检索结果-内蒙古大学图书馆

您好，读者！请登录

内蒙古大学图书馆

首页
概况
党建
资源
服务
科研支持
- 论文收录引用证明
- 科技查新
知识产权
档案馆
帮助

咨询与建议

建议与咨询留下您的常用邮箱和电话号码，以便我们向您反馈解决方案和替代方法

您的常用邮箱：*

您的手机号码：*

问题描述：

当前已输入0个字，您还可以输入200个字

全部搜索
期刊论文
图书
学位论文
标准
纸本馆藏
外文资源发现
数据库导航
超星发现

高级检索

时间限定

出版年份：

文献类型

图书期刊文献学位论文多媒体

馆藏选择

电子馆藏纸本馆藏

核心期刊

全部期刊 SCI 收录期刊 SSCI 收录期刊 EI 收录期刊 CSCD 收录期刊 CSSCI 收录期刊

语言

中文英文

文献类型

期刊文献图书学位论文标准纸本馆藏

帮助

文字说明：

T=题名（书名、题名），A=作者（责任者），K=主题词，P=出版物名称，PU=出版社名称，O=机构（作者单位、学位授予单位、专利申请人），L=中图分类号，C=学科分类号，U=全部字段，Y=年（出版发行年、学位年度、标准发布年）

检索规则说明：

AND代表“并且”；OR代表“或者”；NOT代表“不包含”；(注意必须大写,运算符两边需空一格)

检索范例：

范例一：(K=图书馆学 OR K=情报学) AND A=范并思 AND Y=1982-2016
范例二：P=计算机应用与软件 AND (U=C++ OR U=Basic) NOT K=Visual AND Y=2011-2016

分类表

所选分类

>> <<

限定检索结果

文献类型

414 篇 会议

馆藏范围

414 篇 电子文献
0 种 纸本馆藏

日期分布

学科分类号

404 篇 医学
- 368 篇 药学(可授医学、理...
- 171 篇 中西医结合
- 20 篇 中药学(可授医学、...
- 12 篇 临床医学
- 3 篇 基础医学(可授医学...
- 2 篇 公共卫生与预防医...
- 2 篇 中医学
- 1 篇 医学技术（可授医学...
8 篇 工学
- 6 篇 化学工程与技术
- 1 篇 仪器科学与技术
- 1 篇 材料科学与工程（可...
- 1 篇 控制科学与工程
- 1 篇 生物工程
7 篇 理学
- 3 篇 化学
- 3 篇 生物学
- 1 篇 物理学
5 篇 农学
- 1 篇 作物学
- 1 篇 植物保护
- 1 篇 畜牧学
- 1 篇 兽医学

主题

20 篇 synthesis
17 篇 antitumor
15 篇 apoptosis
15 篇 inhibitor
14 篇 cancer
12 篇 hiv-1
11 篇 anticancer
10 篇 sar
8 篇 inhibitors
8 篇 anti-tumor
7 篇 drug design
7 篇 antitumor activi...
6 篇 virtual screenin...
6 篇 drug discovery
6 篇 antiproliferativ...
5 篇 dapy
5 篇 breast cancer
5 篇 selectivity
5 篇 kinase inhibitor
5 篇 cancer therapy

机构

29 篇 school of pharma...
14 篇 collaborative in...
12 篇 state key labora...
10 篇 department of me...
8 篇 department of me...
8 篇 engineering cent...
7 篇 rega institute f...
7 篇 department of me...
6 篇 school of pharma...
6 篇 high magnetic fi...
6 篇 department of me...
6 篇 department of me...
5 篇 school of pharma...
5 篇 school of pharma...
5 篇 animal science a...
5 篇 department of me...
5 篇 key laboratory o...
4 篇 university of sc...
4 篇 school of pharma...
4 篇 jiangsu key labo...

