Fang Wang

Phenotypic and genotypic features of Alport syndrome in Chinese children.

Effect of glycine substitutions on alpha5(IV) chain structure and structure-phenotype correlations in Alport syndrome.

[Expression of the partial protein encoded by mutated COL4A5 gene and analysis of the structure by circular dichroism].

[Proteins structure changes of COL4A5 gene point mutations and structure-phenotype relations in Alport syndrome].

Detection of mutations in the COL4A5 gene by analyzing cDNA of skin fibroblasts.

[The changing etiology and therapeutic situation of atherosclerotic renal artery stenosis].

Effect of Panax notoginseng saponins on lipopolysaccharide-induced adhesion of leukocytes in rat mesenteric venules.

Inhibition effect of cardiotonic pills on venous thrombosis induced in rat mesentery by photochemical reaction.

Risk factors of diabetic retinopathy in type 2 diabetic patients.

Cardiovascular disease in early stages of chronic kidney disease in a Chinese population.

Community-based screening for chronic kidney disease among populations older than 40 years in Beijing.

Correlation between mRNA expression level of the mutant COL4A5 gene and phenotypes of XLAS females.

Association between carotid artery intima-media thickness and early-stage CKD in a Chinese population.

Metabolic syndrome and chronic kidney disease in a Chinese population aged 40 years and older.

Protective effects of ginsenoside Rb1, ginsenoside Rg1, and notoginsenoside R1 on lipopolysaccharide-induced microcirculatory disturbance in rat mesentery.

[Follow-up study on the pregnancy of an X-linked dominant Alport syndrome female].

Protective effects of dihydroxylphenyl lactic acid and salvianolic acid B on LPS-induced mesenteric microcirculatory disturbance in rats.

[Prenatal diagnosis and genetic counseling of X-linked Alport syndrome in China].

Effect of notoginsenoside R1 on hepatic microcirculation disturbance induced by gut ischemia and reperfusion.

Prevalence and factors associated with CKD: a population study from Beijing.

Prenatal diagnosis and genetic counseling of a Chinese Alport syndrome kindred.

[Nonmuscle myosin heavy chain 9 gene mutations related disease: a family report].

Gender-specific reference value of urine albumin-creatinine ratio in healthy Chinese adults: results of the Beijing CKD survey.

Comparison of the prevalence of chronic kidney disease among different ethnicities: Beijing CKD survey and American NHANES.

The antioxidant Cerebralcare Granule attenuates cerebral microcirculatory disturbance during ischemia-reperfusion injury.

Circulating neutrophil gelatinase-associated lipocalin: a useful biomarker for assessing disease activity of ANCA-associated vasculitis.

The attenuation effect of 3,4-dihydroxy-phenyl lactic acid and salvianolic acid B on venular thrombosis induced in rat mesentery by photochemical reaction.

Meta-analysis of the association between SNPs in TCF7L2 and type 2 diabetes in East Asian population.

[Correlation of plasma thioredoxin reductase activity to growth of H22 hepatocellular carcinoma xenografts in Kunming mice].

Neutrophil degranulation in antineutrophil cytoplasmic antibody-negative pauci-immune crescentic glomerulonephritis.

The first Chinese Pierson syndrome with novel mutations in LAMB2.

Drugs controlling proteinuria of patients with Alport syndrome.

Unusual patterns of neural tube defects in a high risk region of northern China.

Effect of genetic variants in KCNJ11, ABCC8, PPARG and HNF4A loci on the susceptibility of type 2 diabetes in Chinese Han population.

Cardiotonic pills, a compound Chinese medicine, protects ischemia-reperfusion-induced microcirculatory disturbance and myocardial damage in rats.

[Effect of continuous positive airway pressure upon 24 h changes of blood glucose level in patients with obstructive sleep apnea hypopnea syndrome and type 2 diabetes].

Implication of genetic variants near SLC30A8, HHEX, CDKAL1, CDKN2A/B, IGF2BP2, FTO, TCF2, KCNQ1, and WFS1 in type 2 diabetes in a Chinese population.

Cerebralcare Granule, a Chinese herb compound preparation, improves cerebral microcirculatory disorder and hippocampal CA1 neuron injury in gerbils after ischemia-reperfusion.

Level of kidney function correlates with cognitive decline.

Gender differences in age-related decline in glomerular filtration rates in healthy people and chronic kidney disease patients.

[Analysis of clinical manifestations of 159 hospitalized children infected with 2009 novel influenza A (H1N1) virus].

A study of TNF-alpha-238 and -308 polymorphisms with different outcomes of persistent hepatitis B virus infection in China.

Mutation detection of COL4An gene based on mRNA of peripheral blood lymphocytes and prenatal diagnosis of Alport syndrome in China.

[Evaluation of the applicability of three prediction equations for estimating glomerular filtration rate in children with chronic kidney disease].

Reliability and accuracy of Crystaleye spectrophotometric system.

