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Inhibition of Reticulon-1A-Mediated Endoplasmic Reticulum Stress in Early AKI Attenuates Renal Fibrosis Development

Journal of the American Society of Nephrology, 2017-07, Vol.28 (7), p.2007-2021

2017

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Clinical and Histological Features of Phospholipase A2 Receptor-Associated and Thrombospondin Type-I Domain-containing 7A-Associated Idiopathic Membranous Nephropathy: A Single Center Retrospective Study from China

Medical science monitor, 2018-07, Vol.24, p.5076-5083

2018

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Identification and functional characterization of the first deep intronic GLA mutation (IVS4+1326C>T) causing renal variant of Fabry disease

Orphanet journal of rare diseases, 2022-06, Vol.17 (1), p.1-237, Article 237

2022

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Survival Motor Neuron (SMN) Protein Insufficiency Exacerbates Renal Ischemia/Reperfusion Injury

Frontiers in physiology, 2019-05, Vol.10, p.559-559

2019

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Increased CD45RA+ FoxP3(low) regulatory T cells with impaired suppressive function in patients with systemic lupus erythematosus

PloS one, 2012, Vol.7 (4), p.e34662-e34662

2012

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Tissue Proteome of 2-Hydroxyacyl-CoA Lyase Deficient Mice Reveals Peroxisome Proliferation and Activation of ω-Oxidation

International journal of molecular sciences, 2022-01, Vol.23 (2), p.987

2022

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A novel CLCN5 frame shift mutation responsible for Dent disease 1: Case report

Frontiers in pediatrics, 2022-11, Vol.10

2022

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Diagnostic yield of additional exome sequencing after the detection of long continuous stretches of homozygosity (LCSH) in SNP arrays

Journal of human genetics, 2021-04, Vol.66 (4), p.409-417

2021

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ASH2L Is Essential for the Ureteric Bud Lineage Development: SA-OR18

Journal of the American Society of Nephrology, 2022-11, Vol.33 (11S), p.38-39

2022

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ASH2L Controls Ureteric Bud Morphogenesis through the Regulation of RET/GFRA1 Signaling Activity in a Mouse Model

Journal of the American Society of Nephrology, 2023-06, Vol.34 (6), p.988-1002

2023

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Clinical and Genetic Features of Autosomal Dominant Alport Syndrome: A Cohort Study in China: SA-PO559

Journal of the American Society of Nephrology, 2022-11, Vol.33 (11S), p.758-758

2022

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Identification and functional characterization of the first deep intronic GLA mutation

Orphanet journal of rare diseases, 2022-06, Vol.17 (1)

2022

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SPOP suppresses pancreatic cancer progression by promoting the degradation of NANOG

Cell death & disease, 2019-10, Vol.10 (11), p.794-16, Article 794

2019

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THSD7A-associated membranous nephropathy in a patient with neurofibromatosis type 1

European journal of medical genetics, 2018-02, Vol.61 (2), p.84-88

2018

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Increased CD45RA+FoxP3low Regulatory T Cells with Impaired Suppressive Function in Patients with Systemic Lupus Erythematosus

PloS one, 2012-04, Vol.7 (4), p.e34662

2012

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MiR-424 is over-expressed and attenuates ischemia-reperfusion kidney injury via p53 and death receptor 6 pathway

American journal of translational research, 2019-01, Vol.11 (4), p.1965-1979

2019

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Micro RNA-155 inhibitor as a potential therapeutic strategy for the treatment of acute kidney injury (AKI): a nanomedicine perspective

RSC advances, 2018-01, Vol.8 (29), p.1589-15896

2018

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Spraying printing of liquid metal electronics on various clothes to compose wearable functional device

Science China. Technological sciences, 2017-02, Vol.60 (2), p.306-316

2017

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Anomalous magnetic viscosity in relativistic accretion disks

New astronomy, 2013-07, Vol.21, p.40-45

2013

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A novel COL4A1 frameshift mutation in familial kidney disease: the importance of the C-terminal NC1 domain of type IV collagen

Nephrology, dialysis, transplantation, 2016-11, Vol.31 (11), p.1908-1914

2016

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SP014A NOVEL COL4A1 FRAMESHIFT MUTATION AND KIDNEY DISEASE WITHOUT EXTRA-RENAL INVOLVEMENT IN A LARGE TURKISH CYPRIOT FAMILY