作者

35 篇 hongmin liu
11 篇 bin yu
10 篇 xinyong liu
9 篇 zhenfeng chen
9 篇 peng zhan
8 篇 yancheng liu
8 篇 yichao zheng
8 篇 lupei du
8 篇 qidong you
8 篇 hong liang
7 篇 minyong li
7 篇 ge meng
7 篇 maosheng cheng
7 篇 erik de clercq
7 篇 fener chen
7 篇 liangren zhang
6 篇 peng yang
6 篇 christophe panne...
6 篇 dahong li
6 篇 wenjie mei

语言

413 篇 英文
1 篇 中文

检索条件"任意字段=第11届世界华人药物化学研讨会（ISCMC2018）"

共 414 条记录，以下是381-390 订阅

全选清除本页清除全部题录导出标记到"检索档案"

详细简洁

排序：

Regulation mechanism of G9a on glioma and its application as drug targets

Regulation mechanism of G9a on glioma and its application as...

引用

第11届世界华人药物化学研讨会（iscmc 2018）

作者： Lanlan Zang Shukkoor Muhammed Kondengaden Xueyuan Heng Central Laboratory and Key Laboratory of Neurophysiology Linyi People's HospitalShandong University Department of Medicinal Chemistry Key Laboratory of Chemical Biology(Ministry of Education)School of Pharmaceutical SciencesShandong University Chemistry Department and Center for Diagnostics and Therapeutics Georgia State University

Neurogliotna is a disease with high incidence and short survival,the epigenetic phenomena such as abnormal histone modifications and so on are closely related to the occurrence and development of *** are few related studies about the research of G9 a in glioma,its biological effect is not yet *** previous studies showed that G9 a was highly expressed in glioma *** knockdown and overexpression confirmed the effect of G9 a on the proliferation and invasion ability of glioblastoma cells,which have statistical significance,so we put G9 a as a new potential target for the treatment of glioma for further ***,pharmacological experiments using G9 a inhibitors(standard A and G9 a inhibitor DCG066 previously found in our laboratory) showed that DCG066 showed better performance than the standard A's effect in inhibiting the proliferation of cancer cells,decreasing the methylation level of H3 K9,inducing and accelerating apoptosis of cancer *** purpose of this project is to develop novel high-activity G9 a small molecule inhibitors by combining CADD technology,organic synthesis and in vitro pharmacological activity determination and other multidisciplinary methods to optimize the structural transformation of DCG066 based on the chemical environment of protein crystals,and then exploring its mechanism on glioma cell line in *** discovery of a new drug target opens up new ideas for the targeted drug therapy of gliomas and at the same time lays the foundation for the development of more new antitumor drugs.

关键词： Glioma Histone methyltransferase Epigenetics Cell proliferation

来源：评论

学校读者我要写书评

暂无评论

N19 exerts anti-leukemic effects on genetically different AMLcell lines by promoting cell differentiation and apoptosis

N19 exerts anti-leukemic effects on genetically different AM...

引用

第11届世界华人药物化学研讨会（iscmc 2018）

作者： Shehung Chan Hsushan Huang Jihhwa Guh School of Pharmacy Taiwan University Department of Cosmetic Science Providence University The Ph.D.Program for Cancer Biology and Drug Discovery

Leukemia,the disease of hematological malignancies,is characterized by clonal expansion of hematopoietic cells that are uncontrolled proliferation,decreased cell death as well as blocked *** promyelocytic leukemia（APL） has been identified by the unique morphology of promyelocytes in bone *** of the rapid progression of the disease and severe complications,APL is considered as the most malignant type of acute *** there are still numerous safety and tolerability issues with the available clinical anti-APL drugs,the discovery of new therapeutic mechanisms and treatment agents may provide opportunities for the development of curative approaches for *** study examined the anticancer effect of an anthraquinone derivative（N19） in HL-60（FLT3-WT）and MV4-11（FLT3-ITD） cell lines.N19 induced a time-and concentration-dependent cytotoxicity both in HL-60 and MV4-11 cells with IC at low micromolar *** flow cytometric analysis of propidium iodide staining showed that N19 induced a dramatic increase of sub-G1 hypodiploid population（apoptosis） of the cell cycle with an IC of 2 μ*** expression microarray analysis was performed on N19-treated and untreated MV4-11 *** using a fold-change of-1.5 to 1.5 and a FDR P-value of <0.05 identified 240 differentially expressed *** Ontology enrichment analysis revealed that most of the genes were enriched in development transcription regulation of granulocyte development and development c-Kit ligand signaling pathway during *** data were confirmed by Western blot ***,activation of caspase cascades and mitochondria damage markers also *** available data support the anti-leukemic potential of N19.

