Hasil Pencarian - Fu Xiong

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  1. 1
    Urinary Microbial and Metabolomic Profiles in Kidney Stone Disease

    Urinary Microbial and Metabolomic Profiles in Kidney Stone Disease oleh Hong Gao, Jiaqiong Lin, Fu Xiong, Fu Xiong, Zuhu Yu, Shilei Pan, Yuxin Huang

    Diterbitkan 2022-09-01
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  2. 2
    A Novel Mutation in ATRX Causes Alpha-Thalassemia X-Linked Intellectual Disability Syndrome in a Han Chinese Family

    A Novel Mutation in ATRX Causes Alpha-Thalassemia X-Linked Intellectual Disability Syndrome in a Han Chinese Family oleh Shaomin Wu, Shaomin Wu, Yingchun Zheng, Cailing Xu, Jiahui Fu, Fu Xiong, Fu Xiong, Fang Yang

    Diterbitkan 2022-01-01
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  3. 3
    Case Report: First Case of Cefotaxime-Sulbactam-Induced Acute Intravascular Hemolysis in a Newborn With ABO Blood Type Incompatibility by the Mechanism of Non-Immunologic Protein Adsorption

    Case Report: First Case of Cefotaxime-Sulbactam-Induced Acute Intravascular Hemolysis in a Newborn With ABO Blood Type Incompatibility by the Mechanism of Non-Immunologic Protein A... oleh Yuanjun Wu, Yong Wu, Yong Yang, Baochan Chen, Jianqun Li, Ganping Guo, Fu Xiong, Fu Xiong

    Diterbitkan 2021-12-01
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  4. 4
    Case Report: A Novel COL1A1 Missense Mutation Associated With Dentineogenesis Imperfecta Type I

    Case Report: A Novel COL1A1 Missense Mutation Associated With Dentineogenesis Imperfecta Type I oleh Yuting Zeng, Yuhua Pan, Jiayao Mo, Zhiting Ling, Lifang Jiang, Fu Xiong, Fu Xiong, Wenjuan Yan

    Diterbitkan 2021-06-01
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  5. 5
    Familial Translocation t(2;4) (q37.3;p16.3), Resulting in a Partial Trisomy of 2q (or 4p) and a Partial Monosomy of 4p (or 2q), Causes Dysplasia

    Familial Translocation t(2;4) (q37.3;p16.3), Resulting in a Partial Trisomy of 2q (or 4p) and a Partial Monosomy of 4p (or 2q), Causes Dysplasia oleh Jian Wang, Jian Wang, Shiyuan Zhou, Fei He, Xuelian Zhang, Jianqi Lu, Jian Zhang, Feng Zhang, Xiangmin Xu, Xiangmin Xu, Fang Yang, Fu Xiong, Fu Xiong, Fu Xiong

    Diterbitkan 2021-11-01
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  6. 6
    Case Report: A Novel Compound Heterozygous Mutation of the FRMD4A Gene Identified in a Chinese Family With Global Developmental Delay, Intellectual Disability, and Ataxia

    Case Report: A Novel Compound Heterozygous Mutation of the FRMD4A Gene Identified in a Chinese Family With Global Developmental Delay, Intellectual Disability, and Ataxia oleh Yuhua Pan, Xiaoling Guo, Xiaoqiang Zhou, Yue Liu, Jingli Lian, Tingting Yang, Xiang Huang, Fei He, Jian Zhang, Buling Wu, Fu Xiong, Fu Xiong, Fu Xiong, Xingkun Yang

    Diterbitkan 2021-11-01
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  7. 7
    A Heterozygous LMF1 Gene Mutation (c.1523C>T), Combined With an LPL Gene Mutation (c.590G>A), Aggravates the Clinical Symptoms in Hypertriglyceridemia

    A Heterozygous LMF1 Gene Mutation (c.1523C>T), Combined With an LPL Gene Mutation (c.590G>A), Aggravates the Clinical Symptoms in Hypertriglyceridemia oleh Danxia Guo, Yingchun Zheng, Zhongzhi Gan, Yingying Guo, Sijie Jiang, Fang Yang, Fu Xiong, Fu Xiong, Hua Zheng

    Diterbitkan 2022-03-01
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  8. 8
    The molecular mechanism of Gaucher disease caused by compound heterozygous mutations in GBA1 gene

    The molecular mechanism of Gaucher disease caused by compound heterozygous mutations in GBA1 gene oleh Qi Liu, Zongrui Shen, Zongrui Shen, Hong Pan, Shunfei Ma, Shunfei Ma, Fu Xiong, Fu Xiong, Fei He, Fei He

    Diterbitkan 2023-01-01
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  9. 9
    Assessing the robustness of radiomics/deep learning approach in the identification of efficacy of anti–PD-1 treatment in advanced or metastatic non-small cell lung carcinoma patients

