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91.
Elif Bulut Abdulsamet Erden Omer Karadag Kader Karli Oguz Seza Ozen 《Journal of neuroradiology. Journal de neuroradiologie》2019,46(3):193-198
Purpose
To increase the knowledge of central nervous system (CNS) imaging features in deficiency of adenosine deaminase 2 (DADA2) by examining magnetic resonance imaging (MRI) studies of a relatively large number of patients.Methods
We retrospectively examined neuroimages of 12 patients (7 male, 5 female) diagnosed with DADA2. The mean age of the patients at the time of initial brain MRI was 16.7 ± 10.2 years. Seven patients (58.3%) fulfilled the classification criteria of polyarteritis nodosa. Brain MRI studies were assessed with respect to findings of ischemia, intracranial hemorrhages, focal parenchymal signal abnormalities, cerebral/cerebellar volume loss, and abnormal contrast enhancement. Angiographic studies of 7 patients were evaluated for the signs of vasculitis.Results
The most frequent finding was acute and/or chronic lacunar ischemic lesions in the brainstem and/or deep gray matter (n = 9, 75%). Six patients (50%) revealed MRI findings compatible with recurrent ischemic attacks. Small nodular contrast enhancement (n = 2, 16.6%), acute putaminal hemorrhage (n = 1, 8.3%) and findings compatible with posterior reversible encephalopathy syndrome (n = 1, 8.3%) were also detected. Slight-to-moderate diffuse cerebral and/or cerebellar volume loss (n = 7, 58.3%), decreased T1 signal of the bone marrow (n = 6, 50%) and optic atrophy (n = 1, 8.3%) were the other findings on brain MRI. The only abnormal angiographic finding was reduced caliber of the right distal posterior cerebral artery in MRA of a patient (14.6%).Conclusion
DADA2 should be included in the differential diagnosis of young patients presenting with ischemic and/or hemorrhagic lesions located in the brainstem and deep gray matter, especially if they have a family history or additional systemic abnormalities. 相似文献92.
IntroductionAcute intermittent porphyria is a rare autosomal dominant metabolic disease. It is caused by a genetic mutation that results in deficiency of porphobilinogen deaminase enzyme, the third enzyme in heme biosynthesis. Acute intermittent porphyria precipitated by surgery is very rare.Case presentationWe present a 24 year-old woman who developed acute intermittent porphyria five days after right hemi-colectomy. Her presentation included neuro-visceral and psychiatric manifestations, and severe hyponatremia. She received critical care symptomatic management including mechanical ventilation. The diagnosis was based on a positive urine test for porphobilinogen and confirmed by the presence of a heterozygous mutation in the hydroxyrmethylbilane synthase (HMBS) gene (c.760delC p Leu254).DiscussionAcute intermittent porphyria is the most common and life threatining type of acute porphyrias. It is more common in women and usually presents after puberty with acute abdominal pain and diverse neuro-psychiatric manifestations that can be confused with several surgical and medical diseases. Acute intermittent porphyria after surgery is most likely due to postoperative pain and low-calorie intake. Once suspected, prompt ICU management including high calorie intake are necessary to avoid serious complications and mortality before starting definitive treatment with hematin.ConclusionAcute intermittent porphyria should be suspected in any patient, particularly young women, who develop diverse neuro-visceral and psychiatric manifestations and hyponatremia after surgery. 相似文献
93.
94.
Mi-Hyeon You Wang-Joon Kim Wooyoung Shim Sang-Rim Lee Gwang Lee Sangdun Choi Dae-Yong Kim Yong Man Kim Hyunsoo Kim Sang-Uk Han 《Journal of gastroenterology and hepatology》2009,24(8):1393-1400
Background and Aim: Stem cell transplantation offers potential gene therapy for brain tumors. However, this approach has received little attention as a treatment for gastrointestinal tumors. In the present study, we explored the possibility of human bone marrow-derived mesenchymal stem cells (hMSC) producing cytosine deaminase (CD), followed by systemic 5-fluorocytosine (5-FC) administration, showing an antitumor effect on a mouse gastric cancer xenograft.
