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  1. 1
    Research progress on calcineurin inhibitors in the treatment of monogenic steroid resistant nephrotic syndrome

    Article en ligne

  2. 2
    Clinical and pathological features and mutational types of WT1 mutation-associated nephropathy

    Article en ligne

  3. 3
    Co-administration of α-GalCer analog and TLR4 agonist induces robust CD8(+) T-cell responses to PyCS protein and WT-1 antigen and activates memory-like effector NKT cells

    Article en ligne

  4. 4
    The cyclin dependent kinase inhibitor (R)-roscovitine mediates selective suppression of alloreactive human T cells but preserves pathogen-specific and leukemia-specific effectors

    Article en ligne

  5. 5
    Clinical and pathological features of Denys-Drash syndrome report of 3 cases
    Article

  6. 6
    Genetic variations of NPHS2 and WT1 genes in 15 Chinese children with sporadic steroid-resistant nephrotic syndrome
    Article

  7. 7
    WT1 gene and glomerular diseases
    Article

  8. 8
    The clinical and genetic characteristics of nephrotic syndrome in the first year of life
    Article

  9. 9
    Four new cases with WT1 gene mutations in Chinese patients with Wilms' tumor
    Article

  10. 10
    Clinical characteristics and WT1 genetic analysis of patients with steroid-resistant nephrotic syndrome accompanied with genitourinary malformations
    Article

  11. 11
    Metanephric adenoma report of two cases
    Article

  12. 12
    A novel mutation of NPHS2 identified in a Chinese family with steroid-resistant nephrotic syndrome
    Article

  13. 13
    A prospect of molecular biology in the field of urologic oncology mechanisms of carcinogenesis or tumor development in testicular cancer
    Article

  14. 14
    Molecular staging of testicular cancer using polymerase chain reaction of the testicular cancer-specific genes
    Article

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