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Correction: Activation of the IL-17/TRAF6/NF-κB pathway is implicated in Aβ-induced neurotoxicity. 更正:IL-17/TRAF6/NF-κB通路的激活与a β诱导的神经毒性有关。
IF 2.4 4区 医学
BMC Neuroscience Pub Date : 2023-08-24 DOI: 10.1186/s12868-023-00804-5
Yulan Liu, Yang Meng, Chenliang Zhou, Juanjuan Yan, Cuiping Guo, Weiguo Dong
{"title":"Correction: Activation of the IL-17/TRAF6/NF-κB pathway is implicated in Aβ-induced neurotoxicity.","authors":"Yulan Liu, Yang Meng, Chenliang Zhou, Juanjuan Yan, Cuiping Guo, Weiguo Dong","doi":"10.1186/s12868-023-00804-5","DOIUrl":"10.1186/s12868-023-00804-5","url":null,"abstract":"","PeriodicalId":9031,"journal":{"name":"BMC Neuroscience","volume":null,"pages":null},"PeriodicalIF":2.4,"publicationDate":"2023-08-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10463895/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10174268","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Related neural networks underlie suppression of emotion, memory, motor processes as identified by data-driven analysis. 通过数据驱动的分析,相关的神经网络是抑制情绪、记忆和运动过程的基础。
IF 2.4 4区 医学
BMC Neuroscience Pub Date : 2023-08-24 DOI: 10.1186/s12868-023-00812-5
Karisa J Hunt, Lindsay K Knight, Brendan E Depue
{"title":"Related neural networks underlie suppression of emotion, memory, motor processes as identified by data-driven analysis.","authors":"Karisa J Hunt, Lindsay K Knight, Brendan E Depue","doi":"10.1186/s12868-023-00812-5","DOIUrl":"10.1186/s12868-023-00812-5","url":null,"abstract":"<p><strong>Background: </strong>Goal-directed behavior benefits from self-regulation of cognitive and affective processes, such as emotional reactivity, memory retrieval, and prepotent motor response. Dysfunction in self-regulation is a common characteristic of many psychiatric disorders, such as PTSD and ADHD. This study sought to determine whether common intrinsic connectivity networks (ICNs; e.g. default mode network) are involved in the regulation of emotion, motor, and memory processes, and if a data-driven approach using independent component analysis (ICA) would successfully identify such ICNs that contribute to inhibitory regulation.</p><p><strong>Methods: </strong>Eighteen participants underwent neuroimaging while completing an emotion regulation (ER) task, a memory suppression (Think/No-Think; TNT) task, and a motor inhibition (Stop Signal; SS) task. ICA (CONN; MATLAB) was conducted on the neuroimaging data from each task and corresponding components were selected across tasks based on interrelated patterns of activation. Subsequently, ICNs were correlated with behavioral performance variables from each task.</p><p><strong>Results: </strong>ICA indicated a common medial prefrontal network, striatal network, and frontoparietal executive control network, as well as downregulation in task-specific ROIs.</p><p><strong>Conclusions: </strong>These results illustrate that common ICNs were exhibited across three distinct inhibitory regulation tasks, as successfully identified through a data-driven approach (ICA).</p>","PeriodicalId":9031,"journal":{"name":"BMC Neuroscience","volume":null,"pages":null},"PeriodicalIF":2.4,"publicationDate":"2023-08-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10463822/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10109883","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Enhancing structural plasticity of PC12 neurons during differentiation and neurite regeneration with a catalytically inactive mutant version of the zRICH protein. 用催化失活的zRICH蛋白突变体增强PC12神经元在分化和轴突再生过程中的结构可塑性。
IF 2.4 4区 医学
BMC Neuroscience Pub Date : 2023-08-23 DOI: 10.1186/s12868-023-00808-1
Ashoka C Bandla, Aditya S Sheth, Sara M Zarate, Suraj Uskamalla, Elizabeth C Hager, Victor A Villarreal, Maribel González-García, Rafael P Ballestero
