Large concrete pipeline manufacturing equipment and process von JI CHUANZHU, WU XURAN, KUAI XUEFU, WU GUANJUN, ZHANG WEI

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Unraveling the Diagnostic Puzzle: Minor Stroke-Like Lesions and Normal Muscle Histopathology in MELAS Syndrome von Zhao, Ying, Xu, Zhihong, Yan, Chuanzhu, Ji, Kunqian

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Growth Differentiation Factor 15 Is a Novel Diagnostic Biomarker of Mitochondrial Diseases von Ji, Xinbo, Zhao, Lizhen, Ji, Kunqian, Zhao, Yuying, Li, Wei, Zhang, Rui, Hou, Ying, Lu, Jianqiang, Yan, Chuanzhu

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Migratory Rolandic Encephalopathy Caused by the Mitochondrial ND3 Mutation von Ji, Kunqian, Ren, Hong, Zhao, Xiuhe, Yan, Chuanzhu

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ETFDH Mutations and Flavin Adenine Dinucleotide Homeostasis Disturbance Are Essential for Developing Riboflavin‐Responsive Multiple Acyl–Coenzyme A Dehydrogenation Deficiency von Xu, Jingwen, Li, Duoling, Lv, Jingwei, Xu, Xuebi, Wen, Bing, Lin, Pengfei, Liu, Fuchen, Ji, Kunqian, Shan, Jingli, Li, Honghao, Li, Wei, Zhao, Yuying, Zhao, Dandan, Pok, Joo Y., Yan, Chuanzhu

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The clinical and genetic spectrum of mitochondrial diseases in China: A multicenter retrospective cross‐sectional study von Zhao, Yang, Zhao, Xutong, Ji, Kunqian, Wang, Junling, Zhao, Yuying, Lin, Jie, Gang, Qiang, Yu, Meng, Yuan, Yun, Jiang, Haishan, Sun, Chong, Fang, Fang, Yan, Chuanzhu, Wang, Zhaoxia

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Taurine hypomodification underlies mitochondrial tRNATrp-related genetic diseases von Lu, Jia-Li, Dai, Yichen, Ji, Kunqian, Peng, Gui-Xin, Li, Hong, Yan, Chuanzhu, Shen, Bin, Zhou, Xiao-Long

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Novel biallelic mutations in POLG gene: large deletion and missense variant associated with PEO von Lin, Yan, Du, Jixiang, Wang, Wei, Ren, Hong, Zhao, Dandan, Liu, Fuchen, Lin, Pengfei, Ji, Kunqian, Zhao, Yuying, Yan, Chuanzhu

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Fluctuating ataxia caused by mitochondrial tRNA (Lys) gene m.8363G > A variant von Zhao, Ying, Zhao, Bing, Ji, Kunqian, Yan, Chuanzhu

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Reversible cerebral artery constriction accompanied with stroke-like episode in MELAS: A case series von Zhao, Yuying, Yu, Xiaolin, Ji, Kunqian, Lin, Yan, Xu, Xuebi, Wang, Wei, Yan, Chuanzhu

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Skeletal muscle increases FGF21 expression in mitochondrial disorders to compensate for energy metabolic insufficiency by activating the mTOR–YY1–PGC1α pathway von Ji, Kunqian, Zheng, Jinfan, Lv, Jingwei, Xu, Jingwen, Ji, Xinbo, Luo, Yue-Bei, Li, Wei, Zhao, Yuying, Yan, Chuanzhu

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Effect of low-dose rituximab treatment on autoimmune nodopathy with anti-contactin 1 antibody von Hou, Ying, Zhang, Chao, Yu, Xiaolin, Wang, Wenqing, Zhang, Dong, Bai, Yunfei, Yan, Chuanzhu, Ma, Lin, Li, Anning, Ji, Jian, Cao, Lili, Wang, Qinzhou

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Idebenone protects against oxidized low density lipoprotein induced mitochondrial dysfunction in vascular endothelial cells via GSK3β/β-catenin signalling pathways von Lin, Pengfei, Liu, Junling, Ren, Ming, Ji, Kunqian, Li, Ling, Zhang, Bin, Gong, Yaoqin, Yan, Chuanzhu

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Generation of a human induced pluripotent stem cell line (INNDSUi003-A) derived from patient with Becker muscular dystrophy (BMD) von Ji, Xinbo, Wang, Yu, Sun, Ping, Wang, Dongdong, Sun, Xiaohan, Zhang, Rui, Xu, Jingwen, Li, Wei, Liu, Fuchen, Yan, Chuanzhu

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Establishment of an induced pluripotent stem cell (iPSC) line (INNDSUi001-A) from a healthy female Chinese Han von Wang, Dongdong, Zhang, Rui, Wang, Yu, Sun, Ping, Ji, Xinbo, Sun, Xiaohan, Xu, Jingwen, Zhao, Dandan, Yan, Chuanzhu, Liu, Fuchen

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Accuracy of FGF‐21 and GDF‐15 for the diagnosis of mitochondrial disorders: A meta‐analysis von Lin, Yan, Ji, Kunqian, Ma, Xiaotian, Liu, Shuangwu, Li, Wei, Zhao, Yuying, Yan, Chuanzhu

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Late-Onset Leukodystrophy Mimicking Hereditary Spastic Paraplegia without Diffuse Leukodystrophy on Neuroimaging von Zhang, Tongxia, Yan, Chuanzhu, Liu, Yiming, Cao, Lili, Ji, Kunqian, Li, Duoling, Chi, Lingyi, Zhao, Yuying

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Bezafibrate Rescues Mitochondrial Encephalopathy in Mice via Induction of Daily Torpor and Hypometabolic State von Lyu, Jingwei, Zhao, Yuying, Zhang, Na, Xu, Xuebi, Zheng, Rui, Yu, Wenfei, Xin, Wang, Yan, Chuanzhu, Ji, Kunqian

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“Myo-neuropathy” is commonly associated with mitochondrial tRNALysine mutation von Ji, Kunqian, Zhao, Bing, Lin, Yan, Wang, Wei, Liu, Fuchen, Li, Wei, Zhao, Yuying, Yan, Chuanzhu

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A novel nonsense variant in MT-CO3 causes MELAS syndrome von Wang, Wei, Sun, Yuan, Lin, Yan, Xu, Xuebi, Zhao, Dandan, Ji, Kunqian, Li, Wei, Zhao, Yuying, Yan, Chuanzhu

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