Jingjing Wang

Crown Bioscience Inc., Taicang, Jiangsu, China

Affiliated withCrown Bioscience Inc., Taicang, Jiangsu, China Zhejiang University School of Medicine

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JoVE Journal Publications

ArticleTotal : 2	Year
Publication title Cited by 9	2021
Publication title Cited by 4	2023

Other Publications

Article	Year
Efficacy of triptolide for children with moderately severe Henoch-Schönlein purpura nephritis presenting with nephrotic range proteinuria: a prospective and controlled study in China. BioMed research international\| PubMed ID: 24455682	2013
Serum suPAR levels help differentiate steroid resistance from steroid-sensitive nephrotic syndrome in children. Pediatric nephrology (Berlin, Germany)\| PubMed ID: 25034499	2015
Triple immunosuppressive therapy in steroid-resistant nephrotic syndrome children with tacrolimus resistance or tacrolimus sensitivity but frequently relapsing. Nephrology (Carlton, Vic.)\| PubMed ID: 25312783	2015
Evaluation of mycophenolate mofetil or tacrolimus in children with steroid sensitive but frequently relapsing or steroid-dependent nephrotic syndrome. Nephrology (Carlton, Vic.)\| PubMed ID: 26697959	2016
The etiology of congenital nephrotic syndrome: current status and challenges. World journal of pediatrics : WJP\| PubMed ID: 26961288	2016
Coenzyme Q10 supplementation therapy for 2 children with proteinuria renal disease and ADCK4 mutation: Case reports and literature review. Medicine\| PubMed ID: 29382012	2017
Relationships of Cadmium, Lead, and Mercury Levels With Albuminuria in US Adults: Results From the National Health and Nutrition Examination Survey Database, 2009-2012. American journal of epidemiology\| PubMed ID: 30874715	2019
[Analysis of Alport syndrome induced by type IV collagen alpha 5 gene mutation in two families]. Zhejiang da xue xue bao. Yi xue ban = Journal of Zhejiang University. Medical sciences\| PubMed ID: 31901041	2019
Disruption of auto-inhibition underlies conformational signaling of ASIC1a to induce neuronal necroptosis. Nature communications\| PubMed ID: 31980622	2020
Construction of a human cell landscape at single-cell level. Nature\| PubMed ID: 32214235	2020
Case report: a Chinese girl with dent disease 1 and turner syndrome due to a hemizygous CLCN5 gene mutation and Isochromosome (Xq). BMC nephrology\| PubMed ID: 32393202	2020
Comparison of Scanpy-based algorithms to remove the batch effect from single-cell RNA-seq data. Cell regeneration (London, England)\| PubMed ID: 32632608	2020
A single-cell survey of cellular hierarchy in acute myeloid leukemia. Journal of hematology & oncology\| PubMed ID: 32977829	2020
Genome-wide analysis of long non-coding RNAs responsive to multiple nutrient stresses in Arabidopsis thaliana. Functional & integrative genomics\| PubMed ID: 33130916	2021
In situ dissecting the evolution of gene duplication with different histone modification patterns based on high-throughput data analysis in . PeerJ\| PubMed ID: 33505781	2021
Podocyte apoptosis in diabetic nephropathy by BASP1 activation of the p53 pathway via WT1. Acta physiologica (Oxford, England)\| PubMed ID: 33615732	2021
Roxadustat for Renal Anemia in ESRD from PKD Patients: Is It Safe Enough? Journal of the American Society of Nephrology : JASN\| PubMed ID: 33649100	2021
Tracing cell-type evolution by cross-species comparison of cell atlases. Cell reports\| PubMed ID: 33657376	2021
Case Report: Activating Mutation in Patients Presenting With Granulomatosis With Polyangiitis. Frontiers in immunology\| PubMed ID: 33995405	2021
Clinical and Genetic Features in 31 Serial Chinese Children With Gitelman Syndrome. Frontiers in pediatrics\| PubMed ID: 33996672	2021
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 Retrospecti... Frontiers in molecular biosciences\| PubMed ID: 34026823	2021
Primary IgA nephropathy with nephrotic-range proteinuria in Chinese children. Medicine\| PubMed ID: 34032732	2021
Activated phosphoinositide 3-kinase delta syndrome misdiagnosed as anti-neutrophil cytoplasmic antibody-associated vasculitis: a case report. The Journal of international medical research\| PubMed ID: 34039074	2021
Efficacy and safety of Huaiqihuang granule as adjuvant treatment for primary nephrotic syndrome in children: a meta-analysis and systematic review. World journal of pediatrics : WJP\| PubMed ID: 34075551	2021
