全文获取类型
收费全文 | 6899篇 |
免费 | 440篇 |
出版年
2022年 | 31篇 |
2021年 | 99篇 |
2020年 | 52篇 |
2019年 | 73篇 |
2018年 | 119篇 |
2017年 | 86篇 |
2016年 | 140篇 |
2015年 | 214篇 |
2014年 | 259篇 |
2013年 | 394篇 |
2012年 | 378篇 |
2011年 | 395篇 |
2010年 | 237篇 |
2009年 | 220篇 |
2008年 | 333篇 |
2007年 | 370篇 |
2006年 | 329篇 |
2005年 | 309篇 |
2004年 | 343篇 |
2003年 | 306篇 |
2002年 | 309篇 |
2001年 | 202篇 |
2000年 | 217篇 |
1999年 | 175篇 |
1998年 | 97篇 |
1997年 | 89篇 |
1996年 | 76篇 |
1995年 | 59篇 |
1994年 | 55篇 |
1993年 | 51篇 |
1992年 | 98篇 |
1991年 | 127篇 |
1990年 | 109篇 |
1989年 | 106篇 |
1988年 | 90篇 |
1987年 | 85篇 |
1986年 | 80篇 |
1985年 | 83篇 |
1984年 | 69篇 |
1983年 | 65篇 |
1982年 | 35篇 |
1981年 | 24篇 |
1980年 | 20篇 |
1979年 | 42篇 |
1978年 | 30篇 |
1977年 | 31篇 |
1976年 | 21篇 |
1975年 | 21篇 |
1974年 | 24篇 |
1973年 | 30篇 |
排序方式: 共有7339条查询结果,搜索用时 46 毫秒
21.
Nuclear protein antigens to the antinuclear antibodies in serum of non-obese diabetic (NOD) mice were investigated. In the serum of diabetic NOD female mice (20 weeks old), the antinuclear antibodies were detected by indirect immunofluorescence assay using frozen sections of liver of C 57 BL/6 J or NOD mice as antigen. Nuclei were separated from the liver of C 57 BL/6 J mice and solubilized. Solubilized nuclear antigens were analyzed by SDS PAGE-Western immunoblotting techniques. Nuclear protein antigens with molecular weights of 26,000, 32,000 and 65,000 showed strongly positive reactions with the antinuclear antibodies in the serum of the NOD mouse. 相似文献
22.
The possible involvement of fibronectin receptors in growth stimulation was investigated by an analysis of fibronectin-coated latex bead binding to 3T3-L1 cells under various conditions. 3T3-L1 cells, growth-arrested in a medium with a low concentration of calf serum, bound few fibronectin-coated beads. After addition of serum at concentrations of 1.0% or higher, there was a rapid and transient increase in the number of cells with bound beads and a subsequent increase in the incorporation of bromodeoxyuridine (BrdU) into cell nuclei. Incorporation of BrdU was observed in about 60% of the cells with bound beads. Fibroblast growth factor and platelet-derived growth factor at concentrations of 5 ng/ml or higher also enhanced binding of fibronectin-coated beads to cells. Stimulation of bead binding by epidermal growth factor and insulin was weak. Fibroblast growth factor, but not epidermal growth factor, increased the incorporation of BrdU into nuclei. These results indicate a relationship between stimulation of cell proliferation in quiescent cells and increased binding by cells of fibronectin-coated latex beads. 相似文献
23.
Pro----leu change at position 102 of prion protein is the most common but not the sole mutation related to Gerstmann-Str?ussler syndrome 总被引:20,自引:0,他引:20
K Doh-ura J Tateishi H Sasaki T Kitamoto Y Sakaki 《Biochemical and biophysical research communications》1989,163(2):974-979
The host-encoded prion protein (PrP) is a component of transmissible amyloid deposited in the brains affected by Gerstmann-Str?ussler syndrome (GSS). Recently GSS in two unrelated Caucasian families has been reported to be linked to an amino acid change in PrP codon 102, proline to leucine (Leu102). However, it has not been clear whether the change is commonly found to GSS regardless of ethnic origin. We report here that Leu102 is also found in all the Japanese GSS patients tested. Interestingly, one French GSS patient was found to have another change, alanine to valine in codon 117 (Val117), instead of Leu102. Our results indicate that Leu102 is closely related to GSS irrespective of ethnic origin, but not the sole mutation related to GSS. Val117 may also be related to GSS. 相似文献
24.