关键词： Acute promyelocytic leukemia(APL) Anthraquinone derivative(N19) Fms-like tyrosine kinase 3-internal tandem duplication(FLT3-ITD) Microarray Granulocyte develop

来源：评论

学校读者我要写书评

暂无评论

Synthesis and Pinl inhibitory activity of thiazole derivatives

Synthesis and Pinl inhibitory activity of thiazole derivativ...

引用

第11届世界华人药物化学研讨会（iscmc 2018）

作者： Lifei Du Kaiyue Liu Hailong Zhao Jing Jin Guonan Cui Xiaoguang Chen Bailing Xu Institute of Materia Medica Chinese Academy of Medical Sciences & Peking Union Medical College

Pin1（Protein interacting with NIMA1） is a peptidyl proly1 cis-trans isomerase（PPIase） which specifically catalyzes the conformational conversion of the amide bond of pSer/Thr-Pro motifs in its substrate proteins. Proline-directed phosphorylation on Ser or Thr is a common regulation mechanism in cells,thus Pinl plays critical roles in many cellular process including cell cycle progression,cell signaling,cell proliferation etc..Pin1 is overexpressed in various types of cancer cells and overexpression of Pin1 is associated with aggressive tumor progression and poor prognosis in cancer. It has been demonstrated that Pin1 as a molecular switch simultaneously impacts multiple oncogenic signaling pathways in tumor cells,therefore Pin1 is a potential target for antitumor *** to the crystal structures of some small molecule inhibitors complexed with Pinl,we have summarized the features of binding site of catalytic domain,which consists of three subpockets,namely a prolyl pocket,a slightly shallow hydrophobic shelf and a unique phosphate binding pocket Based on our previous work, a series of novel thiazole derivatives containing an oxalic acid or an acetic acid group was designed and *** enzymatic assay was performed against Pin1 and some of compounds displayed potent inhibitory activity with ICvalues at the micromolar *** preliminary SAR and the binding features of the thiazole derivatives were *** demonstrated that the thiazole ring could serve as an appropriate scaffold for discovering structurally novel and drug-like Pinl *** results will provide guidance for further modifications to achieve more potent thiazole derivatives as Pin 1 inhibitors.

关键词： Pin1 thiazole inhibitor

来源：评论

学校读者我要写书评

暂无评论

Establishment of screening platform for small molecular inhibitors of BRD4 and screening and activity evaluation of inhibitors

Establishment of screening platform for small molecular inhi...

引用

第11届世界华人药物化学研讨会（iscmc 2018）

作者： Dandan Shen Shuai Wang Qimeng Song Yichao Zheng Hongmin Liu School of Pharmaceutical Sciences Zhengzhou University Collaborative Innovation Center of New Drug Research and Safety Evaluation

