全文获取类型
收费全文 | 1118篇 |
免费 | 101篇 |
国内免费 | 90篇 |
出版年
2023年 | 14篇 |
2022年 | 23篇 |
2021年 | 53篇 |
2020年 | 36篇 |
2019年 | 42篇 |
2018年 | 37篇 |
2017年 | 33篇 |
2016年 | 43篇 |
2015年 | 67篇 |
2014年 | 58篇 |
2013年 | 76篇 |
2012年 | 92篇 |
2011年 | 87篇 |
2010年 | 35篇 |
2009年 | 49篇 |
2008年 | 50篇 |
2007年 | 44篇 |
2006年 | 54篇 |
2005年 | 31篇 |
2004年 | 21篇 |
2003年 | 25篇 |
2002年 | 33篇 |
2001年 | 26篇 |
2000年 | 29篇 |
1999年 | 16篇 |
1998年 | 16篇 |
1997年 | 39篇 |
1996年 | 32篇 |
1995年 | 21篇 |
1994年 | 15篇 |
1993年 | 21篇 |
1992年 | 18篇 |
1991年 | 8篇 |
1990年 | 3篇 |
1989年 | 10篇 |
1988年 | 5篇 |
1987年 | 6篇 |
1986年 | 8篇 |
1985年 | 5篇 |
1984年 | 5篇 |
1983年 | 5篇 |
1982年 | 6篇 |
1981年 | 2篇 |
1980年 | 2篇 |
1979年 | 2篇 |
1978年 | 2篇 |
1966年 | 1篇 |
1965年 | 1篇 |
1946年 | 2篇 |
排序方式: 共有1309条查询结果,搜索用时 411 毫秒
101.
Zhu Qingjun Yang Yanyan Xiao Yanan Han Wenhui Li Xingyue Wang Wenda Kuang Tingyun Shen Jian-Ren Han Guangye 《Photosynthesis research》2022,152(2):193-206
Photosynthesis Research - Photosystem II (PSII) has a number of hydrogen-bonding networks connecting the manganese cluster with the lumenal bulk solution. The structure of PSII from... 相似文献
102.
103.
Masoud Zamani Esteki Eftychia Dimitriadou Ligia Mateiu Cindy Melotte Niels Van der Aa Parveen Kumar Rakhi Das Koen Theunis Jiqiu Cheng Eric Legius Yves Moreau Sophie Debrock Thomas D’Hooghe Pieter Verdyck Martine De Rycke Karen Sermon Joris R. Vermeesch Thierry Voet 《American journal of human genetics》2015,96(6):894-912
Methods for haplotyping and DNA copy-number typing of single cells are paramount for studying genomic heterogeneity and enabling genetic diagnosis. Before analyzing the DNA of a single cell by microarray or next-generation sequencing, a whole-genome amplification (WGA) process is required, but it substantially distorts the frequency and composition of the cell’s alleles. As a consequence, haplotyping methods suffer from error-prone discrete SNP genotypes (AA, AB, BB) and DNA copy-number profiling remains difficult because true DNA copy-number aberrations have to be discriminated from WGA artifacts. Here, we developed a single-cell genome analysis method that reconstructs genome-wide haplotype architectures as well as the copy-number and segregational origin of those haplotypes by employing phased parental genotypes and deciphering WGA-distorted SNP B-allele fractions via a process we coin haplarithmisis. We demonstrate that the method can be applied as a generic method for preimplantation genetic diagnosis on single cells biopsied from human embryos, enabling diagnosis of disease alleles genome wide as well as numerical and structural chromosomal anomalies. Moreover, meiotic segregation errors can be distinguished from mitotic ones. 相似文献
104.