25.
Rat and human cartilage proteoglycan (aggrecan) gene structure 总被引:1,自引:0,他引:1
26.
27.
Kunio Yonemasu Takako Sasaki Yoshiko Dohi Charles M. Lapière Betty Nusgens 《生物化学与生物物理学报:疾病的分子基础》1990,1096(1):47-51
C1q, a collagen-like complement protein, was purified from the serum of a ddermatosparactic calf which lacks procollagen N-terminal proteinase (pN-proteinase). The specific hemolytic activity of the serum Clq from the dermatosparactic animal was identical to that of C1q from a normal calf. Gel-filtration of serum from dermatosparactic calf, on Sepharose 6B, showed the presence of C1q-antigenic material at only one position which was identical to the elution position of normal bovine C1q. No differdence, under dissociating conditions, could be seen in the size of the chains of C1q in specific immunoprecipitates isolated from the sera of dermatosparactic and normal animals, as judged by polyacrylamidegel electrophoresis (PAGE) in the presence of sodium dodecyl sulfate (SDS). The C1q from the dermatosparactic animal showed the same N-terminal amino acid and typtic-digest peptide pattern on HPLC as C1q from the normal calf. These results strongly suggest that pN-proteinase is not involved in the extracellular processing of C1q. 相似文献
28.
29.
Hiroki Yamaue Hiroshi Tanimura Takuya Tsunoda Makoto Iwahashi Masaji Tani Mikiko Tamai Masaya Inoue 《Biotherapy》1990,2(3):247-259
The tumor-infiltrating lymphocytes (TILs) were cultured with interleukin 2 (IL-2) to induce the activated killer cells possessing autologous tumor-killing activity, and analysed their cell surface phenotypes and assessed anti-tumor killing activity. Furthermore, the activated TILs were transferred into 7 patients adoptively resulting in complete remission in a patient with pancreatic cancer and partial remission in another patient with gastric cancer.The cytotoxic activities of activated TILs at 3 weeks-incubation was 72 ± 15, 42 ± 26, 27 ± 21 and 25 ± 15% against K562, Daudi, KATO-III and autologous tumor, respectively. The negative selection method, indicated that the killer cells recognizing autologous tumor cells consisted of CD4- or CD8-positive T lymphocytes and CD16- or CD56-positive natural killer cells. The activated TILs could not only lyse cultured tumor cell lines, but also autologous tumor cells. 相似文献
30.
Kazuhisa Toyoda Takuya Sugahara Kunio Inouye Koji Yamada Sanetaka Shirahata Hiroki Murakami 《Cytotechnology》1990,3(2):189-197
An immunoglobulin (Ig) production stimulating factor (IPSF) for hybridomas was found in spent medium of the human B lymphoblastoid cell line, HO-323. The IPSF was purified by serial use of DEAE chromatography, ultrafiltration, gel filtration and HPLC-DEAE chromatography. Purified IPSF was estimated to be a 410 k macro molecule by gel filtration, and contained three types of isomers which were separated from each other by native polyacrylamide gel electrophoresis. All of the isomers were, however, assumed to have the same protein components by SDS polyacrylamide gel electrophoresis.The IPSF was effective for human-human and mouse-mouse hybridomas producing IgM, but not for IgG producers in the experimental condition used here. Human-human hybridoma HF10B4, cultured in IPSF-containing medium, produced 20 times more IgM than in IPSF-free medium under serum-free conditions. The IPSF showed very little proliferation stimulating activity on HF10B4 cells. 相似文献