B. Whebe

Autosomal dominant polycystic kidney disease: the changing face of clinical management

A Non-Synonymous Mutation in the Canine Pkd1 Gene Is Associated with Autosomal Dominant Polycystic Kidney Disease in Bull Terriers

Pharmacological management of polycystic kidney disease

SIFT web server: predicting effects of amino acid substitutions on proteins

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

Polycystic kidney disease

Polycystins 1 and 2 mediate mechanosensation in the primary cilium of kidney cells

PKD1 Unusual DNA Conformations Are Recognized by Nucleotide Excision Repair

Clinical Characteristics and Disease Predictors of a Large Chinese Cohort of Patients with Autosomal Dominant Polycystic Kidney Disease

The genetics and physiology of polycystic kidney disease

Treatment of Persistent Gross Hematuria with Tranexamic Acid in Autosomal Dominant Polycystic Kidney Disease

DNA Repair Excision Nuclease Attacks Undamaged DNA

Mutation Analysis of the Entire PKD1 Gene: Genetic and Diagnostic Implications

Evaluating the clinical utility of a molecular genetic test for polycystic kidney disease

Chronic Kidney Disease Diagnosis and Management

A novel evolutionarily conserved domain of cell-adhesion GPCRs mediates autoproteolysis

DGGE screening of PKD1 gene reveals novel mutations in a large cohort of 146 unrelated patients

Novel mutations in the duplicated region of PKD1 gene

Type of PKD1 Mutation Influences Renal Outcome in ADPKD

HLA class II typing and idiopathic IgA nephropathy (IgAN): DQB1*0301, a possible marker of unfavorable outcome

DGGE screening of PKD1 gene reveals novel mutations in a large cohort of 146 unrelated patients