The primary glomerulonephritides: a systems biology approach

Expression of MicroRNAs in the Urinary Sediment of Patients with IgA Nephropathy

(2013) Gang Wang et al.   DISEASE MARKERS

Elevated Levels of miR-146a and miR-155 in Kidney Biopsy and Urine from Patients with IgA Nephropathy

(2013) Gang Wang et al.   DISEASE MARKERS

Renoprotective Effect of Combined Inhibition of Angiotensin-Converting Enzyme and Histone Deacetylase

(2013) Y. Zhong et al.   JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY

Design of the Nephrotic Syndrome Study Network (NEPTUNE) to evaluate primary glomerular nephropathy by a multidisciplinary approach

(2013) Crystal A. Gadegbeku et al.   KIDNEY INTERNATIONAL

Metabolic profiling reveals new serum biomarkers for differentiating diabetic nephropathy

(2012) Akiyoshi Hirayama et al.   ANALYTICAL AND BIOANALYTICAL CHEMISTRY

Systematic variations associated with renal disease uncovered by parallel metabolomics of urine and serum

(2012) Xianfu Gao et al.   BMC Systems Biology

Urinary Proteomics for Early Diagnosis in Diabetic Nephropathy

(2012) P. Zurbig et al.   DIABETES

Genome-wide association study identifies TNFSF13 as a susceptibility gene for IgA in a South Chinese population in smokers

(2012) Chen Yang et al.   IMMUNOGENETICS

Urinary Proteome Analysis by Matrix-Assisted Laser Desorption/Ionization Time-of-Flight Mass Spectrometry with Magnetic Beads for Identifying the Pathologic Presentation of Clinical Early IgA Nephropathy

(2012) Qiang He et al.   Journal of Biomedical Nanotechnology

Autophagy can repair endoplasmic reticulum stress damage of the passive Heymann nephritis model as revealed by proteomics analysis

(2012) Liyuan Wang et al.   Journal of Proteomics

Abnormal miR-148b Expression Promotes Aberrant Glycosylation of IgA1 in IgA Nephropathy

(2012) G. Serino et al.   JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY

A systems approach identifies HIPK2 as a key regulator of kidney fibrosis

(2012) Yuanmeng Jin et al.   NATURE MEDICINE

Pathogenesis of IgA nephropathy

(2012) Kar Neng Lai   Nature Reviews Nephrology

Childhood nephrotic syndrome—current and future therapies

(2012) Larry A. Greenbaum et al.   Nature Reviews Nephrology

APOL1 Null Alleles from a Rural Village in India Do Not Correlate with Glomerulosclerosis

(2012) Duncan B. Johnstone et al.   PLoS One

Proteomics and Systems Biology for Understanding Diabetic Nephropathy

(2012) Jonathan M. Starkey et al.   Journal of Cardiovascular Translational Research

Perspectives on Systems Biology Applications in Diabetic Kidney Disease

(2012) Claudiu V. Komorowsky et al.   Journal of Cardiovascular Translational Research

Systems Pharmacology: Network Analysis to Identify Multiscale Mechanisms of Drug Action

(2011) Shan Zhao et al.   Annual Review of Pharmacology and Toxicology

Urinary proteomics in the assessment of chronic kidney disease

(2011) William Mullen et al.   CURRENT OPINION IN NEPHROLOGY AND HYPERTENSION

COQ6 mutations in human patients produce nephrotic syndrome with sensorineural deafness

(2011) Saskia F. Heeringa et al.   JOURNAL OF CLINICAL INVESTIGATION

Circulating Anti-PLA2R Autoantibodies to Monitor Immunological Activity in Membranous Nephropathy

(2011) P. Cravedi et al.   JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY

Genetic Variation in APOL1 Associates with Younger Age at Hemodialysis Initiation

(2011) Z. Kanji et al.   JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY

APOL1 Genetic Variants in Focal Segmental Glomerulosclerosis and HIV-Associated Nephropathy

(2011) J. B. Kopp et al.   JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY

Rituximab-Induced Depletion of Anti-PLA2R Autoantibodies Predicts Response in Membranous Nephropathy

(2011) L. H. Beck et al.   JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY

Anti-Phospholipase A2 Receptor Antibody in Membranous Nephropathy

(2011) W. Qin et al.   JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY

Exome sequencing identified MYO1E and NEIL1 as candidate genes for human autosomal recessive steroid-resistant nephrotic syndrome

