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861.
Physiological increase in plasma leptin markedly inhibits insulin secretion in vivo 总被引:14,自引:0,他引:14
Cases JA Gabriely I Ma XH Yang XM Michaeli T Fleischer N Rossetti L Barzilai N 《Diabetes》2001,50(2):348-352
The demonstration of leptin receptors on the pancreatic beta-cells suggests the possibility of direct actions of leptin on insulin secretion. In vitro studies on islets or perfused pancreas and beta-cell lines produced inconsistent results. We performed an in vivo study to distinctly examine whether leptin has an effect on glucose-stimulated insulin secretion. Young chronically catheterized Sprague-Dawley rats (n = 28) were subjected to a 4-h hyperglycemic clamp study (approximately 11 mmol/l). At minute 120 to 240, rats were assigned to receive either saline or leptin (0.1, 0.5, and 5 microg x kg(-1) x min) infusion. Leptin decreased plasma insulin levels abruptly, and an approximately twofold decrease in plasma insulin levels compared with saline control was sustained over the 2 h of the study (14.8 +/- 5.8 vs. 34.8 +/- 2.6 ng/ml with leptin and saline infusion, respectively, P < 0.001). Moreover, a dose-dependent decrease in plasma insulin levels was noted (r = -0.731, P < 0.01). Since milrinone, an inhibitor of cAMP phosphodiesterase (PDE) 3, did not reverse the effect of leptin on glucose-induced insulin secretion, its action may be independent of PDE3. These findings suggest that acute physiological increase in plasma leptin levels acutely and significantly inhibits glucose-stimulated insulin secretion in vivo. The site of leptin effects on insulin secretion remains to be determined. 相似文献
862.
The molecular mechanism of dopamine-induced apoptosis: identification and characterization of genes that mediate dopamine toxicity 总被引:1,自引:0,他引:1
Barzilai A Zilkha-Falb R Daily D Stern N Offen D Ziv I Melamed E Shirvan A 《Journal of neural transmission. Supplementum》2000,(60):59-76
Parkinson's disease (PD) is a progressive neurological disorder caused by rather selective degeneration of the dopaminergic (DA) neurons in the substantia nigra. Though subject to intensive research, the etiology of this nigral neuronal loss is still enigmatic and treatment is basically symptomatic. The current major hypothesis suggests that nigral neuronal death in PD is due to excessive oxidative stress generated by auto- and enzymatic oxidation of the endogenous neurotransmitter dopamine (DA), the formation of neuromelanin and presence of high concentrations of iron. We have found that DA toxicity is mediated through its oxidative metabolites. Whereas thiol-containing antioxidants provided marked protection against DA toxicity, ascorbic acid accelerated DA-induced death. Using the differential display approach, we sought to isolate and characterize genes whose expression is altered in response to DA toxicity. We found an upregulation of the collapsin response mediator protein (CRM) and TCP-1delta in sympathetic neurons, which undergo dopamine-induced apoptosis. The isolation of these genes led us to examine the expression and activity of CRM and TCP-1delta related genes. Indeed, we found a significant induction of mRNAs of the secreted collapsin-1 and the mitochondrial stress protein HSP60. Antibodies directed against collapsin-1 provided marked and prolonged protection of several neuronal cell types from dopamine-induced apoptosis. In a parallel study, using antisense technology, we found that inhibition of TCP-1delta expression significantly reduced DA-induced neuronal death. These findings suggest a functional role for collapsin-1 and TCP-1delta as positive mediators of DA-induced neuronal apoptosis. 相似文献
863.
864.
865.
The effects of amyloid-β on the activity and excitability of individual neurons in the early and advanced stages of the pathological progression of Alzheimer's disease remain unknown. We used in vivo intracellular recordings to measure the ongoing and evoked activity of pyramidal neurons in the frontal cortex of APPswe/PS1dE9 transgenic mice and age-matched nontransgenic littermate controls. Evoked excitability was altered in both transgenic groups: neurons in young transgenic mice displayed hypoexcitability, whereas those in older transgenic mice displayed hyperexcitability, suggesting changes in intrinsic electrical properties of the neurons. However, the ongoing activity of neurons in both young and old transgenic groups showed signs of hyperexcitability in the depolarized state of the membrane potential. The membrane potential of neurons in old transgenic mice had an increased tendency to fail to transition to the depolarized state, and the depolarized states had shorter durations on average than did controls. This suggests a combination of both intrinsic electrical and synaptic dysfunctions as mechanisms for activity changes at later stages of the neuropathological progression. 相似文献
866.
