Resultados da busca - Luo, Shiyu
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Correction: Li, et al. LncRNA NEAT1 Silenced miR-133b Promotes Migration and Invasion of Breast Cancer Cells. Int. J. Mol. Sci. 2019, 20, 3616 por Li, Xinping, Deng, Siwei, Pang, Xinyao, Song, Yixiao, Luo, Shiyu, Jin, Liang, Pan, Yi
Publicado em 2020Texto -
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The Phosphatidylcholine Transfer Protein Stard7 is Required for Mitochondrial and Epithelial Cell Homeostasis por Yang, Li, Na, Cheng-Lun, Luo, Shiyu, Wu, David, Hogan, Simon, Huang, Taosheng, Weaver, Timothy E.
Publicado em 2017Texto -
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Striated Preferentially Expressed Protein Kinase (SPEG)-Deficient Skeletal Muscles Display Fewer Satellite Cells with Reduced Proliferation and Delayed Differentiation por Li, Qifei, Lin, Jasmine, Rosen, Samantha M., Zhang, Tian, Kazerounian, Shideh, Luo, Shiyu, Agrawal, Pankaj B.
Publicado em 2020Texto -
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SPEG binds with desmin and its deficiency causes defects in triad and focal adhesion proteins por Luo, Shiyu, Li, Qifei, Lin, Jasmine, Murphy, Quinn, Marty, Isabelle, Zhang, Yuanfan, Kazerounian, Shideh, Agrawal, Pankaj B
Publicado em 2020Texto -
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Development of a Semi-Automatic Segmentation Method for Retinal OCT Images Tested in Patients with Diabetic Macular Edema por Huang, Yijun, Danis, Ronald P., Pak, Jeong W., Luo, Shiyu, White, James, Zhang, Xian, Narkar, Ashwini, Domalpally, Amitha
Publicado em 2013Texto -
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Genetic Testing and Pregnancy Outcome Analysis of 362 Fetuses with Congenital Heart Disease Identified by Prenatal Ultrasound por Luo, Shiyu, Meng, Dahua, Li, Qifei, Hu, Xuehua, Chen, Yuhua, He, Chun, Xie, Bobo, She, Shangyang, Li, Yingfeng, Fu, Chunyun
Publicado em 2018Texto -
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Genetic Testing and Pregnancy Outcome Analysis of 362 Fetuses with Congenital Heart Disease Identified by Prenatal Ultrasound por Luo, Shiyu, Meng, Dahua, Li, Qifei, Hu, Xuehua, Chen, Yuhua, He, Chun, Xie, Bobo, She, Shangyang, Li, Yingfeng, Fu, Chunyun
Publicado em 2018Online -
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Mutation screening of the TPO gene in a cohort of 192 Chinese patients with congenital hypothyroidism por Fu, Chunyun, Xie, Bobo, Zhang, Shujie, Wang, Jin, Luo, Shiyu, Zheng, Haiyang, Su, Jiasun, Hu, Xuyun, Chen, Rongyu, Fan, Xin, Luo, Jingsi, Gu, Xuefan, Chen, Shaoke
Publicado em 2016Texto -
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Maternal uniparental disomy 14 and mosaic trisomy 14 in a Chinese boy with moderate to severe intellectual disability por Zhang, Shujie, Qin, Haisong, Wang, Jin, OuYang, Luping, Luo, Shiyu, Fu, Chunyun, Fan, Xin, Su, Jiasun, Chen, Rongyu, Xie, Bobo, Hu, Xuyun, Chen, Shaoke, Shen, Yiping
Publicado em 2016Texto -
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Newborn screening of glucose-6-phosphate dehydrogenase deficiency in Guangxi, China: determination of optimal cutoff value to identify heterozygous female neonates por Fu, Chunyun, Luo, Shiyu, Li, Qifei, Xie, Bobo, Yang, Qi, Geng, Guoxing, Lin, Caijuan, Su, Jiasun, Zhang, Yue, Wang, Jin, Qin, Zailong, Luo, Jingsi, Chen, Shaoke, Fan, Xin
Publicado em 2018Texto -
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The incidence of congenital hypothyroidism (CH) in Guangxi, China and the predictors of permanent and transient CH por Fu, Chunyun, Luo, Shiyu, Li, Yingfeng, Li, Qifei, Hu, Xuehua, Li, Mengting, Zhang, Yue, Su, Jiasun, Hu, Xuyun, Chen, Yun, Wang, Jin, Xie, Bobo, Luo, Jingsi, Fan, Xin, Chen, Shaoke, Shen, Yiping
Publicado em 2017Texto