{"title":"Enhancing structural plasticity of PC12 neurons during differentiation and neurite regeneration with a catalytically inactive mutant version of the zRICH protein.","authors":"Ashoka C Bandla, Aditya S Sheth, Sara M Zarate, Suraj Uskamalla, Elizabeth C Hager, Victor A Villarreal, Maribel González-García, Rafael P Ballestero","doi":"10.1186/s12868-023-00808-1","DOIUrl":"10.1186/s12868-023-00808-1","url":null,"abstract":"<p><strong>Background: </strong>Studies of the molecular mechanisms of nerve regeneration have led to the discovery of several proteins that are induced during successful nerve regeneration. RICH proteins were identified as proteins induced during the regeneration of the optic nerve of teleost fish. These proteins are 2',3'-cyclic nucleotide, 3'-phosphodiesterases that can bind to cellular membranes through a carboxy-terminal membrane localization domain. They interact with the tubulin cytoskeleton and are able to enhance neuronal structural plasticity by promoting the formation of neurite branches.</p><p><strong>Results: </strong>PC12 stable transfectant cells expressing a fusion protein combining a red fluorescent protein with a catalytically inactive mutant version of zebrafish RICH protein were generated. These cells were used as a model to analyze effects of the protein on neuritogenesis. Differentiation experiments showed a 2.9 fold increase in formation of secondary neurites and a 2.4 fold increase in branching points. A 2.2 fold increase in formation of secondary neurites was observed in neurite regeneration assays.</p><p><strong>Conclusions: </strong>The use of a fluorescent fusion protein facilitated detection of expression levels. Two computer-assisted morphometric analysis methods indicated that the catalytically inactive RICH protein induced the formation of branching points and secondary neurites both during differentiation and neurite regeneration. A procedure based on analysis of random field images provided comparable results to classic neurite tracing methods.</p>","PeriodicalId":9031,"journal":{"name":"BMC Neuroscience","volume":null,"pages":null},"PeriodicalIF":2.4,"publicationDate":"2023-08-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10463786/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10109861","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Retraction Note: Agmatine protects retinal ganglion cells from hypoxia-induced apoptosis in transformed rat retinal ganglion cell line. 注:胍丁氨酸对转化大鼠视网膜神经节细胞系缺氧诱导的细胞凋亡具有保护作用。
IF 2.4 4区 医学
BMC Neuroscience Pub Date : 2023-08-14 DOI: 10.1186/s12868-023-00814-3
Samin Hong, Jong Eun Lee, Chan Yun Kim, Gong Je Seong
{"title":"Retraction Note: Agmatine protects retinal ganglion cells from hypoxia-induced apoptosis in transformed rat retinal ganglion cell line.","authors":"Samin Hong, Jong Eun Lee, Chan Yun Kim, Gong Je Seong","doi":"10.1186/s12868-023-00814-3","DOIUrl":"10.1186/s12868-023-00814-3","url":null,"abstract":"","PeriodicalId":9031,"journal":{"name":"BMC Neuroscience","volume":null,"pages":null},"PeriodicalIF":2.4,"publicationDate":"2023-08-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10426147/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10012146","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Distinct patterns of gene expression in the medial preoptic area are related to gregarious singing behavior in European starlings (Sturnus vulgaris). 欧洲八哥(Sturnus vulgaris)视前内侧区基因表达的不同模式与群居歌唱行为有关。
IF 2.4 4区 医学
BMC Neuroscience Pub Date : 2023-08-03 DOI: 10.1186/s12868-023-00813-4
Brandon J Polzin, Sharon A Stevenson, Stephen C Gammie, Lauren V Riters
{"title":"Distinct patterns of gene expression in the medial preoptic area are related to gregarious singing behavior in European starlings (Sturnus vulgaris).","authors":"Brandon J Polzin, Sharon A Stevenson, Stephen C Gammie, Lauren V Riters","doi":"10.1186/s12868-023-00813-4","DOIUrl":"10.1186/s12868-023-00813-4","url":null,"abstract":"<p><strong>Background: </strong>Song performed in flocks by European starlings (Sturnus vulgaris), referred to here as gregarious song, is a non-sexual, social behavior performed by adult birds. Gregarious song is thought to be an intrinsically reinforced behavior facilitated by a low-stress, positive affective state that increases social cohesion within a flock. The medial preoptic area (mPOA) is a region known to have a role in the production of gregarious song. However, the neurochemical systems that potentially act within this region to regulate song remain largely unexplored. In this study, we used RNA sequencing to characterize patterns of gene expression in the mPOA of male and female starlings singing gregarious song to identify possibly novel neurotransmitter, neuromodulator, and hormonal pathways that may be involved in the production of gregarious song.