Sebastiani Paola Song Zeyuan Ellis Dylan Tian Qu Schwaiger-Haber Michaela Stancliffe Ethan Lustgarten Michael S. Funk Cory C. Baloni Priyanka Yao Cong-Hui Joshi Shakchhi Marron Megan M. Gurinovich Anastasia Li Mengze Leshchyk Anastasia Xiang Qingyan Andersen Stacy L. Feitosa Mary F. Ukraintseva Svetlana Soerensen Mette Fiehn Oliver Ordovas Jose M. Haigis Marcia Monti Stefano Barzilai Nir Milman Sofiya Ferrucci Luigi Rappaport Noa Patti Gary J. Perls Thomas T. 《Age (Dordrecht, Netherlands)》2023,45(1):415-426
GeroScience - With the goal of identifying metabolites that significantly correlate with the protective e2 allele of the apolipoprotein E (APOE) gene, we established a consortium of five studies of... 相似文献
867.
Lykke Sylow Thomas E. Jensen Maximilian Kleinert Joshua R. Mouatt Stine J. Maarbjerg Jacob Jeppesen Clara Prats Tim T. Chiu Shlomit Boguslavsky Amira Klip Peter Schjerling Erik A. Richter 《Diabetes》2013,62(4):1139-1151
In skeletal muscle, the actin cytoskeleton-regulating GTPase, Rac1, is necessary for insulin-dependent GLUT4 translocation. Muscle contraction increases glucose transport and represents an alternative signaling pathway to insulin. Whether Rac1 is activated by muscle contraction and regulates contraction-induced glucose uptake is unknown. Therefore, we studied the effects of in vivo exercise and ex vivo muscle contractions on Rac1 signaling and its regulatory role in glucose uptake in mice and humans. Muscle Rac1-GTP binding was increased after exercise in mice (∼60–100%) and humans (∼40%), and this activation was AMP-activated protein kinase independent. Rac1 inhibition reduced contraction-stimulated glucose uptake in mouse muscle by 55% in soleus and by 20–58% in extensor digitorum longus (EDL; P < 0.01). In agreement, the contraction-stimulated increment in glucose uptake was decreased by 27% (P = 0.1) and 40% (P < 0.05) in soleus and EDL muscles, respectively, of muscle-specific inducible Rac1 knockout mice. Furthermore, depolymerization of the actin cytoskeleton decreased contraction-stimulated glucose uptake by 100% and 62% (P < 0.01) in soleus and EDL muscles, respectively. These are the first data to show that Rac1 is activated during muscle contraction in murine and human skeletal muscle and suggest that Rac1 and possibly the actin cytoskeleton are novel regulators of contraction-stimulated glucose uptake.Muscle contraction, like insulin, increases glucose uptake into skeletal muscle (1,2). Insulin and muscle contraction both stimulate the translocation of vesicles containing the glucose transporter GLUT4 from intracellular compartments to the sarcolemma and T tubules, allowing glucose to enter the cell via facilitated diffusion (3–5). However, the proximal signaling pathways of contraction and insulin are distinct. Muscle contraction has no effect on the insulin-signaling pathway (6,7), and muscle-specific knockout of the insulin receptor (8), or inhibition of phosphatidyl inositol 3-kinase with wortmannin (9) does not impair contraction-stimulated glucose uptake. Exercise has an insulin-sensitizing effect, suggesting that these two pathways may regulate similar unidentified distal signaling steps (10,11).Activation of AMP-activated protein kinase (AMPK) and calcium-dependent signaling, such as protein kinase Cs (PKCs) and calcium-calmodulin–dependent kinases, has traditionally been believed to induce glucose uptake during muscle contraction (3,12). However, the functional significance of these pathways is not fully understood. It is likely that so far unrecognized mechanisms regulated by AMPK, PKCs, calcium, liver kinase B1, stretch, reactive oxygen, and nitrogen species, or other yet unidentified pathways, participate in the regulation of glucose uptake during muscle contraction (3,13).One such candidate is Rac1 (Ras-related C3 botulinum toxin substrate 1), a small Rho family GTPase that regulates various cellular processes, including dynamic assembly and disassembly of the actin cytoskeleton (14,15). Rac1 is activated by insulin and induces actin cytoskeleton remodeling at the plasma membrane (15,16). Rac1-dependent rearrangement of the actin cytoskeleton is necessary for insulin-stimulated GLUT4 translocation in L6 myotubes (16–18).Even though Rac1 has traditionally only been implicated in insulin signaling, the contraction-related protein, AMPK, has been proposed to activate Rac1 in cultured muscle cells (19), endothelial cells (20), and macrophages (21). The primary aim of the present investigation was to explore whether insulin-independent stimuli, such as exercise in vivo and muscle contractions in vitro, activate Rac1 in skeletal muscle. Because Rac1 activation is necessary for insulin-stimulated GLUT4 translocation (22), we further aimed to investigate the involvement of Rac1 in AICAR- and contraction-stimulated glucose uptake. We hypothesized that Rac1 is activated by muscle contraction and that this activation plays a role in contraction-induced glucose uptake. 相似文献
868.
