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Jinghua Hu – författare

Visar alla böcker från författaren Jinghua Hu. Handla med fri frakt och snabb leverans.

4 produkter

  1. Yong Yu, Jinghua Hu - Polycystic Kidney Disease, E-bok. Tillgänglighet: Lägg i varukorg

    Polycystic Kidney Disease

    Av Yong Yu, Jinghua Hu

    E-bok, 2019

    814 kr

    Lägg i varukorg

    This volume focuses on the investigatory methods applied to autosomal dominant polycystic kidney disease (ADPKD), one of the most common human genetic diseases. ADPKD is caused by mutations in PKD1 and TRPP2, two integral membrane proteins that function as receptor/ion channels in primary cilia of …

  2. Yong Yu, Jinghua Hu - Polycystic Kidney Disease, E-bok. Tillgänglighet: Lägg i varukorg

    Polycystic Kidney Disease

    Av Yong Yu, Jinghua Hu

    E-bok, 2019

    838 kr

    Lägg i varukorg

    This volume focuses on the investigatory methods applied to autosomal dominant polycystic kidney disease (ADPKD), one of the most common human genetic diseases. ADPKD is caused by mutations in PKD1 and TRPP2, two integral membrane proteins that function as receptor/ion channels in primary cilia of …

  3. Jinghua Hu, Yong Yu - Polycystic Kidney Disease, Häftad. Tillgänglighet: Lägg i varukorg

    Polycystic Kidney Disease

    Av Jinghua Hu, Yong Yu

    Häftad, 2021

    710 kr

    Lägg i varukorg

    This volume focuses on the investigatory methods applied to autosomal dominant polycystic kidney disease (ADPKD), one of the most common human genetic diseases. ADPKD is caused by mutations in PKD1 and TRPP2, two integral membrane proteins that function as receptor/ion channels in primary cilia of …

  4. Jinghua Hu, Yong Yu - Polycystic Kidney Disease, Inbunden. Tillgänglighet: Lägg i varukorg

    Polycystic Kidney Disease

    Av Jinghua Hu, Yong Yu

    Inbunden, 2019

    2192 kr

    Lägg i varukorg

    This volume focuses on the investigatory methods applied to autosomal dominant polycystic kidney disease (ADPKD), one of the most common human genetic diseases. ADPKD is caused by mutations in PKD1 and TRPP2, two integral membrane proteins that function as receptor/ion channels in primary cilia of …