首页 > 最新文献

Journal of biological regulators and homeostatic agents最新文献

英文 中文
Expression of NLR and IL-1β and their predictive efficacy value in acute myocardial infarction patients treated with aspirin combined with clopidogrel. 阿司匹林联合氯吡格雷治疗急性心肌梗死患者NLR和IL-1β的表达及其预测疗效
IF 3.2 4区 医学 Q4 ENDOCRINOLOGY & METABOLISM Pub Date : 2021-08-27 Epub Date: 2021-08-26 DOI: 10.23812/21-88-L
Q Ma, W N Li, H Y Liu, H Y Zhang, J Y Dong, X L Tian
{"title":"Expression of NLR and IL-1β and their predictive efficacy value in acute myocardial infarction patients treated with aspirin combined with clopidogrel.","authors":"Q Ma, W N Li, H Y Liu, H Y Zhang, J Y Dong, X L Tian","doi":"10.23812/21-88-L","DOIUrl":"https://doi.org/10.23812/21-88-L","url":null,"abstract":"","PeriodicalId":15084,"journal":{"name":"Journal of biological regulators and homeostatic agents","volume":"35 4","pages":""},"PeriodicalIF":3.2,"publicationDate":"2021-08-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39345270","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Levodropropizine in children: over thirty years of clinical experience. 左丙嗪治疗儿童:30多年临床经验。
IF 3.2 4区 医学 Q4 ENDOCRINOLOGY & METABOLISM Pub Date : 2021-08-27 Epub Date: 2021-08-06 DOI: 10.23812/21-176-L
G Ciprandi, A Licari, M A Tosca, G L Marseglia
{"title":"Levodropropizine in children: over thirty years of clinical experience.","authors":"G Ciprandi, A Licari, M A Tosca, G L Marseglia","doi":"10.23812/21-176-L","DOIUrl":"https://doi.org/10.23812/21-176-L","url":null,"abstract":"","PeriodicalId":15084,"journal":{"name":"Journal of biological regulators and homeostatic agents","volume":"35 4","pages":""},"PeriodicalIF":3.2,"publicationDate":"2021-08-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39281203","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Targeted regulation of BBOX1-AS1 on miR-361-3p and its effect on the biological function of non-small cell lung cancer cell. BBOX1-AS1靶向调控miR-361-3p及其对非小细胞肺癌细胞生物学功能的影响
IF 3.2 4区 医学 Q4 ENDOCRINOLOGY & METABOLISM Pub Date : 2021-08-27 Epub Date: 2021-07-19 DOI: 10.23812/21-143-L
Y F Lian, X M Jiang, L H Sui, X J Shi
{"title":"Targeted regulation of BBOX1-AS1 on miR-361-3p and its effect on the biological function of non-small cell lung cancer cell.","authors":"Y F Lian, X M Jiang, L H Sui, X J Shi","doi":"10.23812/21-143-L","DOIUrl":"https://doi.org/10.23812/21-143-L","url":null,"abstract":"","PeriodicalId":15084,"journal":{"name":"Journal of biological regulators and homeostatic agents","volume":"35 4","pages":""},"PeriodicalIF":3.2,"publicationDate":"2021-08-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39199070","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 4
Analysis of long non-coding RNA expression profiles in disuse osteoporosis using microarray and bioinformatics. 利用微阵列和生物信息学分析废用性骨质疏松症的长链非编码RNA表达谱。
IF 3.2 4区 医学 Q4 ENDOCRINOLOGY & METABOLISM Pub Date : 2021-08-27 Epub Date: 2021-07-23 DOI: 10.23812/21-246-A
W Z Wei, B Li, J X Lin, J Zhao, X F Zhang, X Q Wang, Z Lv, J Liu

Disuse osteoporosis (DOP) is one of the major consequences of long space flights. DOP also occurs in patients with spinal cord injuries and prolonged bedridden states that can have a severe impact on human health. Bone marrow mesenchymal stem cells (BMSCs) are multipotent stromal cells that play an important role in bone homeostasis. Long non-coding RNAs (lncRNAs) are involved in regulating osteogenic differentiation of BMSCs, and their abnormal expression might lead to the formation of orthopedic diseases. However, the specific mechanism of DOP has not yet been elucidated. All sequencing data were obtained