Rachel Grossman MD Erez Nossek MD Razi Sitt MSW Daniel Hayat MD Tal Shahar MD Ori Barzilai MD Tal Gonen MA Akiva Korn MMedSc Gal Sela MA Zvi Ram MD 《Annals of surgical oncology》2013,20(5):1722-1728
Background
Awake-craniotomy allows maximal tumor resection, which has been associated with extended survival. The feasibility and safety of awake-craniotomy and the effect of extent of resection on survival in the elderly population has not been established. The aim of this study was to compare surgical outcome of elderly patients undergoing awake-craniotomy to that of younger patients.Methods
Outcomes of consecutive patients younger and older than 65 years who underwent awake-craniotomy at a single institution between 2003 and 2010 were retrospectively reviewed. The groups were compared for clinical variables and surgical outcome parameters, as well as overall survival.Results
A total of 334 young (45.4 ± 13.2 years, mean ± SD) and 90 elderly (71.7 ± 5.1 years) patients were studied. Distribution of gender, mannitol treatment, hemodynamic stability, and extent of tumor resection were similar. Significantly more younger patients had a better preoperative Karnofsky Performance Scale score (>70) than elderly patients (P = 0.0012). Older patients harbored significantly more high-grade gliomas (HGG) and brain metastases, and fewer low-grade gliomas (P < 0.0001). No significantly higher rate of mortality, or complications were observed in the elderly group. Age was associated with increased length of stay (4.9 ± 6.3 vs. 6.6 ± 7.5 days, P = 0.01). Maximal extent of tumor resection in patients with HGG was associated with prolonged survival in the elderly patients.Conclusions
Awake-craniotomy is a well-tolerated and safe procedure, even in elderly patients. Gross total tumor resection in elderly patients with HGG was associated with prolonged survival. The data suggest that favorable prognostic factors for patients with malignant brain tumors are also valid in elderly patients. 相似文献869.
Childhood obesity 总被引:4,自引:0,他引:4
Speiser PW Rudolf MC Anhalt H Camacho-Hubner C Chiarelli F Eliakim A Freemark M Gruters A Hershkovitz E Iughetti L Krude H Latzer Y Lustig RH Pescovitz OH Pinhas-Hamiel O Rogol AD Shalitin S Sultan C Stein D Vardi P Werther GA Zadik Z Zuckerman-Levin N Hochberg Z;Obesity Consensus Working Group 《The Journal of clinical endocrinology and metabolism》2005,90(3):1871-1887
In March 2004 a group of 65 physicians and other health professionals representing nine countries on four continents convened in Israel to discuss the widespread public health crisis in childhood obesity. Their aim was to explore the available evidence and develop a consensus on the way forward. The process was rigorous, although time and resources did not permit the development of formal evidence-based guidelines. In the months before meeting, participants were allocated to seven groups covering prevalence, causes, risks, prevention, diagnosis, treatment, and psychology. Through electronic communication each group selected the key issues for their area, searched the literature, and developed a draft document. Over the 3-d meeting, these papers were debated and finalized by each group before presenting to the full group for further discussion and agreement. In developing a consensus statement, this international group has presented the evidence, developed recommendations, and provided a platform aimed toward future corrective action and ongoing debate in the international community. 相似文献
870.
Anisimov VN Bartke A Barzilai N Batin MA Blagosklonny MV Brown-Borg H Budovskaya Y Campisi J Friguet B Fraifeld V Franceschi C Gems D Gladyshev V Gorbunova V Gudkov AV Kennedy B Konovalenko M Kraemer B Moskalev A Petropoulos I Pasyukova E Rattan S Rogina B Seluanov A Shaposhnikov M Shmookler Reis R Tavernarakis N Vijg J Yashin A Zimniak P 《Aging》2012,4(5):305-317