BRIM has two BRD domain which can recognize the histone acetylation modification,mediating interaction of ***4 is abnormal expression in a variety of tumors,including almost all kinds of blood tumors and solid *** inhibitors can be used for research and treatment of many ***,BRIM can be used as a drug target and the discovery of inhibitors is a great significance for the prevention and treatment of ***,two active domains of BRD4 were chosen to establish pGEX4 T-1-BRD4（BD1） and pGEX4 T-1-BRD4（BD2） prokaryotic expression vector,and prokaryotic expression system and affinity chromatography purification were used to get BRD4（BD1） and BRD4（BD2）recombinant *** recombinant proteins were evaluated by HTRF method and reaction conditions were *** these,positive compound JQ-1 were used to evaluate the system and get better results.A high throughput screening platform for BRD4 small molecule inhibitors was successfully *** a series of compounds were screened and evaluated the BRD4 inhibitory ***-722 potently inhibited BRD4(IC = 2 μM).Mechanistically,WS-722 can inhibit BRD4 activity and down-regulate the expression of its target gene c-myc in leukemia THP-1 *** also induced expression of CD11 b and CD 14 in THP-1 cells,promoted the differentiation of leukemia cells,and show better antitumor activity,which lays a foundation for the discovery and optimization of such new BRD4 inhibitors in the future.

关键词： BRD4 prokaryotic expression HTRF inhibitors screening

来源：评论

学校读者我要写书评

暂无评论

Total synthesis of jolkinolide analogues as potential anti-cancer agents

Total synthesis of jolkinolide analogues as potential anti-c...

引用

第11届世界华人药物化学研讨会（iscmc 2018）

作者： Ke Wang Juancheng Yang Xiaoming Wu Dayong Zhang Yangchang Wu Department of Medicinal Chemistry China Pharmaceutical University Center for Drug Discovery China Pharmaceutical University Graduate Institute of Natural Products Kaohsiung Medical University Research Center for Natural Products & Drug Development Kaohsiung Medical University

Jolkinolides are a series naturally ent-abietane diterpenes with potent antitumor *** isolated from genusEuphorbia,a Traditional Chinese Medicine（TCM）,which is used for treating "dampness toxin",swollen sores and *** antitumor activity of Euphorbia was mainly attributed to the presence of abietane diterpenes,many of which possessα,β-unsaturated lactone structures. Jolkinolides,include jolkinolide A,B and E,represents a subgroup of naturally occurring abietane lactones exhibiting significant antitumor ***,synthesis and structure-activity relationship remain *** et *** the total synthesis of（±）-jolkinolide A,B and E from10-methoxycarbonyl-β-onone in twenty *** our study for synthesizing jolkinolides,construction of D ring,including γ-ylidenebutenolide moiety was anticipated through intramolecular Wittig-Horner reaction developed by Katsumura et al. Stevioside was chosen as the raw material to synthesize natural jolkinolide A and B because it is not only shared the structural similarity to the jolkinolides but also had the same fused A and B *** efficient strategy for synthesis of Jolkinolides A and B from easily available material Steviol in 10 and 11 steps with total yields over 10%.19-substitued jolkinolides were also synthesized from stevioside. 3,19-substitued jolkinolides were synthesized from Andrographolide,which also able to transfer the functional groups similar to stevioside. In addition,we synthesized more than 30 jolkinolide derivatives and established the 3 D-QSAR model for the study of structure-activity *** derivativeswere evaluated for their cytotoxicity activity in NTUB1,T24,and J82 bladder cancer ***,the anti-tumor activity of 19-（Benzyloxy）-19-oxojolkinolide B（compound J24） was investigated using xenograft animal *** result showed that J24 had an effective antitumor activity in nude mice.

关键词： Euphorbia flscheriana Jolkinolide 3D-QSAR Cytotoxicity Anti-tumor

来源：评论

学校读者我要写书评

暂无评论

Anti-histone deacetylase and reversing cisplatin resistance of adamantane based N-hydroxypropenamides in lung cancer cells

Anti-histone deacetylase and reversing cisplatin resistance ...