from Gene Expression Omnibus (GEO) datasets. The limma package of R was applied to identify DEmRNAs and DElncRNAs. Pearson correlation coefficients (PCC) between DElncRNADEmRNA expression levels were calculated. Functional annotation was performed for DEmRNAs coexpressed with DElncRNAs. In addition, the Cytohubba plug-in in Cytoscape was applied to determine the top 10 hub genes. Finally, connectivity map (CMap) analysis was used to identify potential therapeutic drugs for DOP. The gene expression data, GSE100930 and GSE17696, were retrieved from the GEO database. A total of 2,212 differentially expressed mRNAs (DEmRNAs) and 22 differentially expressed lncRNAs (DElncRNAs) were obtained. Gene ontology (GO) functional terms, Kyoto Encyclopedia of Genes, and Genomes (KEGG) pathway enrichment analysis reveal 30 significant GO terms and 13 significant pathways. A coding-non-coding gene co-expression (CNC) network was constructed to study the potential role of hub-DElncRNAs and their co-expressed DEmRNAs in DOP. The lncRNAs, GSNAS1, SNHG12, and EPB41LA4A-AS1, were significant in the CNC network and potential regulators of DOP development. Three bioactive compounds (scoulerine, kinetin riboside, dexanabinol) with potential therapeutic significance for DOP were obtained through the Connectivity Map (CMAP) analysis. Our study revealed a new mechanism for a lineage shift of bone marrow mesenchymal stem cells under microgravity, and linked the function of protein-coding mRNAs with ncRNAs, which may contribute to the development of new therapies for DOP.

废用性骨质疏松症(DOP)是长期太空飞行的主要后果之一。DOP也发生在脊髓损伤和长期卧床不起的患者身上,这可能对人体健康产生严重影响。骨髓间充质干细胞(BMSCs)是一种多能基质细胞,在骨稳态中起重要作用。长链非编码rna (Long non-coding RNAs, lncRNAs)参与骨髓间充质干细胞成骨分化的调控,其表达异常可能导致骨科疾病的形成。然而,DOP的具体机制尚未阐明。所有测序数据均来自Gene Expression Omnibus (GEO)数据集。使用R的limma包来鉴定demrna和delncrna。计算delncrnademmrna表达水平之间的Pearson相关系数(PCC)。对与DElncRNAs共表达的demrna进行功能注释。此外,利用Cytoscape中的Cytohubba插件确定前10个枢纽基因。最后,通过连接图(CMap)分析确定DOP的潜在治疗药物。基因表达数据GSE100930和GSE17696从GEO数据库中检索。共获得2212个差异表达mrna (DEmRNAs)和22个差异表达lncRNAs (DElncRNAs)。基因本体(GO)功能术语,京都基因百科全书和基因组(KEGG)途径富集分析揭示了30个重要的GO术语和13个重要的通路。构建编码-非编码基因共表达(CNC)网络,研究hub-DElncRNAs及其共表达的demmrnas在DOP中的潜在作用。lncrna GSNAS1、SNHG12和EPB41LA4A-AS1在CNC网络和DOP发展的潜在调节因子中具有重要意义。通过连接图(CMAP)分析,获得3种对DOP具有潜在治疗意义的生物活性化合物(scoulerine, kinetin核糖体,dexanabinol)。我们的研究揭示了微重力下骨髓间充质干细胞谱系转移的新机制,并将蛋白质编码mrna与ncRNAs的功能联系起来,这可能有助于开发新的治疗DOP的方法。
{"title":"Analysis of long non-coding RNA expression profiles in disuse osteoporosis using microarray and bioinformatics.","authors":"W Z Wei,&nbsp;B Li,&nbsp;J X Lin,&nbsp;J Zhao,&nbsp;X F Zhang,&nbsp;X Q Wang,&nbsp;Z Lv,&nbsp;J Liu","doi":"10.23812/21-246-A","DOIUrl":"https://doi.org/10.23812/21-246-A","url":null,"abstract":"<p><p>Disuse osteoporosis (DOP) is one of the major consequences of long space flights. DOP also occurs in patients with spinal cord injuries and prolonged bedridden states that can have a severe impact on human health. Bone marrow mesenchymal stem cells (BMSCs) are multipotent stromal cells that play an important role in bone homeostasis. Long non-coding RNAs (lncRNAs) are involved in regulating osteogenic differentiation of BMSCs, and their abnormal expression might lead to the formation of orthopedic diseases. However, the specific mechanism of DOP has not yet been elucidated. All sequencing data were obtained from Gene Expression Omnibus (GEO) datasets. The limma package of R was applied to identify DEmRNAs and DElncRNAs. Pearson correlation coefficients (PCC) between DElncRNADEmRNA expression levels were calculated. Functional annotation was performed for DEmRNAs coexpressed with DElncRNAs. In