Mortality and renal function decline among a community-based Chinese population with normal or mildly impaired renal function.

[Prokaryotic expression for fusion protein of human metapneumovirus and its preliminary application as an antigen for antibody detection].

Reference intervals for serum creatinine with enzymatic assay and evaluation of four equations to estimate glomerular filtration rate in a healthy Chinese adult population.

Characterization of human metapneumovirus from pediatric patients with acute respiratory infections in a 4-year period in Beijing, China.

Development and validation of a new dry weight estimation method using single frequency bioimpedance in hemodialysis patients.

The association between plasma uric acid and renal function decline in a Chinese population-based cohort.

[Analysis of clinical manifestations of hospitalized children infected with seasonal influenza A virus and 2009 novel influenza A (H1N1) virus in Beijing].

The protective effect of Cerebralcare Granule® on brain edema, cerebral microcirculatory disturbance, and neuron injury in a focal cerebral ischemia rat model.

Attitudes toward genetic diagnosis and prenatal diagnosis of X-linked Alport syndrome in China.

Prevalence of chronic kidney disease in China: a cross-sectional survey.

[Relationship between V617F mutation and 46/1 haplotype in JAK2 gene in patients with chronic myeloproliferative diseases and frequencies of 46/1 haplotype in different Chinese nationalities].

Common variants of the UMOD promoter associated with blood pressure in a community-based Chinese cohort.

[Features of proteinuria in Chinese male patients with Alport syndrome].

Prevalence and significance of Hepatitis B reverse transcriptase mutants in different disease stages of untreated patients.

Genotype-phenotype correlations in 17 Chinese patients with autosomal recessive Alport syndrome.

Skin biopsy is a practical approach for the clinical diagnosis and molecular genetic analysis of X-linked Alport's syndrome.

[Application of multiplex ligation-dependent probe amplification in gene diagnosis of X-linked Alport syndrome].

Association study of NRXN3 polymorphisms with schizophrenia and risperidone-induced bodyweight gain in Chinese Han population.

Association of MTHFR C677T polymorphism with schizophrenia and its effect on episodic memory and gray matter density in patients.

Common genetic variants of the human uromodulin gene regulate transcription and predict plasma uric acid levels.

Novel OCRL mutations in Chinese children with Lowe syndrome.

Plasma soluble urokinase receptor levels are increased but do not distinguish primary from secondary focal segmental glomerulosclerosis.

[Hereditary kidney diseases in children].

Genetic variation in attachment glycoprotein genes of human respiratory syncytial virus subgroups a and B in children in recent five consecutive years.

Leprosy presented as cutaneous erythema.

A large-scale screen for coding variants predisposing to psoriasis.

Further evidence for genetic association of CACNA1C and schizophrenia: new risk loci in a Han Chinese population and a meta-analysis.

Awareness of CKD in China: a national cross-sectional survey.

Prevalence, awareness, treatment, and control of hypertension in China: results from a national survey.

[Comparison of phenotypic features between patients with X-linked and autosomal recessive Alport syndrome].

[Clinical characteristies of atypical hemolytie uremic syndrome associated with H factor antibody in children].

Urinary soluble urokinase receptor levels are elevated and pathogenic in patients with primary focal segmental glomerulosclerosis.

Clinical characteristics and mutation analysis of three Chinese children with autosomal recessive polycystic kidney disease.

Effect and mechanism of tacrolimus on melanogenesis on A375 human melanoma cells.

Evaluating landscape options for corridor restoration between giant panda reserves.

Status of non-steroidal anti-inflammatory drugs use and its association with chronic kidney disease: a cross-sectional survey in China.

Reading performance is enhanced by visual texture discrimination training in Chinese-speaking children with developmental dyslexia.

Functional screen reveals essential roles of miR-27a/24 in differentiation of embryonic stem cells.

Targeting the microRNA-21/AP1 axis by 5-fluorouracil and pirarubicin in human hepatocellular carcinoma.

A simple and sensitive LC-MS/MS method for the determination of sotalol in rat plasma.

[Relationship between hyperuricemia and primary nephrotic syndrome in children].

[Analysis of the clinical audiological characteristics in 92 Chinese Alport syndrome cases].

Chemotherapy-Induced miRNA-29c/Catenin-δ Signaling Suppresses Metastasis in Gastric Cancer.

Serum Level of Fibroblast Growth Factor 21 Is Independently Associated with Acute Myocardial Infarction.

Genetic and Functional Evidence Supports LPAR1 as a Susceptibility Gene for Hypertension.

Long-term treatment by ACE inhibitors and angiotensin receptor blockers in children with Alport syndrome.

Levels of Serum Phosphorus and Cardiovascular Surrogate Markers.

Acute kidney injury in China: a cross-sectional survey.

A pharmacogenomic study revealed an association between SLC6A4 and risperidone-induced weight gain in Chinese Han population.

