全文获取类型
收费全文 | 73篇 |
免费 | 6篇 |
出版年
2021年 | 7篇 |
2020年 | 1篇 |
2018年 | 1篇 |
2017年 | 2篇 |
2016年 | 3篇 |
2015年 | 2篇 |
2014年 | 2篇 |
2013年 | 2篇 |
2012年 | 5篇 |
2011年 | 6篇 |
2010年 | 1篇 |
2009年 | 4篇 |
2008年 | 1篇 |
2007年 | 2篇 |
2006年 | 2篇 |
2005年 | 1篇 |
2004年 | 2篇 |
2003年 | 1篇 |
2002年 | 2篇 |
2001年 | 2篇 |
2000年 | 2篇 |
1999年 | 2篇 |
1998年 | 10篇 |
1997年 | 2篇 |
1996年 | 2篇 |
1986年 | 1篇 |
1982年 | 2篇 |
1980年 | 1篇 |
1977年 | 3篇 |
1976年 | 2篇 |
1972年 | 2篇 |
1971年 | 1篇 |
排序方式: 共有79条查询结果,搜索用时 15 毫秒
61.
Ponnulakshmi Rajagopal Selvaraj Jayaraman Shazia Fathima JH Saravanan Radhakrishnan Patil Ashlesh Laxman Vijaya Prakash Krishnan Muthaiah Satyendra Chandra Tripathi TS Gugapriya Aaditya Madhusudan Tarnekar Gayatri Girish Muthiyan Vishwajit Ravindra Deshmukh Bharat Ramrao Sontakke Kirubhanand Chandrashekar 《Bioinformation》2021,17(11):928
62.
Chella Perumal Palanisamy Shazia Fathima JH Ramya Sekar Ponnulakshmi Rajagopal Selvaraj Jeyaraman 《Bioinformation》2021,17(7):705
It is of interest to document the inhibition of A2780 cell proliferation using Mollugo nudicaulis Lam.(M.nudicaulis) extract by MTT assay and by monitoring the CXCR4 and HER2 expression through RT-PCR analysis. Results shown that the n-hexane extract of M.nudicaulis have anticancer activity IC50 values of 32.46±0.92 µg/mL on A2780 cell lines. It is further found that the CXCR4 and HER2 mRNA and protein expression were significantly reduced in M.nudicaulis treated A2780 cell lines. Thus, the n-hexane extract of M.nudicaulis is a natural source of bioactive compounds as potential anticancer agents. 相似文献
63.
Proliferation of three murine marrow-derived stromal cell lines, LC1, LC2, and LC3, depended on initial cell density. For LC2 and LC3, the cell density-dependence was negated by conditioned-media, indicating growth dependence on a soluble growth factor. For LC1, conditioned-media failed to stimulate proliferation, suggesting growth dependence on direct cell-cell contact. 相似文献
64.
Choline acetyltransferase activity of spinal cord cell cultures increased by co-culture with muscle and by muscle-conditioned medium 总被引:9,自引:3,他引:6
下载免费PDF全文
![点击此处可从《The Journal of cell biology》网站下载免费的PDF全文](/ch/ext_images/free.gif)
Activity of the enzyme choline acetyltransferase (CAT), which mediates the synthesis of the neurotransmitter, acetylcholine, was increased up to 20- fold in spinal cord (SC) cells grown in culture with muscle cells for 2 wk. This increase was directly related to the duration of co-culture as well as to the cell density of both the SC and muscle involved and was not affected by the presence of the acetylcholine receptor blocking agent, α-bungarotoxin. Glutamic acid decarboxylase (GAD) activity was often markedly decreased in SC-muscle cultures while the activities of acetylcholinesterase and several other enzymes were little changed. Increased CAT activity was also observed when SC cultures were maintained in medium which had been conditioned by muscle cells or by undifferentiated cells from embryonic muscle. Muscle-conditioned medium (CM) did not affect the activities of SC cell GAD or acetylcholinesterase. Dilution or concentration of the CM directly affected its ability to increase SC CAT activity , as did the duration and timing of exposure of the SC cells to the CM. The medium could be conditioned by muscle cells in the presence or absence of serum, and remained effective after dialysis or heating to 58 degrees C. Membrane filtration data were consistent with the conclusion that the active material(s) in CM had a molecular weight in excess of 50,000 daltons. We conclude that large molecular weight material that is released by muscle cells is capable of producing a specific increase in CAT activity of SC cells. 相似文献
65.
66.
Stable expression of mammalian beta 1,4-galactosyltransferase extends the N-glycosylation pathway in insect cells 总被引:5,自引:2,他引:3
An established lepidopteran insect cell line (Sf9) was cotransfected with
expression plasmids encoding neomycin phosphotransferase and bovine beta
1,4-galactosyltransferase. Neomycin-resistant transformants were selected,
assayed for beta 1,4-galactosyltransferase activity, and the transformant
with the highest level of enzymatic activity was characterized. Southern
blots indicated that this transformed Sf9 cell derivative contained
multiple copies of the galactosyltransferase- encoding expression plasmid
integrated at a single site in its genome. One-step growth curves showed
that these cells supported normal levels of baculovirus replication.
Baculovirus infection of the transformed cells stimulated beta
1,4-galactosyltransferase activity almost 5-fold by 12 h postinfection.
This was followed by a gradual decline in activity, but the infected cells
still had about as much activity as uninfected controls as late as 48 h
after infection and they were able to produce a beta 1,4-galactosylated
virion glycoprotein during infection. Infection of the transformed cells
with a conventional recombinant baculovirus expression vector encoding
human tissue plasminogen activator also resulted in the production of a
galactosylated end-product. These results demonstrate that stable
transformation can be used to add a functional mammalian
glycosyltransferase to lepidopteran insect cells and extend their N-
glycosylation pathway. Furthermore, stably-transformed insect cells can be
used as modified hosts for conventional baculovirus expression vectors to
produce foreign glycoproteins with "mammalianized" glycans which more
closely resemble those produced by higher eucaryotes.
相似文献
67.
JH Curtis 《BMJ (Clinical research ed.)》1998,317(7162):856-857
68.
69.
长春市儿童医院1998~2001年婴幼儿杯状病毒腹泻流行病学研究 总被引:54,自引:3,他引:51
人类杯状病毒(human calicivirus,HuCV)是引起儿童和成人非菌性胃肠炎的主要病原之一.为了掌握HuCV在我国的流行情况,1998年7月至2001年6月,从长春市儿童医院2343例5岁以下腹泻患儿中共收集粪便标本1264份,其中1056份来自2135例住院患儿.对轮状病毒检测为阴性的588份标本,经多价酶免疫试验(EIA)和两组引物反转录-聚合酶链反应(RT-PCR)检测HuCV,202份为阳性,其中住院患儿标本178份,HuCV检出率为16.9%.HuCV腹泻以2岁以下儿童为主(占96%),流行高峰季节为11月至次年3月.选择17株HuCV进行分子鉴定,15株属GⅡ-4群,1株属GⅡ-3群,另1株属GⅠ-2群,表明GⅡ-4群HuCV是我国流行的优势株.根据HuCV住院患儿的监测资料初步估计,HuCV腹泻住院率约为0.5‰~2.4‰.讨论了长春地区HuCV的流行趋势和疾病负担.以上结果为我国HuCV腹泻的预防和控制提供了科学依据. 相似文献
70.
Subbaramaiah K Yoshimatsu K Scherl E Das KM Glazier KD Golijanin D Soslow RA Tanabe T Naraba H Dannenberg AJ 《The Journal of biological chemistry》2004,279(13):12647-12658