引用

第11届世界华人药物化学研讨会（iscmc 2018）

作者： Xuefei Bao Yuhong Sun Changshun Bao Jiayu Zhang Shenglan Zou Jingyu Yang Chunfu Wu Lihui Wang Guoliang Chen Key Laboratory of Structure-Based Drugs Design and Discovery of Ministry of Education Shenyang Pharmaceutical University Department of Pharmacology Shenyang Pharmaceutical University Benxi Institute of Pharmaceutical Research Shenyang Pharmaceutical University

The expression level of P-gp increased with the evolution of NSCLC,which was a consequence of the acquired ***,several studies had shown,except P-gp,the aberrant epigenetic regulations also played a crucial role in cisplatin resistance of *** moieties and nitrogen atoms appeared to be essential for the substrate recognition of ***,non-planar adamantane moieties were employed to replace the terminal phenyl group of belinostat and small alky1 groups including methyl and ethyl were introduced in the nitrogen of sulfonamide.A series of novel N-hydroxypropenamides containing adamantane moiety were identified and most of them exhibited HDAC inhibitory action and eminent reversal of cisplatin resistance in NSCLC cell ***2 yme-based data showed that most of synthesized compounds could inhibit HDAC activity with the inhibitory rate more than 80%at 10 μ***-based results demonstrated that the treatment with synthesized compounds resulted in an increase of Ac-H4 and p21 in AS49 cells,which conformed the anti-HDAC activity of those ***,we assessed the reversal effect of those compounds and found several compounds display an anti-resistant effect in lung cancer *** compared to belinostat and cisplatin,compound 8 f(（E）-3-(4-(N-(（3 s,5 s,7 s）-adamantan-l-y1>N-methylsulfamoyl)phenyl)-N-hydroxyacrylamide) showed improved inhibitory activity against AS49/CDDP cell lines with IC value of 5.76 μM.,and far lower resistance index of 1.24.

关键词： HDAC cisplatin resistance N-hydroxypropenamide molecular docking lung cancer

来源：评论

学校读者我要写书评

暂无评论

Design,synthesis and in vitro activity of novel triazine-based LSD1 inhibitors

Design,synthesis and in vitro activity of novel triazine-bas...

引用

第11届世界华人药物化学研讨会（iscmc 2018）

作者： Ying Liu Longfei Zhao Jianjia Liang Zhusong Cao Xiaojing Li Le Yang Bo Wang Fengzhi Suo Jinyi Wang Ruihua Yang Yu Ke Liying Ma Hongmin Liu School of Pharmaceutical Sciences Zhengzhou University Collaborative Innovation Center of New Drug Research and Safety Evaluation

LSD1 plays an important role in the development and progression of *** the basis of the study of LSD1 inhibitor system,two series new compounds with homo-triazine skeleton were designed and *** the LSD1 inhibitory activity,small molecule-induced apoptosis mechanism,computer simulation of molecular docking of above derivatives were further *** specific contents are as follows:1,3,5-triazine derivatives containing1,2,3-triazole,including bismorpholino group of structural units and monomorpholino group structural units 1,3,5-triazine derivatives were designed and synthesized.31 new compounds were synmesized *** above-mentioned 31 compounds were evaluated for LSD1 enzyme inhibitory activity and found that some of them had certain LSD1 inhibitory activity,and the IC50 of compound 5 h to LSD1 reached 1.005μ*** anti-tumor activity of LSD 1-inhibiting compounds was evaluated in *** was confirmed that these compounds had certain proliferation inhibitory activity on LSD1 overexpressing cancer *** molecular analogue docking experiments were carried out for the typical derivatives with better *** binding mode of the compounds with different chain lengths and LSD1 was *** further analysis of the structure-activity relationship of the compounds,the LSD1 agents provide the direction and *** conclusion,two series of compounds have been designed and synmesized with a total of31 new structures in this *** compounds are novel and easy to be *** results showed that the structure of this compound had certain LSD1 inhibitory activity and antitumor activity in *** kind of structure has a good prospect of research and development

关键词： 1,3,5-triazine LSD1 structure-activity relationship anti-tumor

来源：评论

学校读者我要写书评

暂无评论

Design,synthesis and biological activities of 2,3-dihydroquinazolin-4(1H)-one derivatives as TRPM2 inhibitors

Design,synthesis and biological activities of 2,3-dihydroqui...

