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Silencing miRNA-324-3p protects against cerebral ischemic injury via regulation of the GATA2/A1R axis 被引量:3
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作者 An-Qi Zhang Lu wang +11 位作者 yi-xiu wang Shan-Shan Hong Yu-Shan Zhong Ru-Yi Yu Xin-Lu Wu Bing-Bing Zhou Qi-Min Yu Hai-Feng Fu Shuang-Dong Chen Yun-Chang Mo Qin-Xue Dai Jun-Lu wang 《Neural Regeneration Research》 SCIE CAS CSCD 2022年第11期2504-2511,共8页
Previous studies have suggested that miR-324-3p is related to the pathophysiology of cerebral ischemia,but the mechanism underlying this relationship is unclea r.In this study,we found that miR-324-3p expression was d... Previous studies have suggested that miR-324-3p is related to the pathophysiology of cerebral ischemia,but the mechanism underlying this relationship is unclea r.In this study,we found that miR-324-3p expression was decreased in patients with acute ischemic stroke and in in vitro and in vivo models of ischemic stro ke.miR-324-3p agomir potentiated ischemic brain damage in rats subjected to middle cerebral artery occlusion,as indicated by increased infarct volumes and cell apoptosis rates and greater neurological deficits.In a PC12 cell oxygen-glucose deprivation/reoxygenation model,a miR-324-3 p mimic decreased cell viability and expression of the anti-apoptotic protein BCL2 and increased expression of the pro-apoptotic protein BAX and rates of cell apoptosis,whereas treatment with a miR-324-3p inhibitor had the opposite effects.Silencing miR-324-3p increased adenosine A1 receptor(A1R)expression thro ugh regulation of GATA binding protein 2(GATA2).These findings suggest that silencing miR-324-3p reduces ischemic brain damage via the GATA2/A1R axis. 展开更多
关键词 acute ischemic stroke adenosine A1 receptor apoptosis cerebral ischemia-reperfusion injury cortical neurons GATA2 middle cerebral artery occlusion miR-324-3p oxygen-glucose deprivation/reoxygenation PC12 cells
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Prenatal diagnosis of congenital chloride diarrhea by whole exome sequencing in four Chinese families and prenatal genotype–phenotype association study
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作者 Ying-Fei Shao Hong wang +2 位作者 yi-xiu wang Le-Ping Shao Sai wang 《World Journal of Pediatrics》 SCIE CAS CSCD 2023年第2期200-207,共8页
Congenital chloride diarrhea(CCD;OMIM 214700)is an intestinal disease of an electrolyte defect characterized by dilated bowel loops,maternal polyhydramnios,premature birth,and lack of infant meconium[l].The incidence ... Congenital chloride diarrhea(CCD;OMIM 214700)is an intestinal disease of an electrolyte defect characterized by dilated bowel loops,maternal polyhydramnios,premature birth,and lack of infant meconium[l].The incidence of CCD is variable worldwide.Most cases are sporadic;however,there are three high-incidence areas,Finland,Poland,and Saudi Arabia.In addition,large genetic heterogeneity has been reported in about 300 sporadic patients with CCD from other ethnic groups[2-4].Undiagnosed or untreated CCD can be lethal within the first year of life,but with adequate treatment,patients are usually able to survive into adulthood[5,6]. 展开更多
关键词 diagnosis DIARRHEA CONGENITAL
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