Methods: We first explored the ability of hMSC, coated with fluorescent dye, to migrate to human gastric cancer MKN45 cells in vitro and in vivo . We then used hMSC in which a gene expressed the prodrug-activating enzyme CD, which can convert the prodrug 5-FC into the cytotoxic agent 5-fluorouracil (5-FU), and further investigated the potential of these cells to deliver the CD gene and to reduce tumor growth in nude mice. The migratory capacity of hMSC was confirmed by an in vitro migration assay, as well as in an in vivo model of nude mice bearing subcutaneous tumors of MKN45 cells when hMSC were injected.
Results: The migration ability of hMSC towards MKN45 cells was confirmed by migration assay. Effective conversion of 5-FC to 5-FU by hMSC transfected with the CD gene (CD-hMSC) showed therapeutic anticancer potential in a MKN45 cell co-culture system, as confirmed by thin layer chromatography. Nude mice bearing MKN45 tumors were intravenously injected with CD-hMSC, followed by systemic 5-FC treatment (500 mg/kg/day) for 7 days. Tumor volumes and weights of mice injected with CD-hMSC decreased significantly after treatment with 5-FC. However, the 5-FC-treated group without CD-hMSC injection showed neither a decrease in tumor volume nor bodyweight loss.
Conclusion: The CD-hMSC system showed anticancer therapeutic potential, and minimized the side-effects of 5-FU. 相似文献
Methods: We first explored the ability of hMSC, coated with fluorescent dye, to migrate to human gastric cancer MKN45 cells in vitro and in vivo . We then used hMSC in which a gene expressed the prodrug-activating enzyme CD, which can convert the prodrug 5-FC into the cytotoxic agent 5-fluorouracil (5-FU), and further investigated the potential of these cells to deliver the CD gene and to reduce tumor growth in nude mice. The migratory capacity of hMSC was confirmed by an in vitro migration assay, as well as in an in vivo model of nude mice bearing subcutaneous tumors of MKN45 cells when hMSC were injected.
Results: The migration ability of hMSC towards MKN45 cells was confirmed by migration assay. Effective conversion of 5-FC to 5-FU by hMSC transfected with the CD gene (CD-hMSC) showed therapeutic anticancer potential in a MKN45 cell co-culture system, as confirmed by thin layer chromatography. Nude mice bearing MKN45 tumors were intravenously injected with CD-hMSC, followed by systemic 5-FC treatment (500 mg/kg/day) for 7 days. Tumor volumes and weights of mice injected with CD-hMSC decreased significantly after treatment with 5-FC. However, the 5-FC-treated group without CD-hMSC injection showed neither a decrease in tumor volume nor bodyweight loss.
Conclusion: The CD-hMSC system showed anticancer therapeutic potential, and minimized the side-effects of 5-FU. 相似文献
95.
目的:探讨腺病毒介导的mdr1启动子调控胞嘧啶脱氨酶∷尿嘧啶磷酸核糖转移酶(CD∷UPP)融合基因联合5-氟胞嘧啶(5-FC)对紫杉醇耐药卵巢癌细胞的特异性杀伤作用。方法:扩增、纯化含有mdr1-CD∷UPP基因的重组腺病毒,转染人卵巢癌紫杉醇耐药细胞株A2780/Taxol和亲本细胞株A2780,RT-PCR检测mdr1和CD∷UPP基因的表达水平;之后加入5-FC,MTT法检测细胞抑制情况及旁观者效应,并观察腺病毒转染后裸鼠移植瘤的生长情况。结果:mdr1和CD∷UPP基因在A2780/Taxol细胞中可稳定表达,转染后A2780/Taxol组的细胞生长明显低于A2780组;转基因的A2780/Taxol细胞联合5-FC后可通过旁观者效应杀伤周围未转基因的耐药细胞;耐药组移植瘤生长明显受到抑制,肿瘤体积为(569.10±187.93)mm3,对照组肿瘤体积为(2111.98±230.82)mm3,差异有统计学意义(P<0.01)。结论:mdr1启动子可调控CD∷UPP基因特异性表达并特异性杀伤紫杉醇耐药卵巢癌细胞。 相似文献
96.
