Gui sen Li

Summary

Country: China

Publications

  1. pmc The genetic variants at the HLA-DRB1 gene are associated with primary IgA nephropathy in Han Chinese
    Yang Jiyun
    Center for Human Molecular Biology and Genetics, Sichuan Academy of Medical Science and Sichuan Provincial People s Hospital, Chengdu, Sichuan, 617002, China
    BMC Med Genet 13:33. 2012
  2. pmc Malnutrition and inflammation in acute kidney injury due to earthquake-related crush syndrome
    Gui sen Li
    Department of Nephrology, Institute of Nephrology, Sichuan Academy of Medical Sciences and Sichuan Provincial People s Hospital, Chengdu, Sichuan, China
    BMC Nephrol 11:4. 2010
  3. pmc Do the mutations of C1GALT1C1 gene play important roles in the genetic susceptibility to Chinese IgA nephropathy?
    Gui sen Li
    Renal Division, Department of Internal Medicine, Peking University First Hospital, and Peking University Institute of Nephrology, Beijing, PR China
    BMC Med Genet 10:101. 2009
  4. ncbi request reprint [The correlation between NPHS2 polymorphism and IgA nephropathy in northern Chinese patients]
    Lei Yu
    The First Hospital of Peking University, Peking University Institute of Nephrology, Beijing, China
    Zhonghua Nei Ke Za Zhi 50:851-5. 2011
  5. doi request reprint Genetic effect of the NPHS2 gene variants on proteinuria in minimal change disease and immunoglobulin A nephropathy
    Li Zhu
    Renal Division, Department of Internal Medicine, Peking University First Hospital, Peking University Institute of Nephrology, Key Laboratory of Renal Disease, Ministry of Health of China, Beijing, China
    Nephrology (Carlton) 14:728-34. 2009
  6. ncbi request reprint Variants of the ST6GALNAC2 promoter influence transcriptional activity and contribute to genetic susceptibility to IgA nephropathy
    Gui sen Li
    Renal Division, Department of Internal Medicine, Peking University First Hospital, Beijing, China
    Hum Mutat 28:950-7. 2007
  7. ncbi request reprint [Variable number of tandem repeats polymorphism of MUC20 is associated with the progression of IgA nephropathy]
    Gui sen Li
    Renal Division of Peking University First Hospital, and Peking University Institute of Nephrology, Beijing 100034, China
    Zhonghua Yi Xue Za Zhi 85:1333-8. 2005
  8. ncbi request reprint [The prevention of crush syndrome related medical problems after earthquake]
    Li Wang
    Department of Nephrology, Sichuan People s Hospital, Sichuan Academy of Medical Science, Chengdu 610072, China
    Zhonghua Nei Ke Za Zhi 47:711-4. 2008
  9. ncbi request reprint [Association of NPHS1 gene polymorphism with IgA nephropathy]
    Lei Yu
    Renal Division of First Hospital, Institute of Nephrology, Peking University, Beijing 100034, China
    Zhonghua Yi Xue Za Zhi 89:881-5. 2009

Collaborators

Detail Information

Publications9

  1. pmc The genetic variants at the HLA-DRB1 gene are associated with primary IgA nephropathy in Han Chinese
    Yang Jiyun
    Center for Human Molecular Biology and Genetics, Sichuan Academy of Medical Science and Sichuan Provincial People s Hospital, Chengdu, Sichuan, 617002, China
    BMC Med Genet 13:33. 2012
    ..Familial clustering of patients with IgAN suggests a genetic predisposition...
  2. pmc Malnutrition and inflammation in acute kidney injury due to earthquake-related crush syndrome
    Gui sen Li
    Department of Nephrology, Institute of Nephrology, Sichuan Academy of Medical Sciences and Sichuan Provincial People s Hospital, Chengdu, Sichuan, China
    BMC Nephrol 11:4. 2010
    ..This study describes the clinical characteristics of malnutrition and inflammation in patients with AKI and CS due to the Wenchuan earthquake...
  3. pmc Do the mutations of C1GALT1C1 gene play important roles in the genetic susceptibility to Chinese IgA nephropathy?
    Gui sen Li
    Renal Division, Department of Internal Medicine, Peking University First Hospital, and Peking University Institute of Nephrology, Beijing, PR China
    BMC Med Genet 10:101. 2009
    ..Cosmc, encoded by C1GALT1C1 gene, was indispensable to beta1,3 galactosylation of IgA1. We designed a serial study to investigate the relationship between the mutations of C1GALT1C1 gene and the genetic susceptibility to IgAN...
  4. ncbi request reprint [The correlation between NPHS2 polymorphism and IgA nephropathy in northern Chinese patients]
    Lei Yu
    The First Hospital of Peking University, Peking University Institute of Nephrology, Beijing, China
    Zhonghua Nei Ke Za Zhi 50:851-5. 2011
    ....
  5. doi request reprint Genetic effect of the NPHS2 gene variants on proteinuria in minimal change disease and immunoglobulin A nephropathy
    Li Zhu
    Renal Division, Department of Internal Medicine, Peking University First Hospital, Peking University Institute of Nephrology, Key Laboratory of Renal Disease, Ministry of Health of China, Beijing, China
    Nephrology (Carlton) 14:728-34. 2009
    ....
  6. ncbi request reprint Variants of the ST6GALNAC2 promoter influence transcriptional activity and contribute to genetic susceptibility to IgA nephropathy
    Gui sen Li
    Renal Division, Department of Internal Medicine, Peking University First Hospital, Beijing, China
    Hum Mutat 28:950-7. 2007
    ....
  7. ncbi request reprint [Variable number of tandem repeats polymorphism of MUC20 is associated with the progression of IgA nephropathy]
    Gui sen Li
    Renal Division of Peking University First Hospital, and Peking University Institute of Nephrology, Beijing 100034, China
    Zhonghua Yi Xue Za Zhi 85:1333-8. 2005
    ..In this study we determined the distribution of MUC20 VNTR polymorphism in the healthy population, and the association between the MUC20 VNTR polymorphism and the pathogenesis or progression of IgAN...
  8. ncbi request reprint [The prevention of crush syndrome related medical problems after earthquake]
    Li Wang
    Department of Nephrology, Sichuan People s Hospital, Sichuan Academy of Medical Science, Chengdu 610072, China
    Zhonghua Nei Ke Za Zhi 47:711-4. 2008
    ..Managing these critical issues appropriately is essential for effective treatment of the crush syndrome...
  9. ncbi request reprint [Association of NPHS1 gene polymorphism with IgA nephropathy]
    Lei Yu
    Renal Division of First Hospital, Institute of Nephrology, Peking University, Beijing 100034, China
    Zhonghua Yi Xue Za Zhi 89:881-5. 2009
    ..To investigate the association of the polymorphism of NPHS1, coding gene of nephrin, with the degree of proteinuria, renal function, and prognosis of IgA nephropathy (IgAN) in patients in north China...