全文获取类型
收费全文 | 20622篇 |
免费 | 2603篇 |
国内免费 | 1466篇 |
专业分类
耳鼻咽喉 | 157篇 |
儿科学 | 368篇 |
妇产科学 | 371篇 |
基础医学 | 4060篇 |
口腔科学 | 1056篇 |
临床医学 | 2294篇 |
内科学 | 2551篇 |
皮肤病学 | 203篇 |
神经病学 | 783篇 |
特种医学 | 399篇 |
外国民族医学 | 5篇 |
外科学 | 2116篇 |
综合类 | 3504篇 |
现状与发展 | 6篇 |
预防医学 | 682篇 |
眼科学 | 1665篇 |
药学 | 1905篇 |
5篇 | |
中国医学 | 534篇 |
肿瘤学 | 2027篇 |
出版年
2024年 | 47篇 |
2023年 | 413篇 |
2022年 | 583篇 |
2021年 | 1068篇 |
2020年 | 933篇 |
2019年 | 894篇 |
2018年 | 884篇 |
2017年 | 995篇 |
2016年 | 1050篇 |
2015年 | 1247篇 |
2014年 | 1827篇 |
2013年 | 1959篇 |
2012年 | 1424篇 |
2011年 | 1606篇 |
2010年 | 1297篇 |
2009年 | 1091篇 |
2008年 | 1157篇 |
2007年 | 1075篇 |
2006年 | 867篇 |
2005年 | 763篇 |
2004年 | 637篇 |
2003年 | 527篇 |
2002年 | 355篇 |
2001年 | 286篇 |
2000年 | 230篇 |
1999年 | 167篇 |
1998年 | 172篇 |
1997年 | 150篇 |
1996年 | 115篇 |
1995年 | 113篇 |
1994年 | 82篇 |
1993年 | 89篇 |
1992年 | 68篇 |
1991年 | 78篇 |
1990年 | 60篇 |
1989年 | 50篇 |
1988年 | 50篇 |
1987年 | 31篇 |
1986年 | 28篇 |
1985年 | 43篇 |
1984年 | 40篇 |
1983年 | 25篇 |
1982年 | 21篇 |
1981年 | 24篇 |
1980年 | 20篇 |
1979年 | 17篇 |
1978年 | 13篇 |
1977年 | 6篇 |
1976年 | 7篇 |
1975年 | 3篇 |
排序方式: 共有10000条查询结果,搜索用时 46 毫秒
71.
Tamaki Sasaki Tetsuya Sato Yoshiyuki Jyo Nobuya Tanda Hitoshi Tamai Gengo Osawa 《Clinical and experimental nephrology》1997,1(1):32-40
Background We previously found that glomerular epithelial cells play an important role in the formation of adhesive lesions. Glomerular
sclerotic lesions develop after the inital adhesive lesions.
Methods Two series of experiments were done with spontaneously diabetic WBN/Kob rats. These rats develop segmental glomerular sclerotic
lesions with aging. The first series of experiments was intended to clarify the kinetics of glomerular cells on progressive
glomerular damage in these rats. The second series of experiments was designed to study the relationship between proliferation
(judged by % bromodeoxyuridine-positive cells) of glomerlar epithelial cells and sclerotic lesions with adhesions.
Results In the first series, rats having increased proteinuria showed segmental glomerular sclerotic lesions with adhesions. At the
same time, increased labeling indices of tuft cells and epithelial cells of Bowman's capsule were observed. In the second
series, no significant increase in the labeling indices of tuft cells with sclerotic lesions was observed, compared to tuft
cells without sclerotic lesions. In sclerotic lesions with adhesion, bromodeoxyurdine-positive cells were observed that were
not distinguishable as podocytes or epithelial cells of Bowman's capsule. The highest labelling index was noted in the epithelial
cells of Bowman's capsules with sclerosis.
Conclusion This study shows that the proliferation of glomerular epithelial cells (mainly epithelial cells of Bowman's capsule) occurs
in glomerular sclerotic lesions with adhesions. 相似文献
72.
