Simultaneous saccharification and protein enrichment fermentation of sugar beet pulp 总被引:1,自引:0,他引:1
Summary A product with 40 % protein content was obtained from sugar beet pulp (1.25–2.0 mm) in 48 h one stage (simultaneous) saccharification/fermentation process under optimized conditions using a specific enzyme mixture andCandida
tropicalis strain, also saving about 40 % enzymes in comparison to a 2-stage process. 相似文献
9.
A minority of 46,XX true hermaphrodites are positive for the Y-DNA sequence including SRY 总被引:4,自引:0,他引:4
Ken McElreavey Raphaël Rappaport Eric Vilain Nacer Abbas François Richaud Stéphen Lortat-Jacob Roland Berger Maryvonne LeConiat Chafika Boucekkine Kiran Kucheria Samia Temtamy Claire Nihoul-Fekete Raja Brauner Marc Fellous 《Human genetics》1992,90(1-2):121-125
Summary A total of 30 cases of 46,XX true hermaphroditism was analysed for Y-DNA sequences including the recently cloned gene for male testis-determination SRY. In 3 cases, a portion of the Y chromosome including SRY was present and, in 2 cases, was localised, to Xp22 by in situ hybridisation. Since previous studies have shown that the majority of XX males are generated by an X-Y chromosomal interchange, the Xp22 position of the Yp material suggests that certain cases of hermaphroditism can arise by the same meiotic event. The phenotype in the 3 SRY-positive cases may be caused by X-inactivation resulting in somatic mosaicism of testis-determining factor expression giving rise to both testicular and ovarian tissues. Autosomal or X-linked mutation(s) elsewhere in the sex-determining pathway may explain the phenotype observed in the remaining 27 SRY-negative cases. 相似文献
10.
Intact isolated rat hepatocytes show a small amount of specific 125I-labeled hyaluronic acid (HA) binding. However, in the presence of digitonin, a very large increase in the specific binding of 125I-HA is observed. Chondroitin sulfate, heparin and dextran sulfate were as effective as unlabeled HA in competing for 125I-HA binding to permeabilized hepatocytes, indicating that the binding sites may have a general specificity for glycosaminoglycans. After rat hepatocytes had been homogenized in a hypotonic buffer, more than 98% of the 125I-HA binding activity could be pelleted by centrifugation at 100,000 x g for 1 h. Mild alkaline treatment of hepatocyte membranes did not release 125I-HA binding activity, suggesting that the HA binding site is an integral membrane molecule. Furthermore, trypsin treatment of deoxycholate-extracted membranes destroyed the binding activity, as assessed by a dot-blot assay. This suggests that a protein component in the membrane is necessary for 125I-HA binding activity. Rat fibrinogen could be a possible candidate for the HA binding activity because HA binds specifically to human fibrinogen (LeBoeuf et al. (1986) J. Biol. Chem. 261, 12 586). Also, fibrinogen can be found in a quasi-crystalline form in rat hepatocytes and could be pelleted with the membranes. Rat fibrinogen was not responsible for the 125I-HA binding activity, since (1) purified rat fibrinogen did not bind to 125I-HA, and (2) immunoprecipitation of rat fibrinogen from hepatocyte extracts did not decrease the 125I-HA binding of these extracts. We conclude that the internal HA binding sites are membrane- or cytoskeleton-associated proteins and are neither cytosolic proteins nor fibrinogen. 相似文献