引用

第11届世界华人药物化学研讨会（iscmc 2018）

作者： Han Zhang Huan Liu Xiao Luo Wei Yang Peilin Yu Liangren Zhang Lihe Zhang State Key Laboratory of Natural and Biomimetic Drugs School of Pharmaceutical SciencesPeking University Department of Toxicology School of Public HealthZhejiang University Department of Neurobiology School of MedicineZhejiang University

Transient receptor potential melastatin 2（TRPM2）,a Ca-permeable cationic channel,plays critical roles in insulin release,cytokine production,body temperature regulation and cell death as a reactive oxygen species（ROS） and temperature sensor .However,few TRPM2 inhibitors have been reported,especially TRP-subtype selective inhibitors,which hampers the investigation and validation of TRPM2 as a drug target .To discover novel TRPM2 inhibitors,3 D similarity-based virtual screening method was employed,by which2,3-dihydroquinazolin-4（1 H）-one derivative H1 was identified as a TRPM2 inhibitor.A series of novel 2,3-dihydroquinazolin-4（1 H）-one derivatives were subsequently synthesized and *** inhibitory activities against the TRPM2 channel were evaluated by calcium imaging and electrophysiology *** of the compounds exhibited significant inhibitory activity,especially D9 which showed an IC of 3.7 μM against the TRPM2 *** importantly,this compound showed specificity to the TRPM2 channel without affecting the TRPM8 *** addition,naphthyl at 3'-position,methyl at 6-position and chlorine or bromine at 8-position of the 2,3-dihydroquinazolin-4（1 H）-one were favorable for the inhibitory activity and the chirality had no influence on inhibitory *** summarized structure-activity relationship（SAR） provides valuable insights for further development of specific TRPM2 targeted inhibitors.

关键词： TRPM2 2,3-dihydroquinazolin-4(1H)-ones inhibitors SAR virtual screening

来源：评论

学校读者我要写书评

暂无评论

Targeted inhibition of Rictor/mTORC2 suppresses tumorigenesis and enhances the therapeutic efficacy of mTOR inhibitors in esophageal squamous cell carcinoma

Targeted inhibition of Rictor/mTORC2 suppresses tumorigenesi...

引用

第11届世界华人药物化学研讨会（iscmc 2018）

作者： Mengying Zhang Yandan Ren Yang Wang Tianli Fan Ang Jia Guiqin Hou Zhaoming Lu School of Pharmaceutical Sciences Zhengzhou University Department of Pharmacology School of Basic MedicineZhengzhou University Collaborative Innovation Center of Cancer Chemoprevention

Esophageal squamous cell carcinoma(ESCC) is one of popular malignant tumors in *** dysregulation of mTOR pathway had been confirmed in many human cancers including ESCC and the antitumor effect of RAD001,the inhibitor of mTORCl,was weakened because the negative feedback *** this study,we explore the potential role of mTORC2 as a therapeutic target in ***,we demonstrated that mTORC2 subunit Rictor and p-Akt(Ser473) are more frequently activated in ESCC tissues than that in normal esophageal tissues,and their overexpression correlates with the TNM phase of ESCC ***,inhibition of mTORCl and mTORC2 by PP242 exhibits more efficacious anti-proliferative effect against ESCC cells than ***,shRNA-mediated stable knockdown of Rictor inhibits proliferation and migration as well as induces cell cycle arrest and apoptosis of ESCC ***,stable knockdown of Rictor significantly suppresses the RAD001-induced feedback activation of Akt/PRAS40 signaling,and thus potentiating the antitumor effect of RAD001 and PP242 both in vitro and in *** findings highlight selective targeting mTORC2 could be a promising therapeutic strategy for future treatment of ESCC.