</p><p><strong>Results: </strong>Differential gene expression analysis and rank rank hypergeometric analysis indicated that dopaminergic, cholinergic, and GABAergic systems were associated with the production of gregarious song, with multiple receptor genes (e.g., DRD2, DRD5, CHRM4, GABRD) upregulated in the mPOA of starlings who sang at high rates. Additionally, co-expression network analyses identified co-expressing gene clusters of glutamate signaling-related genes associated with song. One of these clusters contained five glutamate receptor genes and two glutamate scaffolding genes and was significantly enriched for genetic pathways involved in neurodevelopmental disorders associated with social deficits in humans. Two of these genes, GRIN1 and SHANK2, were positively correlated with performance of gregarious song.</p><p><strong>Conclusions: </strong>This work provides new insights into the role of the mPOA in non-sexual, gregarious song in starlings and highlights candidate genes that may play a role in gregarious social interactions across vertebrates. The provided data will also allow other researchers to compare across species to identify conserved systems that regulate social behavior.</p>","PeriodicalId":9031,"journal":{"name":"BMC Neuroscience","volume":null,"pages":null},"PeriodicalIF":2.4,"publicationDate":"2023-08-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10399071/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9936834","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1
Differential effects of two phosphodiesterase 4 inhibitors against lipopolysaccharide-induced neuroinflammation in mice. 两种磷酸二酯酶4抑制剂对脂多糖诱导的小鼠神经炎症的不同作用。
IF 2.4 4区 医学
BMC Neuroscience Pub Date : 2023-07-31 DOI: 10.1186/s12868-023-00810-7
Dong Ho Kang, Sunjoo Ahn, Jung Woo Chae, Jin Sook Song
{"title":"Differential effects of two phosphodiesterase 4 inhibitors against lipopolysaccharide-induced neuroinflammation in mice.","authors":"Dong Ho Kang,&nbsp;Sunjoo Ahn,&nbsp;Jung Woo Chae,&nbsp;Jin Sook Song","doi":"10.1186/s12868-023-00810-7","DOIUrl":"https://doi.org/10.1186/s12868-023-00810-7","url":null,"abstract":"<p><strong>Background: </strong>Several phosphodiesterase 4 (PDE4) inhibitors have emerged as potential therapeutics for central nervous system (CNS) diseases. This study investigated the pharmacological effects of two selective PDE4 inhibitors, roflumilast and zatolmilast, against lipopolysaccharide-induced neuroinflammation.</p><p><strong>Results: </strong>In BV-2 cells, the PDE4 inhibitor roflumilast reduced the production of nitric oxide and tumor necrosis factor-α (TNF-α) by inhibiting NF-κB phosphorylation. Moreover, mice administered roflumilast had significantly reduced TNF-α, interleukin-1β (IL-1β), and IL-6 levels in plasma and brain tissues. By contrast, zatolmilast, a PDE4D inhibitor, showed no anti-neuroinflammatory effects in vitro or in vivo. Next, in vitro and in vivo pharmacokinetic studies of these compounds in the brain were performed. The apparent permeability coefficients of 3 µM roflumilast and zatolmilast were high (> 23 × 10<sup>-6</sup> cm/s) and moderate (3.72-7.18 × 10<sup>-6</sup> cm/s), respectively, and increased in a concentration-dependent manner in the MDR1-MDCK monolayer. The efflux ratios were < 1.92, suggesting that these compounds are not P-glycoprotein substrates. Following oral administration, both roflumilast and zatolmilast were slowly absorbed and eliminated, with time-to-peak drug concentrations of 2-2.3 h and terminal half-lives of 7-20 h. Assessment of their brain dispositions revealed the unbound brain-to-plasma partition coefficients of roflumilast and zatolmilast to be 0.17 and 0.18, respectively.</p><p><strong>Conclusions: </strong>These findings suggest that roflumilast, but not zatolmilast, has the potential for use as a therapeutic agent against neuroinflammatory diseases.</p>","PeriodicalId":9031,"journal":{"name":"BMC Neuroscience","volume":null,"pages":null},"PeriodicalIF":2.4,"publicationDate":"2023-07-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10391911/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9994943","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1
Transcriptome analysis reveals the neuroprotective effect of Dlg4 against fastigial nucleus stimulation-induced ischemia/reperfusion injury in rats. 转录组分析揭示了Dlg4对大鼠顶核刺激引起的缺血再灌注损伤的神经保护作用。
