Hasil Pencarian - Qihua Fu

Perbaiki Hasil
  1. 1
    FGD5-AS1 Is a Hub lncRNA ceRNA in Hearts With Tetralogy of Fallot Which Regulates Congenital Heart Disease Genes Transcriptionally and Epigenetically

    FGD5-AS1 Is a Hub lncRNA ceRNA in Hearts With Tetralogy of Fallot Which Regulates Congenital Heart Disease Genes Transcriptionally and Epigenetically oleh Xingyu Zhang, Xingyu Zhang, Yunqian Gao, Xiaoping Zhang, Xiaoqing Zhang, Ying Xiang, Qihua Fu, Qihua Fu, Qihua Fu, Bo Wang, Bo Wang, Zhuoming Xu

    Diterbitkan 2021-05-01
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  2. 2
    Long Noncoding RNA lnc-TSSK2-8 Activates Canonical Wnt/β-Catenin Signaling Through Small Heat Shock Proteins HSPA6 and CRYAB

    Long Noncoding RNA lnc-TSSK2-8 Activates Canonical Wnt/β-Catenin Signaling Through Small Heat Shock Proteins HSPA6 and CRYAB oleh Jingjing Fa, Jingjing Fa, Xiaoqing Zhang, Xiaoping Zhang, Ming Qi, Xingyu Zhang, Qihua Fu, Qihua Fu, Qihua Fu, Zhuoming Xu, Yunqian Gao, Yunqian Gao, Bo Wang, Bo Wang

    Diterbitkan 2021-05-01
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  3. 3
    Corrigendum to “Generation of a homozygous CRISPR/Cas9-mediated knockout human iPSC line for PTCH1 gene” [Stem Cell Res. 56 (2021) 102517]

    Corrigendum to “Generation of a homozygous CRISPR/Cas9-mediated knockout human iPSC line for PTCH1 gene” [Stem Cell Res. 56 (2021) 102517] oleh Bailing Zu, Xiaoqing Zhang, Guoling You, Qihua Fu

    Diterbitkan 2022-07-01
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  4. 4
    Generation of a homozygous CRISPR/Cas9-mediated knockout human iPSC line for PTCH1 gene

    Generation of a homozygous CRISPR/Cas9-mediated knockout human iPSC line for PTCH1 gene oleh Bailing Zu, Xiaoqing Zhang, Guoling You, Qihua Fu

    Diterbitkan 2021-10-01
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  5. 5
    The clinical application and laboratory management of molecular genetic diagnosis in children's hospital

    The clinical application and laboratory management of molecular genetic diagnosis in children's hospital oleh Wenjie Bao, Qihua Fu, Xiaoqing Zhang, Xi Mo, Tingting Yu

    Diterbitkan 2024-06-01
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  6. 6
    Development of two different pharmacogenomics detection methods for second-generation antipsychotic drugs quetiapine and aripiprazole

    Development of two different pharmacogenomics detection methods for second-generation antipsychotic drugs quetiapine and aripiprazole oleh Lichen Zhang, Xingyu Zhang, Xiaoqing Zhang, Guoling You, Qihua Fu

    Diterbitkan 2020-03-01
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  7. 7
    A Novel Missense Mutation of GATA4 in a Chinese Family with Congenital Heart Disease.

    A Novel Missense Mutation of GATA4 in a Chinese Family with Congenital Heart Disease. oleh Xiaoqing Zhang, Jian Wang, Bo Wang, Sun Chen, Qihua Fu, Kun Sun

    Diterbitkan 2016-01-01
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  8. 8
    Blood arsenic exposure levels of preschool children and dietary factors analysis

    Blood arsenic exposure levels of preschool children and dietary factors analysis oleh Junxia LIU, Zhenyan GAO, Ju WANG, Chenyin DONG, Chonghuai YAN, Qihua FU

    Diterbitkan 2020-11-01
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  9. 9
    Molecular Characteristic and Virulence Gene Profiles of Community-associated Methicillin-Resistant Staphylococcus aureus Isolates from Pediatric Patients in Shanghai, China

    Molecular Characteristic and Virulence Gene Profiles of Community-associated Methicillin-Resistant Staphylococcus aureus Isolates from Pediatric Patients in Shanghai, China oleh Xing Wang, Xia Li, Wei Liu, Weichun Huang, Qihua Fu, MIN LI

    Diterbitkan 2016-11-01
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  10. 10
    Identification of miRNA–mRNA–TFs Regulatory Network and Crucial Pathways Involved in Tetralogy of Fallot

    Identification of miRNA–mRNA–TFs Regulatory Network and Crucial Pathways Involved in Tetralogy of Fallot oleh Guoling You, Guoling You, Bailing Zu, Bo Wang, Qihua Fu, Fen Li

