ISRN biochemistry最新文献

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Analysis of mathematical modelling on potentiometric biosensors. 电位生物传感器的数学建模分析。
ISRN biochemistry Pub Date : 2014-05-07 eCollection Date: 2014-01-01 DOI: 10.1155/2014/582675
N Mehala, L Rajendran
{"title":"Analysis of mathematical modelling on potentiometric biosensors.","authors":"N Mehala,&nbsp;L Rajendran","doi":"10.1155/2014/582675","DOIUrl":"https://doi.org/10.1155/2014/582675","url":null,"abstract":"<p><p>A mathematical model of potentiometric enzyme electrodes for a nonsteady condition has been developed. The model is based on the system of two coupled nonlinear time-dependent reaction diffusion equations for Michaelis-Menten formalism that describes the concentrations of substrate and product within the enzymatic layer. Analytical expressions for the concentration of substrate and product and the corresponding flux response have been derived for all values of parameters using the new homotopy perturbation method. Furthermore, the complex inversion formula is employed in this work to solve the boundary value problem. The analytical solutions obtained allow a full description of the response curves for only two kinetic parameters (unsaturation/saturation parameter and reaction/diffusion parameter). Theoretical descriptions are given for the two limiting cases (zero and first order kinetics) and relatively simple approaches for general cases are presented. All the analytical results are compared with simulation results using Scilab/Matlab program. The numerical results agree with the appropriate theories. </p>","PeriodicalId":90189,"journal":{"name":"ISRN biochemistry","volume":"2014 ","pages":"582675"},"PeriodicalIF":0.0,"publicationDate":"2014-05-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1155/2014/582675","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"33298678","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 6
Tumor microenvironment: a new treatment target for cancer. 肿瘤微环境:癌症治疗的新靶点
ISRN biochemistry Pub Date : 2014-04-10 eCollection Date: 2014-01-01 DOI: 10.1155/2014/351959
Ming-Ju Tsai, Wei-An Chang, Ming-Shyan Huang, Po-Lin Kuo
{"title":"Tumor microenvironment: a new treatment target for cancer.","authors":"Ming-Ju Tsai,&nbsp;Wei-An Chang,&nbsp;Ming-Shyan Huang,&nbsp;Po-Lin Kuo","doi":"10.1155/2014/351959","DOIUrl":"https://doi.org/10.1155/2014/351959","url":null,"abstract":"<p><p>Recent advances in cancer therapy encounter a bottleneck. Relapsing/recurrent disease almost always developed eventually with resistance to the initially effective drugs. Tumor microenvironment has been gradually recognized as a key contributor for cancer progression, epithelial-mesenchymal transition of the cancer cells, angiogenesis, cancer metastasis, and development of drug resistance, while dysregulated immune responses and interactions between various components in the microenvironment all play important roles. Future development of anticancer treatment should take tumor microenvironment into consideration. Besides, we also discuss the limitations of current pre-clinical testing models that mainly come from the impossibility in simulating all detailed carcinogenic mechanisms in human, especially failure to create the same tumor microenvironment. With the cumulating knowledge about tumor microenvironment, the design of a novel anticancer therapy may be facilitated and may have better chance for success in cancer eradication. </p>","PeriodicalId":90189,"journal":{"name":"ISRN biochemistry","volume":"2014 ","pages":"351959"},"PeriodicalIF":0.0,"publicationDate":"2014-04-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1155/2014/351959","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"33273616","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 111
New Lipase for Biodiesel Production: Partial Purification and Characterization of LipSB 25-4. 用于生物柴油生产的新型脂肪酶:LipSB 25-4的部分纯化与表征
ISRN biochemistry Pub Date : 2014-03-10 eCollection Date: 2014-01-01 DOI: 10.1155/2014/289749