addition, the Cytohubba plug-in in Cytoscape was applied to determine the top 10 hub genes. Finally, connectivity map (CMap) analysis was used to identify potential therapeutic drugs for DOP. The gene expression data, GSE100930 and GSE17696, were retrieved from the GEO database. A total of 2,212 differentially expressed mRNAs (DEmRNAs) and 22 differentially expressed lncRNAs (DElncRNAs) were obtained. Gene ontology (GO) functional terms, Kyoto Encyclopedia of Genes, and Genomes (KEGG) pathway enrichment analysis reveal 30 significant GO terms and 13 significant pathways. A coding-non-coding gene co-expression (CNC) network was constructed to study the potential role of hub-DElncRNAs and their co-expressed DEmRNAs in DOP. The lncRNAs, GSNAS1, SNHG12, and EPB41LA4A-AS1, were significant in the CNC network and potential regulators of DOP development. Three bioactive compounds (scoulerine, kinetin riboside, dexanabinol) with potential therapeutic significance for DOP were obtained through the Connectivity Map (CMAP) analysis. Our study revealed a new mechanism for a lineage shift of bone marrow mesenchymal stem cells under microgravity, and linked the function of protein-coding mRNAs with ncRNAs, which may contribute to the development of new therapies for DOP.</p>","PeriodicalId":15084,"journal":{"name":"Journal of biological regulators and homeostatic agents","volume":"35 4","pages":""},"PeriodicalIF":3.2,"publicationDate":"2021-08-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39211883","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1
Identification of miRNAs, mRNAs, lncRNAs, and circRNAs associated with hepatocellular carcinoma recurrence after interferon treatment. 干扰素治疗后肝癌复发相关mirna、mrna、lncrna和circrna的鉴定
IF 3.2 4区 医学 Q4 ENDOCRINOLOGY & METABOLISM Pub Date : 2021-08-27 Epub Date: 2021-07-23 DOI: 10.23812/21-173-A
W P Zhu, X G He, H X Zhu, L R Wang, Z H Lin, M Wang, L Wang

To study the molecular mechanism of interferon-alpha (IFN-α) in the treatment of hepatocellular carcinoma (HCC) and the molecular markers that can predict the therapeutic effect, differentially expressed (DE)-miRNAs, -mRNAs, -lncRNAs, and -circRNAs were screened between 12 samples collected from 4 patients who had not received treatment (control), 4 patients who had received recombinant human interferon a-2b treatment (case1), and 4 patients who had relapsed after receiving recombinant human interferon a-2b treatment (case2). Enrichment analyses were performed to determine the principal functions of the DE-RNAs. We also constructed protein-protein interactions (PPI) and competing endogenous RNA (ceRNA) networks. In addition, a series-cluster analysis was performed to analyze changes in gene expression across different groups of HCC. Furthermore, the expression of the genes were verified in the Cancer Genome Atlas (TCGA) database. A total of 36 union DE-miRNAs, 175 union DE-mRNAs, 65 union DE-lncRNAs, and 52 union DE-circRNAs were obtained between the control vs case1, and case2 vs case1 groups. DE-mRNAs were mainly involved in the mitochondrial inner membrane. DE-circRNAs were mainly enriched in the Golgi apparatus. ceRNA network contained 68 DE-mRNAs, 26 DE-miRNAs, 45 DE-lncRNAs, and 23 DE-circRNAs. A total of 24 DE-miRNAs, 175 DE-mRNAs, 65 DE-lncRNAs, and 52 DE-circRNAs were classified into eight profiles, respectively. A total of 26 genes showed a significant correlation with prognosis of HCC (p < 0.05). Some genes may be used to predict the efficacy of IFN-α in the treatment of HCC. The results may lay a foundation for investigating the different sensitivities of IFN-α in the treatment of HCC.

