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MicroRNA-340-5p inhibits endothelial apoptosis, inflammatory response, and pro-coagulation by targeting KDM4C in anti-neutrophil cytoplasmic antibody (ANCA)-mediated glomerulonephritis through activation of B cells

Autoimmunity (Chur, Switzerland), 2021-08, Vol.54 (6), p.343-352

2021

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MiR-130a-5p prevents angiotensin II-induced podocyte apoptosis by modulating M-type phospholipase A2 receptor

Cell cycle (Georgetown, Tex.), 2018-11, Vol.17 (21-22), p.2484-2495

2018

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Evidence from mendelian randomization identifies several causal relationships between primary membranous nephropathy and gut microbiota

Renal failure, 2024-12, Vol.46 (1), p.2349136-2349136

2024

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Long non-coding RNA Neat1 triggers renal tubular epithelial cell apoptosis via activating BH3-only protein in membranous nephropathy

Autoimmunity (Chur, Switzerland), 2021-11, Vol.54 (8), p.539-546

2021

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Urinary exosomal miRNA-451a can be used as a potential noninvasive biomarker for diagnosis, reflecting tubulointerstitial damage and therapeutic response in IgA nephropathy

Renal failure, 2024-12, Vol.46 (1), p.2319326-2319326

2024

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Mitochondrial DNA copy number in peripheral blood of IgA nephropathy: a cross-sectional study

Renal failure, 2023-12, Vol.45 (1), p.2182133-2182133

2023

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Retinal disease in the C3 glomerulopathies and the risk of impaired vision

Ophthalmic genetics, 2016-10, Vol.37 (4), p.369-376

2016

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Novel immune cross-talk between inflammatory bowel disease and IgA nephropathy

Renal failure, 2024-12, Vol.46 (1), p.2337288-2337288

2024

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Epigenome-wide association study and network analysis for IgA Nephropathy from CD19+ B-cell in Chinese Population

Epigenetics, 2021-12, Vol.16 (12), p.1283-1294

2021

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The association between therapeutic outcomes and VEGF G-1154A and C-936T gene polymorphisms in patients with glomerulonephritis

Renal failure, 2014-07, Vol.36 (6), p.904-907

2014

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Associations between m-type phospholipase A2 receptor,human leukocyte antigen gene polymorphisms and idiopathic membranous nephropathy

Bioengineered, 2021-01, Vol.12 (1), p.8833-8844

2021

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Tetrandrine may treat membranous glomerulopathy via P13K/Akt signaling pathway regulation: therapeutic mechanism validation using Heymann nephritis rat model

Bioengineered, 2021-01, Vol.12 (1), p.6499-6515

2021

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3' untranslated region variants in DEFA5 gene associated with susceptibility to IgA nephropathy in the Chinese Han population

Biomarkers in medicine, 2022-11, Vol.16 (16), p.1151-1159

2022

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Pseudolinear C4d deposits in a hereditary glomerulopathy caused by a rare NC1 collagen-4-alpha-5 missense mutation: a "new disease entity"?

Ultrastructural pathology, 2019-09, Vol.43 (4-5), p.209-215

2019

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Lack of effect of the MEFV E148Q polymorphism on IL-1β in Henoch-Schönlein purpura

Scandinavian journal of rheumatology, 2011-05, Vol.40 (3), p.238-239

2011

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Biomarkers in IgA nephropathy

Biomarkers in medicine, 2014-12, Vol.8 (10), p.1263-1277

2014

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The Transition from Thin Basement Membranes to Typical Alport Syndrome Morphology in Children

Fetal and pediatric pathology, 2016-11, Vol.35 (6), p.369-375

2016

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Association of AGT M235T gene polymorphism with HSP/HSPN risk

Renal failure, 2015-02, Vol.37 (1), p.16-21

2015

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Urinary messenger RNA of the receptor activator of NF-kappaB could be used to differentiate between minimal change disease and membranous nephropathy

Biomarkers, 2014-11, Vol.19 (7), p.597-603

2014

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Association of uteroglobin G38A gene polymorphism with IgA nephropathy risk: an updated meta-analysis

