Search Results - "Qiu, Liru"

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    Endocytosis of albumin by podocytes elicits an inflammatory response and induces apoptotic cell death by Okamura, Kayo, Dummer, Patrick, Kopp, Jeffrey, Qiu, Liru, Levi, Moshe, Faubel, Sarah, Blaine, Judith

    Published in PloS one (28-01-2013)
    “…The presence of albuminuria is strongly associated with progression of chronic kidney disease. While albuminuria has been shown to injure renal proximal…”
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    CUBN gene mutations may cause focal segmental glomerulosclerosis (FSGS) in children by Yang, Jing, Xu, Yongli, Deng, Linxia, Zhou, Luowen, Qiu, Liru, Zhang, Yu, Zhou, Jianhua

    Published in BMC nephrology (03-01-2022)
    “…Imerslund-Gräsbeck Syndrome (IGS) is mainly caused by CUBN gene biallelic mutations. Proteinuria accompanies IGS specific symptoms in about half of the…”
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    Mutations in the NUP93, NUP107 and NUP160 genes cause steroid-resistant nephrotic syndrome in Chinese children by Han, Yanxinli, Sha, Hongyu, Yang, Yuan, Yu, Zhuowei, Zhou, Lanqi, Wang, Yi, Yang, Fengjie, Qiu, Liru, Zhang, Yu, Zhou, Jianhua

    Published in Italian journal of pediatrics (22-04-2024)
    “…The variants of nucleoporins are extremely rare in hereditary steroid-resistant nephrotic syndrome (SRNS). Most of the patients carrying such variants progress…”
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    Steroid-resistant nephrotic syndrome associated with certain SGPL1 variants in a family: Case report and literature review by Yang, Siying, He, Yonghua, Zhou, Jianhua, Yuan, Huiqing, Qiu, Liru

    Published in Frontiers in pediatrics (16-02-2023)
    “…Steroid-resistant nephrotic syndrome (SRNS) is a clinical syndrome characterized by the lack of response to standard steroid therapy, usually progressing to…”
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    Long-Term Clinical and Immunological Impact of Severe COVID-19 on a Living Kidney Transplant Recipient – A Case Report by Qiu, Liru, Zhang, Ji, Huang, Yafei, Chen, Gen, Chen, Zhishui, Ming, Changsheng, Lu, Xia, Gong, Nianqiao

    Published in Frontiers in immunology (08-09-2021)
    “…The long-term impact of COVID-19 on transplant recipients remains unknown. We describe the case of a 30-year-old male kidney transplant recipient from Wuhan,…”
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    Liver X receptors preserve renal glomerular integrity under normoglycaemia and in diabetes in mice by Patel, Monika, Wang, Xiaoxin X., Magomedova, Lilia, John, Rohan, Rasheed, Adil, Santamaria, Hannah, Wang, Weidong, Tsai, Ricky, Qiu, Liru, Orellana, Arturo, Advani, Andrew, Levi, Moshe, Cummins, Carolyn L.

    Published in Diabetologia (01-02-2014)
    “…Aims/hypothesis Liver X receptors (LXRs) α and β are nuclear hormone receptors that are widely expressed in the kidney. They promote cholesterol efflux from…”
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    Global Existence and Uniform Energy Decay Rates for the Semilinear Parabolic Equation with a Memory Term and Mixed Boundary Condition by Fang, Zhong Bo, Qiu, Liru

    Published in Abstract and Applied Analysis (01-01-2013)
    “…This work is concerned with a mixed boundary value problem for the semilinear parabolic equation with a memory term and generalized Lewis functions which…”
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    Recommendations for the Diagnosis, Prevention, and Control of Coronavirus Disease-19 in Children—The Chinese Perspectives by Fang, Feng, Chen, Yu, Zhao, Dongchi, Liu, Tonglin, Huang, Yongjian, Qiu, Liru, Hao, Yan, Hu, Xiaolin, Yin, Wei, Liu, Zhisheng, Jin, Runming, Ning, Qin, Cheung, Pik-to, Liu, Chunfeng, Shu, Sainan, Wang, Tianyou, Luo, Xiaoping

    Published in Frontiers in pediatrics (05-11-2020)
    “…Ever since SARS-CoV-2 began infecting people by the end of 2019, of whom some developed severe pneumonia (about 5%), which could be fatal (case fatality…”
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    SGLT2 Protein Expression Is Increased in Human Diabetic Nephropathy by Wang, Xiaoxin X., Levi, Jonathan, Luo, Yuhuan, Myakala, Komuraiah, Herman-Edelstein, Michal, Qiu, Liru, Wang, Dong, Peng, Yingqiong, Grenz, Almut, Lucia, Scott, Dobrinskikh, Evgenia, D'Agati, Vivette D., Koepsell, Hermann, Kopp, Jeffrey B., Rosenberg, Avi Z., Levi, Moshe

    Published in The Journal of biological chemistry (01-03-2017)
    “…There is very limited human renal sodium gradient-dependent glucose transporter protein (SGLT2) mRNA and protein expression data reported in the literature…”
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    Are They Just Two Children COVID-19 Cases Confused With Flu? by Zou, Biao, Ma, Di, Li, Yinhu, Qiu, Liru, Chen, Yu, Hao, Yan, Luo, Xiaoping, Shu, Sainan

    Published in Frontiers in pediatrics (05-06-2020)
    “…COVID-19, an emerging infectious disease, has quickly spread all over the world. All human populations are susceptible to this disease. Here we present two…”
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    Simultaneous mutations of LAMB2 and NPHP1genes in a Chinese girl with isolated congenital nephrotic syndrome: a case report by Qiu, Liru, Zhou, Jianhua

    Published in BMC pediatrics (22-03-2016)
    “…LAMB2 mutations cause Pierson syndrome (OMIM 609049), an autosomal recessive genetic disease typically characterized by congenital nephrotic syndrome (CNS) and…”
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    Zero‐contrast PTRA and stenting for child with TRAS: A case report by Xie, Yang, He, Xingwei, Qiu, Liru, Zeng, Hesong

    Published in Pediatric transplantation (01-03-2022)
    “…Background Kidney transplantation is often complicated by TRAS, and PTRA can effectively treat it. However, PTRA is not appropriate for patients with CKD…”
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    Early onset stage III diabetic nephropathy in a child with Prader-Willi syndrome treated with dulaglutide: a case report by He, Yonghua, Xu, Rongrong, Ma, Xueqing, Zhou, Jianhua, Qiu, Liru

    Published in Translational pediatrics (31-05-2024)
    “…Prader-Willi syndrome (PWS) is a multisystem genetic disorder caused by chromosomal imprinting gene defects, with approximately 70% of cases resulting from…”
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    Clinical, histological and molecular characteristics of Alport syndrome in Chinese children by Zhou, Lanqi, Xi, Bijun, Xu, Yongli, Han, Yanxinli, Yang, Yuan, Yang, Jing, Wang, Yi, Qiu, Liru, Zhang, Yu, Zhou, Jianhua

    Published in Journal of nephrology (01-06-2023)
    “…Background Alport syndrome is caused by COL4A3, COL4A4, or COL4A5 gene mutations. The present study aims to compare the clinicopathological features, gene…”
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