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91.
We investigated the mechanisms for glucocorticoid regulation of rat renal NaK-ATPase activity. Our findings suggest that the magnitudes of corticosterone-induced increases in
1 mRNA and
1 mRNA levels are similar in the kidney of the adult adrenalectomized rats. The results also suggest that corticosterone restores NaK-ATPase activity in adrenalectomized rats prior to any enhanced sodium delivery. 相似文献
92.
93.
The influence of a) tissue culture medium (RPMI), b) homologous plasma (HP), and c) fetal calf serum (FCS) on lymphocytic cortisol metabolism was compared to that of phosphate buffered saline alone. RPMI was found to enhance the conversion rate 1.71 times, whereas HP and FCS enhanced it about 3.2 times. Raising the temperature of the HP and FCS to 100 degrees C before incubation reduced the enhancing effect to the level of that obtained with RPMI. 相似文献
94.
We investigated the mechanisms for glucocorticoid regulation of rat renal NaK-ATPase activity. Our findings suggest that the magnitudes of corticosterone-induced increases in alpha 1 mRNA and beta 1 mRNA levels are similar in the kidney of the adult adrenalectomized rats. The results also suggest that corticosterone restores NaK-ATPase activity in adrenalectomized rats prior to any enhanced sodium delivery. 相似文献
95.
Evolution of tumours and the impact of molecular oncology 总被引:3,自引:0,他引:3
It is generally accepted that tumours arise through the accumulation of several changes affecting the control of cell growth. Recent advances in molecular biology have made it possible to define some of these changes in molecular terms and to trace the steps by which certain tumours evolve. 相似文献
96.
Herman MA Peroni OD Villoria J Schön MR Abumrad NA Blüher M Klein S Kahn BB 《Nature》2012,484(7394):333-338
97.
Pérez-Mancera PA Rust AG van der Weyden L Kristiansen G Li A Sarver AL Silverstein KA Grützmann R Aust D Rümmele P Knösel T Herd C Stemple DL Kettleborough R Brosnan JA Li A Morgan R Knight S Yu J Stegeman S Collier LS ten Hoeve JJ de Ridder J Klein AP Goggins M Hruban RH Chang DK Biankin AV Grimmond SM;Australian Pancreatic Cancer Genome Initiative Wessels LF Wood SA Iacobuzio-Donahue CA Pilarsky C Largaespada DA Adams DJ Tuveson DA 《Nature》2012,486(7402):266-270
Pancreatic ductal adenocarcinoma (PDA) remains a lethal malignancy despite much progress concerning its molecular characterization. PDA tumours harbour four signature somatic mutations in addition to numerous lower frequency genetic events of uncertain significance. Here we use Sleeping Beauty (SB) transposon-mediated insertional mutagenesis in a mouse model of pancreatic ductal preneoplasia to identify genes that cooperate with oncogenic Kras(G12D) to accelerate tumorigenesis and promote progression. Our screen revealed new candidate genes for PDA and confirmed the importance of many genes and pathways previously implicated in human PDA. The most commonly mutated gene was the X-linked deubiquitinase Usp9x, which was inactivated in over 50% of the tumours. Although previous work had attributed a pro-survival role to USP9X in human neoplasia, we found instead that loss of Usp9x enhances transformation and protects pancreatic cancer cells from anoikis. Clinically, low USP9X protein and messenger RNA expression in PDA correlates with poor survival after surgery, and USP9X levels are inversely associated with metastatic burden in advanced disease. Furthermore, chromatin modulation with trichostatin A or 5-aza-2'-deoxycytidine elevates USP9X expression in human PDA cell lines, indicating a clinical approach for certain patients. The conditional deletion of Usp9x cooperated with Kras(G12D) to accelerate pancreatic tumorigenesis in mice, validating their genetic interaction. We propose that USP9X is a major tumour suppressor gene with prognostic and therapeutic relevance in PDA. 相似文献
98.
C Kaschka-Dierich A Adams T Lindahl G W Bornkamm G Bjursell G Klein B C Giovanella S Singh 《Nature》1976,260(5549):302-306
Tumour biopsies from Burkitt lymphoma patients, as well as human nasopharyngeal carcinoma cells growing in athymic mice, contain Epstein-Barr virus DNA as covalently closed circular DNA. In addition integrated viral DNA sequences seem to be present. 相似文献
99.
Sue A. Binkley D. C. Klein Joan L. Weller 《Cellular and molecular life sciences : CMLS》1973,29(11):1339-1340
Zusammenfassung Nachweis, dass Ratten, aus normaler Lichtperiode abrupt in Dunkelheit versetzt, keine Zunahme der NATase-Aktivität im Pinealorgan zeigen und dass Isoproterenol-Injektion die Zunahme der NATase auslöst.
Support was provided to S. B. by NIH Postdoctoral Fellowship No. 1 FO2 HD 52858-01.
We thankW. Langebartel andM. Veltrum. 相似文献
Support was provided to S. B. by NIH Postdoctoral Fellowship No. 1 FO2 HD 52858-01.
We thankW. Langebartel andM. Veltrum. 相似文献
100.