Journal of receptors and signal transduction, 2015-04, Vol.35 (2), p.115-121

2015

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Familial MPGN - a case series: a clinical description of familial membranoproliferative glomerulonephritis amongst three Irish families

Renal failure, 2014-09, Vol.36 (8), p.1333-1336

2014

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Association of angiotensinogen gene M235T polymorphism with the risk of IgA nephropathy: a meta-analysis

Renal failure, 2014-04, Vol.36 (3), p.466-472

2014

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Association of BH3 interacting domain death agonist (BID) gene polymorphisms with proteinuria of immunoglobulin A nephropathy

Scandinavian journal of clinical and laboratory investigation, 2014-06, Vol.74 (4), p.329-335

2014

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Association of Megsin gene polymorphism with IgA nephropathy risk

Journal of receptors and signal transduction, 2015-04, Vol.35 (2), p.122-126

2015

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Toll-like receptor 9 SNPs are susceptible to the development and progression of membranous glomerulonephritis: 27 years follow-up in Taiwan

Renal failure, 2013-11, Vol.35 (10), p.1370-1375

2013

Volltextzugriff (PDF)

1 – 25 von 103

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MicroRNA-340-5p inhibits endothelial apoptosis, inflammatory response, and pro-coagulation by targeting KDM4C in anti-neutrophil cytoplasmic antibody (ANCA)-mediated glomerulonephritis through activation of B cells

MiR-130a-5p prevents angiotensin II-induced podocyte apoptosis by modulating M-type phospholipase A2 receptor

Evidence from mendelian randomization identifies several causal relationships between primary membranous nephropathy and gut microbiota

Long non-coding RNA Neat1 triggers renal tubular epithelial cell apoptosis via activating BH3-only protein in membranous nephropathy

Urinary exosomal miRNA-451a can be used as a potential noninvasive biomarker for diagnosis, reflecting tubulointerstitial damage and therapeutic response in IgA nephropathy

Mitochondrial DNA copy number in peripheral blood of IgA nephropathy: a cross-sectional study

Retinal disease in the C3 glomerulopathies and the risk of impaired vision

Novel immune cross-talk between inflammatory bowel disease and IgA nephropathy

Epigenome-wide association study and network analysis for IgA Nephropathy from CD19+ B-cell in Chinese Population

The association between therapeutic outcomes and VEGF G-1154A and C-936T gene polymorphisms in patients with glomerulonephritis

Associations between m-type phospholipase A2 receptor,human leukocyte antigen gene polymorphisms and idiopathic membranous nephropathy

Tetrandrine may treat membranous glomerulopathy via P13K/Akt signaling pathway regulation: therapeutic mechanism validation using Heymann nephritis rat model

3' untranslated region variants in DEFA5 gene associated with susceptibility to IgA nephropathy in the Chinese Han population

Pseudolinear C4d deposits in a hereditary glomerulopathy caused by a rare NC1 collagen-4-alpha-5 missense mutation: a "new disease entity"?

Lack of effect of the MEFV E148Q polymorphism on IL-1β in Henoch-Schönlein purpura

Biomarkers in IgA nephropathy

The Transition from Thin Basement Membranes to Typical Alport Syndrome Morphology in Children

Association of AGT M235T gene polymorphism with HSP/HSPN risk

Urinary messenger RNA of the receptor activator of NF-kappaB could be used to differentiate between minimal change disease and membranous nephropathy

Association of uteroglobin G38A gene polymorphism with IgA nephropathy risk: an updated meta-analysis

Familial MPGN - a case series: a clinical description of familial membranoproliferative glomerulonephritis amongst three Irish families

Association of angiotensinogen gene M235T polymorphism with the risk of IgA nephropathy: a meta-analysis

Association of BH3 interacting domain death agonist (BID) gene polymorphisms with proteinuria of immunoglobulin A nephropathy

Association of Megsin gene polymorphism with IgA nephropathy risk

Toll-like receptor 9 SNPs are susceptible to the development and progression of membranous glomerulonephritis: 27 years follow-up in Taiwan

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