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101.
Shiau Yun Chong Catherine R. Chittleborough Tess Gregory Murthy N. Mittinty John W. Lynch Lisa G. Smithers 《PloS one》2016,11(3)
Cognitive development might be influenced by parenting practices and child temperament. We examined whether the associations between parental warmth, control and intelligence quotient (IQ) may be heightened among children in difficult temperament. Participants were from the Avon Longitudinal Study of Parents and Children (n = 7,044). Temperament at 6 months was measured using the Revised Infant Temperament Questionnaire and classified into ‘easy’ and ‘difficult’. Parental warmth and control was measured at 24 to 47 months and both were classified into 2 groups using latent class analyses. IQ was measured at 8 years using the Wechsler Intelligence Scale for Children and dichotomized (<85 and ≥85) for analyzing effect-measure modification by temperament. Linear regression adjusted for multiple confounders and temperament showed lower parental warmth was weakly associated with lower IQ score [β = -0.52 (95% CI 1.26, 0.21)], and higher parental control was associated with lower IQ score [β = -2.21 (-2.95, -1.48)]. Stratification by temperament showed no increased risk of having low IQ in temperamentally difficult children [risk ratio (RR) = 0.97 95% CI 0.65, 1.45)] but an increased risk among temperamentally easy children (RR = 1.12 95% CI 0.95, 1.32) when parental warmth was low. There was also no increased risk of having low IQ in temperamentally difficult children (RR = 1.02 95% CI 0.69, 1.53) but there was an increased risk among temperamentally easy children (RR = 1.30 95% CI 1.11, 1.53) when parental control was high. For both parental warmth and control, there was some evidence of negative effect-measure modification by temperament on the risk-difference scale and the risk-ratio scale. It may be more appropriate to provide parenting interventions as a universal program rather than targeting children with difficult temperament. 相似文献
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Sunita M. C. De Sousa Liam C. McIntyre Chan-Eng Chong Hamish S. Scott 《BMC endocrine disorders》2016,16(1):58
Background
The 46,XY female is characterised by a male karyotype and female phenotype arising due to any interruption in the sexual development pathways in utero. The cause is usually genetic and various genes are implicated.Case presentation
Herein we describe a 46,XY woman who was first diagnosed with androgen insensitivity syndrome (testicular feminisation) at 18 years; however, this was later questioned due to the presence of intact Müllerian structures. The clinical phenotype suggested several susceptibility genes including SRY, DHH, NR5A1, NR0B1, AR, AMH, and AMHR2. To study candidate genes simultaneously, we performed whole genome sequencing. This revealed a novel and likely pathogenic missense variant (p.Arg130Pro, c.389G>C) in SRY, one of the major genes implicated in complete gonadal dysgenesis, hence securing this condition over androgen insensitivity syndrome as the cause of the patient’s disorder of sexual development.Conclusion
This case highlights the emerging clinical utility of whole genome sequencing as a tool in differentiating disorders of sexual development.104.