为了研究干扰素-α (IFN-α)在肝细胞癌(HCC)治疗中的分子机制及预测疗效的分子标志物,我们从4例未接受治疗的患者(对照组)、4例接受重组人干扰素a-2b治疗的患者(case1)中收集12份样本,筛选差异表达(DE)-miRNAs、- mrna、-lncRNAs和-circRNAs。接受重组人干扰素a-2b治疗后复发4例(case2)。进行富集分析以确定de - rna的主要功能。我们还构建了蛋白质-蛋白质相互作用(PPI)和竞争内源性RNA (ceRNA)网络。此外,我们还进行了系列聚类分析,以分析不同HCC组中基因表达的变化。此外,这些基因的表达在癌症基因组图谱(TCGA)数据库中得到验证。在对照组与case1组、case2组与case1组之间共获得36个联合de - mirna、175个联合de - mrna、65个联合de - lncrna和52个联合de - circrna。de - mrna主要参与线粒体内膜。de - circrna主要富集在高尔基体中。ceRNA网络包含68个de - mrna, 26个de - mirna, 45个de - lncrna和23个de - circrna。共有24个de - mirna、175个de - mrna、65个de - lncrna和52个de - circrna分别被划分为8个谱。26个基因与HCC预后有显著相关性(p < 0.05)。一些基因可用于预测IFN-α治疗HCC的疗效。研究结果可为探讨IFN-α在HCC治疗中的不同敏感性奠定基础。
{"title":"Identification of miRNAs, mRNAs, lncRNAs, and circRNAs associated with hepatocellular carcinoma recurrence after interferon treatment.","authors":"W P Zhu,&nbsp;X G He,&nbsp;H X Zhu,&nbsp;L R Wang,&nbsp;Z H Lin,&nbsp;M Wang,&nbsp;L Wang","doi":"10.23812/21-173-A","DOIUrl":"https://doi.org/10.23812/21-173-A","url":null,"abstract":"<p><p>To study the molecular mechanism of interferon-alpha (IFN-α) in the treatment of hepatocellular carcinoma (HCC) and the molecular markers that can predict the therapeutic effect, differentially expressed (DE)-miRNAs, -mRNAs, -lncRNAs, and -circRNAs were screened between 12 samples collected from 4 patients who had not received treatment (control), 4 patients who had received recombinant human interferon a-2b treatment (case1), and 4 patients who had relapsed after receiving recombinant human interferon a-2b treatment (case2). Enrichment analyses were performed to determine the principal functions of the DE-RNAs. We also constructed protein-protein interactions (PPI) and competing endogenous RNA (ceRNA) networks. In addition, a series-cluster analysis was performed to analyze changes in gene expression across different groups of HCC. Furthermore, the expression of the genes were verified in the Cancer Genome Atlas (TCGA) database. A total of 36 union DE-miRNAs, 175 union DE-mRNAs, 65 union DE-lncRNAs, and 52 union DE-circRNAs were obtained between the control vs case1, and case2 vs case1 groups. DE-mRNAs were mainly involved in the mitochondrial inner membrane. DE-circRNAs were mainly enriched in the Golgi apparatus. ceRNA network contained 68 DE-mRNAs, 26 DE-miRNAs, 45 DE-lncRNAs, and 23 DE-circRNAs. A total of 24 DE-miRNAs, 175 DE-mRNAs, 65 DE-lncRNAs, and 52 DE-circRNAs were classified into eight profiles, respectively. A total of 26 genes showed a significant correlation with prognosis of HCC (p < 0.05). Some genes may be used to predict the efficacy of IFN-α in the treatment of HCC. The results may lay a foundation for investigating the different sensitivities of IFN-α in the treatment of HCC.</p>","PeriodicalId":15084,"journal":{"name":"Journal of biological regulators and homeostatic agents","volume":"35 4","pages":""},"PeriodicalIF":3.2,"publicationDate":"2021-08-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39212757","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1
Efficacy of early oral and perioral physiotherapy on feeding autonomy in preterm infants: results of randomized controlled trials. 早期口服和口周物理治疗对早产儿自主喂养的影响:随机对照试验的结果。
