Related references
Note: Only part of the references are listed.The Nuclear Poly(A)-Binding Protein Interacts with the Exosome to Promote Synthesis of Noncoding Small Nucleolar RNAs
Jean-Francois Lemay et al.
MOLECULAR CELL (2010)
Native Functions of the Androgen Receptor Are Essential to Pathogenesis in a Drosophila Model of Spinobulbar Muscular Atrophy
Natalia B. Nedelsky et al.
NEURON (2010)
SCA1-like Disease in Mice Expressing Wild-Type Ataxin-1 with a Serine to Aspartic Acid Replacement at Residue 776
Lisa Duvick et al.
NEURON (2010)
PolyQ Disease: Too Many Qs, Too Much Function?
Ian H. Kratter et al.
NEURON (2010)
Prevention of oculopharyngeal muscular dystrophy by muscular expression of Llama single-chain intrabodies in vivo
Aymeric Chartier et al.
HUMAN MOLECULAR GENETICS (2009)
Tools for the study of ribosome-borne protein folding activity
Cécile Voisset et al.
Biotechnology Journal (2008)
Protein folding by domain v of Escherichia coli 23S rRNA:: Specificity of RNA-protein interactions
Dibyendu Samanta et al.
JOURNAL OF BACTERIOLOGY (2008)
Antihypertensive Drug Guanabenz Is Active In Vivo against both Yeast and Mammalian Prions
Deborah Tribouillard-Tanvier et al.
PLOS ONE (2008)
Protein Folding Activity of Ribosomal RNA Is a Selective Target of Two Unrelated Antiprion Drugs
Deborah Tribouillard-Tanvier et al.
PLOS ONE (2008)
A folded and functional protein domain in an amyloid-like fibril
Mirko Sackewitz et al.
PROTEIN SCIENCE (2008)
Effect of oculopharyngeal muscular dystrophy-associated extension of seven alanines on the fibrillation properties of the N-terminal domain of PABPN1
Grit Lodderstedt et al.
FEBS JOURNAL (2007)
A Drosophila model of oculopharyngeal muscular dystrophy reveals intrinsic toxicity of PABPN1
Aymeric Chartier et al.
EMBO JOURNAL (2006)
Trehalose reduces aggregate formation and delays pathology in a transgenic mouse model of oculopharyngeal muscular dystrophy
JE Davies et al.
HUMAN MOLECULAR GENETICS (2006)
Induction of HSP70 expression and recruitment of HSC70 and HSP70 in the nucleus reduce aggregation of a polyalanine expansion mutant of PABPN1 in HeLa cells
QS Wang et al.
HUMAN MOLECULAR GENETICS (2005)
An essential cytoplasmic function for the nuclear poly(A) binding protein, PABP2, in poly(A) tall length control and early development in Drosophila
B Benoit et al.
DEVELOPMENTAL CELL (2005)
Doxycycline attenuates and delays toxicity of the oculopharyngeal muscular dystrophy mutation in transgenic mice
JE Davies et al.
NATURE MEDICINE (2005)
In vivo aggregation properties of the nuclear poly(A)-binding protein PABPN1
JP Tavanez et al.
RNA (2005)
Oculopharyngeal muscular dystrophy-like nuclear inclusions are present in normal magnocellular neurosecretory neurons of the hypothalamus
MT Berciano et al.
HUMAN MOLECULAR GENETICS (2004)
Trehalose alleviates polyglutamine-mediated pathology in a mouse model of Huntington disease
M Tanaka et al.
NATURE MEDICINE (2004)
Congo red, doxycycline, and HSP70 overexpression reduce aggregate formation and cell death in cell models of oculopharyngeal muscular dystrophy
YP Bao et al.
JOURNAL OF MEDICAL GENETICS (2004)
Inclusion body formation reduces levels of mutant huntingtin and the risk of neuronal death
M Arrasate et al.
NATURE (2004)
Structure and function of poly(A) binding proteins
U Kühn et al.
BIOCHIMICA ET BIOPHYSICA ACTA-GENE STRUCTURE AND EXPRESSION (2004)
Can flies help humans treat neurodegenerative diseases?
JL Marsh et al.
BIOESSAYS (2004)
Involvement of the ubiquitin-proteasome pathway and molecular chaperones in oculopharyngeal muscular dystrophy
A Abu-Baker et al.
HUMAN MOLECULAR GENETICS (2003)
Isolation of drugs active against mammalian prions using a yeast-based screening assay
S Bach et al.
NATURE BIOTECHNOLOGY (2003)
The RNA binding domains of the nuclear poly(A)-binding protein
U Kühn et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2003)
Trinucleotide expansions leading to an extended poly-L-alanine segment in the poly (A) binding protein PABPN1 cause fibril formation
T Scheuermann et al.
PROTEIN SCIENCE (2003)
Oculopharyngeal muscular dystrophy: a late-onset polyalanine disease
B Brais
CYTOGENETIC AND GENOME RESEARCH (2003)
Biomedicine - Toxic proteins in neurodegenerative disease
JP Taylor et al.
SCIENCE (2002)
23S rRNA assisted folding of cytoplasmic malate dehydrogenase is distinctly different from its self-folding
SC Sanyal et al.
NUCLEIC ACIDS RESEARCH (2002)
Oligomerization of polyalanine expanded PABPN1 facilitates nuclear protein aggregation that is associated with cell death
XP Fan et al.
HUMAN MOLECULAR GENETICS (2001)
Nuclear inclusions in oculopharyngeal muscular dystrophy consist of poly(A) binding protein 2 aggregates which sequester poly(A) RNA
A Calado et al.
HUMAN MOLECULAR GENETICS (2000)
Ribosome-mediated folding of partially unfolded ricin A-chain
RH Argent et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2000)
Share Paper