TB-Ab、ADA、和CEA对良恶性胸水鉴别诊断价值 总被引:2,自引:0,他引:2
[目的]探讨胸水结核抗体(TB-Ab-IgG)、腺苷脱氨酶(ADA)、癌胚抗原(CEA)联合检测对良恶性胸腔积液的鉴别诊断价值。[方法]采用斑点金免疫渗滤试验(DIGFA)、酶连续监测法和酶联免疫(ELISA)双抗体夹心法对119例胸腔积液患者行胸水/血清TB-Ab-IgG、ADA和CEA检测分析。[结果]97例结核性胸膜炎患者胸水、血清中TB-Ab-IgG的阳性率分别为61.9%(60/97)和70.1%(68/97),特异性分别为90.1%(20/22)和86.4%(19/22)。ADA活性在结核性和癌性胸腔积液中分别为(59.58±29.85)U/L和(15.31±7.36)U/L(P﹤0.01)。以P-ADA﹥40 U/L做为诊断结核的临界值,其敏感性为79.3%,特异性为86.4%;以P-ADA/S-ADA﹥1为临界值,其敏感性为97.7%,特异性为95.5%。CEA在结核性和癌性胸腔积液中的阳性率分别为8.20%和63.6%,特异性91.8%(89/97)。[结论]胸水和血清TB-Ab-IgG、ADA、CEA联合检测对良恶性胸腔积液具有诊断与鉴别诊断价值。 相似文献
97.
多种雷公藤单体抑制HL-60细胞腺苷脱氨酶活性 总被引:4,自引:0,他引:4
目的研究多种雷公藤单体对HL-60细胞腺苷脱氨酶(ADA)的影响和诱导细胞凋亡作用。方法分别用雷公藤春碱、雷公藤内酯甲、雷公藤乙素、雷公藤黄素、雷公藤呋喃南蛇碱、雷公藤定碱(10mg/L、1mg/L、0.1mg/L)与HL-60细胞共孵育24h后测定ADA活性,选出抑制作用最强的雷公藤内酯甲。将HL-60细胞与雷公藤内酯甲10mg/L、1mg/L、0.1mg/L以及0.1mg/L雷公藤内酯甲+腺苷0.5mmol/L、腺苷0.5mmol/L共孵育24h后测定细胞凋亡率。结果①雷公藤内酯甲和雷公藤呋喃南蛇碱均能明显抑制HL-60细胞ADA活性(P〈0.01),抑制作用与浓度成正比;雷公藤春碱仅在10mg/L浓度时有明显的ADA抑制作用(P〈0.01);雷公藤黄素、雷公藤定碱与雷公藤乙素无明显ADA抑制作用(P〉0.05)。②HL-60细胞与雷公藤内酯甲10mg/L、1mg/L作用均可见明显的凋亡,单加内酯甲0.1mg/L时或单加腺苷时与对照组比较凋亡率无显著差异,但同时再加入腺苷有很高的凋亡率,两者有协同作用。结论雷公藤内酯甲、雷公藤呋喃南蛇碱和雷公藤春碱等雷公藤单体在一定浓度下对HL-60细胞ADA有抑制作用,可能是ADA一种抑制剂。雷公藤内酯甲在抑制细胞ADA活性的同时也造成明显的细胞凋亡。 相似文献
98.
