Involvement of the modifier gene of a human Mendelian disorder in a negative selection process.
BACKGROUND:Identification of modifier genes and characterization of their effects represent major challenges in human genetics. SAA1 is one of the few modifiers identified in humans: this gene influences the risk of renal amyloidosis (RA) in patients with familial Mediterranean fever (FMF), a Mendel...
Main Authors: | Isabelle Jéru, Hasmik Hayrapetyan, Philippe Duquesnoy, Emmanuelle Cochet, Jean-Louis Serre, Josué Feingold, Gilles Grateau, Tamara Sarkisian, Marc Jeanpierre, Serge Amselem |
---|---|
Format: | Article |
Language: | English |
Published: |
Public Library of Science (PLoS)
2009-10-01
|
Series: | PLoS ONE |
Online Access: | http://europepmc.org/articles/PMC2765618?pdf=render |
Similar Items
-
Role of IL-1b in NLRP12-associated autoinflammatory disorders and resistance to anti-IL-1 therapy
by: Marlin Sandrine, et al.
Published: (2011-09-01) -
Involvement of the same TNFR1 residue in mendelian and multifactorial inflammatory disorders.
by: Isabelle Jéru, et al.
Published: (2013-01-01) -
The risk of familial Mediterranean fever in MEFV heterozygotes: a statistical approach.
by: Isabelle Jéru, et al.
Published: (2013-01-01) -
Expression of SAA1, SAA2 and SAA4 genes in human primary monocytes and monocyte-derived macrophages.
by: Claire Jumeau, et al.
Published: (2019-01-01) -
Genes that bias Mendelian segregation.
by: Pierre Grognet, et al.
Published: (2014-01-01)