2024-03-28T10:17:10Z
http://repoint.unil.ch/oaiprovider/
oai:serval.unil.ch:BIB_3F5DA390795D
2024-03-23T02:15:35Z
openaire
documents
urnserval
serval:BIB_3F5DA390795D
Absence of the Fragile X Mental Retardation Protein results in defects of RNA editing of neuronal mRNAs in mouse.
10.1080/15476286.2017.1338232
28640668
000422628400015
Filippini
A.
author
Bonini
D.
author
Lacoux
C.
author
Pacini
L.
author
Zingariello
M.
author
Sancillo
L.
author
Bosisio
D.
author
Salvi
V.
author
Mingardi
J.
author
La Via
L.
author
Zalfa
F.
author
Bagni
C.
author
Barbon
A.
author
article
2017-11-02
2017-11-02
RNA biology
1555-8584
1547-6286
journal
14
11
1580-1591
Adenosine Deaminase/genetics
Adenosine Deaminase/metabolism
Animals
Cell Nucleus/metabolism
Cell Nucleus/ultrastructure
Cerebral Cortex/metabolism
Cerebral Cortex/pathology
Disease Models, Animal
Fragile X Mental Retardation Protein/genetics
Fragile X Mental Retardation Protein/metabolism
Fragile X Syndrome/genetics
Fragile X Syndrome/metabolism
Fragile X Syndrome/pathology
Gene Deletion
Hippocampus/metabolism
Hippocampus/pathology
Humans
Male
Mice
Mice, Knockout
Neurons/metabolism
Neurons/pathology
Phenotype
Primary Cell Culture
Protein Binding
RNA Editing
RNA, Messenger/genetics
RNA, Messenger/metabolism
RNA-Binding Proteins/genetics
RNA-Binding Proteins/metabolism
ADAR2
FMRP
Fragile X syndrome
RNA editing
eng
60_published
peer-reviewed
Publication types: Journal Article ; Research Support, Non-U.S. Gov't
Publication Status: ppublish
https://serval.unil.ch/notice/serval:BIB_3F5DA390795D
https://serval.unil.ch/resource/serval:BIB_3F5DA390795D.P001/REF.pdf
http://nbn-resolving.org/urn/resolver.pl?urn=urn:nbn:ch:serval-BIB_3F5DA390795D7
Creative Commons : Attribution-NonCommercial-NoDerivatives 4.0 International