Loss of Podocyte Dysferlin Expression Is Associated With Minimal Change Nephropathy
- 31 July 2006
- journal article
- Published by Elsevier in American Journal of Kidney Diseases
- Vol. 48 (1) , 143-150
- https://doi.org/10.1053/j.ajkd.2006.04.074
Abstract
No abstract availableKeywords
This publication has 15 references indexed in Scilit:
- Protein and gene analyses of dysferlinopathy in a large group of Japanese muscular dystrophy patientsJournal of the Neurological Sciences, 2003
- Defective membrane repair in dysferlin-deficient muscular dystrophyNature, 2003
- A novel, blood‐based diagnostic assay for limb girdle muscular dystrophy 2B and miyoshi myopathyAnnals of Neurology, 2001
- The sarcolemmal proteins dysferlin and caveolin-3 interact in skeletal muscleHuman Molecular Genetics, 2001
- Molecular basis of muscular dystrophiesMuscle & Nerve, 2000
- The Third Human FER-1-like Protein Is Highly Similar to DysferlinGenomics, 2000
- Myoferlin, a candidate gene and potential modifier of muscular dystrophyHuman Molecular Genetics, 2000
- A mutation in OTOF, encoding otoferlin, a FER-1-like protein, causes DFNB9, a nonsyndromic form of deafnessNature Genetics, 1999
- Dysferlin, a novel skeletal muscle gene, is mutated in Miyoshi myopathy and limb girdle muscular dystrophyNature Genetics, 1998
- A gene related to Caenorhabditis elegans spermatogenesis factor fer-1 is mutated in limb-girdle muscular dystrophy type 2BNature Genetics, 1998