The role of Fragile X mental retardation protein in Drosophila cleavage furrow formation
Reduced activity of Fragile X mental retardation protein (FMRP) in brain neurons results in the most common form of heritable mental retardation in humans, Fragile X Syndrome (FXS). FMRP is a selective RNA-binding protein that is implicated in the translational regulation of specific mRNAs in neuro...
Main Author: | Monzo, Kate Frances |
---|---|
Other Authors: | Sisson, John Charles |
Format: | Others |
Language: | English |
Published: |
2010
|
Subjects: | |
Online Access: | http://hdl.handle.net/2152/ETD-UT-2009-12-411 |
Similar Items
-
Modeling Fragile X Syndrome in Drosophila
by: Małgorzata Drozd, et al.
Published: (2018-04-01) -
Fragile X Syndrome in Mentally Retarded Patients from Latvia
by: Daneberga Zanda, et al.
Published: (2009-01-01) -
Novel Features of dFMR1, the Drosophila Orthologue of the Fragile X Mental Retardation Protein
by: Annette Schenck, et al.
Published: (2002-10-01) -
Síndrome frágil X Fragile X syndrome
by: Miguel Lugones Botell, et al.
Published: (2006-09-01) -
Rôles fonctionnels de la SUMOylation de FMRP « Fragile X Mental Retardation Protein »
by: Khayachi, Anouar
Published: (2015)