关键词： Esophageal squamous cell carcinoma Rictor Akt RAD001 PP242

来源：评论

学校读者我要写书评

暂无评论

Effects of clostridium butyricum on growth performance,serum biochemical parameters,antioxidant capacity and immune function of weaning calves

Effects of clostridium butyricum on growth performance,serum...

引用

第11届世界华人药物化学研讨会（iscmc 2018）

作者： Wenxi Li Enyue Yao Xin Liu Zhou Shuang Zhang Liyang Zhang Yonggen Animal Science and Technology Collage Northeast Agricultural University

Clostridium butyrate as a new microecological preparation has the characteristics of heat resistance,acid resistance and antibiotic *** butyrate is not only effective in the treatment of human intestinal tract disorder,acute and chronic diarrhea,but also can regulate the microecological balance of intestinal microflora,reduce diarrhea rate and improve production performance in poultry ***,whether or not Clostridium butyricum will play a role in calves remains to be *** experiment was conducted to investigate the effects of Clostridium butyricum on growth performance,serum biochemical parameters,antioxidant capacity and immune function of weaning *** Holstein calves of about 50 days old with similar body weight and health condition were randomly assigned to 2 groups with 6 replicates per group and one calf per replicate for a 20-day *** treatments were:basal diet（control group,CON） and basal diet supplemented with 2.0×10～8 cfu/kg Clostridium butyricum（Clostridium butyricum group,CB）.The results showed as follows:1) The average daily gain（ADG） of calves in CB was significantly higher than that in CON（P<0.05）;the feed efficiency of CB was higher than that of CON（P=0.09） and the diarrhea rate of calves in CB was 3.62%lower than that of CON.2)the contents of serum cholesterol（CHOL） and high-density lipoprotein（HDL） in CB decreased significantly（P<0.05） and low density lipoprotein（LDL） tended to be lower than that of CON（P=0.07） at 20 d.3) At 10 d,the content of glutathione（GSH） in CB was higher than Con（P = 0.06）;at 20 d,Clostridium butyricum treatment extremely significantly decreased the content of malondialdehyde（MDA） in serum（P<0.01）.4) CB could significantly increase the contents of immunoglobulin A（IgA）,immunoglobulin M（IgM）,immunoglobulin G（IgG） in serum of calves at 20 d（PO.01）.（Conclusion） It is concluded that adding Clostridium butyricum into the diet for weaning calves can improve growth performanc

关键词： calf Clostridium butyrate growth performance antioxidant capacity immune function

来源：评论

学校读者我要写书评

暂无评论

没有更多数据了...

全选清除本页清除全部题录导出标记到“检索档案”

共42页 << < 33 34 35 36 37 38 39 40 41 42 > >>

检索报告对象比较合并检索0

隐藏清空

合并搜索

回到顶部

执行限定条件

内容：

评分：

请选择保存的检索档案：

请选择收藏分类：

订阅名称：

通借通还

温馨提示：

图书名称：

借书校区：

取书校区：

手机号码：

邮箱地址：

一卡通帐号：

电话和邮箱必须正确填写，我们会与您联系确认。

联系人：

所在院系：

联系邮箱：

联系电话：

内蒙古自治区呼和浩特市赛罕区大学西街235号邮编: 010021

建议与咨询 留下您的常用邮箱和电话号码，以便我们向您反馈解决方案和替代方法

时间限定

文献类型

馆藏选择

核心期刊

语言

文献类型

帮助

文字说明：

检索规则说明：

检索范例：

分类表

所选分类

限定检索结果

文献类型

馆藏范围

日期分布

学科分类号

主题

机构

作者

语言

请选择保存的检索档案： 新增检索档案 确定 取消

请选择收藏分类： 新增自定义分类 确定 取消

通借通还

建议与咨询留下您的常用邮箱和电话号码，以便我们向您反馈解决方案和替代方法

请选择保存的检索档案：

请选择收藏分类：