相关参考文献
注意：仅列出部分参考文献，下载原文获取全部文献信息。Interaction of musleblind, CUG-BP1 and hnRNP H proteins in DM1-associated aberrant IR splicing
Sharan Paul et al.
EMBO JOURNAL (2006)
Reversible model of RNA toxicity and cardiac conduction defects in myotonic dystrophy
Mani S. Mahadevan et al.
NATURE GENETICS (2006)
MBNL1 and CUGBP1 modify expanded CUG-induced toxicity in a Drosophila model of myotonic dystrophy type 1
Maria de Haro et al.
HUMAN MOLECULAR GENETICS (2006)
DM2 intronic expansions:: evidence for CCUG accumulation without flanking sequence or effects on ZNF9 mRNA processing or protein expression
Jamie M. Margolis et al.
HUMAN MOLECULAR GENETICS (2006)
Glorund, a Drosophila hnRNP F/H homolog, is an ovarian repressor of nanos translation
Y Kalifa et al.
DEVELOPMENTAL CELL (2006)
Colocalization of muscleblind with RNA foci is separable from mis-regulation of alternative splicing in myotonic dystrophy
TH Ho et al.
JOURNAL OF CELL SCIENCE (2005)
Myotonic dystrophy associated expanded CUG repeat muscleblind positive ribonuclear foci are not toxic to Drosophila
JM Houseley et al.
HUMAN MOLECULAR GENETICS (2005)
HnRNP H inhibits nuclear export of mRNA containing expanded CUG repeats and a distal branch point sequence
DH Kim et al.
NUCLEIC ACIDS RESEARCH (2005)
The Spinocerebellar Ataxia 8 noncoding RNA causes neurodegeneration and associates with staufen in Drosophila
M Mutsuddi et al.
CURRENT BIOLOGY (2004)
The Drosophila Bruno paralogue Bru-3 specifically binds the EDEN translational repression element
J Delaunay et al.
NUCLEIC ACIDS RESEARCH (2004)
A targeted gain of function screen in the embryonic CNS of Drosophila
VL McGovern et al.
MECHANISMS OF DEVELOPMENT (2003)
Modelling human diseases in Drosophila and Caenorhabditis
CJ O'Kane
SEMINARS IN CELL & DEVELOPMENTAL BIOLOGY (2003)
Transgenic mouse models for myotonic dystrophy type 1 (DM1)
DG Wansink et al.
CYTOGENETIC AND GENOME RESEARCH (2003)
Living synaptic vesicle marker: Synaptotagmin-GFP
YQ Zhang et al.
GENESIS (2002)
EDEN-dependent translational repression of maternal mRNAs is conserved between Xenopus and Drosophila
N Ezzeddine et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2002)
Mice transgenic for the human myotonic dystrophy region with expanded CTG repeats display muscular and brain abnormalities
H Seznec et al.
HUMAN MOLECULAR GENETICS (2001)
The myotonic dystrophy expanded CUG repeat tract is necessary but not sufficient to disrupt C2C12 myoblast differentiation
JD Amack et al.
HUMAN MOLECULAR GENETICS (2001)
Myotonic dystrophy type 2 caused by a CCTG expansion in intron 1 of ZNF9
CL Liquori et al.
SCIENCE (2001)
Myotonic dystrophy in transgenic mice expressing an expanded CUG repeat
A Mankodi et al.
SCIENCE (2000)
Large, expanded repeats in SCA8 are not confined to patients with cerebellar ataxia
PF Worth et al.
NATURE GENETICS (2000)
Recruitment of human muscleblind proteins to (CUG)(n) expansions associated with myotonic dystrophy
JW Miller et al.
EMBO JOURNAL (2000)
分享论文
