Jingjing Wang

Efficacy of triptolide for children with moderately severe Henoch-Schönlein purpura nephritis presenting with nephrotic range proteinuria: a prospective and controlled study in China.

Serum suPAR levels help differentiate steroid resistance from steroid-sensitive nephrotic syndrome in children.

Triple immunosuppressive therapy in steroid-resistant nephrotic syndrome children with tacrolimus resistance or tacrolimus sensitivity but frequently relapsing.

Evaluation of mycophenolate mofetil or tacrolimus in children with steroid sensitive but frequently relapsing or steroid-dependent nephrotic syndrome.

The etiology of congenital nephrotic syndrome: current status and challenges.

Coenzyme Q10 supplementation therapy for 2 children with proteinuria renal disease and ADCK4 mutation: Case reports and literature review.

Relationships of Cadmium, Lead, and Mercury Levels With Albuminuria in US Adults: Results From the National Health and Nutrition Examination Survey Database, 2009-2012.

[Analysis of Alport syndrome induced by type IV collagen alpha 5 gene mutation in two families].

Disruption of auto-inhibition underlies conformational signaling of ASIC1a to induce neuronal necroptosis.

Construction of a human cell landscape at single-cell level.

Case report: a Chinese girl with dent disease 1 and turner syndrome due to a hemizygous CLCN5 gene mutation and Isochromosome (Xq).

Comparison of Scanpy-based algorithms to remove the batch effect from single-cell RNA-seq data.

A single-cell survey of cellular hierarchy in acute myeloid leukemia.

Genome-wide analysis of long non-coding RNAs responsive to multiple nutrient stresses in Arabidopsis thaliana.

In situ dissecting the evolution of gene duplication with different histone modification patterns based on high-throughput data analysis in .

Podocyte apoptosis in diabetic nephropathy by BASP1 activation of the p53 pathway via WT1.

Roxadustat for Renal Anemia in ESRD from PKD Patients: Is It Safe Enough?

Tracing cell-type evolution by cross-species comparison of cell atlases.

Case Report: Activating Mutation in Patients Presenting With Granulomatosis With Polyangiitis.

Clinical and Genetic Features in 31 Serial Chinese Children With Gitelman Syndrome.

Efficacy and Safety of Combination Treatment With Apatinib and Osimertinib After Osimertinib Resistance in Epidermal Growth Factor Receptor-Mutant Non-small Cell Lung Carcinoma-A Retrospective Analysis of a Multicenter Clinical Study.

Primary IgA nephropathy with nephrotic-range proteinuria in Chinese children.

Activated phosphoinositide 3-kinase delta syndrome misdiagnosed as anti-neutrophil cytoplasmic antibody-associated vasculitis: a case report.

Efficacy and safety of Huaiqihuang granule as adjuvant treatment for primary nephrotic syndrome in children: a meta-analysis and systematic review.

The immune cell landscape of peripheral blood mononuclear cells from PNS patients.

Seven novel podocyte autoantibodies were identified to diagnosis a new disease subgroup-autoimmune Podocytopathies.

Characterization of the Zebrafish Cell Landscape at Single-Cell Resolution.

Growth Retardation in the Course of Fanconi Syndrome Caused by the 4977-bp Mitochondrial DNA Deletion: A Case Report.

Evaluation of a new frequency-volume chart for children with primary monosymptomatic nocturnal enuresis: a prospective, comparative study.

The important roles and molecular mechanisms of annexin A autoantibody in children with nephrotic syndrome.

Clinical Manifestations of Alport Syndrome-Diffuse Leiomyomatosis Patients With Contiguous Gene Deletions in and .

Mosaic in Polycystic Kidneys Caused Aberrant Protein Expression in the Mitochondria and Lysosomes.

Description of the Molecular and Phenotypic Spectrum of Lesch-Nyhan Disease in Eight Chinese Patients.

Systematic identification of cell-fate regulatory programs using a single-cell atlas of mouse development.

Construction of the axolotl cell landscape using combinatorial hybridization sequencing at single-cell resolution.

Cell landscape of larval and adult Xenopus laevis at single-cell resolution.

Glomerular IgA Deposition and Serum Antineutrophil Cytoplasmic Antibody Positivity in a Child With Dystrophic Epidermolysis Bullosa: Case Report and Literature Review.

Genotype-Phenotype Correlation Reanalysis in 83 Chinese Cases with Mutations.

Author Correction: Systematic identification of cell-fate regulatory programs using a single-cell atlas of mouse development.

Construction of a cross-species cell landscape at single-cell level.

Vasculitis after COVID-19 Vaccination.

Pediatric membranous nephropathy: In the novel antigens era.

Publisher Correction: Cell landscape of larval and adult Xenopus laevis at single-cell resolution.

Deep learning of cross-species single-cell landscapes identifies conserved regulatory programs underlying cell types.

COVID-19 Breakthrough Infections in Vaccinated Kidney Transplant Recipients.

Successful Treatment of New-Onset Pediatric Nephrotic Syndrome With Rituximab as a First-Line Therapy.

Hutchinson-Gilford progeria syndrome complicated with stroke: A report of 2 cases and literature review.

Growth hormone treatment in pre-pubertal short Chinese children with chronic kidney disease prior to transplantation.

Metabolomic profiles in serum and urine uncover novel biomarkers in children with nephrotic syndrome.

De novo 11q13.3q13.4 deletion in a patient with Fanconi renotubular syndrome and intellectual disability: Case report and review of literature.

Textbook outcomes in liver surgery for gallbladder cancer patients treated with curative-intent resection: a multicenter observational study.

An analytical framework for decoding cell type-specific genetic variation of gene regulation.