Aysel Ugur, Nurdan Sarac, Rukiye Boran, Berk Ayaz, Ozgur Ceylan, Gulten Okmen
{"title":"New Lipase for Biodiesel Production: Partial Purification and Characterization of LipSB 25-4.","authors":"Aysel Ugur,&nbsp;Nurdan Sarac,&nbsp;Rukiye Boran,&nbsp;Berk Ayaz,&nbsp;Ozgur Ceylan,&nbsp;Gulten Okmen","doi":"10.1155/2014/289749","DOIUrl":"https://doi.org/10.1155/2014/289749","url":null,"abstract":"<p><p>The lipolytic activities of 300 Streptomyces isolates were determined in Tributyrin and Rhodamine-B Agar. Lipase activities were also measured with p-nitrophenyl palmitate (p-NPP) as a substrate. The strain of Streptomyces bambergiensis OC 25-4 used in this study was selected among 300 strains of Streptomyces from MUCC as the best lipase producer. The incubation conditions were optimized and the inoculum amount, incubation period, effect of carbon and nitrogen sources, and rates of MgSO4 and CaCO3 were investigated. LipSB 25-4 (the lipase produced by S. bambergiensis OC 25-4 strain) was partially purified with ammonium sulphate precipitation, dialysis, and gel filtration chromatography 2.73-fold and with 92.12 U/mg specific activity. The optimal pH and temperature for LipSB 25-4 were determined as 8.0 and 50°C, respectively. The lipase has high stability in all pH and temperature values used in this study. While LipSB 25-4 was slightly activated in the presence of β-mercaptoethanol, it was slightly reduced by PMSF. The enzyme conserved approximately 75% of its activity at the end of 60 h, in the presence of methanol and ethanol. Since LipSB 25-4 displays high activity in the thermophilic conditions and stability in the presence of organic solvents, this lipase can catalyse the biodiesel production from olive oil by the transesterification reactions. </p>","PeriodicalId":90189,"journal":{"name":"ISRN biochemistry","volume":"2014 ","pages":"289749"},"PeriodicalIF":0.0,"publicationDate":"2014-03-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1155/2014/289749","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"33273614","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 38
Synthetic melatoninergic ligands: achievements and prospects. 合成褪黑激素配体:进展与展望。
ISRN biochemistry Pub Date : 2014-02-23 eCollection Date: 2014-01-01 DOI: 10.1155/2014/843478
N V Kostiuk, M B Belyakova, D V Leshchenko, V V Zhigulina, M V Miniaev
{"title":"Synthetic melatoninergic ligands: achievements and prospects.","authors":"N V Kostiuk,&nbsp;M B Belyakova,&nbsp;D V Leshchenko,&nbsp;V V Zhigulina,&nbsp;M V Miniaev","doi":"10.1155/2014/843478","DOIUrl":"https://doi.org/10.1155/2014/843478","url":null,"abstract":"<p><p>Pineal hormone melatonin is widely used in the treatment of disorders of circadian rhythms. The presence of melatonin receptors in various animal tissues motivates the use of this hormone in some other diseases. For this reason, in recent years investigators continued the search for synthetic analogues of melatonin which are metabolically stable and selective to receptors. This review includes recent information about the most famous melatonin analogues, their structure, properties, and physiological features of the interaction with melatonin receptors. </p>","PeriodicalId":90189,"journal":{"name":"ISRN biochemistry","volume":"2014 ","pages":"843478"},"PeriodicalIF":0.0,"publicationDate":"2014-02-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1155/2014/843478","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"33273617","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 5
Kinetic Characterization and Effect of Immobilized Thermostable β-Glucosidase in Alginate Gel Beads on Sugarcane Juice. 海藻酸盐凝胶珠固定化耐热β-葡萄糖苷酶对甘蔗汁的动力学表征及影响。
ISRN biochemistry Pub Date : 2014-02-20 eCollection Date: 2014-01-01 DOI: 10.1155/2014/178498
Keerti, Anuradha Gupta, Vinod Kumar, Ashutosh Dubey, A K Verma