The immune cell landscape of peripheral blood mononuclear cells from PNS patients. Scientific reports\| PubMed ID: 34158604	2021
Seven novel podocyte autoantibodies were identified to diagnosis a new disease subgroup-autoimmune Podocytopathies. Clinical immunology (Orlando, Fla.)\| PubMed ID: 34600127	2021
Characterization of the Zebrafish Cell Landscape at Single-Cell Resolution. Frontiers in cell and developmental biology\| PubMed ID: 34660600	2021
Growth Retardation in the Course of Fanconi Syndrome Caused by the 4977-bp Mitochondrial DNA Deletion: A Case Report. Children (Basel, Switzerland)\| PubMed ID: 34682152	2021
Evaluation of a new frequency-volume chart for children with primary monosymptomatic nocturnal enuresis: a prospective, comparative study. World journal of pediatrics : WJP\| PubMed ID: 34716893	2021
The important roles and molecular mechanisms of annexin A autoantibody in children with nephrotic syndrome. Annals of translational medicine\| PubMed ID: 34734004	2021
Clinical Manifestations of Alport Syndrome-Diffuse Leiomyomatosis Patients With Contiguous Gene Deletions in and . Frontiers in medicine\| PubMed ID: 34778325	2021
Mosaic in Polycystic Kidneys Caused Aberrant Protein Expression in the Mitochondria and Lysosomes. Frontiers in medicine\| PubMed ID: 34977057	2021
Description of the Molecular and Phenotypic Spectrum of Lesch-Nyhan Disease in Eight Chinese Patients. Frontiers in genetics\| PubMed ID: 35559039	2022
Systematic identification of cell-fate regulatory programs using a single-cell atlas of mouse development. Nature genetics\| PubMed ID: 35817981	2022
Construction of the axolotl cell landscape using combinatorial hybridization sequencing at single-cell resolution. Nature communications\| PubMed ID: 35869072	2022
Cell landscape of larval and adult Xenopus laevis at single-cell resolution. Nature communications\| PubMed ID: 35879314	2022
Glomerular IgA Deposition and Serum Antineutrophil Cytoplasmic Antibody Positivity in a Child With Dystrophic Epidermolysis Bullosa: Case Report and Literature Review. Frontiers in pediatrics\| PubMed ID: 35899130	2022
Genotype-Phenotype Correlation Reanalysis in 83 Chinese Cases with Mutations. Genetics research\| PubMed ID: 35919034	2022
Author Correction: Systematic identification of cell-fate regulatory programs using a single-cell atlas of mouse development. Nature genetics\| PubMed ID: 35922581	2022
Construction of a cross-species cell landscape at single-cell level. Nucleic acids research\| PubMed ID: 35929025	2023
Vasculitis after COVID-19 Vaccination. Current rheumatology reviews\| PubMed ID: 35980076	2023
Pediatric membranous nephropathy: In the novel antigens era. Frontiers in immunology\| PubMed ID: 36016931	2022
Publisher Correction: Cell landscape of larval and adult Xenopus laevis at single-cell resolution. Nature communications\| PubMed ID: 36050298	2022
Deep learning of cross-species single-cell landscapes identifies conserved regulatory programs underlying cell types. Nature genetics\| PubMed ID: 36229673	2022
COVID-19 Breakthrough Infections in Vaccinated Kidney Transplant Recipients. Vaccines\| PubMed ID: 36423007	2022
Successful Treatment of New-Onset Pediatric Nephrotic Syndrome With Rituximab as a First-Line Therapy. Kidney international reports\| PubMed ID: 36506238	2022
Hutchinson-Gilford progeria syndrome complicated with stroke: A report of 2 cases and literature review. Frontiers in pediatrics\| PubMed ID: 36523395	2022
Growth hormone treatment in pre-pubertal short Chinese children with chronic kidney disease prior to transplantation. Pediatric research\| PubMed ID: 36539574	2023
Metabolomic profiles in serum and urine uncover novel biomarkers in children with nephrotic syndrome. European journal of clinical investigation\| PubMed ID: 36856027	2023
De novo 11q13.3q13.4 deletion in a patient with Fanconi renotubular syndrome and intellectual disability: Case report and review of literature. Frontiers in pediatrics\| PubMed ID: 37152320	2023
Textbook outcomes in liver surgery for gallbladder cancer patients treated with curative-intent resection: a multicenter observational study. International journal of surgery (London, England)\| PubMed ID: 37288584	2023
An analytical framework for decoding cell type-specific genetic variation of gene regulation. Nature communications\| PubMed ID: 37391400	2023