全文获取类型
收费全文 | 784篇 |
免费 | 0篇 |
专业分类
电工技术 | 3篇 |
化学工业 | 2篇 |
金属工艺 | 1篇 |
轻工业 | 1篇 |
一般工业技术 | 1篇 |
冶金工业 | 774篇 |
自动化技术 | 2篇 |
出版年
2011年 | 1篇 |
2010年 | 1篇 |
2009年 | 1篇 |
2007年 | 1篇 |
2006年 | 2篇 |
2005年 | 1篇 |
2003年 | 4篇 |
1999年 | 21篇 |
1998年 | 209篇 |
1997年 | 108篇 |
1996年 | 91篇 |
1995年 | 56篇 |
1994年 | 29篇 |
1993年 | 39篇 |
1992年 | 8篇 |
1991年 | 10篇 |
1990年 | 10篇 |
1989年 | 16篇 |
1988年 | 16篇 |
1987年 | 13篇 |
1986年 | 18篇 |
1985年 | 14篇 |
1983年 | 3篇 |
1982年 | 8篇 |
1981年 | 5篇 |
1980年 | 13篇 |
1978年 | 1篇 |
1977年 | 30篇 |
1976年 | 49篇 |
1975年 | 3篇 |
1965年 | 2篇 |
1955年 | 1篇 |
排序方式: 共有784条查询结果,搜索用时 15 毫秒
61.
MC Mahon MP Driscoll WJ Glover KM Borchert ZT Kelleher GJ Smith WB Coleman 《Canadian Metallurgical Quarterly》1999,14(2):337-346
We have previously identified and mapped a locus within human chromosome 11p11.2-p12 that suppresses the tumorigenic potential of a rat liver tumor cell line (termed GN6TF) which contains well defined chromosomal aberrations involving rat chromosomes 1, 4, 7, and 10. In the present study, we investigated the potential of this human 11p11.2-p12 liver tumor suppressor locus to suppress the tumorigenic potential of two other rat liver tumor cell lines (GN3TG and GP10TA) following microcell-mediated introduction of human chromosome 11. These tumor cell lines are aneuploid and contain chromosomal abnormalities that are similar to the GN6TF tumor line. The tumorigenic potential and other phenotypic characteristics of GN3TG-11neo and GP10TA-11neo microcell hybrid (MCH) cell lines were variable, and dependent upon the status of the introduced human chromosome 11. MCH cell lines that retained the region of 11p11. 2-p12 delineated by microsatellite markers D11S1385 and D11S903 exhibited suppression of tumorigenicity in vivo (decrease in tumorigenicity and/or elongation of latency), whereas, the tumorigenic potential of one MCH line that lacked markers in this region of human 11p11.2-p12, but retained flanking markers, was not changed from that of the parental tumor cell line. The chromosomal interval between microsatellite markers D11S1385 and D11S903 encompasses the previously localized minimal liver tumor suppressor region, suggesting that a common locus is responsible for tumor suppression among the rat liver tumor cell lines examined. The results of the present study have verified the presence of a liver tumor suppressor locus within human 11p11.2-p12, and have identified a substantial number of microsatellite markers that are closely linked to this tumor suppressor region. These chromosomal markers will facilitate positional cloning of candidate genes from this region, and may prove useful for determining the involvement of this locus in the pathogenesis of human liver cancer. 相似文献
62.
63.
64.
65.
PR Burchat GJ Feldman T Barklow AM Boyarski DL Burke JM Dorfan L Gladney G Hanson K Hayes RJ Hollebeek WR Innes JA Jaros D Karlen AJ Lankford RR Larsen BW LeClaire NS Lockyer V Lüth C Matteuzzi RA Ong ML Perl B Richter K Riles MC Ross JM Yelton C Zaiser GS Abrams D Amidei AR Baden J Boyer F Butler G Gidal MS Gold G Goldhaber L Golding J Haggerty D Herrup I Juricic JA Kadyk ME Nelson PC Rowson H Schellman WB Schmidke PD Sheldon GH Trilling de la Vaissiere C DR Wood ME Levi T Schaad 《Canadian Metallurgical Quarterly》1987,35(1):27-41
66.
67.
WB Strong 《Canadian Metallurgical Quarterly》1999,20(1):1-3; discussion 89
68.
Soluble factors from serum such as lysophosphatidic acid (LPA) are thought to activate the small GTP-binding protein Rho based on their ability to induce actin stress fibers and focal adhesions in a Rho-dependent manner. Cell adhesion to extracellular matrices (ECM) has also been proposed to activate Rho, but this point has been controversial due to the difficulty of distinguishing changes in Rho activity from the structural contributions of ECM to the formation of focal adhesions. To address these questions, we established an assay for GTP-bound cellular Rho. Plating Swiss 3T3 cells on fibronectin-coated dishes elicited a transient inhibition of Rho, followed by a phase of Rho activation. The activation phase was greatly enhanced by serum. In serum-starved adherent cells, LPA induced transient Rho activation, whereas in suspended cells Rho activation was sustained. Furthermore, suspended cells showed higher Rho activity than adherent cells in the presence of serum. These data indicate the existence of an adhesion-dependent negative-feedback loop. We also observed that both cytochalasin D and colchicine trigger Rho activation despite their opposite effects on stress fibers and focal adhesions. Our results show that ECM, cytoskeletal structures and soluble factors all contribute to regulation of Rho activity. 相似文献
69.
70.
Significant spinal deformity is particularly common in nonambulatory patients with myelodysplasia. Progressive deformity may be caused by congenital anomalies, paralytic collapse, hip contractures, or spinal cord tethering. Existing or projected functional impairment should be the principle indication for treatment. Surgical treatment is complicated by poor soft tissue coverage, associated contractures, lack of sensation, weak bone, and absence of posterior elements. Successful fusion can be achieved by circumferential (anterior and posterior) fusion and current rigid segmental instrumentation. The unique deformities and bony anatomy require individualized techniques to achieve fixation. 相似文献