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Jingyuan Xie

Showing results (1-10 of 150) with videos related to

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Journal of the American Society of Nephrology : JASN|September 28, 2023
Uncovering Rare Coding Variants in IgA NephropathyJian Liu, Jingyuan Xie
Contributions to Nephrology|May 22, 2013
Primary glomerulonephritis in mainland China: an overviewJingyuan Xie, Nan Chen
The New England Journal of Medicine|July 2, 2020
Roxadustat for Anemia in Patients with Chronic Kidney Disease. ReplyJingyuan Xie, Nan Chen
Zhonghua Nei Ke Za Zhi|August 14, 2015
[Genetic basis of glomerulonephritis is gradually explored]Jingyuan Xie, Nan Chen
Contributions to Nephrology|May 22, 2013
Genetic studies of IgA nephropathy: what have we learned from genome-wide association studiesJingyuan Xie, Samantha Shapiro, Ali Gharavi
Orphanet Journal of Rare Diseases|August 7, 2025
Autosomal dominant tubulointerstitial kidney disease-UMOD: a short reviewPanpan Qiao, Zhaohui Wang, Jingyuan Xie
Biomedicines|June 27, 2024
Exploration of Gene Therapy for Alport SyndromeYafei Zhao, Qimin Zheng, Jingyuan Xie
Kidney Diseases (Basel, Switzerland)|February 22, 2021
Hypoxia-Inducible Factor-Proline Hydroxylase Inhibitor in the Treatment of Renal AnemiaXiaofan Hu, Jingyuan Xie, Nan Chen
Kidney International|May 2, 2026
Bilateral staghorn calculi in primary hyperoxaluria type 1Chunli Zhang, Ninghao Lu, Jingyuan Xie
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|February 1, 2019
[Advances in research on gene and cell therapy for type IV collagen related hereditary kidney diseases]Yifan Shi, Jingyuan Xie, Jingzhi Zhang, et al.
Pageof 15

Showing results (1-10 of 150) with videos related to

Sort By:
Pageof 15
Journal of the American Society of Nephrology : JASN|September 28, 2023
Uncovering Rare Coding Variants in IgA NephropathyJian Liu, Jingyuan Xie
Contributions to Nephrology|May 22, 2013
Primary glomerulonephritis in mainland China: an overviewJingyuan Xie, Nan Chen
The New England Journal of Medicine|July 2, 2020
Roxadustat for Anemia in Patients with Chronic Kidney Disease. ReplyJingyuan Xie, Nan Chen
Zhonghua Nei Ke Za Zhi|August 14, 2015
[Genetic basis of glomerulonephritis is gradually explored]Jingyuan Xie, Nan Chen
Contributions to Nephrology|May 22, 2013
Genetic studies of IgA nephropathy: what have we learned from genome-wide association studiesJingyuan Xie, Samantha Shapiro, Ali Gharavi
Orphanet Journal of Rare Diseases|August 7, 2025
Autosomal dominant tubulointerstitial kidney disease-UMOD: a short reviewPanpan Qiao, Zhaohui Wang, Jingyuan Xie
Biomedicines|June 27, 2024
Exploration of Gene Therapy for Alport SyndromeYafei Zhao, Qimin Zheng, Jingyuan Xie
Kidney Diseases (Basel, Switzerland)|February 22, 2021
Hypoxia-Inducible Factor-Proline Hydroxylase Inhibitor in the Treatment of Renal AnemiaXiaofan Hu, Jingyuan Xie, Nan Chen
Kidney International|May 2, 2026
Bilateral staghorn calculi in primary hyperoxaluria type 1Chunli Zhang, Ninghao Lu, Jingyuan Xie
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|February 1, 2019
[Advances in research on gene and cell therapy for type IV collagen related hereditary kidney diseases]Yifan Shi, Jingyuan Xie, Jingzhi Zhang, et al.
Pageof 15