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Correlation between spina bifida manifesta in fetal rats and c-Jun N-terminal kinase signaling
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作者 Yinghuan Ma Yongxin Bao +3 位作者 Chenghao Li Fubin Jiao Hongjie Xin Zhengwei Yuan 《Neural Regeneration Research》 SCIE CAS CSCD 2012年第32期2485-2491,共7页
Fetal rat models with neural tube defects were established by injection with retinoic acid at 10 days after conception. The immunofluorescence assay and western blot analysis showed that the number of caspase-3 positi... Fetal rat models with neural tube defects were established by injection with retinoic acid at 10 days after conception. The immunofluorescence assay and western blot analysis showed that the number of caspase-3 positive cells in myeloid tissues for spina bifida manifesta was increased. There was also increased phosphorylation of c-Jun N-terminal kinase, a member of the mitogen activated protein kinase family. The c-Jun N-terminal kinase phosphorylation level was positively correlated with caspase-3 expression in myeloid tissues for spina bifida manifesta. Experimental findings indicate that abnormal apoptosis is involved in retinoic acid-induced dominant spina bifida formation in fetal rats, and may be associated with the c-Jun N-terminal kinase signal transduction pathway. 展开更多
关键词 retinoic acid neural tube defects myeloid tissues caspase-3 apoptotic kinase c-Jun N-terminal kinase mitogen-activated protein kinase neural development REGENERATION neural regeneration
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Adrenal Myelolipoma Associated with Spherocytosis:An Extremely Rare Case
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作者 Youness Chakir El Mahdi Graiouid +3 位作者 Jandou Issam Mohamed Dakir Adil Debbagh Rachid Aboutaieb 《Case Reports in Clinical Medicine》 2019年第11期281-284,共4页
Adrenal myelolipoma is a benign, non-secreting tumor composed of adipose and myeloid tissue that can be complicated by retroperitoneal pain or hemorrhage. Its diagnosis is carried by the computed tomography (CT) and c... Adrenal myelolipoma is a benign, non-secreting tumor composed of adipose and myeloid tissue that can be complicated by retroperitoneal pain or hemorrhage. Its diagnosis is carried by the computed tomography (CT) and confirmed histologically. Surgery may be necessary in case of large volume, symptomatic mass or complication. We report the case of a 36-year-old patient who has a combination of myelolipoma and hereditary spherocytosis, which is extremely rare in the world literature. Computed tomography guided the diagnosis and surgical excision was performed because of the volume of the mass and its symptomatic nature. The evolution at two years was without recurrences. 展开更多
关键词 Non-Secreting Tumor Adipose tissue myeloid tissue Adrenal Myelolipoma
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