IF 2.4 4区 医学
BMC Neuroscience Pub Date : 2023-07-31 DOI: 10.1186/s12868-023-00811-6
Jinggui Gao, Xiaomin Pang, Lei Zhang, Shenghua Li, Zhenxiu Qin, Xiaoyun Xie, Jingli Liu
{"title":"Transcriptome analysis reveals the neuroprotective effect of Dlg4 against fastigial nucleus stimulation-induced ischemia/reperfusion injury in rats.","authors":"Jinggui Gao,&nbsp;Xiaomin Pang,&nbsp;Lei Zhang,&nbsp;Shenghua Li,&nbsp;Zhenxiu Qin,&nbsp;Xiaoyun Xie,&nbsp;Jingli Liu","doi":"10.1186/s12868-023-00811-6","DOIUrl":"https://doi.org/10.1186/s12868-023-00811-6","url":null,"abstract":"<p><strong>Background: </strong>Previous studies have demonstrated that electrical stimulation of the cerebellar fastigial nucleus (FNS) can considerably decrease infarction volume and improve neurofunction restoration following cerebral ischemia. Nevertheless, the molecular mechanism of the neuroprotective effect of FNS is still vague.</p><p><strong>Methods: </strong>In this study, we developed a rat model of ischemia/reperfusion that included 1 h FNS followed by reperfusion for 3, 6, 12, 24, and 72 h. The expression profile of molecular alterations in brain tissues was obtained by transcriptome sequencing at five different time points. The function and pathway of miRNA expression pattern and core genes were annotated by Allen Brain Atlas, STRING database and Cytoscape software, so as to explore the mechanism of FNS-mediated neuroprotection.</p><p><strong>Results: </strong>The results indicated that FNS is associated with the neurotransmitter cycle pathway. FNS may regulate the release of monoamine neurotransmitters in synaptic vesicles by targeting the corresponding miRNAs through core Dlg4 gene, stimulate the Alternative polyadenylation (APA) incident's anti -apoptosis effect on the brain, and stimulate the interaction activation of neurons in cerebellum, cortex/thalamus and other brain regions, regulate neurovascular coupling, and reduce cerebral damage.</p><p><strong>Conclusion: </strong>FNS may activate neuronal and neurovascular coupling by regulating the release of neurotransmitters in synaptic vesicles through the methylation of core Dlg4 gene and the corresponding transcription factors and protein kinases, inducing the anti-apoptotic mechanism of APA events. The findings from our investigation offer a new perspective on the way brain tissue responds to FNS-driven neuroprotection.</p>","PeriodicalId":9031,"journal":{"name":"BMC Neuroscience","volume":null,"pages":null},"PeriodicalIF":2.4,"publicationDate":"2023-07-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10391810/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9994944","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Hydrogen alleviated cognitive impairment and blood‒brain barrier damage in sepsis-associated encephalopathy by regulating ABC efflux transporters in a PPARα-dependent manner. 氢以ppar α依赖的方式调节ABC外排转运蛋白,减轻败血症相关脑病的认知障碍和血脑屏障损伤。
IF 2.4 4区 医学
BMC Neuroscience Pub Date : 2023-07-20 DOI: 10.1186/s12868-023-00795-3
Yuanyuan Bai, Wen Mi, Xiaoyin Meng, Beibei Dong, Yi Jiang, Yuechun Lu, Yonghao Yu
{"title":"Hydrogen alleviated cognitive impairment and blood‒brain barrier damage in sepsis-associated encephalopathy by regulating ABC efflux transporters in a PPARα-dependent manner.","authors":"Yuanyuan Bai,&nbsp;Wen Mi,&nbsp;Xiaoyin Meng,&nbsp;Beibei Dong,&nbsp;Yi Jiang,&nbsp;Yuechun Lu,&nbsp;Yonghao Yu","doi":"10.1186/s12868-023-00795-3","DOIUrl":"https://doi.org/10.1186/s12868-023-00795-3","url":null,"abstract":"<p><p>Hydrogen (H<sub>2</sub>) can protect against blood‒brain barrier (BBB) damage in sepsis-associated encephalopathy (SAE), but the mechanism is still unclear. We examined whether it is related to PPARα and its regulatory targets, ABC efflux transporters. After injection with DMSO/GW6471 (a PPARα inhibitor), the mice subjected to sham/caecal ligation and puncture (CLP) surgery were treated with H<sub>2</sub> for 60 min postoperation. Additionally, bEnd.3 cells were grown in DMSO/GW6471-containing or saline medium with LPS. In addition to the survival rates, cognitive function was assessed using the Y-maze and fear conditioning tests. Brain tissues were stained with TUNEL and Nissl staining. Additionally, inflammatory mediators (TNF-α, IL-6, HMGB1, and IL-1β) were evaluated with ELISA, and