Amanote Research
Register
Sign In
A Cluster of Mutations in the UMOD Gene Causes Familial Juvenile Hyperuricemic Nephropathy With Abnormal Expression of Uromodulin
Journal of the American Society of Nephrology : JASN
- United States
doi 10.1097/01.asn.0000092147.83480.b5
Full Text
Open PDF
Abstract
Available in
full text
Categories
Medicine
Nephrology
Date
November 1, 2003
Authors
K. Dahan
Publisher
American Society of Nephrology (ASN)
Related search
Familial Juvenile Hyperuricemic Nephropathy Type 1
First Report of Familial Juvenile Hyperuricemic Nephropathy (FJHN) in Iran Caused by a Novel De Novo Mutation (E197X) in UMOD
Journal of Molecular and Genetic Medicine
Novel Uromodulin Mutation Causing Familial Juvenile Hyperuricemia Nephropathy to Lead Its Impaired Protein Stability and Cellular Apoptosis.
GOUT AND NUCLEIC ACID METABOLISM
Febuxostat Attenuates ER Stress Mediated Kidney Injury in a Rat Model of Hyperuricemic Nephropathy
Oncotarget
Oncology
Abnormal miR-148b Expression Promotes Aberrant Glycosylation of IgA1 in IgA Nephropathy
Journal of the American Society of Nephrology : JASN
Medicine
Nephrology
Metabolic Changes in Patients With Familial Pituitary Adenomas Associated With Mutations in the AIP Gene
Obesity and Metabolism
Internal Medicine
Nutrition
Endocrinology
Public Health
Environmental
Dietetics
Occupational Health
Metabolism
Diabetes
Familial Juvenile Degeneration of the Macula
British Journal of Ophthalmology
Molecular Neuroscience
Ophthalmology
Sensory Systems
Cellular
Mutations in DDR2 Gene Cause SMED With Short Limbs and Abnormal Calcifications
American Journal of Human Genetics
Genetics
Clinical Expression of Familial Hypercholesterolemia in Clusters of Mutations of the LDL Receptor Gene That Cause a Receptor-Defective or Receptor-Negative Phenotype
Arteriosclerosis, Thrombosis, and Vascular Biology
Cardiovascular Medicine
Cardiology