羊膜负载骨髓间充质干细胞与表皮细胞对放创性皮肤损伤促愈合研究 总被引:14,自引:3,他引:11
目的探讨治疗放创性全厚皮肤缺损创面的方法及效果. 方法贵州小香猪8只,每只背部脊柱两侧均有放创性全层皮肤缺损圆形创面(Ф3.67cm)各3个,共48个创面.将经处理的人羊膜(human amniotic mambrane, HAM)分别负载自体骨髓间充质干细胞(mesenchymal stem cells, MSCs)和表皮细胞,移植到其左侧24个创面作为实验组(A组);以单纯无种植细胞的HAM敷盖其右侧前16个创面(B组);以单纯油纱布敷盖其右侧后8个创面(C组).B、C作为对照组.观察移植后1~3周内各组创面愈合、肉芽组织生长及上皮化等情况,并进行创面组织HE染色及vWF免疫组织化学检测.用图像分析法测算各组各时间点创面平均面积(cm2),并计算其愈合百分率. 结果 C组于伤后 22~23天愈合,B组于伤后19~21天愈合;A组于伤后15~17天愈合,较B、C组分别提前6~7天和5~6天,愈合质量好.移植15~17天,A组与B、C组创面平均残留面积及愈合面积百分率比较,差异有统计学意义(P<0.01). A组创面的新生上皮已完全覆盖整个创面,肉芽组织生长旺盛,肉芽组织中vWF、成纤维细胞和毛细血管含量丰富,可见胶原沉积;B、C组创面仍见许多炎性细胞浸润,肉芽组织中vWF、成纤维细胞和毛细血管含量少,胶原沉积不明显. 结论 HAM负载自体MSCs和表皮细胞植入对放创性全厚皮肤缺损创面有较好的促愈合作用,愈合质量较高. 相似文献
73.
人骨髓间充质干细胞向多巴胺神经元分化的体外研究 总被引:2,自引:0,他引:2
目的探讨人骨髓间充质干细胞(hMSC)向神经元和多巴胺神经元分化的潜能。方法分离和纯化hMSCs;在体外以WHI-P131预处理和碱性成纤维细胞生长因子预诱导后,全反式维甲酸和胶质细胞源性神经营养因子联合诱导hMSCs向神经元和多巴胺神经元分化。光镜下观察其分化过程中hMSCs的形态变化,免疫组化检测诱导前后细胞是否表达神经元和多巴胺能神经元标志蛋白。结果诱导后的hMSCs能分化成为具有典型神经元形态的细胞,并明显表达抗人神经巢蛋白(nestin)[(54.2±3.7)%]和神经元特异性烯醇化酶(NSE)[(77.0±5.7)%],低表达胶质纤维酸性蛋白(GFAP)[(8.8±2.4)%];对照组细胞这些表达均为阴性;而且相当部分hMSCs表达酪氨酸羟化酶(TH)[(36.5±15.8)%]和多巴胺转运体(DAT)[(26.0±14.2)%]。结论在适当条件下,hMSCs可分化成为神经元样细胞和多巴胺神经元样细胞。 相似文献
74.
VEGF基因体外转染大鼠骨髓间充质干细胞的实验研究 总被引:1,自引:0,他引:1
目的:探讨脂质体介导血管内皮细胞生长因子(VEGF)基因转染大鼠骨髓间充质干细胞(MSCS)应用于基因治疗的可行性、安全性。方法:体外分离、培养、鉴定MSCs,PcDNA3.1(-)/VEGF165质粒转染MSCs,转染后用免疫荧光和ELISA检测MSCs表达VEGF蛋白的情况,MTT检测MSCs对VEGF质粒转染的敏感性。结果:骨髓中分离得到MSCs,流式细胞检测显示MSCs不表达CD34和CD45,但表达CD90。透射电镜观察可见细胞浆中含大量粗面内质网和分泌颗粒。VEGF基因转染MSCs后第5天抗VEGF免疫荧光染色约90%的MSCs呈阳性,ELISA检测结果显示PcDNA3.1(-)/VEGF165质粒转染组细胞培养上清液中VEGF含量明显高于对照组,并于转染后第5天达到峰值。MTT检测结果显示VEGF质粒转染对MSCs增殖无影响。结论:MSC可作为VEGF基因转染的靶细胞用于基因治疗。 相似文献
75.
76.
高奉浔 《中国人民解放军军医大学学报》1989,(1)
Eight cases of mesenchymal chondrosarcoma either of skeletal(5 cases) or extrasketetalorigin (3 cases) are reported. According to histopathological and diagnostic criteria,mesenchymal chondrosarcoma were classified into two types cartilage isiand cell type andundifierentiated small cell type It is believed that the application of this classification in the study ofmesenchymal chondrosarcoma is helptul the estimation of its malignancy and choice of treatmentas well al in the prediction of its prognosis. Mesenchymal chondrosarcoma is a highly malignant neoplasm with poor prognosis. None ofthe patients in this series survived more than five years after they were diagnosed. The diffentialdiagnosis of malignant lymphoma, chondrosarcoma, hemangiopericytosarcoma, etc. was discussed.My data support the assumption that mesenchymal chondrosarcoma originates from the secondarymesenchyme rather than the primary mesenchyme. 相似文献
77.