Clinical Features and Outcomes in Patients With Membranous Nephropathy and Crescent Formation.

[Retrospective study of primary IgA nephropathy with crescent formation and/or rapidly progressive glomerulonephritis in children].

[Clinical and genetic features of X-linked Alport syndrome in men positive for the collagen Ⅳ α5 chain in epidermal basement membrane].

A Pilot Study of Quantitative Loop-mediated Isothermal Amplification-guided Target Therapies for Hospital-acquired Pneumonia.

[Analysis of influencing factors on rehabilitation effects for 1 422 preschool deaf children following cochlear implantation].

Patients With Combined Membranous Nephropathy and Focal Segmental Glomerulosclerosis Have Comparable Clinical and Autoantibody Profiles With Primary Membranous Nephropathy: A Retrospective Observational Study.

Clinical Significance of IgM and C3 Glomerular Deposition in Primary Focal Segmental Glomerulosclerosis.

Mice with mutant Inf2 show impaired podocyte and slit diaphragm integrity in response to protamine-induced kidney injury.

Efficacy and safety of fenofibrate as an add-on in patients with elevated triglyceride despite receiving statin treatment.

Combination of Gram Stain, Sputum Culture, and Molecular Method for Diagnosis and Guiding Target Therapies of Bacterial Pneumonia.

Mineral and Bone Disorder and Its Association with Cardiovascular Parameters in Chinese Patients with Chronic Kidney Disease.

Spatial Co-Occurrence and Activity Patterns of Mesocarnivores in the Temperate Forests of Southwest China.

MHC Class II Risk Alleles and Amino Acid Residues in Idiopathic Membranous Nephropathy.

Chromatin-remodelling factor Brg1 regulates myocardial proliferation and regeneration in zebrafish.

A Neutralized Noncharged Polyethylenimine-Based System for Efficient Delivery of siRNA into Heart without Toxicity.

Incidence, Development, and Prognosis of Diabetic Kidney Disease in China: Design and Methods.

Electrophysiological basis of reading related phonological impairment in Chinese speakers with schizophrenia: An ERP study.

Spectrum of mutations in Chinese children with steroid-resistant nephrotic syndrome.

The RNA-binding protein QKI5 regulates primary miR-124-1 processing via a distal RNA motif during erythropoiesis.

Conservation planning beyond giant pandas: the need for an innovative telecoupling framework.

Diagnosis and treatment of Dent disease in 10 Chinese boys.

Strategies and cost-effectiveness evaluation of persistent albuminuria screening among high-risk population of chronic kidney disease.

Renal replacement therapy in acute kidney injury from a Chinese cross-sectional study: patient, clinical, socioeconomic and health service predictors of treatment.

China Kidney Disease Network (CK-NET) 2014 Annual Data Report.

Dent disease: Same mutation but different phenotypes in two brothers in China.

Reduced Kidney Function, Albuminuria, and Risks for All-cause and Cardiovascular Mortality in China: A Population-based Cohort Study.

Accelerated podocyte detachment and progressive podocyte loss from glomeruli with age in Alport Syndrome.

Circulating Antibodies against Thrombospondin Type-I Domain-Containing 7A in Chinese Patients with Idiopathic Membranous Nephropathy.

Low-dose cyclosporine in treatment of membranous nephropathy with nephrotic syndrome: effectiveness and renal safety.

The kinetics of white blood cell and the predictive factors of leukocytosis under oral or intravenous arsenic as the first-line treatment for acute promyelocytic leukemia.

Germline cytotoxic lymphocytes defective mutations in Chinese patients with lymphoma.

Rituximab for non-responsive idiopathic membranous nephropathy in a Chinese cohort.

Value of the Oxford classification of IgA nephropathy in children with Henoch-Schönlein purpura nephritis.

Steroid-resistant nephrotic syndrome caused by co-inheritance of mutations at and genes in two Chinese siblings.

Genetic screening and functional analysis of CASP9 mutations in a Chinese cohort with neural tube defects.

Hearing loss prevalence and risk factors among older adults in China.

Simultaneous determination of Vitamin A, 25-hydroxyl vitamin D α-tocopherol in small biological fluids by liquid chromatography-tandem mass spectrometry.

Mortality risk of chronic kidney disease: A comparison between the adult populations in urban China and the United States.

Alport syndrome: a unified classification of genetic disorders of collagen IV α345: a position paper of the Alport Syndrome Classification Working Group.

The ratio of urinary α1-microglobulin to microalbumin can be used as a diagnostic criterion for tubuloproteinuria.

An alternative way to increase the power gain of resonant rings.

Next-generation CRISPR/Cas9 transcriptional activation in using flySAM.

Urinary epidermal growth factor as a prognostic marker for the progression of Alport syndrome in children.

Clinical and prognostic significance of glomerular C1q deposits in primary MN.

Investigation of the Propagation of Stress Wave in Nickel-Titanium Shape Memory Alloys.