Development of antifouling strategies requires knowledge of how fouling organisms would respond to climate change associated environmental stressors. Here, a calcareous tube built by the tubeworm, Hydroides elegans, was used as an example to evaluate the individual and interactive effects of ocean acidification (OA), warming and reduced salinity on the mechanical properties of a tube. Tubeworms produce a mechanically weaker tube with less resistance to simulated predator attack under OA (pH 7.8). Warming (29°C) increased tube volume, tube mineral density and the tube’s resistance to a simulated predatory attack. A weakening effect by OA did not make the removal of tubeworms easier except for the earliest stage, in which warming had the least effect. Reduced salinity (27 psu) did not affect tubes. This study showed that both mechanical analysis and computational modeling can be integrated with biofouling research to provide insights into how fouling communities might develop in future ocean conditions. 相似文献
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目的:探讨褪黑素对脊髓损伤大鼠突触可塑性的影响及磷脂酰肌醇3-激酶/张力蛋白同源基因/蛋白激酶B(PI3K/PTEN/AKT)信号途径在其中的作用。方法:选择4月龄SPF级雄性SD大鼠48只,将其随机分为对照组(CON)、模型组(SCI)、褪黑素组(MT)和褪黑素受体拮抗剂组(LUZ),每组12只大鼠。对照组大鼠背部切口后缝合,余下各组大鼠使用改良的Allen's法建立T9水平的脊髓损伤模型。模型建立后,褪黑素组及褪黑素受体拮抗剂组每天腹腔注射褪黑素及褪黑素抑制剂,剂量为12.5 mg·kg~(-1)·d~(-1),对照组和模型组每天注射同体积的生理盐水。治疗后第3、7、14、21、28天进行BBB评分,实验结束处死大鼠取胸椎8-10节段脊髓组织,分别采用免疫组化方法测尼氏小体数量及Western Blot检测PTEN、Synapsin、PSD-95、Gap-43、Akt蛋白的表达。结果:与SCI模型大鼠相比,MT给药干预14 d后的SCI大鼠BBB评分及痛觉压力值均明显降低(P0.05),尼氏小体灰度值提高(P 0.05),PTEN、Synapsin、PSD-95、Gap-43、Akt蛋白的表达均显著上调(P 0.05)。结论:MT可能通过激活PI3K/PTEN/Akt信号途径,上调突触可塑性相关蛋白的表达,促进SCI大鼠突触修复。 相似文献
108.
Jia‐Min Wang An‐Fang Huang Wang‐Dong Xu Lin‐Chong Su 《Journal of cellular and molecular medicine》2019,23(12):7926-7932
Interleukin‐29 (IL‐29) is a newly discovered member of type III interferon. It mediates signal transduction via binding to its receptor complex and activates downstream signalling pathways, and therefore induces the generation of inflammatory components. Recent studies reported that expression of IL‐29 is dysregulated in inflammatory autoimmune diseases, such as rheumatoid arthritis, systemic lupus erythematosus, osteoarthritis, Sjögren's syndrome, psoriasis and systemic sclerosis. Furthermore, functional analysis revealed that IL‐29 may involve in the pathogenesis of the inflammatory autoimmune disorders. In this review, we will systematically review the current knowledge about IL‐29. The information collected revealed the regulatory role of IL‐29 and may give important implications for its potential in clinical treatment. 相似文献
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Yang‐ling Li Ke Ding Xiu Hu Lin‐wen Wu Dong‐mei Zhou Ming‐jun Rao Neng‐ming Lin Chong Zhang 《Journal of cellular and molecular medicine》2019,23(11):7427-7437
DYRK1A is considered a potential cancer therapeutic target, but the role of DYRK1A in NSCLC oncogenesis and treatment requires further investigation. In our study, high DYRK1A expression was observed in tumour samples from patients with lung cancer compared with normal lung tissues, and the high levels of DYRK1A were related to a reduced survival time in patients with lung cancer. Meanwhile, the DYRK1A inhibitor harmine could suppress the proliferation of NSCLC cells compared to that of the control. As DYRK1A suppression might be effective in treating NSCLC, we next explored the possible specific molecular mechanisms that were involved. We showed that DYRK1A suppression by siRNA could suppress the levels of EGFR and Met in NSCLC cells. Furthermore, DYRK1A siRNA could inhibit the expression and nuclear translocation of STAT3. Meanwhile, harmine could also regulate the STAT3/EGFR/Met signalling pathway in human NSCLC cells. AZD9291 is effective to treat NSCLC patients with EGFR‐sensitivity mutation and T790 M resistance mutation, but the clinical efficacy in patients with wild‐type EGFR remains modest. We showed that DYRK1A repression could enhance the anti‐cancer effect of AZD9291 by inducing apoptosis and suppressing cell proliferation in EGFR wild‐type NSCLC cells. In addition, harmine could enhance the anti‐NSCLC activity of AZD9291 by modulating STAT3 pathway. Finally, harmine could enhance the anti‐cancer activity of AZD9291 in primary NSCLC cells. Collectively, targeting DYRK1A might be an attractive target for AZD9291 sensitization in EGFR wild‐type NSCLC patients. 相似文献