全文获取类型
收费全文 | 84篇 |
免费 | 5篇 |
出版年
2019年 | 1篇 |
2018年 | 2篇 |
2016年 | 3篇 |
2015年 | 1篇 |
2014年 | 2篇 |
2013年 | 4篇 |
2012年 | 5篇 |
2011年 | 3篇 |
2010年 | 3篇 |
2009年 | 1篇 |
2008年 | 3篇 |
2007年 | 6篇 |
2006年 | 1篇 |
2005年 | 4篇 |
2004年 | 4篇 |
2003年 | 4篇 |
2001年 | 2篇 |
2000年 | 2篇 |
1999年 | 1篇 |
1998年 | 8篇 |
1997年 | 3篇 |
1996年 | 3篇 |
1995年 | 1篇 |
1994年 | 2篇 |
1992年 | 3篇 |
1991年 | 4篇 |
1990年 | 1篇 |
1989年 | 1篇 |
1987年 | 1篇 |
1986年 | 2篇 |
1985年 | 2篇 |
1984年 | 3篇 |
1983年 | 1篇 |
1979年 | 1篇 |
1978年 | 1篇 |
排序方式: 共有89条查询结果,搜索用时 16 毫秒
31.
32.
Gene duplications in the TL region of the mouse major histocompatibility complex 总被引:1,自引:0,他引:1
下载免费PDF全文
![点击此处可从《The EMBO journal》网站下载免费的PDF全文](/ch/ext_images/free.gif)
U Hammerling H Ronne E Widmark B Servenius M Denaro L Rask P A Peterson 《The EMBO journal》1985,4(6):1431-1434
We have isolated a class I gene from the TL region of the A/J mouse. The gene, T2A, is a homologue of the C57BL/10 mouse gene T2. In the process of mapping this gene we screened a number of BALB/c class I cosmid clusters with a T2A flanking probe. Several of the hybridizing clusters were found to contain identical DNA segments and could therefore be linked together into one single BALB/c TL region which appears to be identical to the TL region of the C57BL/10 mouse. However, two of the hybridizing clusters do not overlap with the C57BL/10 TL region. It appears that these two clusters represent a partial duplication of the TL region in the BALB/c mouse. 相似文献
33.
Intra-specific heterogeneity of the rDNA internal transcribed spacer in the Simulium damnosum (Diptera: Simuliidae) complex 总被引:3,自引:0,他引:3
The internal transcribed spacer (ITS) of the rRNA gene cluster has been
used as a model for the study of the action of concerted evolution and
molecular drive on repeated sequence families. In contrast to this general
finding, preliminary DNA sequence analysis of cloned representatives of the
ITS from the West African black fly species complex Simulium damnosum s.1.
demonstrated extensive intra-individual and intra-specific polymorphisms.
Variability in the ITS was primarily confined to the ITS1 domain. The
degree and type of intra-individual and intra-specific variability within
the ITS was further characterized using gel electrophoresis, DNA
hybridization, and heteroduplex analysis of the PCR products generated from
the ITS1 domain. ITS1 copies from individual S. damnosum s.1. differed in
length and sequence composition. These results, when taken together,
demonstrate that a large degree of intra-individual and intra-specific
heterogeneity exists in the ITS of S. damnosum s.1. The intra-individual
heterogeneity was greater in the savanna-dwelling than forest-dwelling
sibling species of S. damnosum s.1. This heterogeneity may be due in part
to inter-breeding among sympatric sibling species, coupled with disturbance
of S. damnosum s.1. populations resulting from intensive vector control
efforts.
相似文献
34.
Deepa Indira Shankara Narayanan Varadarajan Santhik Subhasingh Lupitha Asha Lekshmi Krupa Ann Mathew Aneesh Chandrasekharan Prakash Rajappan Pillai Ishaque Pulikkal Kadamberi Indu Ramachandran Hari Sekar Anurup Kochucherukkan Gopalakrishnan Santhoshkumar TR 《European journal of cell biology》2018,97(1):1-14
The selective autophagic removal of mitochondria called mitophagy is an essential physiological signaling for clearing damaged mitochondria and thus maintains the functional integrity of mitochondria and cells. Defective mitophagy is implicated in several diseases, placing mitophagy as a target for drug development. The identification of key regulators of mitophagy as well as chemical modulators of mitophagy requires sensitive and reliable quantitative approaches. Since mitophagy is a rapidly progressing event and sub-microscopic in nature, live cell image-based detection tools with high spatial and temporal resolution is preferred over end-stage assays. We describe two approaches for measuring mitophagy in mammalian cells using stable cells expressing EGFP-LC3 – Mito-DsRed to mark early phase of mitophagy and Mitochondria-EGFP – LAMP1-RFP stable cells for late events of mitophagy. Both the assays showed good spatial and temporal resolution in wide-field, confocal and super-resolution microscopy with high-throughput adaptable capability. A limited compound screening allowed us to identify a few new mitophagy inducers. Compared to the current mitophagy tools, mito-Keima or mito-QC, the assay described here determines the direct delivery of mitochondrial components to the lysosome in real time mode with accurate quantification if monoclonal cells expressing a homogenous level of both probes are established. Since the assay described here employs real-time imaging approach in a high-throughput mode, the platform can be used both for siRNA screening or compound screening to identify key regulators of mitophagy at decisive stages. 相似文献
35.
Luciano Gastaldo Romeo Ciabatti Francesco Assi Ermenegildo Restelli Jurgen K. Kettenring Luigi F. Zerilli Gabriella Romanò Maurizio Denaro Bruno Cavalleri 《Journal of industrial microbiology & biotechnology》1992,11(1):13-18
Summary WhenActinoplanes strain ATCC 33076, the producer of A-16686 A1, A2 and A3 complex, is fermented in a suitable medium three additional factors, designated A1, A2 and A3 are produced. These were isolated and characterized, and were shown to differ from the parent components of the original complex by lacking one mannose unit. Bioconversion of A factors into A factors was achieved by incubation with the mycelium ofActinoplanes ATCC 33076. Factor A2 has better antibacterial activity than A2 against some bacteria. 相似文献
36.
37.
38.
39.
40.
Saccà F Puorro G Antenora A Marsili A Denaro A Piro R Sorrentino P Pane C Tessa A Brescia Morra V Cocozza S De Michele G Santorelli FM Filla A 《PloS one》2011,6(3):e17627