Nephrology, dialysis, transplantation, 2015-05, Vol.30 (suppl_3), p.iii385-iii385

2015

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Whole exome sequencing reveals novel COL4A3 and COL4A4 mutations and resolves diagnosis in Chinese families with kidney disease

BMC nephrology, 2014-11, Vol.15 (1), p.175-175

2014

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Increased CD45RA.sup.+FoxP3.sup.low Regulatory T Cells with Impaired Suppressive Function in Patients with Systemic Lupus Erythematosus

PloS one, 2012-04, Vol.7 (4), p.e34662

2012

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Whole exome sequencing reveals novel COL4A3 and COL4A4mutations and resolves diagnosis in Chinese families with kidney disease

BMC nephrology, 2014-11, Vol.15 (1), Article 175

2014

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Fossil Liverworts from the Lower Cretaceous Huolinhe Formation in Inner Mongolia, China

Acta geologica Sinica (Beijing), 2016-06, Vol.90 (3), p.838-846

English ed., 2016

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Inhibition of Reticulon-1A-Mediated Endoplasmic Reticulum Stress in Early AKI Attenuates Renal Fibrosis Development

Clinical and Histological Features of Phospholipase A2 Receptor-Associated and Thrombospondin Type-I Domain-containing 7A-Associated Idiopathic Membranous Nephropathy: A Single Center Retrospective Study from China

Identification and functional characterization of the first deep intronic GLA mutation (IVS4+1326C>T) causing renal variant of Fabry disease

Survival Motor Neuron (SMN) Protein Insufficiency Exacerbates Renal Ischemia/Reperfusion Injury

Increased CD45RA+ FoxP3(low) regulatory T cells with impaired suppressive function in patients with systemic lupus erythematosus

Tissue Proteome of 2-Hydroxyacyl-CoA Lyase Deficient Mice Reveals Peroxisome Proliferation and Activation of ω-Oxidation

A novel CLCN5 frame shift mutation responsible for Dent disease 1: Case report

Diagnostic yield of additional exome sequencing after the detection of long continuous stretches of homozygosity (LCSH) in SNP arrays

ASH2L Is Essential for the Ureteric Bud Lineage Development: SA-OR18

ASH2L Controls Ureteric Bud Morphogenesis through the Regulation of RET/GFRA1 Signaling Activity in a Mouse Model

Clinical and Genetic Features of Autosomal Dominant Alport Syndrome: A Cohort Study in China: SA-PO559

Identification and functional characterization of the first deep intronic GLA mutation

SPOP suppresses pancreatic cancer progression by promoting the degradation of NANOG

THSD7A-associated membranous nephropathy in a patient with neurofibromatosis type 1

Increased CD45RA+FoxP3low Regulatory T Cells with Impaired Suppressive Function in Patients with Systemic Lupus Erythematosus

MiR-424 is over-expressed and attenuates ischemia-reperfusion kidney injury via p53 and death receptor 6 pathway

Micro RNA-155 inhibitor as a potential therapeutic strategy for the treatment of acute kidney injury (AKI): a nanomedicine perspective

Spraying printing of liquid metal electronics on various clothes to compose wearable functional device

Anomalous magnetic viscosity in relativistic accretion disks

A novel COL4A1 frameshift mutation in familial kidney disease: the importance of the C-terminal NC1 domain of type IV collagen

SP014A NOVEL COL4A1 FRAMESHIFT MUTATION AND KIDNEY DISEASE WITHOUT EXTRA-RENAL INVOLVEMENT IN A LARGE TURKISH CYPRIOT FAMILY

Whole exome sequencing reveals novel COL4A3 and COL4A4 mutations and resolves diagnosis in Chinese families with kidney disease

Increased CD45RA.sup.+FoxP3.sup.low Regulatory T Cells with Impaired Suppressive Function in Patients with Systemic Lupus Erythematosus

Whole exome sequencing reveals novel COL4A3 and COL4A4mutations and resolves diagnosis in Chinese families with kidney disease

Fossil Liverworts from the Lower Cretaceous Huolinhe Formation in Inner Mongolia, China

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