(2011) Simone Sanna-Cherchi et al.   KIDNEY INTERNATIONAL

Systems biology of kidney diseases

(2011) John Cijiang He et al.   KIDNEY INTERNATIONAL

A systems view of genetics in chronic kidney disease

(2011) Benjamin J. Keller et al.   KIDNEY INTERNATIONAL

A genome-wide association study in Han Chinese identifies multiple susceptibility loci for IgA nephropathy

(2011) Xue-Qing Yu et al.   NATURE GENETICS

Genome-wide association study identifies susceptibility loci for IgA nephropathy

(2011) Ali G Gharavi et al.   NATURE GENETICS

INF2Mutations in Charcot–Marie–Tooth Disease with Glomerulopathy

(2011) Olivia Boyer et al.   NEW ENGLAND JOURNAL OF MEDICINE

MYO1EMutations and Childhood Familial Focal Segmental Glomerulosclerosis

(2011) Caterina Mele et al.   NEW ENGLAND JOURNAL OF MEDICINE

Focal Segmental Glomerulosclerosis

(2011) Vivette D. D'Agati et al.   NEW ENGLAND JOURNAL OF MEDICINE

Risk HLA-DQA1 and PLA2R1 Alleles in Idiopathic Membranous Nephropathy

(2011) Horia C. Stanescu et al.   NEW ENGLAND JOURNAL OF MEDICINE

A Molecular Profile of Focal Segmental Glomerulosclerosis from Formalin-Fixed, Paraffin-Embedded Tissue

(2010) Jeffrey B. Hodgin et al.   AMERICAN JOURNAL OF PATHOLOGY

Detection of microRNAs in dried serum blots

(2010) Santosh Kumar Patnaik et al.   ANALYTICAL BIOCHEMISTRY

Insulin-like growth factor binding protein-1 levels are increased in patients with IgA nephropathy

(2010) Koki Tokunaga et al.   BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS

Systems pathology

(2010) Michael J. Donovan et al.   CANCER

The MicroRNA Spectrum in 12 Body Fluids

(2010) J. A. Weber et al.   CLINICAL CHEMISTRY

HLA Has Strongest Association with IgA Nephropathy in Genome-Wide Analysis

(2010) J. Feehally et al.   JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY

Altered modulation of WNT–β-catenin and PI3K/Akt pathways in IgA nephropathy

(2010) Sharon N. Cox et al.   KIDNEY INTERNATIONAL

Patients with Epstein–Fechtner syndromes owing to MYH9 R702 mutations develop progressive proteinuric renal disease

(2010) Takashi Sekine et al.   KIDNEY INTERNATIONAL

Genetic kidney diseases

(2010) Friedhelm Hildebrandt   LANCET

Review: The role of microRNAs in kidney disease

(2010) JORDAN YZ LI et al.   NEPHROLOGY

A Molecular Signature of Proteinuria in Glomerulonephritis

(2010) Heather N. Reich et al.   PLoS One

Association of Trypanolytic ApoL1 Variants with Kidney Disease in African Americans

(2010) G. Genovese et al.   SCIENCE

Role of systems pharmacology in understanding drug adverse events

(2010) Seth I. Berger et al.   Wiley Interdisciplinary Reviews-Systems Biology and Medicine

MicroRNAs and Their Role in Progressive Kidney Diseases

(2009) M. Kato et al.   Clinical Journal of the American Society of Nephrology

Molecular genetic analysis of podocyte genes in focal segmental glomerulosclerosis—a review

(2009) M. M. Löwik et al.   EUROPEAN JOURNAL OF PEDIATRICS

Mutations in the formin gene INF2 cause focal segmental glomerulosclerosis

(2009) Elizabeth J Brown et al.   NATURE GENETICS

Microarray and Bioinformatics Analysis of Gene Expression in Experimental Membranous Nephropathy

(2009) Peter V. Hauser et al.   NEPHRON EXPERIMENTAL NEPHROLOGY

M-Type Phospholipase A2Receptor as Target Antigen in Idiopathic Membranous Nephropathy

(2009) Laurence H. Beck et al.   NEW ENGLAND JOURNAL OF MEDICINE

MYH9 is associated with nondiabetic end-stage renal disease in African Americans

(2008) W H Linda Kao et al.   NATURE GENETICS

MYH9 is a major-effect risk gene for focal segmental glomerulosclerosis

(2008) Jeffrey B Kopp et al.   NATURE GENETICS

Biomarker discovery in glomerular diseases using urinary proteomics

(2008) Visith Thongboonkerd   Proteomics Clinical Applications

Urine protein profile of IgA nephropathy patients may predict the response to ACE-inhibitor therapy

(2007) Maria Teresa Rocchetti et al.   PROTEOMICS