目的探讨腺苷脱氨酶(ADA)在结核性胸膜炎中的临床意义。方法测定32例结核性胸膜炎患者与28例恶性胸腔积液患者的胸水、血液、支气管肺泡灌洗液(BALF)中腺苷脱氨酶(ADA)的水平。结果结核性胸膜炎患者的胸水腺苷脱氨酶(ADA)平均值为(46.68±1.64)u/L,恶性胸腔积液患者的胸水腺苷脱氨酶(ADA)平均值为(24.76±2.34)u/L,两者相比差异有显著性P〈0.01,结核性胸膜炎患者的血液腺苷脱氨酶(A-DA)平均值为(23.46±1.28)u/L,恶性胸腔积液患者的血液腺苷脱氨酶(ADA)平均值为(22.76±1.34)u/L,两者相比差异无显著性(P〉0.05),结核性胸膜炎患者的支气管肺泡灌洗液(BALF)中腺苷脱氨酶(ADA)平均值为(22.56±1.17)u/L。恶性胸腔积液患者的支气管肺泡灌洗液(BALF)中腺苷脱氨酶(ADA)平均值为(21.96±1.85)u/L,两者相比差异无显著性(P〉0.05),结核性胸膜炎患者的胸水腺苷脱氨酶(ADA)/血液腺苷脱氨酶(ADA)平均值(A1)为(1.82±0.26),结核性胸膜炎患者的胸水腺苷脱氨酶(ADA)/支气管肺泡灌洗液(BALF)中腺苷脱氨酶(ADA)平均值(A2)为(1.78±0.29),两者相比差异无显著性(P〉0.05),恶性胸水患者的胸水腺苷脱氨酶(ADA)/血液腺苷脱氨酶(ADA)平均值(B1)为(1.02±0.16),恶性胸膜炎患者的胸水腺苷脱氨酶(ADA)/支气管肺泡灌洗液(BALF)中腺苷脱氨酶(ADA)平均值(B2)为(0.98±0.26),两者相比差异无显著性(P〉0.05),但A1与B1,A2与B2相比差异有显著性(P〈0.01)。结论腺苷脱氨酶对诊断结核性胸膜炎有特异性,胸水腺苷脱氨酶(ADA)/血液腺苷脱氨酶(ADA)平均值(A1),胸水腺苷脱氨酶(ADA)/支气管肺泡灌洗液(BALF)中腺苷脱氨酶(ADA)的平均值(A2)在1.8左右有一定的临床价值。 相似文献
99.
目的:构建人端粒酶逆转录酶(hTERT)启动子驱动的含胞嘧啶脱氨酶(CD)基因的复制缺陷型腺病毒载体,使CD基因只能在端粒酶阳性的细胞表达.方法:采用细胞内同源重组法构建出hTERT启动子调控的携带CD基因的复制缺陷型腺病毒Ad-hTERTp-CD,经PCR鉴定正确后进行扩增、纯化和滴度测定.分别将腺病毒感染人卵巢癌细胞株SKOV3及人胚肺成纤维细胞,MTT法检测受染细胞的存活率.结果:构建的重组腺病毒中带有hTERT启动子及CD基因.用不同滴度的重组腺病毒以及不同浓度的5-FC作用于SKOV3细胞后,MTT法检测到细胞的存活率随着病毒滴度和5-FC浓度的增加而不断降低;而同样的处理对人胚肺成纤维细胞的也有部分杀伤作用,但远较SKOV3细胞弱,差异有统计学意义(P<0.01).结论:本实验构建的由hTERT启动子调控的携带CD基因的复制缺陷型腺病毒Ad-hTERTp-CD对SKOV3细胞具有靶向杀伤的能力. 相似文献
100.
İlker Durak Hasan Biri İmge B. Ergüder Erdinç Devrim Çağrı Şenocak Aslıhan Avcı 《Medicinal chemistry research》2007,16(6):259-265
Aim Possible effects of garlic (Allium sativum) and black grape (Fructus vitis minuta) with known antioxidant potential on adenosine deaminase (ADA) activities were investigated in cancerous and noncancerous
human bladder tissues.
Methods The effects of garlic and black grape extracts on adenosine deaminase (ADA) activities were measured in 20 pairs of cancer
and adjacent normal human bladder tissues with and without pre-incubation with garlic and black grape extracts at different
concentrations.
Results No significant difference was observed between ADA activities in cancerous and non cancerous bladder tissues without plant
extract (5.85 ± 3.78 versus 7.63 ± 2.88, respectively). At the 1/3 and 1/1 plant extract/bladder tissue homogenate ratios,
the garlic extract completely abolished the ADA activity in both cancerous and noncancerous tissues. At the 1/3 plant extract/bladder
tissue homogenate ratio, the black grape extract decreased the activity significantly as compared to without extract (2.01 ± 1.30
versus 5.85 ± 3.78; p < 0.05 for cancerous tissue and 2.10 ± 1.66 versus 7.63 ± 2.88; p < 0.05 for noncancerous tissue) and, at the 1/1 plant extract/bladder tissue homogenate ratio, completely abolished the activity.
Conclusion Our results show that garlic and black grape have potential to inhibit ADA activity in both cancerous and adjacent normal
human bladder tissues.We suggest that this might be rational basis for the uses of garlic and black grape in the complementary
therapy of urinary bladder cancer. 相似文献