全文获取类型
收费全文 | 12307篇 |
免费 | 1202篇 |
国内免费 | 864篇 |
专业分类
耳鼻咽喉 | 75篇 |
儿科学 | 142篇 |
妇产科学 | 81篇 |
基础医学 | 1441篇 |
口腔科学 | 143篇 |
临床医学 | 1490篇 |
内科学 | 1764篇 |
皮肤病学 | 117篇 |
神经病学 | 612篇 |
特种医学 | 421篇 |
外国民族医学 | 9篇 |
外科学 | 1316篇 |
综合类 | 2478篇 |
现状与发展 | 3篇 |
一般理论 | 1篇 |
预防医学 | 875篇 |
眼科学 | 286篇 |
药学 | 1326篇 |
6篇 | |
中国医学 | 781篇 |
肿瘤学 | 1006篇 |
出版年
2024年 | 45篇 |
2023年 | 171篇 |
2022年 | 455篇 |
2021年 | 547篇 |
2020年 | 416篇 |
2019年 | 444篇 |
2018年 | 442篇 |
2017年 | 355篇 |
2016年 | 349篇 |
2015年 | 486篇 |
2014年 | 638篇 |
2013年 | 600篇 |
2012年 | 778篇 |
2011年 | 845篇 |
2010年 | 591篇 |
2009年 | 458篇 |
2008年 | 492篇 |
2007年 | 602篇 |
2006年 | 589篇 |
2005年 | 540篇 |
2004年 | 516篇 |
2003年 | 687篇 |
2002年 | 642篇 |
2001年 | 544篇 |
2000年 | 395篇 |
1999年 | 358篇 |
1998年 | 186篇 |
1997年 | 191篇 |
1996年 | 136篇 |
1995年 | 139篇 |
1994年 | 123篇 |
1993年 | 92篇 |
1992年 | 89篇 |
1991年 | 89篇 |
1990年 | 69篇 |
1989年 | 57篇 |
1988年 | 55篇 |
1987年 | 47篇 |
1986年 | 39篇 |
1985年 | 26篇 |
1984年 | 14篇 |
1983年 | 6篇 |
1982年 | 7篇 |
1981年 | 4篇 |
1980年 | 4篇 |
1979年 | 10篇 |
1978年 | 1篇 |
1977年 | 1篇 |
1968年 | 1篇 |
1966年 | 2篇 |
排序方式: 共有10000条查询结果,搜索用时 0 毫秒
991.
Watts LM Manchem VP Leedom TA Rivard AL McKay RA Bao D Neroladakis T Monia BP Bodenmiller DM Cao JX Zhang HY Cox AL Jacobs SJ Michael MD Sloop KW Bhanot S 《Diabetes》2005,54(6):1846-1853
Glucocorticoids (GCs) increase hepatic gluconeogenesis and play an important role in the regulation of hepatic glucose output. Whereas systemic GC inhibition can alleviate hyperglycemia in rodents and humans, it results in adrenal insufficiency and stimulation of the hypothalamic-pituitary-adrenal axis. In the present study, we used optimized antisense oligonucleotides (ASOs) to cause selective reduction of the glucocorticoid receptor (GCCR) in liver and white adipose tissue (WAT) and evaluated the resultant changes in glucose and lipid metabolism in several rodent models of diabetes. Treatment of ob/ob mice with GCCR ASOs for 4 weeks resulted in approximately 75 and approximately 40% reduction in GCCR mRNA expression in liver and WAT, respectively. This was accompanied by approximately 65% decrease in fed and approximately 30% decrease in fasted glucose levels, a 60% decrease in plasma insulin concentration, and approximately 20 and 35% decrease in plasma resistin and tumor necrosis factor-alpha levels, respectively. Furthermore, GCCR ASO reduced hepatic glucose production and inhibited hepatic gluconeogenesis in liver slices from basal and dexamethasone-treated animals. In db/db mice, a similar reduction in GCCR expression caused approximately 40% decrease in fed and fasted glucose levels and approximately 50% reduction in plasma triglycerides. In ZDF and high-fat diet-fed streptozotocin-treated (HFD-STZ) rats, GCCR ASO treatment caused approximately 60% reduction in GCCR expression in the liver and WAT, which was accompanied by a 40-70% decrease in fasted glucose levels and a robust reduction in plasma triglyceride, cholesterol, and free fatty acids. No change in circulating corticosterone levels was seen in any model after GCCR ASO treatment. To further demonstrate that GCCR ASO does not cause systemic GC antagonism, normal Sprague-Dawley rats were challenged with dexamethasone after treating with GCCR ASO. Dexamethasone increased the expression of GC-responsive genes such as PEPCK in the liver and decreased circulating lymphocytes. GCCR ASO treatment completely inhibited the increase in dexamethasone-induced PEPCK expression in the liver without causing any change in the dexamethasone-induced lymphopenia. These studies demonstrate that tissue-selective GCCR antagonism with ASOs may be a viable therapeutic strategy for the treatment of the metabolic syndrome. 相似文献
992.
993.
994.
995.