    Assessing the robustness of radiomics/deep learning approach in the identification of efficacy of anti–PD-1 treatment in advanced or metastatic non-small cell lung carcinoma patien... oleh Qianqian Ren, Qianqian Ren, Fu Xiong, Fu Xiong, Peng Zhu, Xiaona Chang, Guobin Wang, Nan He, Qianna Jin, Qianna Jin

    Diterbitkan 2022-08-01
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  10. 10
    Case Report: Two cases of advanced primary cardiac angiosarcoma treated with anlotinib and a retrospective analysis of the literature

    Case Report: Two cases of advanced primary cardiac angiosarcoma treated with anlotinib and a retrospective analysis of the literature oleh Pan Yang, Fu Xiong, Bingjing Zhu, Liang Gong, Chunlan Tang

    Diterbitkan 2024-03-01
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  11. 11
    Mechanism and Influential Factors of the Stability of Hydrophobic Starch Pickering Emulsion Gels

    Mechanism and Influential Factors of the Stability of Hydrophobic Starch Pickering Emulsion Gels oleh GUO Lu, HUANG Liang, ZHANG Bin, FU Xiong, HUANG Qiang

    Diterbitkan 2023-01-01
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  12. 12
    Correlation between serum vitamin D level and acute invasive enteritis in children

    Correlation between serum vitamin D level and acute invasive enteritis in children oleh Lingrong Yang, Yu Fang, Jinyu Zheng, Qiaoying Zhu, Li Tang, Fu Xiong

    Diterbitkan 2024-09-01
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  13. 13
    Four novel mutations identified in the COL4A3, COL4A4 and COL4A5 genes in 10 families with Alport syndrome

    Four novel mutations identified in the COL4A3, COL4A4 and COL4A5 genes in 10 families with Alport syndrome oleh Duocai Wang, Meize Pan, Hang Li, Minchun Li, Ping Li, Fu Xiong, Hongbo Xiao

    Diterbitkan 2024-07-01
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  14. 14
    Chemical Composition, Antioxidant and Hypoglycemic Activities of Phenolic Fractions from Sargassum pallidum

    Chemical Composition, Antioxidant and Hypoglycemic Activities of Phenolic Fractions from Sargassum pallidum oleh XIE Xing, WANG Siyu, WANG Peixin, ZHANG Lu, TU Zongcai, CHEN Chun, FU Xiong

    Diterbitkan 2023-05-01
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  15. 15
    Correction of Sample-Time Error for Time-Interleaved Sampling System Using Cubic Spline Interpolation

    Correction of Sample-Time Error for Time-Interleaved Sampling System Using Cubic Spline Interpolation oleh Qin Guo-jie, Liu Guo-man, Gao Mei-guo, Fu Xiong-jun, Xu Peng

    Diterbitkan 2014-08-01
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  16. 16
    A case of spontaneous hepatic hemangioma rupture: Successful management with transarterial chemoembolization alone

    A case of spontaneous hepatic hemangioma rupture: Successful management with transarterial chemoembolization alone oleh Yanyan Cao, Fu Xiong, Bin Xiong, Yong Wang, Feng Yuan, Yanqiao Ren, Chuansheng Zheng

    Diterbitkan 2019-08-01
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  17. 17
    Functional Analysis of Ectodysplasin-A Mutations in X-Linked Nonsyndromic Hypodontia and Possible Involvement of X-Chromosome Inactivation

    Functional Analysis of Ectodysplasin-A Mutations in X-Linked Nonsyndromic Hypodontia and Possible Involvement of X-Chromosome Inactivation oleh Yuhua Pan, Ting Lu, Ling Peng, Qi Zeng, Xiangyu Huang, Xinchen Yao, Buling Wu, Fu Xiong

    Diterbitkan 2021-01-01
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  18. 18
    Identification of a novel nonsense mutation in α-galactosidase A that causes Fabry disease in a Chinese family

    Identification of a novel nonsense mutation in α-galactosidase A that causes Fabry disease in a Chinese family oleh Yushi Peng, Meize Pan, Yuchen Wang, Zongrui Shen, Jian Xu, Fu Xiong, Hongbo Xiao, Yun Miao

    Diterbitkan 2024-12-01
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  19. 19
    Vacuolar protein sorting 4B regulates the proliferation and odontoblastic differentiation of human dental pulp stem cells through the Wnt-β-catenin signalling pathway

    Vacuolar protein sorting 4B regulates the proliferation and odontoblastic differentiation of human dental pulp stem cells through the Wnt-β-catenin signalling pathway oleh Yuhua Pan, Ting Lu, Ling Peng, Zhao Chen, Meiyi Li, Kaiying Zhang, Fu Xiong, Buling Wu

    Diterbitkan 2019-12-01
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  20. 20
    A new prediction model of hepatocellular carcinoma based on N7-methylguanosine modification

    A new prediction model of hepatocellular carcinoma based on N7-methylguanosine modification oleh Li Yang, Yi-ran Wang, Zhi-qiang Mou, Ping-fu Xiong, Kun Deng, Jian Wen, Jing Li

    Diterbitkan 2023-04-01
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