Search Results - "Luo, Jie-Wei" :: K.UTB vyhledávací portál | TBU Library Retrieval Portal

Medial retropharyngeal nodal region sparing radiotherapy versus standard radiotherapy in patients with nasopharyngeal carcinoma: open label, non-inferiority, multicentre, randomised, phase 3 trial

Medial retropharyngeal nodal region sparing radiotherapy versus standard radiotherapy in patients with nasopharyngeal carcinoma: open label, non-inferiority, multicentre, randomised, phase 3 trial

by Mao, Yan-Ping, Wang, Shun-Xin, Gao, Tian-Sheng, Zhang, Ning, Liang, Xiao-Yu, Xie, Fang-Yun, Zhang, Yuan, Zhou, Guan-Qun, Guo, Rui, Luo, Wei-Jie, Li, Yong-Jie, Liang, Shao-Qiang, Lin, Li, Li, Wen-Fei, Liu, Xu, Xu, Cheng, Chen, Yu-Pei, Lv, Jia-Wei, Huang, Shao-Hui, Liu, Li-Zhi, Li, Ji-Bin, Tang, Ling-Long, Chen, Lei, Sun, Ying, Ma, Jun
Published in BMJ (Online) (06.02.2023)

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Clinical phenotype and genetic function analysis of a rare family with hereditary leiomyomatosis and renal cell carcinoma complicated with Birt-Hogg-Dubé syndrome

Clinical phenotype and genetic function analysis of a rare family with hereditary leiomyomatosis and renal cell carcinoma complicated with Birt-Hogg-Dubé syndrome

by Pan, Hong-Hong, Ruan, Dan-Dan, Wu, Min, Chen, Ting, Lu, Tao, Gan, Yu-Mian, Wang, Chen, Liao, Li-Sheng, Lin, Xin-Fu, Chen, Xin, Zhu, Yao-Bin, Fang, Zhu-Ting, Yu, Qing-Hua, Yang, Guo-Kai, Ye, Lie-Fu, Luo, Jie-Wei
Published in Journal of medical genetics (01.12.2023)

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Clinical phenotype and genetic function analysis of a family with hypomyelinating leukodystrophy-7 caused by POLR3A mutation

Clinical phenotype and genetic function analysis of a family with hypomyelinating leukodystrophy-7 caused by POLR3A mutation

by Ruan, Dan-dan, Ruan, Xing-lin, Wang, Ruo‑li, Lin, Xin-fu, Zhang, Yan-ping, Lin, Bin, Li, Shi-jie, Wu, Min, Chen, Qian, Zhang, Jian-hui, Cheng, Qiong, Zhang, Yi-wu, Lin, Fan, Luo, Jie-wei, Zheng, Zheng, Li, Yun-fei
Published in Scientific reports (01.04.2024)

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Pharmarcomechanical thrombectomy combined with transluminal balloon angioplasty for treating transplant renal vein thrombosis

Pharmarcomechanical thrombectomy combined with transluminal balloon angioplasty for treating transplant renal vein thrombosis

by Wu, Shao-Jie, Zhang, Chi, Wu, Min, Ruan, Dan-dan, Zhang, Yan-ping, Lin, Bin, Tang, Yi, Chen, Xin, Wang, Chen, Pan, Hong-hong, Zhu, Qing-guo, Luo, Jie-wei, Ye, Lie-fu, Fang, Zhu-ting
Published in Scientific reports (12.10.2023)

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A novel compound heterozygous variant linked to hematuria in a family with hereditary factor VII deficiency

A novel compound heterozygous variant linked to hematuria in a family with hereditary factor VII deficiency

by Hu, Ya‐Nan, Gan, Yu‐Mian, Zhang, Yan‐Ping, Ruan, Dan‐Dan, Zhu, Yao‐Bin, Lin, Xin‐Fu, Fang, Zhu‐Ting, Liao, Li‐Sheng, Tang, Fa‐Qiang, Luo, Jie‐Wei
Published in The journal of gene medicine (01.02.2022)

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The value of computed tomography angiography for evaluation of left atrial enlargement in patients with persistent atrial fibrillation