Liu BY Wang CC Lau TK Chu CY Phil M Pang CP Rogers MS Leung TN 《American journal of obstetrics and gynecology》2005,192(1):289-294
OBJECTIVE: The purpose of this study was to compare the umbilical arterial 8-iso-prostaglandin F2alpha, concentrations between pregnancies that were complicated by moderate or thick meconium-stained liquor and those with clear liquor. STUDY DESIGN: Umbilical cord arterial blood samples were collected from 247 singleton pregnancies with either moderate or thick meconium-stained liquor at any stage of labor or clear liquor at all stages of labor for the determination of the total 8-iso-prostaglandins F2alpha concentration. RESULTS: The median total 8-iso-prostaglandins F2alpha concentration of the meconium-stained liquor group was significantly higher than that of the control group (719.2 vs 115.8 pg/mL). Among the meconium-stained liquor group, those who had a change from "clear liquor" at early labor to "moderate/ thick meconium-stained liquor" at late first stage or at delivery (late meconium-stained liquor group) had higher 8-iso-prostaglandins F2alpha concentration, compared with those who had moderate/ thick meconium-stained liquor since early labor (early meconium-stained liquor group; 959.8 vs 499.9 pg/mL). With the use of multiple regression analysis, meconium-stained liquor, duration of second stage of labor, and abnormal fetal heart tracings were independent determinants of cord blood 8-iso-prostaglandins F2alpha concentration. CONCLUSION: Moderate or thick meconium-stained liquor is an independent factor for increased oxidative stress in pregnancy. 相似文献
996.
997.
X-linked adrenoleukodystrophy is a neurodegenerative disorder caused by mutations in the adrenoleukodystrophy (ALD) protein gene ABCD1. This study used direct sequencing of genomic polymerase chain reaction products to perform mutational analysis of ABCD1 in 34 unrelated Chinese X-linked adrenoleukodystrophy patients and 27 of their maternal relatives. Thirty-two different mutations were identified in 34 patients. Most of the mutations (62.5%, 20/32) were missense mutations, six of which are novel. One novel single nucleotide polymorphism, c.1047 C>A, was also found in three patients and their mothers, which can also be observed in 1 of 120 normal control alleles. Two synonymous mutations (p.L516L and p.V349V) appeared in two unrelated patients, and no other mutations were evident after screening the gene's 10 exons. Seventeen of the probands' mothers were found to be heterozygous for the same mutations present in their sons' ABCD1 gene. Eight of the 10 screened sisters and cousins were identified as carriers. There were no hot spot mutations in the ABCD1 gene of Chinese patients with X-linked adrenoleukodystrophy. However, over half of the mutations (19/34) were located in exon 1 and exon 6, suggesting possible hot exons. No obvious relationship between genotype and phenotype was observed. 相似文献
998.
999.
Rett综合征的临床特征及MeCP2的基因型与表型的关系研究 总被引:8,自引:4,他引:4
目的 总结Rett综合征(RTT)的临床特点,探讨甲基化CpG结合蛋白2(MeCP2)基因突变型与表型的关系。方法 北京大学第一医院儿科1987年以来诊断的RTT66例,每1~2年对本组患儿进行1次临床随访,并观察左旋肉碱的治疗反应。应用PCR、测序方法对39例患儿进行突变基因分析。结果 患儿3~38个月起病,59例(89%)患儿于7个月~6岁丧失手的功能,66例(100%)患儿1—5岁出现手的刻板动作,56例(85%)患儿11个月~8岁语言完全丧失,21%的患儿于2岁9个月~15岁丧失原已获得的行走能力。头围小、惊厥、呼吸节律异常、咬牙、脊柱侧凸或后凸均很常见。左旋肉碱治疗17例,8周后6例症状改善。39例进行.MeCP2基因分析者中有25例(64%)发现突变,其中2例无义突变C502T(氨基酸改变R168X)患儿均死亡,2例C397T(氨基酸改变R133C)和1例A398T(氨基酸改变R133H)突变者均保留语言。结论 RTI。特征性的表现为头围增长缓慢,手的失用与刻板动作,语言倒退,左旋肉碱可以改善部分患儿的临床症状。MeCP2基因型与表型之间有一定的相关性。 相似文献
1000.
Prenatal exposure to excessive glucocorticoids may alter the developing fetus inducing metabolic and endocrine imbalance in various organs, including the kidney. This study aimed at evaluating whether prenatal exposure to high levels of glucocorticoids adversely affects renal cell survival and predisposes to renal cell death. Pregnant rats were injected with 0.1 mg/kg dexamethasone (DEX) i.p. from day 1 of gestation. Renal proximal tubular cells (PTCs) were prepared from 20-day-old offspring in the DEX (DEX cells) and control groups (CON cells). After 4 days' culture, cells were exposed to uropathogenic Escherichia coli ARD6 toxins at concentrations known to induce apoptotic cell death. We found that cell death rate was significantly higher in DEX than in CON cells. Cells exhibited morphological and biochemical features of apoptosis. Conversely, the activity of the antioxidant enzyme catalase was significantly increased in renal cortex homogenate from 20-day-old DEX rats. The antioxidant vitamin E did not prevent apoptosis. These results indicate that prenatal exposure to high levels of glucocorticoids induces alterations in renal PTCs rendering them more sensitive to E. coli toxins via nonoxidative stress. With the increasing use of multiple doses of glucocorticoids in preterm infants, the possibility that antenatal glucocorticoids may lead to renal adverse consequences is of clinical relevance. 相似文献