IF 3.2 4区 医学 Q4 ENDOCRINOLOGY & METABOLISM Pub Date : 2021-08-27 Epub Date: 2021-08-25 DOI: 10.23812/21-199-L
M S Cori, P E Ferrara, P Papacci, F Serrao, A Di Polito, A Del Vecchio, I Bastoni, C Di Paola, U Moscato, S Codazza, G Ferriero, G Vento, G Ronconi
{"title":"Efficacy of early oral and perioral physiotherapy on feeding autonomy in preterm infants: results of randomized controlled trials.","authors":"M S Cori,&nbsp;P E Ferrara,&nbsp;P Papacci,&nbsp;F Serrao,&nbsp;A Di Polito,&nbsp;A Del Vecchio,&nbsp;I Bastoni,&nbsp;C Di Paola,&nbsp;U Moscato,&nbsp;S Codazza,&nbsp;G Ferriero,&nbsp;G Vento,&nbsp;G Ronconi","doi":"10.23812/21-199-L","DOIUrl":"https://doi.org/10.23812/21-199-L","url":null,"abstract":"","PeriodicalId":15084,"journal":{"name":"Journal of biological regulators and homeostatic agents","volume":"35 4","pages":""},"PeriodicalIF":3.2,"publicationDate":"2021-08-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39341764","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Identification of circRNA-mediated competing endogenous RNA network in the development of bladder urothelial carcinoma. circrna介导的内源性竞争RNA网络在膀胱尿路上皮癌发展中的鉴定。
IF 3.2 4区 医学 Q4 ENDOCRINOLOGY & METABOLISM Pub Date : 2021-08-27 DOI: 10.23812/21-117-L
S P Shao, R J Zhao, S Lu, L P Wen, J J Ni, K M Zhu, W D Han
{"title":"Identification of circRNA-mediated competing endogenous RNA network in the development of bladder urothelial carcinoma.","authors":"S P Shao,&nbsp;R J Zhao,&nbsp;S Lu,&nbsp;L P Wen,&nbsp;J J Ni,&nbsp;K M Zhu,&nbsp;W D Han","doi":"10.23812/21-117-L","DOIUrl":"https://doi.org/10.23812/21-117-L","url":null,"abstract":"","PeriodicalId":15084,"journal":{"name":"Journal of biological regulators and homeostatic agents","volume":"35 4","pages":""},"PeriodicalIF":3.2,"publicationDate":"2021-08-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39355543","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Level changes of serum high-sensitivity C-reactive protein and vascular endothelial growth factor in patients with St-segment elevation myocardial infarction after percutaneous coronary intervention. st段抬高型心肌梗死患者经皮冠状动脉介入治疗后血清高敏c反应蛋白和血管内皮生长因子水平的变化
IF 3.2 4区 医学 Q4 ENDOCRINOLOGY & METABOLISM Pub Date : 2021-07-30 DOI: 10.23812/21-SI1-4
H G Wang, X H Ji, C C Wang, X L Tian
{"title":"Level changes of serum high-sensitivity C-reactive protein and vascular endothelial growth factor in patients with St-segment elevation myocardial infarction after percutaneous coronary intervention.","authors":"H G Wang,&nbsp;X H Ji,&nbsp;C C Wang,&nbsp;X L Tian","doi":"10.23812/21-SI1-4","DOIUrl":"https://doi.org/10.23812/21-SI1-4","url":null,"abstract":"","PeriodicalId":15084,"journal":{"name":"Journal of biological regulators and homeostatic agents","volume":"35 Special on Internal Medicine n.1","pages":""},"PeriodicalIF":3.2,"publicationDate":"2021-07-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39273732","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
microRNA-486-5p functions as a tumor suppressor in gastric carcinoma via directly targeting KDM5B. microRNA-486-5p通过直接靶向KDM5B在胃癌中发挥抑瘤作用。
IF 3.2 4区 医学 Q4 ENDOCRINOLOGY & METABOLISM Pub Date : 2021-07-30 DOI: 10.23812/21-SI1-2
Y B Li, X Y Fan, L Ning, S K Li, Z P Yu