Xinqiong Huang Yujie Qian Hainan Wu Xiaoxue Xie Qin Zhou Ying Wang Weilu Kuang Lin Shen Kai Li Juan Su Liangfang Shen Xiang Chen 《The journal of histochemistry and cytochemistry》2015,63(2):88-98
Radiotherapy is the first-line treatment for all stages of cervical cancer, whether it is used for radical or palliative therapy. However, radioresistance of cervical cancer remains a major therapeutic problem. Consequently, we explored if E-cadherin (a marker of epithelial-mesenchymal transition) and osteopontin could predict radioresistance in patients with locally advanced cervical squamous cell carcinoma (LACSCC). Patients were retrospectively reviewed and 111 patients divided into two groups (radiation-resistant and radiation-sensitive groups) according to progression-free survival (PFS). In pretreated paraffin-embedded tissues, we evaluated E-cadherin and osteopontin expression using immunohistochemical staining. The percentage of patients with high osteopontin but low E-cadherin expression in the radiation-resistant group was significantly higher than those in the radiation-sensitive group (p<0.001). These patients also had a lower 5-year PFS rate (p<0.001). Our research suggests that high osteopontin but low E-cadherin expression can be considered as a negative, independent prognostic factor in patients with LACSCC ([Hazard ratios (95% CI) 6.766 (2.940, 15.572)], p<0.001). 相似文献
105.
Lin Wei Jiuxiang Gao Shumin Zhang Sijin Wu Zeping Xie Guiying Ling Yi-Qun Kuang Yongliang Yang Haining Yu Yipeng Wang 《The Journal of biological chemistry》2015,290(27):16633-16652
Cathelicidins are a family of gene-encoded peptide effectors of innate immunity found exclusively in vertebrates. They play pivotal roles in host immune defense against microbial invasions. Dozens of cathelicidins have been identified from several vertebrate species. However, no cathelicidin from marine reptiles has been characterized previously. Here we report the identification and characterization of a novel cathelicidin (Hc-CATH) from the sea snake Hydrophis cyanocinctus. Hc-CATH is composed of 30 amino acids, and the sequence is KFFKRLLKSVRRAVKKFRKKPRLIGLSTLL. Circular dichroism spectroscopy and structure modeling analysis indicated that Hc-CATH mainly assumes an amphipathic α-helical conformation in bacterial membrane-mimetic solutions. It possesses potent broad-spectrum and rapid antimicrobial activity. Meanwhile, it is highly stable and shows low cytotoxicity toward mammalian cells. The microbial killing activity of Hc-CATH is executed through the disruption of cell membrane and lysis of bacterial cells. In addition, Hc-CATH exhibited potent anti-inflammatory activity by inhibiting the LPS-induced production of nitric oxide (NO) and pro-inflammatory cytokines such as TNF-α, IL-1β, and IL-6. Hc-CATH directly binds with LPS to neutralize its toxicity, and it also binds to Toll-like receptor 4 (TLR4/MD2 complex), which therefore inhibits the binding of LPS to TLR4/MD2 complex and the subsequent activation of LPS-induced inflammatory response pathways. Taken together, our study demonstrates that Hc-CATH, the first cathelicidin from sea snake discovered to have both antimicrobial and anti-inflammatory activity, is a potent candidate for the development of peptide antibiotics. 相似文献
106.
107.
108.
109.
Identification of Campylobacter jejuni and determination of point mutations associated with macrolide resistance using a multiplex TaqMan MGB real‐time PCR 下载免费PDF全文
110.
Kuang H Zhao S Chen W Ma W Yong Q Xu L Wang L Xu C 《Biosensors & bioelectronics》2011,26(5):2495-2499
A novel, rapid DNA detection method based on fluorescence quenching of quantum dots (QDs) by gold nanoparticles (GNPs) through polymerase chain reaction (PCR) was developed. In proof-of-concept experiments, the length of the amplicon DNA ranging from 152 to 1003 base pairs (bp) could be determined based on quenched fluorescence intensity with 136 bp as the lower limit of effective range. And the real sample detections were also achieved successfully by this developed method. Therefore, this DNA detection method has the potential to be the powerful gene diagnostic tool. 相似文献