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Membranous lupus nephritis secondary to secukinumab therapy: A case report and literature review

Lupus, 2024-05, Vol.33 (6), p.644-649

2024

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Systematic review and meta-analysis of the clinical features of MGRS

BMC nephrology, 2024-01, Vol.25 (1), p.22-22, Article 22

2024

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The Novel Apolipoprotein E Mutation ApoE Chengdu (c.518T＞C, p.L173P) in a Chinese Patient with Lipoprotein Glomerulopathy

Journal of Atherosclerosis and Thrombosis, 2018/08/01, Vol.25(8), pp.733-740

2018

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Reverse complete heart block using transcutaneous pacing and repeated plasmapheresis in a neonate with lupus: a case report

Pediatric rheumatology online journal, 2023-11, Vol.21 (1), p.135-135, Article 135

2023

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Pembrolizumab induced-C3 glomerulonephritis and RBC cast nephropathy: a case report

BMC nephrology, 2023-05, Vol.24 (1), p.145-145, Article 145

2023

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Integration of multiomics analysis to reveal the major pathways of vitamin A deficiency aggravates acute respiratory distress syndrome in neonatal rats

Scientific reports, 2023-12, Vol.13 (1), p.22643-22643, Article 22643

2023

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Regulation of Cholesterol Homeostasis by a Novel Long Non-coding RNA LASER

Scientific reports, 2019-05, Vol.9 (1), p.7693, Article 7693

2019

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Lipoprotein glomerulopathy induced by ApoE Kyoto mutation in ApoE-deficient mice

Journal of translational medicine, 2021-03, Vol.19 (1), p.97-97, Article 97

2021

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The Novel Apolipoprotein E Mutation ApoE Chengdu (c.518T>C, p.L173P) in a Chinese Patient with Lipoprotein Glomerulopathy

Journal of Atherosclerosis and Thrombosis, 2018, Vol.25 (8), p.733-740

2018

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U-shaped association between hemoglobin levels and albuminuria in US adults: a cross-sectional study

International urology and nephrology, 2024-09

2024

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Association of SCNN1A Single Nucleotide Polymorphisms with neonatal respiratory distress syndrome

Scientific reports, 2015-11, Vol.5 (1), p.17317-17317, Article 17317

2015

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Cholesteryl ester transfer protein inhibitors in the treatment of dyslipidemia: a systematic review and meta-analysis

PloS one, 2013-10, Vol.8 (10), p.e77049

2013

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Myoglobin clearance by continuous venous-venous haemofiltration in rhabdomyolysis with acute kidney injury: A case series

Injury, 2012-05, Vol.43 (5), p.619-623

2012

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Glycochenodeoxycholate induces rat alveolar epithelial type II cell death and inhibits surfactant secretion in vitro

Free radical biology & medicine, 2012-07, Vol.53 (1), p.122-128

2012

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Dendritic cells transduced with TEM8 recombinant adenovirus prevents hepatocellular carcinoma angiogenesis and inhibits cells growth

Vaccine, 2010-10, Vol.28 (43), p.7130-7135

2010

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Mammalian target of rapamycin complex 1 activation in podocytes promotes cellular crescent formation

American journal of physiology. Renal physiology, 2014-11, Vol.307 (9), p.F1023-F1032

2014

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Unique imaging findings in fibromuscular dysplasia of renal arteries: A case report

Medicine (Baltimore), 2018-11, Vol.97 (46), p.e12815-e12815

2018

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Identification of novel mutations in Chinese Hans with autosomal dominant polycystic kidney disease

BMC medical genetics, 2011-12, Vol.12 (1), p.164-164, Article 164

2011

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A novel ADCK4 mutation in a Chinese family with ADCK4-Associated glomerulopathy

Biochemical and biophysical research communications, 2018-11, Vol.506 (3), p.444-449

2018

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A novel HNF1B mutation p.R177Q in autosomal dominant tubulointerstitial kidney disease and maturity-onset diabetes of the young type 5: A pedigree-based case report

Medicine (Baltimore), 2020-07, Vol.99 (31), p.e21438-e21438

2020

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Infections in crush syndrome: a retrospective observational study after the Wenchuan earthquake

Emergency medicine journal : EMJ, 2011-01, Vol.28 (1), p.14-17

2011

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Activation of liver X receptor attenuates endothelin-1 expression in vascular endothelial cells

The international journal of biochemistry & cell biology, 2012-12, Vol.44 (12), p.2299-2307

2012

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A case of malignant hypertension with thrombotic microangiopathy

Internal medicine journal, 2018-03, Vol.48 (3), p.361-362

2018

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Identification of c.146G > A mutation in a Fabry patient and its correction by customized Cas9 base editors in vitro

International journal of biological macromolecules, 2024-10, p.136922, Article 136922

2024

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CELF2 Deficiency Demonstrates Autism-Like Behaviors and Interferes with Late Development of Cortical Neurons in Mice

Molecular neurobiology, 2024-06

2024

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Membranous lupus nephritis secondary to secukinumab therapy: A case report and literature review

Systematic review and meta-analysis of the clinical features of MGRS

The Novel Apolipoprotein E Mutation ApoE Chengdu (c.518T＞C, p.L173P) in a Chinese Patient with Lipoprotein Glomerulopathy

Reverse complete heart block using transcutaneous pacing and repeated plasmapheresis in a neonate with lupus: a case report

Pembrolizumab induced-C3 glomerulonephritis and RBC cast nephropathy: a case report

Integration of multiomics analysis to reveal the major pathways of vitamin A deficiency aggravates acute respiratory distress syndrome in neonatal rats

Regulation of Cholesterol Homeostasis by a Novel Long Non-coding RNA LASER

Lipoprotein glomerulopathy induced by ApoE Kyoto mutation in ApoE-deficient mice

The Novel Apolipoprotein E Mutation ApoE Chengdu (c.518T>C, p.L173P) in a Chinese Patient with Lipoprotein Glomerulopathy

U-shaped association between hemoglobin levels and albuminuria in US adults: a cross-sectional study

Association of SCNN1A Single Nucleotide Polymorphisms with neonatal respiratory distress syndrome

Cholesteryl ester transfer protein inhibitors in the treatment of dyslipidemia: a systematic review and meta-analysis

Myoglobin clearance by continuous venous-venous haemofiltration in rhabdomyolysis with acute kidney injury: A case series

Glycochenodeoxycholate induces rat alveolar epithelial type II cell death and inhibits surfactant secretion in vitro

Dendritic cells transduced with TEM8 recombinant adenovirus prevents hepatocellular carcinoma angiogenesis and inhibits cells growth

Mammalian target of rapamycin complex 1 activation in podocytes promotes cellular crescent formation

Unique imaging findings in fibromuscular dysplasia of renal arteries: A case report

Identification of novel mutations in Chinese Hans with autosomal dominant polycystic kidney disease

A novel ADCK4 mutation in a Chinese family with ADCK4-Associated glomerulopathy

A novel HNF1B mutation p.R177Q in autosomal dominant tubulointerstitial kidney disease and maturity-onset diabetes of the young type 5: A pedigree-based case report

Infections in crush syndrome: a retrospective observational study after the Wenchuan earthquake

Activation of liver X receptor attenuates endothelin-1 expression in vascular endothelial cells

A case of malignant hypertension with thrombotic microangiopathy

Identification of c.146G > A mutation in a Fabry patient and its correction by customized Cas9 base editors in vitro

CELF2 Deficiency Demonstrates Autism-Like Behaviors and Interferes with Late Development of Cortical Neurons in Mice

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