{"title":"microRNA-486-5p functions as a tumor suppressor in gastric carcinoma via directly targeting KDM5B.","authors":"Y B Li,&nbsp;X Y Fan,&nbsp;L Ning,&nbsp;S K Li,&nbsp;Z P Yu","doi":"10.23812/21-SI1-2","DOIUrl":"https://doi.org/10.23812/21-SI1-2","url":null,"abstract":"","PeriodicalId":15084,"journal":{"name":"Journal of biological regulators and homeostatic agents","volume":"35 Special on Internal Medicine n.1","pages":""},"PeriodicalIF":3.2,"publicationDate":"2021-07-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39259071","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
The role of lutein in cerebral ischemia-reperfusion injury in rats and its mechanism. 叶黄素在大鼠脑缺血再灌注损伤中的作用及其机制。
IF 3.2 4区 医学 Q4 ENDOCRINOLOGY & METABOLISM Pub Date : 2021-07-30 DOI: 10.23812/21-SI1-3
A X Yang, C Y Liu, H Y Liu, T T Li, B F Ren, P P Qiao
{"title":"The role of lutein in cerebral ischemia-reperfusion injury in rats and its mechanism.","authors":"A X Yang,&nbsp;C Y Liu,&nbsp;H Y Liu,&nbsp;T T Li,&nbsp;B F Ren,&nbsp;P P Qiao","doi":"10.23812/21-SI1-3","DOIUrl":"https://doi.org/10.23812/21-SI1-3","url":null,"abstract":"","PeriodicalId":15084,"journal":{"name":"Journal of biological regulators and homeostatic agents","volume":"35 Special on Internal Medicine n.1","pages":""},"PeriodicalIF":3.2,"publicationDate":"2021-07-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39273731","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
期刊
Journal of biological regulators and homeostatic agents
全部 Acc. Chem. Res. ACS Applied Bio Materials ACS Appl. Electron. Mater. ACS Appl. Energy Mater. ACS Appl. Mater. Interfaces ACS Appl. Nano Mater. ACS Appl. Polym. Mater. ACS BIOMATER-SCI ENG ACS Catal. ACS Cent. Sci. ACS Chem. Biol. ACS Chemical Health & Safety ACS Chem. Neurosci. ACS Comb. Sci. ACS Earth Space Chem. ACS Energy Lett. ACS Infect. Dis. ACS Macro Lett. ACS Mater. Lett. ACS Med. Chem. Lett. ACS Nano ACS Omega ACS Photonics ACS Sens. ACS Sustainable Chem. Eng. ACS Synth. Biol. Anal. Chem. BIOCHEMISTRY-US Bioconjugate Chem. BIOMACROMOLECULES Chem. Res. Toxicol. Chem. Rev. Chem. Mater. CRYST GROWTH DES ENERG FUEL Environ. Sci. Technol. Environ. Sci. Technol. Lett. Eur. J. Inorg. Chem. IND ENG CHEM RES Inorg. Chem. J. Agric. Food. Chem. J. Chem. Eng. Data J. Chem. Educ. J. Chem. Inf. Model. J. Chem. Theory Comput. J. Med. Chem. J. Nat. Prod. J PROTEOME RES J. Am. Chem. Soc. LANGMUIR MACROMOLECULES Mol. Pharmaceutics Nano Lett. Org. Lett. ORG PROCESS RES DEV ORGANOMETALLICS J. Org. Chem. J. Phys. Chem. J. Phys. Chem. A J. Phys. Chem. B J. Phys. Chem. C J. Phys. Chem. Lett. Analyst Anal. Methods Biomater. Sci. Catal. Sci. Technol. Chem. Commun. Chem. Soc. Rev. CHEM EDUC RES PRACT CRYSTENGCOMM Dalton Trans. Energy Environ. Sci. ENVIRON SCI-NANO ENVIRON SCI-PROC IMP ENVIRON SCI-WAT RES Faraday Discuss. Food Funct. Green Chem. Inorg. Chem. Front. Integr. Biol. J. Anal. At. Spectrom. J. Mater. Chem. A J. Mater. Chem. B J. Mater. Chem. C Lab Chip Mater. Chem. Front. Mater. Horiz. MEDCHEMCOMM Metallomics Mol. Biosyst. Mol. Syst. Des. Eng. Nanoscale Nanoscale Horiz. Nat. Prod. Rep. New J. Chem. Org. Biomol. Chem. Org. Chem. Front. PHOTOCH PHOTOBIO SCI PCCP Polym. Chem.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1