The value of computed tomography angiography for evaluation of left atrial enlargement in patients with persistent atrial fibrillation

by Lin, Fang-Fang, Chen, Qian, Wu, Qiu-Yan, Li, Shi-Jie, Zhu, Yao-Bin, Tang, Yi, Xue, Yun-Jing, Luo, Jie-Wei, Li, Zuo-An, Chen, Hong-Yi
Published in BMC cardiovascular disorders (19.09.2024)

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TMEM45A is involved in renal fibrosis in rats by regulating Jagged1/Notch pathway

TMEM45A is involved in renal fibrosis in rats by regulating Jagged1/Notch pathway

by Lan, Jian-Zi, Pan, Qi, Tao, Qing, Shi, Xin, Wang, Wei-Zhun, Xu, Bo-Wen, Luo, Jie-Wei
Published in Frontiers in bioscience (01.01.2020)

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Genetic analysis of sick sinus syndrome in a family harboring compound CACNA1C and TTN mutations

Genetic analysis of sick sinus syndrome in a family harboring compound CACNA1C and TTN mutations

by Zhu, Yao-Bin, Luo, Jie-Wei, Jiang, Fen, Liu, Gui
Published in Molecular medicine reports (01.05.2018)

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Potential regulatory role of the Nrf2/HMGB1/TLR4/NF-κB signaling pathway in lupus nephritis

Potential regulatory role of the Nrf2/HMGB1/TLR4/NF-κB signaling pathway in lupus nephritis

by Li, Shi-jie, Ruan, Dan-dan, Wu, Wei-zhen, Wu, Min, Wu, Qiu-yan, Wang, Han-lu, Ji, Yuan-yuan, Zhang, Yan-ping, Lin, Xin-fu, Fang, Zhu-ting, Liao, Li-sheng, Luo, Jie-wei, Gao, Mei-zhu, Wu, Jia-bin
Published in Pediatric Rheumatology (23.10.2023)

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Case report and analysis: Behçet’s disease with lower extremity vein thrombosis and pseudoaneurysm

Case report and analysis: Behçet’s disease with lower extremity vein thrombosis and pseudoaneurysm

by Wang, Han-Lu, Zhang, Jian-Hui, Wu, Yi-Cheng, Lin, Jia-Li, Tang, Yi, Liao, Li-Sheng, Luo, Jie-Wei, Yu, Qing-Hua, Fang, Zhu-Ting
Published in Frontiers in immunology (29.08.2022)

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Review and Analysis of Two Gitelman Syndrome Pedigrees Complicated with Proteinuria or Hashimoto’s Thyroiditis Caused by Compound Heterozygous SLC12A3 Mutations

Review and Analysis of Two Gitelman Syndrome Pedigrees Complicated with Proteinuria or Hashimoto’s Thyroiditis Caused by Compound Heterozygous SLC12A3 Mutations

by Zhang, Jian-hui, Ruan, Dan-dan, Hu, Ya-nan, Ruan, Xing-lin, Zhu, Yao-bin, Yang, Xiao, Wu, Jia-bin, Lin, Xin-fu, Luo, Jie-wei, Tang, Fa-qiang
Published in BioMed research international (10.05.2021)

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Function of PHEX mutations p.Glu145 and p.Trp749Arg in families with X-linked hypophosphatemic rickets by the negative regulation mechanism on FGF23 promoter transcription

Function of PHEX mutations p.Glu145 and p.Trp749Arg in families with X-linked hypophosphatemic rickets by the negative regulation mechanism on FGF23 promoter transcription

by Gan, Yu-mian, Zhang, Yan-ping, Ruan, Dan-dan, Huang, Jian-bin, Zhu, Yao-bin, Lin, Xin-fu, Xiao, Xiao-ping, Cheng, Qiong, Geng, Zhen-bo, Liao, Li-sheng, Tang, Fa-qiang, Luo, Jie-wei
Published in Cell death & disease (02.06.2022)

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Expression Profiles and Prognostic Value of Multiple Inhibitory Checkpoints in Head and Neck Lymphoepithelioma-Like Carcinoma

Expression Profiles and Prognostic Value of Multiple Inhibitory Checkpoints in Head and Neck Lymphoepithelioma-Like Carcinoma

by Zou, Wen-Qing, Luo, Wei-Jie, Feng, Yan-Fen, Liu, Fang, Liang, Shao-Bo, Fang, Xue-Liang, Liang, Ye-Lin, Liu, Na, Wang, Ya-Qin, Mao, Yan-Ping
Published in Frontiers in immunology (24.01.2022)