PPARα, ZO-1, occludin, VE-cadherin, P-gp, BCRP and MRP2 were detected using Western blotting. BBB destruction was assessed by brain water content and Evans blue (EB) extravasation. Finally, we found that H<sub>2</sub> improved survival rates and brain dysfunction and decreased inflammatory cytokines. Furthermore, H<sub>2</sub> decreased water content in the brain and EB extravasation and increased ZO-1, occludin, VE-cadherin and ABC efflux transporters regulated by PPARα. Thus, we concluded that H<sub>2</sub> decreases BBB permeability to protect against brain dysfunction in sepsis; this effect is mediated by PPARα and its regulation of ABC efflux transporters.</p>","PeriodicalId":9031,"journal":{"name":"BMC Neuroscience","volume":null,"pages":null},"PeriodicalIF":2.4,"publicationDate":"2023-07-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10360271/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10244675","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Mini review: Current status and perspective of S100B protein as a biomarker in daily clinical practice for diagnosis and prognosticating of clinical outcome in patients with neurological diseases with focus on acute brain injury. 综述:S100B蛋白在神经系统疾病(以急性脑损伤为重点)临床诊断和预后预测中的应用现状及展望。
IF 2.4 4区 医学
BMC Neuroscience Pub Date : 2023-07-20 DOI: 10.1186/s12868-023-00807-2
Tammam Abboud, Veit Rohde, Dorothee Mielke
{"title":"Mini review: Current status and perspective of S100B protein as a biomarker in daily clinical practice for diagnosis and prognosticating of clinical outcome in patients with neurological diseases with focus on acute brain injury.","authors":"Tammam Abboud, Veit Rohde, Dorothee Mielke","doi":"10.1186/s12868-023-00807-2","DOIUrl":"10.1186/s12868-023-00807-2","url":null,"abstract":"<p><p>Prognosticating the clinical outcome of neurological diseases is essential to guide treatment and facilitate decision-making. It usually depends on clinical and radiological findings. Biomarkers have been suggested to support this process, as they are deemed objective measures and can express the extent of tissue damage or reflect the degree of inflammation. Some of them are specific, and some are not. Few of them, however, reached the stage of daily application in clinical practice. This mini review covers available applications of the S100B protein in prognosticating clinical outcome in patients with various neurological disorders, particularly in those with traumatic brain injury, spontaneous subarachnoid hemorrhage and ischemic stroke. The aim is to provide an understandable picture of the clinical use of the S100B protein and give a brief overview of the current limitations that require future solutions.</p>","PeriodicalId":9031,"journal":{"name":"BMC Neuroscience","volume":null,"pages":null},"PeriodicalIF":2.4,"publicationDate":"2023-07-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10360330/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10011974","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1
Correction to: Similar cortical morphometry trajectories from 5 to 9 years in children with perinatal HIV who started treatment before age 2 years and uninfected controls. 更正:在2岁前开始治疗的围产期艾滋病毒感染儿童和未感染对照组中,5至9岁的皮质形态测量轨迹相似。
IF 2.4 4区 医学
BMC Neuroscience Pub Date : 2023-07-12 DOI: 10.1186/s12868-023-00802-7
Emmanuel C Nwosu, Martha J Holmes, Mark F Cotton, Els Dobbels, Francesca Little, Barbara Laughton, Andre van der Kouwe, Frances Robertson, Ernesta M Meintjes
{"title":"Correction to: Similar cortical morphometry trajectories from 5 to 9 years in children with perinatal HIV who started treatment before age 2 years and uninfected controls.","authors":"Emmanuel C Nwosu,&nbsp;Martha J Holmes,&nbsp;Mark F Cotton,&nbsp;Els Dobbels,&nbsp;Francesca Little,&nbsp;Barbara Laughton,&nbsp;Andre van der Kouwe,&nbsp;Frances Robertson,&nbsp;Ernesta M Meintjes","doi":"10.1186/s12868-023-00802-7","DOIUrl":"https://doi.org/10.1186/s12868-023-00802-7","url":null,"abstract":"","PeriodicalId":9031,"journal":{"name":"BMC Neuroscience","volume":null,"pages":null},"PeriodicalIF":2.4,"publicationDate":"2023-07-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10337162/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10192273","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
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