{"title":"Kinetic Characterization and Effect of Immobilized Thermostable β-Glucosidase in Alginate Gel Beads on Sugarcane Juice.","authors":"Keerti,&nbsp;Anuradha Gupta,&nbsp;Vinod Kumar,&nbsp;Ashutosh Dubey,&nbsp;A K Verma","doi":"10.1155/2014/178498","DOIUrl":"https://doi.org/10.1155/2014/178498","url":null,"abstract":"<p><p>A thermostable β-glucosidase was effectively immobilized on alginate by the method of gel entrapment. After optimization of immobilized conditions, recovered enzyme activity was 60%. Optimum pH, temperature, kinetic parameters, thermal and pH stability, reusability, and storage stability were investigated. The K m and V max for immobilized β-glucosidase were estimated to be 5.0 mM and 0.64 U/ml, respectively. When comparing, free and immobilized enzyme, change was observed in optimum pH and temperature from 5.0 to 6.0 and 60°C to 80°C, respectively. Immobilized enzyme showed an increase in pH stability over the studied pH range (3.0-10.0) and stability at temperature up to 80°C. The storage stability and reusability of the immobilized β-glucosidase were improved significantly, with 12.09% activity retention at 30°C after being stored for 25 d and 17.85% residual activity after being repeatedly used for 4 times. The effect of both free and immobilized β-glucosidase enzyme on physicochemical properties of sugarcane juice was also analyzed. </p>","PeriodicalId":90189,"journal":{"name":"ISRN biochemistry","volume":"2014 ","pages":"178498"},"PeriodicalIF":0.0,"publicationDate":"2014-02-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1155/2014/178498","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"33298677","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 83
Transsulfuration Is a Significant Source of Sulfur for Glutathione Production in Human Mammary Epithelial Cells. 转硫是人类乳腺上皮细胞中产生谷胱甘肽的重要硫源。
ISRN biochemistry Pub Date : 2014-01-01 DOI: 10.1155/2013/637897
Andrea D Belalcázar, John G Ball, Leslie M Frost, Monica A Valentovic, John Wilkinson
{"title":"Transsulfuration Is a Significant Source of Sulfur for Glutathione Production in Human Mammary Epithelial Cells.","authors":"Andrea D Belalcázar,&nbsp;John G Ball,&nbsp;Leslie M Frost,&nbsp;Monica A Valentovic,&nbsp;John Wilkinson","doi":"10.1155/2013/637897","DOIUrl":"https://doi.org/10.1155/2013/637897","url":null,"abstract":"<p><p>The transsulfuration pathway, through which homocysteine from the methionine cycle provides sulfur for cystathionine formation, which may subsequently be used for glutathione synthesis, has not heretofore been identified as active in mammary cells. Primary human mammary epithelial cells (HMEC's) were labeled with <sup>35</sup>S-methionine for 24 hours following pretreatment with a vehicle control, the cysteine biosynthesis inhibitor propargylglycine or the gamma-glutamylcysteine synthesis inhibitor buthionine sulfoximine. Cell lysates were prepared and reacted with glutathione-S-transferase and the fluorescent labeling compound monochlorobimane to form a fluorescent glutathione-bimane conjugate. Comparison of fluorographic and autoradiographic images indicated that glutathione had incorporated <sup>35</sup>S-methionine demonstrating that functional transsulfuration occurs in mammary cells. Pathway inhibitors reduced incorporation by roughly 80%. Measurement of glutathione production in HMEC's treated with and without hydrogen peroxide and/or pathway inhibitors indicates that the transsulfuration pathway plays a significant role in providing cysteine for glutathione production both normally and under conditions of oxidant stress.</p>","PeriodicalId":90189,"journal":{"name":"ISRN biochemistry","volume":"2013 ","pages":"637897"},"PeriodicalIF":0.0,"publicationDate":"2014-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1155/2013/637897","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"32179817","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 35
Production of Alkaline Protease by Solvent-Tolerant Alkaliphilic Bacillus circulans MTCC 7942 Isolated from Hydrocarbon Contaminated Habitat: Process Parameters Optimization. 从受碳氢化合物污染的生境中分离出来的耐溶剂嗜碱性芽孢杆菌 MTCC 7942 生产碱性蛋白酶:工艺参数优化。
ISRN biochemistry Pub Date : 2013-11-28 eCollection Date: 2013-01-01 DOI: 10.1155/2013/942590
Ulhas Patil, Ambalal Chaudhari
