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Establishment of bovine expanded potential stem cells

Proceedings of the National Academy of Sciences - PNAS, 2021-04, Vol.118 (15), p.1

2021

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Reducing GEF-H1 Expression Inhibits Renal Cyst Formation, Inflammation, and Fibrosis via RhoA Signaling in Nephronophthisis

International journal of molecular sciences, 2023-02, Vol.24 (4), p.3504

2023

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MicroRNAs and Polycystic Kidney Disease

Kidney medicine, 2020-11, Vol.2 (6), p.762-770

2020

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An Nphp1 knockout mouse model targeting exon 2–20 demonstrates characteristic phenotypes of human nephronophthisis

Human molecular genetics, 2021-12, Vol.31 (2), p.232-243

2021

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Clinical features of children with pulmonary microscopic polyangiitis: report of 9 cases

PloS one, 2015-04, Vol.10 (4), p.e0124352-e0124352

2015

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821 Kibra mediates the activation of hippo by classic signal pathway related to NPHP1 defect

Nephrology, dialysis, transplantation, 2024-05, Vol.39 (Supplement_1)

2024

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COQ2 mutation associated isolated nephropathy in two siblings from a Chinese pedigree

Renal failure, 2021-01, Vol.43 (1), p.97-101

2021

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The Accumulation of VEGFA in the Glomerular Basement Membrane and Its Relationship with Podocyte Injury and Proteinuria in Alport Syndrome

PloS one, 2015-08, Vol.10 (8), p.e0135648-e0135648

2015

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Analysis of SALL1 gene variant in a boy with Townes-Brocks syndrome without anal atresia

Zhonghua yi xue yi chuan xue za zhi, 2022-04, Vol.39 (4), p.401

2022

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High mutation rate of NPHP3 in 18 Chinese infantile nephronophthisis patients

Nephrology (Carlton, Vic.), 2016-03, Vol.21 (3), p.209-216

2016

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Identification of renal cyst cells of type I Nephronophthisis by single-nucleus RNA sequencing

Frontiers in cell and developmental biology, 2023-07, Vol.11, p.1192935-1192935

2023

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Dent Disease in Chinese Children and Findings from Heterozygous Mothers: Phenotypic Heterogeneity, Fetal Growth, and 10 Novel Mutations

The Journal of pediatrics, 2016-07, Vol.174, p.204-210.e1

2016

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滇东-黔西煤层气井排采动态影响因素及初始排水速度优化步骤

煤炭学报, 2018-06, Vol.43 (6), p.1716-1727

2018

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The Clinical and Genetic Features in Chinese Children With Steroid-Resistant or Early-Onset Nephrotic Syndrome: A Multicenter Cohort Study

Frontiers in medicine, 2022-06, Vol.9, p.885178-885178

2022

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391 Calpain inhibition enhances autophagy-lysosomal pathway and ameliorates tubulointerstitial fibrosis in Nphp1-targeted models

Nephrology, dialysis, transplantation, 2024-05, Vol.39 (Supplement_1)

2024

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Novel mutation of TCIRG1 and clinical pictures of two infantile malignant osteopetrosis patients

Journal of bone and mineral metabolism, 2011-03, Vol.29 (2), p.251-256

2011

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Overexpression of smad7 inhibits the TGF-β/Smad signaling pathway and EMT in NPHP1-defective MDCK cells

Biochemical and biophysical research communications, 2021-12, Vol.582, p.57-63

2021

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Cyclosporine A relieved proteinuria and hypoproteinemia in DGKE nephropathy

Clinica chimica acta, 2021-07, Vol.518, p.78-82

2021

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Novel compound mutations of SMARCAL1 associated with severe Schimke immuno-osseous dysplasia in a Chinese patient

Nephrology, dialysis, transplantation, 2010-05, Vol.25 (5), p.1697-1702

2010

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A novel ITGA3 homozygous splice mutation in an ILNEB syndrome child with slow progression

Clinica chimica acta, 2021-12, Vol.523, p.430-436

2021

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Clinical and pathological features and varied mutational spectra of pathogenic genes in 55 Chinese patients with nephronophthisis

Clinica chimica acta, 2020-07, Vol.506, p.136-144

2020

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SP6 controls human cytotrophoblast fate decisions and trophoblast stem cell establishment by targeting MSX2 regulatory elements

Developmental cell, 2024-06, Vol.59 (12), p.1506-1522.e11

2024

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WT1 mutation-associated nephropathy: a single-center experience

Clinical nephrology, 2017-05, Vol.87 (2017) (5), p.245

2017

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Association between endothelin-A receptor gene polymorphisms in locus rs10305936 and primary nephrotic syndrome in children

Life sciences (1973), 2013-12, Vol.93 (25-26), p.e75-e76

2013

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Twenty-eight-year review of childhood renal diseases from renal biopsy data: A single centre in China

Nephrology (Carlton, Vic.), 2016-12, Vol.21 (12), p.1003-1009

2016

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Establishment of bovine expanded potential stem cells

Reducing GEF-H1 Expression Inhibits Renal Cyst Formation, Inflammation, and Fibrosis via RhoA Signaling in Nephronophthisis

MicroRNAs and Polycystic Kidney Disease

An Nphp1 knockout mouse model targeting exon 2–20 demonstrates characteristic phenotypes of human nephronophthisis

Clinical features of children with pulmonary microscopic polyangiitis: report of 9 cases

821 Kibra mediates the activation of hippo by classic signal pathway related to NPHP1 defect

COQ2 mutation associated isolated nephropathy in two siblings from a Chinese pedigree

The Accumulation of VEGFA in the Glomerular Basement Membrane and Its Relationship with Podocyte Injury and Proteinuria in Alport Syndrome

Analysis of SALL1 gene variant in a boy with Townes-Brocks syndrome without anal atresia

High mutation rate of NPHP3 in 18 Chinese infantile nephronophthisis patients

Identification of renal cyst cells of type I Nephronophthisis by single-nucleus RNA sequencing

Dent Disease in Chinese Children and Findings from Heterozygous Mothers: Phenotypic Heterogeneity, Fetal Growth, and 10 Novel Mutations

滇东-黔西煤层气井排采动态影响因素及初始排水速度优化步骤

The Clinical and Genetic Features in Chinese Children With Steroid-Resistant or Early-Onset Nephrotic Syndrome: A Multicenter Cohort Study

391 Calpain inhibition enhances autophagy-lysosomal pathway and ameliorates tubulointerstitial fibrosis in Nphp1-targeted models

Novel mutation of TCIRG1 and clinical pictures of two infantile malignant osteopetrosis patients

Overexpression of smad7 inhibits the TGF-β/Smad signaling pathway and EMT in NPHP1-defective MDCK cells

Cyclosporine A relieved proteinuria and hypoproteinemia in DGKE nephropathy

Novel compound mutations of SMARCAL1 associated with severe Schimke immuno-osseous dysplasia in a Chinese patient

A novel ITGA3 homozygous splice mutation in an ILNEB syndrome child with slow progression

Clinical and pathological features and varied mutational spectra of pathogenic genes in 55 Chinese patients with nephronophthisis

SP6 controls human cytotrophoblast fate decisions and trophoblast stem cell establishment by targeting MSX2 regulatory elements

WT1 mutation-associated nephropathy: a single-center experience

Association between endothelin-A receptor gene polymorphisms in locus rs10305936 and primary nephrotic syndrome in children

Twenty-eight-year review of childhood renal diseases from renal biopsy data: A single centre in China

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