目的 探讨在“2× 4”矫治技术中弓丝弯制的方法及原理。方法 替牙牙合时期前牙反牙合患者 2 4例 ,使用粗弓丝 ,在其弓丝上弯制各种曲形 ,并根据不同错牙合类型 ,处理各种曲与牙齿、带环关系 ,防止出现磨牙旋转移动等异常。结果 2~ 6个月纠正反牙合 ,2 4例替牙牙合时期反牙合患者得以早期矫治。结论 本方法矫治时间短 ,效果明显 ,操作简单 ,能够达到较为理想的矫治效果 相似文献
78.
A low concentration of transition metal ions Co2+ and Ni2+ increases the inward current density in neurons from the land snail Helix aspersa. The currents were measured using a single electrode voltage-clamp/internal perfusion method under conditions in which the external Na+ was replaced by Tris+, the predominant external current carrying cation was Ca2+, and the internal perfusate contained 120 mM Cs+/0 K+; 30 mM tetraethylammonium (TEA) was added externally to block K+ current. In the presence of Co2+ (3 mM) or Ni2+ (0.5 mM) inward Ca2+ currents were stimulated normally by voltage-dependent activation of Ca2+ channels. There was a 5-10% decrease in the rate of rise of the inward current. The principal effect of Co2+ and Ni2+ in increasing the current density seems to be a decrease in the rate at which the inward currents decline during a depolarizing voltage pulse. The results may be due to a decrease in a voltage-dependent or Ca(2+)-dependent outward current and/or an inhibition of Ca2+ channel inactivation. Outward current under these conditions (zero internal K+) was significant and most likely due to Cs+ efflux through the voltage-activated or Ca(2+)-activated nonspecific cation channels. Co2+ is an extremely effective blocker of this outward current. These results are not an artifact of internal perfusion or the special ionic conditions. Intracellular recording of unperfused neurons in normal Helix Ringer's solution showed that the Ca(2+)-dependent action potential duration was increased significantly by low concentrations of Co2+. This result is consistant with the Co(2+)-dependent increase in inward (depolarizing) current seen in voltage-clamp experiments. 相似文献
79.
为研究和比较化学致癌物对人呼吸道上皮细胞和纤维母细胞的损伤及损伤后DNA修复合成的差异,作者用直接致癌物4-硝基喹啉-1-氧化物(4-NQO)和间接致癌物3,4-苯并芘(BaP)处理人胚鼻咽、气管上皮细胞和纤维母细胞,用放射自显影术测定这3种细胞的非时序脱氧核糖核酸合成(UDS)。用4-NQO处理后,这3种细胞的UDS均呈明显的剂量依赖(dose dePendency)关系,但气管和鼻咽上皮细胞UDS平均分别是纤维母细胞的3.0和2.4倍。用BaP处理后,气管和鼻咽上皮细胞UDS呈现明显的剂量依赖关系,而纤维母细胞未见这种关系。气管和鼻咽上皮细胞的UDS平均分别是纤维母细胞的8.6和3.0倍。 相似文献
80.
It is documented that alkaline phosphatase (AP) plays an important role in bone mineralization. Considering that TN-AP is
expressed in periodontal ligament fibroblasts, renal epithelial cells, and vascular endothelial cells, and that TN-AP is both
a calcium-/phosphate-binding protein and a phosphohydrolytic enzyme, we hypothesize that membrane-bound AP also plays an important
role in the initiation of physiological and pathological mineralizations in tissues other than bone and cartilage. To test
this hypothesis, nonosteoblast cell lines, including a fibroblast line, a renal epithelial line, and a capillary endothelial
line, were stably transfected to express high levels of rat bone AP on their cell surfaces. These rat bone AP-expressing cells
were then cultured on filter membranes in the presence or absence of β-glycerol phosphate. von Kossa staining for calcium
phosphate and transmission electron microscopy with electron diffraction analysis for minerals were employed to investigate
the effect of membrane AP on extracellular calcium phosphate mineralization. Our results indicated that AP expression on these
nonosteoblast-like cell surfaces have induced extracellular hydroxyapatite (HAP) mineralization. Our findings support the
concept that membrane-bound AP contributes to extracellular apatitic mineralization by mechanisms that do not necessarily
involve its hydrolase activity. They also suggest that AP might be important for the initiation of pathological mineralization
in nonosteogenic tissues.
Received: 11 January 1996 / Accepted: 31 October 1996 相似文献