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Mutational Analysis of a Familial Adenomatous Polyposis Pedigree with Bile Duct Polyp Phenotype

Mutational Analysis of a Familial Adenomatous Polyposis Pedigree with Bile Duct Polyp Phenotype

by Xie, Li-jun, Ruan, Dan-dan, Zhang, Jian-hui, Li, Yi, Chen, Li, Yan, Mao-lin, Yu, Ming-dian, Luo, Jie-wei, Zhang, Hui-zhen
Published in Canadian journal of gastroenterology & hepatology (2021)

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Effect of superselective prostatic artery embolization on benign prostatic hyperplasia

Effect of superselective prostatic artery embolization on benign prostatic hyperplasia

by Tang, Yi, Zhang, Jian-Hui, Zhu, Yao-bin, Wu, Shao-Jie, Cai, Sen-Lin, Zhou, Yan-Feng, Qian, Xin, Luo, Jie-Wei, Fang, Zhu-Ting
Published in Abdominal imaging (01.04.2021)

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Retrospective observation of the efficacy and safety of prostatic artery embolization combined with transurethral resection of the prostate and simple transurethral resection of the prostate in the treatment of large (> 100 mL) benign prostatic hyperplasia

Retrospective observation of the efficacy and safety of prostatic artery embolization combined with transurethral resection of the prostate and simple transurethral resection of the prostate in the treatment of large (> 100 mL) benign prostatic hyperplasia

by Tang, Yi, Wang, Ruo-li, Ruan, Dan-dan, Chen, Xin, Zhou, Yan-feng, Wu, Shao-jie, Cai, Sen‑lin, Zhang, Jian-hui, Yang, Feng-guang, Luo, Jie-wei, Fang, Zhu-ting
Published in Abdominal imaging (01.12.2021)

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Different phenotypes of neurological diseases, including alternating hemiplegia of childhood and rapid-onset dystonia-parkinsonism, caused by de novo ATP1A3 mutation in a family

Different phenotypes of neurological diseases, including alternating hemiplegia of childhood and rapid-onset dystonia-parkinsonism, caused by de novo ATP1A3 mutation in a family

by Wei, Wen, Zheng, Xiu-fen, Ruan, Dan-dan, Gan, Yu-mian, Zhang, Yan-ping, Chen, Ying, Lin, Xin-fu, Tang, Fa-qiang, Luo, Jie-wei, Li, Yun-fei
Published in Neurological sciences (01.04.2022)

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Screening and function discussion of a hereditary renal tubular acidosis family pathogenic gene

Screening and function discussion of a hereditary renal tubular acidosis family pathogenic gene

by Chen, Li, Wang, Han-Lu, Zhu, Yao-Bin, Jin, Zhao, Huang, Jian-Bin, Lin, Xin-Fu, Luo, Jie-Wei, Fang, Zhu-Ting
Published in Cell death & disease (02.03.2020)

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An integrated model of the gross tumor volume of cervical lymph nodes and pretreatment plasma Epstein–Barr virus DNA predicts survival of nasopharyngeal carcinoma in the intensity-modulated radiotherapy era: a big-data intelligence platform-based analysis

An integrated model of the gross tumor volume of cervical lymph nodes and pretreatment plasma Epstein–Barr virus DNA predicts survival of nasopharyngeal carcinoma in the intensity-modulated radiotherapy era: a big-data intelligence platform-based analysis

by Li, Jun-Yan, Huang, Cheng-Long, Luo, Wei-Jie, Zhang, Yuan, Tang, Ling-Long, Peng, Hao, Sun, Ying, Chen, Yu-Pei, Ma, Jun
Published in Therapeutic advances in medical oncology (2019)

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Identification and characterization of two SERPINC1 mutations causing congenital antithrombin deficiency

Identification and characterization of two SERPINC1 mutations causing congenital antithrombin deficiency

by Wang, Han-Lu, Ruan, Dan-Dan, Wu, Min, Ji, Yuan-Yuan, Hu, Xing-Xing, Wu, Qiu-Yan, Zhang, Yan-Ping, Lin, Bin, Hu, Ya-Nan, Wang, Hang, Tang, Yi, Fang, Zhu-Ting, Luo, Jie-Wei, Liao, Li-Sheng, Gao, Mei-Zhu
Published in Thrombosis journal (09.01.2023)

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