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National Clinical Research Center of Kidney Diseases,
Jinling Hospital,
National Clinical Research Center of Kidney Diseases, Jinling Hospital
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Novel mutations of ABCB6 associated with autosomal dominant dyschromatosis universalis hereditaria.
PloS one , 2013 | Pubmed ID: 24224009
[Comparative study on da Vince robotic and laparoscopic radical gastrectomy for gastric cancer].
Zhonghua wei chang wai ke za zhi = Chinese journal of gastrointestinal surgery May, 2014 | Pubmed ID: 24859955
Role of intestinal flora imbalance in pathogenesis of pouchitis.
Asian Pacific journal of tropical medicine Aug, 2016 | Pubmed ID: 27569889
The analysis of risk factors for diabetic nephropathy progression and the construction of a prognostic database for chronic kidney diseases.
Journal of translational medicine Aug, 2019 | Pubmed ID: 31409386
Mindfulness interventions for rheumatoid arthritis: A systematic review and meta-analysis.
Complementary therapies in clinical practice May, 2020 | Pubmed ID: 31957665
Generation of induced pluripotent stem cell line (NCKDi001-A) from a 19-year-old patient with a novel COL4A5 gene mutation in Alport syndrome.
Stem cell research Dec, 2020 | Pubmed ID: 33128955
Hydrogen Sulfide Is a Regulator of Hemoglobin Oxygen-Carrying Capacity via Controlling 2,3-BPG Production in Erythrocytes.
Oxidative medicine and cellular longevity , 2021 | Pubmed ID: 33628390
Generation of the induced pluripotent stem cell line (NCKDi002-A) from a 22-year-old patient with Focal Segmental Glomerular Sclerosis carrying a heterozygous mutation in WT1 gene.
Stem cell research May, 2021 | Pubmed ID: 33780729
Endogenous Hydrogen Sulfide Is an Important Factor in Maintaining Arterial Oxygen Saturation.
Frontiers in pharmacology , 2021 | Pubmed ID: 34135757
Generation of an induced pluripotent stem cell line (ZJUi007-A) from a 11-year-old patient of Fabry disease.
Stem cell research Aug, 2021 | Pubmed ID: 34365103
Establishment of an induced pluripotent stem cell line (NCKDi003-A) from a patient with X-linked Dent disease (X-Dent) carrying the hemizygote mutation p. T277P (c. 829A > C) in the CLCN5 gene.
Stem cell research Oct, 2021 | Pubmed ID: 34547705
Generation of the induced pluripotent stem cell line (NCKDi004-A) from a 17-year-old patient with Alport syndrome carrying a homozygous mutation in COL4A3 gene.
Stem cell research Oct, 2021 | Pubmed ID: 34626894
Establishment of the induced pluripotent stem cell line (NCKDi005-A) from a male patient with Alport syndrome carrying a homozygous frameshift mutation in the COL4A4 gene.
Stem cell research Jan, 2022 | Pubmed ID: 34942480
Nanjing University School of Medicine
Langping Gao*,1,2,
Yue Wang*,3,
Gang Wang4,
Hangdi Wu2,
Qingtao Yan1,
Jingjing Wang1,
Fei Liu1,
Haidong Fu1,
Wei Li5,
Lidan Hu1,
Jianhua Mao1,2
1Department of Nephrology, The Children's Hospital, Zhejiang University School of Medicine,
2, Zhejiang University School of Medicine,
3, Hubei Normal University,
4National Clinical Research Center of Kidney Diseases, Jinling Hospital, Nanjing University School of Medicine,
5Clinical Laboratory, The Children’s Hospital, Zhejiang University School of Medicine, National Clinical Research Center for Child Health
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