Epistatic role of the MYH9/APOL1 region on familial hematuria genes.
Familial hematuria (FH) is explained by at least four different genes (see below). About 50% of patients develop late proteinuria and chronic kidney disease (CKD). We hypothesized that MYH9/APOL1, two closely linked genes associated with CKD, may be associated with adverse progression in FH. Our stu...
Main Authors: | Konstantinos Voskarides, Panayiota Demosthenous, Louiza Papazachariou, Maria Arsali, Yiannis Athanasiou, Michalis Zavros, Kostas Stylianou, Dimitris Xydakis, Eugenios Daphnis, Daniel P Gale, Patrick H Maxwell, Avraam Elia, Cristian Pattaro, Alkis Pierides, Constantinos Deltas |
---|---|
Format: | Article |
Language: | English |
Published: |
Public Library of Science (PLoS)
2013-01-01
|
Series: | PLoS ONE |
Online Access: | http://europepmc.org/articles/PMC3597641?pdf=render |
Similar Items
-
Frequency of COL4A3/COL4A4 mutations amongst families segregating glomerular microscopic hematuria and evidence for activation of the unfolded protein response. Focal and segmental glomerulosclerosis is a frequent development during ageing.
by: Louiza Papazachariou, et al.
Published: (2014-01-01) -
COL4A5 and LAMA5 variants co-inherited in familial hematuria: digenic inheritance or genetic modifier effect?
by: Konstantinos Voskarides, et al.
Published: (2018-05-01) -
A functional variant in NEPH3 gene confers high risk of renal failure in primary hematuric glomerulopathies. Evidence for predisposition to microalbuminuria in the general population.
by: Konstantinos Voskarides, et al.
Published: (2017-01-01) -
New insights into the molecular regulation of kidney disease: contributions of APOL1 and MYH9
by: Bondzie, Philip Apraku
Published: (2016) -
A miR-1207-5p binding site polymorphism abolishes regulation of HBEGF and is associated with disease severity in CFHR5 nephropathy.
by: Gregory Papagregoriou, et al.
Published: (2012-01-01)