{"title":"Production of Alkaline Protease by Solvent-Tolerant Alkaliphilic Bacillus circulans MTCC 7942 Isolated from Hydrocarbon Contaminated Habitat: Process Parameters Optimization.","authors":"Ulhas Patil, Ambalal Chaudhari","doi":"10.1155/2013/942590","DOIUrl":"10.1155/2013/942590","url":null,"abstract":"<p><p>In the present investigation, a newly isolated organic solvent-tolerant and alkaliphilic bacterial strain was reported from a hydrocarbon (gasoline and diesel) contaminated soil collected from the petrol station, Shirpur (India). The strain was identified as Bacillus circulans MTCC 7942, based on phenotype, biochemical, and phylogenetic analysis of 16S rRNA gene sequence. The capability of Bacillus circulans to secrete an extracellular, thermostable, alkaline protease and grow in the presence of organic solvents was explored. Bacillus circulans produced maximum alkaline protease (412 U/mL) in optimized medium (g/L): soybean meal, 15; starch, 10; KH2PO4, 1; MgSO4·7H2O, 0.05; CaCl2, 1; Na2CO3, 8; pH 10.0 at 37°C and 100 rpm. The competence of strain to grow in various organic solvents-n-octane, dodecane, n-decane, N,N-dimethylformamide, n-hexane, and dimethyl sulfoxide, establishes its potential as solvent-stable protease source for the possible applications in nonaqueous reactions and fine chemical synthesis. </p>","PeriodicalId":90189,"journal":{"name":"ISRN biochemistry","volume":"2013 ","pages":"942590"},"PeriodicalIF":0.0,"publicationDate":"2013-11-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4392993/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"33272054","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Variable-temperature size exclusion chromatography for the study of the structural changes in g-quadruplex. 变温粒径排除色谱法研究g-四联体的结构变化。
ISRN biochemistry Pub Date : 2013-11-10 eCollection Date: 2013-01-01 DOI: 10.1155/2013/631875
Sanae Benabou, Ramon Eritja, Raimundo Gargallo
{"title":"Variable-temperature size exclusion chromatography for the study of the structural changes in g-quadruplex.","authors":"Sanae Benabou,&nbsp;Ramon Eritja,&nbsp;Raimundo Gargallo","doi":"10.1155/2013/631875","DOIUrl":"https://doi.org/10.1155/2013/631875","url":null,"abstract":"<p><p>The conformational equilibria of a guanine-rich sequence found at the promoter region of the human c-kit oncogene are studied by means of circular dichroism spectroscopy (CD) and variable-temperature size exclusion chromatography (SEC). It is shown that the wild sequence ckit21 exists as a mixture of monomeric and multimeric G-quadruplexes. Appropriate mutation of several bases in the wild sequence produces the shift from parallel to antiparallel G-quadruplex, as well as the disappearance of multimeric species. The shift from the antiparallel to the parallel conformation induced by temperature is reflected in both CD and SEC profiles. </p>","PeriodicalId":90189,"journal":{"name":"ISRN biochemistry","volume":"2013 ","pages":"631875"},"PeriodicalIF":0.0,"publicationDate":"2013-11-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1155/2013/631875","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"33272052","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 3
Serum prolidase activity, oxidant and antioxidant status in nonulcer dyspepsia and healthy volunteers. 非溃疡性消化不良和健康志愿者血清脯氨酸酶活性、氧化剂和抗氧化状态的研究。
ISRN biochemistry Pub Date : 2013-10-29 eCollection Date: 2013-01-01 DOI: 10.1155/2013/182601
Shweta Kumari, Akhilesh Kumar Verma, Sumit Rungta, Rahul Mitra, Ragini Srivastava, Narender Kumar