    Diterbitkan 2020-06-01
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  11. 11
    Copy number variation analysis in Chinese children with complete atrioventricular canal and single ventricle

    Copy number variation analysis in Chinese children with complete atrioventricular canal and single ventricle oleh Xingyu Zhang, Bo Wang, Guoling You, Ying Xiang, Qihua Fu, Yongguo Yu, Xiaoqing Zhang

    Diterbitkan 2021-10-01
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  12. 12
    Molecular Characteristics of Community-Associated Staphylococcus aureus Isolates From Pediatric Patients With Bloodstream Infections Between 2012 and 2017 in Shanghai, China

    Molecular Characteristics of Community-Associated Staphylococcus aureus Isolates From Pediatric Patients With Bloodstream Infections Between 2012 and 2017 in Shanghai, China oleh Xing Wang, Qian Liu, He Zhang, Xia Li, Weichun Huang, Qihua Fu, Min Li

    Diterbitkan 2018-06-01
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  13. 13
    Accurate diagnosis of spinal muscular atrophy and 22q11.2 deletion syndrome using limited deoxynucleotide triphosphates and high-resolution melting

    Accurate diagnosis of spinal muscular atrophy and 22q11.2 deletion syndrome using limited deoxynucleotide triphosphates and high-resolution melting oleh Xiaoqing Zhang, Bo Wang, Lichen Zhang, Guoling You, Robert A. Palais, Luming Zhou, Qihua Fu

    Diterbitkan 2018-06-01
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  14. 14
    Identification of TBX2 and TBX3 variants in patients with conotruncal heart defects by target sequencing

    Identification of TBX2 and TBX3 variants in patients with conotruncal heart defects by target sequencing oleh Huilin Xie, Erge Zhang, Nanchao Hong, Qihua Fu, Fen Li, Sun Chen, Yu Yu, Kun Sun

    Diterbitkan 2018-09-01
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  15. 15
    Variants in a cis-regulatory element of TBX1 in conotruncal heart defect patients impair GATA6-mediated transactivation

    Variants in a cis-regulatory element of TBX1 in conotruncal heart defect patients impair GATA6-mediated transactivation oleh Xuechao Jiang, Tingting Li, Sijie Liu, Qihua Fu, Fen Li, Sun Chen, Kun Sun, Rang Xu, Yuejuan Xu

    Diterbitkan 2021-07-01
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  16. 16
    Integrated analysis of copy number variation-associated lncRNAs identifies candidates contributing to the etiologies of congenital kidney anomalies

    Integrated analysis of copy number variation-associated lncRNAs identifies candidates contributing to the etiologies of congenital kidney anomalies oleh Yibo Lu, Yiyang Zhou, Jing Guo, Ming Qi, Yuwan Lin, Xingyu Zhang, Ying Xiang, Qihua Fu, Bo Wang

    Diterbitkan 2023-07-01
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  17. 17
    Novel mutations in the SCNN1A gene causing Pseudohypoaldosteronism type 1.

    Novel mutations in the SCNN1A gene causing Pseudohypoaldosteronism type 1. oleh Jian Wang, Tingting Yu, Lei Yin, Jing Li, Li Yu, Ye Shen, Yongguo Yu, Yongnian Shen, Qihua Fu

    Diterbitkan 2013-01-01
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  18. 18
    HBprem: A database of transcription, translation, and posttranscriptional and posttranslational modifications in hepatoblastoma

    HBprem: A database of transcription, translation, and posttranscriptional and posttranslational modifications in hepatoblastoma oleh Hang Song, Zhixuan Bian, Siwei Mao, Jiabei Zhu, Yue Zhang, Song Gu, Minzhi Yin, Qihua Fu, Qiuhui Pan

    Diterbitkan 2020-06-01
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  19. 19
    Copy number variation-associated lncRNAs may contribute to the etiologies of congenital heart disease

    Copy number variation-associated lncRNAs may contribute to the etiologies of congenital heart disease oleh Yibo Lu, Qing Fang, Ming Qi, Xiaoliang Li, Xingyu Zhang, Yuwan Lin, Ying Xiang, Qihua Fu, Bo Wang

    Diterbitkan 2023-02-01
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  20. 20
    Identification of the genetic basis of sporadic polydactyly in China by targeted sequencing

    Identification of the genetic basis of sporadic polydactyly in China by targeted sequencing oleh Bailing Zu, Xiaoqing Zhang, Yunlan Xu, Ying Xiang, Zhigang Wang, Haiqing Cai, Bo Wang, Guoling You, Qihua Fu

    Diterbitkan 2021-01-01
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