Lidan Hu

Department of Nephrology, Zhejiang University School of Medicine

Affiliated withZhejiang University School of Medicine The Children's Hospital, Zhejiang University School of Medicine

Research Area

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JoVE Journal Publications

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

Other Publications

Article	Year
Establishment of an induced pluripotent stem cell line (NCKDi003-A) from a patient with X-linked Dent disease (X-Dent) carrying the hemizygote mutation p. T277P (c. 829A > C) in the CLCN5 ge... Stem cell research\| PubMed ID: 34547705	2021
Bacterial and Fungal Infections Promote the Bone Erosion Progression in Acquired Cholesteatoma Revealed by Metagenomic Next-Generation Sequencing. Frontiers in microbiology\| PubMed ID: 34803987	2021
Cataract-Causing S93R Mutant Destabilized Structural Conformation of βB1 Crystallin Linking With Aggregates Formation and Cellular Viability. Frontiers in molecular biosciences\| PubMed ID: 35359596	2022
A novel cataract-causing mutation Ile82Met of γA crystallin trends to aggregate with unfolding intermediate. International journal of biological macromolecules\| PubMed ID: 35513103	2022
Stress granules in the spinal muscular atrophy and amyotrophic lateral sclerosis: The correlation and promising therapy. Neurobiology of disease\| PubMed ID: 35568100	2022
A protocol for the generation of patient-specific iPSC lines from peripheral blood mononuclear cells. STAR protocols\| PubMed ID: 35834385	2022
Clinical Metagenomic Next-Generation Sequencing for Diagnosis of Secondary Glaucoma in Patients With Cytomegalovirus-Induced Corneal Endotheliitis. Frontiers in microbiology\| PubMed ID: 35865935	2022
Heteromeric formation with βA3 protects the low thermal stability of βB1-L116P. The British journal of ophthalmology\| PubMed ID: 36126102	2022
Clinical characteristics and in silico analysis of congenital pseudarthrosis of the tibia combined with neurofibromatosis type 1 caused by a novel mutation. Frontiers in genetics\| PubMed ID: 36246612	2022
Clinical Characteristics and In Silico Analysis of Cystinuria Caused by a Novel Mutation. Genes\| PubMed ID: 36421847	2022
Cysteine Pathogenic Variants of PMM2 Are Sensitive to Environmental Stress with Loss of Structural Stability. Oxidative medicine and cellular longevity\| PubMed ID: 36743691	2023
Metabolomic profiles in serum and urine uncover novel biomarkers in children with nephrotic syndrome. European journal of clinical investigation\| PubMed ID: 36856027	2023
Cross-cancer pleiotropic analysis identifies three novel genetic risk loci for colorectal cancer. Human molecular genetics\| PubMed ID: 36928917	2023
N6-methyladenosine related gene expression signatures for predicting the overall survival and immune responses of patients with colorectal cancer. Frontiers in genetics\| PubMed ID: 36936424	2023
Multiple functions of stress granules in viral infection at a glance. Frontiers in microbiology\| PubMed ID: 36937261	2023
Determinants of depression, problem behavior, and cognitive level of adolescents in China: Findings from a national, population-based cross-sectional study. Frontiers in psychiatry\| PubMed ID: 37091712	2023
Cataract-causing variant Q70P damages structural stability of βB1-crystallin and increases its tendency to form insoluble aggregates. International journal of biological macromolecules\| PubMed ID: 37148932	2023
A quantitative planar array screen of 440 proteins uncovers novel serum protein biomarkers of idiopathic nephrotic syndrome. MedComm\| PubMed ID: 37180824	2023
Early onset of nephrogenic diabetes insipidus due to fabry disease in a child with N215S mutation: Case report and literature review. Heliyon\| PubMed ID: 37205992	2023
Network pharmacology and biochemical experiments reveal the antiapoptotic mechanism of huperzine A for treating diabetic retinopathy. The British journal of ophthalmology\| PubMed ID: 37339867	2023
Health-related quality of life of children with Williams syndrome and caregivers in China. Frontiers in public health\| PubMed ID: 37361163	2023
A Review of Inactivated COVID-19 Vaccine Development in China: Focusing on Safety and Efficacy in Special Populations. Vaccines\| PubMed ID: 37376434	2023
Inhibition of squalene epoxidase linking with PI3K/AKT signaling pathway suppresses endometrial cancer. Cancer science\| PubMed ID: 37438885	2023
Atopic dermatitis and chronic kidney disease: a bidirectional Mendelian randomization study. Frontiers in medicine\| PubMed ID: 37441684	2023
Low skeletal muscle mass as an early sign in children with fabry disease. Orphanet journal of rare diseases\| PubMed ID: 37480128	2023
Cysteine mutations impair the structural stability of phosphomannomutase 2 (PMM2) in glycosylation-associated metabolic disorders. Genes & diseases\| PubMed ID: 37492729	2023
The 18th amino acid glycine plays an essential role in maintaining the structural stabilities of γS-crystallin linking with congenital cataract. International journal of biological macromolecules\| PubMed ID: 37586630	2023
Cataract-causing mutations S78F and S78P of γD-crystallin decrease protein conformational stability and drive aggregation. International journal of biological macromolecules\| PubMed ID: 37739288	2023