{"title":"Serum prolidase activity, oxidant and antioxidant status in nonulcer dyspepsia and healthy volunteers.","authors":"Shweta Kumari,&nbsp;Akhilesh Kumar Verma,&nbsp;Sumit Rungta,&nbsp;Rahul Mitra,&nbsp;Ragini Srivastava,&nbsp;Narender Kumar","doi":"10.1155/2013/182601","DOIUrl":"https://doi.org/10.1155/2013/182601","url":null,"abstract":"<p><p>Helicobacter pylori (H. pylori) infection is associated with increased oxidative stress and serum prolidase activity (SPA) in many diseases. We aimed to observe SPA and oxidative stress in nonulcer dyspepsia (NUD) infected with and without H. pylori among eastern Indians. 106 patients with H. pylori positive NUD, 82 patients with H. pylori negative NUD, and 50 healthy individuals were selected. SPA, total antioxidant capacity (TAOC), and total oxidant status (TOS) were measured with the use of spectrophotometer and an automated measurement method. SPA, TOS, and oxidative stress index (OSI) were significantly higher in patients with H. pylori positive than H. pylori negative NUD and healthy individuals (all P < 0.0001), whereas TAOC was significantly lower (P < 0.0001). Nonsignificant, increased SPA (P value = 0.6083) and decreased TAOC (P value = 0.1186) were observed in patients with H. pylori negative NUD than healthy individuals, while increased TOS and OSI were significant (P < 0.0001). Weak, nonsignificant correlations were observed between serum prolidase activity and TAOC, TOS, and OSI in H. pylori positive cases. Thus, increased SPA along with increased oxidative stress was observed, which seem to be closely associated with H. pylori infection. SPA and oxidative stress seem to be used as biomarkers for H. pylori infection in NUD. </p>","PeriodicalId":90189,"journal":{"name":"ISRN biochemistry","volume":"2013 ","pages":"182601"},"PeriodicalIF":0.0,"publicationDate":"2013-10-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1155/2013/182601","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"33272134","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 12
Evaluation of the In Vitro Efficacy of Artemisia annua, Rumex abyssinicus, and Catha edulis Forsk Extracts in Cancer and Trypanosoma brucei Cells. 黄花蒿、阿比西尼亚和长春花提取物对肿瘤和布鲁氏锥虫细胞体外抑制作用的研究。
ISRN biochemistry Pub Date : 2013-09-22 eCollection Date: 2013-01-01 DOI: 10.1155/2013/910308
Netsanet Worku, Andualem Mossie, August Stich, Arwid Daugschies, Susanne Trettner, Nasr Y A Hemdan, Gerd Birkenmeier
{"title":"Evaluation of the In Vitro Efficacy of Artemisia annua, Rumex abyssinicus, and Catha edulis Forsk Extracts in Cancer and Trypanosoma brucei Cells.","authors":"Netsanet Worku,&nbsp;Andualem Mossie,&nbsp;August Stich,&nbsp;Arwid Daugschies,&nbsp;Susanne Trettner,&nbsp;Nasr Y A Hemdan,&nbsp;Gerd Birkenmeier","doi":"10.1155/2013/910308","DOIUrl":"https://doi.org/10.1155/2013/910308","url":null,"abstract":"<p><p>The current drugs against sleeping sickness are derived from cancer chemotherapeutic approaches. Herein, we aimed at evaluating the in vitro effect of alcoholic extracts of Artemisia annua (AMR), Rumex abyssinicus (RMA), and Catha edulis Forsk (CEF) on proliferation/viability of 1321N1 astrocytoma, MCF-7 breast cancer, THP-1 leukemia, and LNCaP, Du-145, and PC-3 prostate cancer cells and on Trypanosoma brucei cells. Proliferation of tumor cells was evaluated by WST-1 assay and viability/behaviour of T. brucei by cell counting and light microscopy. CEF was the most efficient growth inhibitor in comparison to AMR and RMA. Nevertheless, in LNCaP and THP-1 cells, all extracts significantly inhibited tumor growth at 3 μg/mL. All extracts inhibited proliferation of T. brucei cells in a concentration-dependent manner. Microscopic analysis revealed that 95% of the T. brucei cells died when exposed to 33 μg/mL CEF for 3 hrs. Similar results were obtained using 33 μg/mL AMR for 6 hrs. In case of RMA, however, higher concentrations were necessary to obtain similar effects on T. brucei. This demonstrates the antitumor efficacy of these extracts as well as their ability to dampen viability and proliferation of T. brucei, suggesting a common mechanism of action on highly proliferative cells, most probably by targeting cell metabolism. </p>","PeriodicalId":90189,"journal":{"name":"ISRN biochemistry","volume":"2013 ","pages":"910308"},"PeriodicalIF":0.0,"publicationDate":"2013-09-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4392988/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"33272053","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 27
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