|1.||Schwarz, Elisabeth: 4 articles (11/2015 - 02/2008)|
|2.||Bag, Jnanankur: 4 articles (01/2009 - 12/2005)|
|3.||Wang, Qishan: 3 articles (05/2008 - 12/2005)|
|4.||Golbik, Ralph: 2 articles (11/2015 - 02/2008)|
|5.||Hause, Gerd: 2 articles (11/2015 - 06/2012)|
|6.||Winter, Reno: 2 articles (11/2015 - 06/2012)|
|7.||Kühn, Uwe: 2 articles (06/2012 - 02/2008)|
|8.||Gray, Nicola K: 2 articles (04/2009 - 06/2006)|
|9.||Beauchemin, Chantal: 2 articles (07/2008 - 10/2007)|
|10.||Laliberté, Jean-François: 2 articles (07/2008 - 10/2007)|
09/01/2010 - "Surprisingly, poly(A)-binding protein 1 (PABP1), a predominantly cytoplasmic protein that is required for efficient translation initiation, is partially relocated to the nucleus during HSV-1 infection. "
09/01/2010 - "Poly(A)-binding protein 1 partially relocalizes to the nucleus during herpes simplex virus type 1 infection in an ICP27-independent manner and does not inhibit virus replication."
01/01/2009 - "Degradation of cellular mRNAs during Kaposi's sarcoma-associated herpesvirus infection is associated with hyperadenylation of transcripts and a relocalization of cytoplasmic poly(A)-binding proteins to the nucleus."
10/01/2007 - "The poly(A) binding protein is internalized in virus-induced vesicles or redistributed to the nucleolus during turnip mosaic virus infection."
01/01/2005 - "AMV CP is proposed to initiate infection by mimicking the function of the poly(A)-binding protein."
|2.||Oculopharyngeal Muscular Dystrophy
11/01/2006 - "Cultures of myoblasts isolated from cricopharyngeal muscles from patients with oculopharyngeal muscular dystrophy (OPMD) have been performed to study the effect of the expanded (GCG)8-13 repeat, located on the poly(A) binding protein nuclear-1 (PABPN1), on satellite cell phenotype. "
06/01/2013 - "Oculopharyngeal muscular dystrophy (OPMD) is caused by trinucleotide repeat expansion mutations in Poly(A) binding protein 1 (PABPN1). "
06/29/2012 - "Oculopharyngeal muscular dystrophy is a late-onset disease caused by an elongation of a natural 10-alanine segment within the N-terminal domain of the nuclear poly(A)-binding protein 1 (PABPN1) to maximally 17 alanines. "
05/01/2005 - "Intranuclear inclusions constitute a pathological hallmark of oculopharyngeal muscular dystrophy (OPMD), a dominantly inherited disease caused by (GCG) repeat expansions in the gene that encodes for nuclear poly(A) binding protein (PABPN1). "
09/01/2003 - "We reported a 52-year-old woman with oculopharyngeal muscular dystrophy (OPMD) harboring expanded (GCG) 13 mutation of the poly (A) binding protein 2 gene. "
01/01/2009 - "Expression of poly(A)-binding protein is upregulated during recovery from heat shock in HeLa cells."
11/01/1995 - "Parallel analysis of the poly(A)-binding protein detects no change in its abundance during heat shock or subsequent recovery. "
05/11/1994 - "An artifactual appearance that poly(A)-binding protein is specifically degraded by heat shock can result. "
05/11/1994 - "Heat shock-induced repression of proteolysis: poly(A)-binding protein degradation patterns can illusorily suggest its specific loss during heat shock."
10/01/1985 - "Heat shock increases the synthesis of the poly(A)-binding protein in HeLa cells."
01/01/2014 - "An evolutionarily conserved interaction of tumor suppressor protein Pdcd4 with the poly(A)-binding protein contributes to translation suppression by Pdcd4."
03/26/2010 - "MLLE (previously known as PABC) is a peptide-binding domain that is found in poly(A)-binding protein (PABP) and EDD (E3 isolated by differential display), a HECT E3 ubiquitin ligase also known as HYD (hyperplastic discs tumor suppressor) or UBR5. "
12/01/2008 - "TD-NEM (transcription-dependent nuclear export motif), a newly characterized nuclear export signal, mediates efficient nuclear export of several proteins including the von Hippel-Lindau (VHL) tumor suppressor and the poly(A)-binding protein (PABP1) in a manner that is dependent on ongoing RNA polymerase II (RNA PolII)-dependent transcription. "
04/01/2005 - "Five downregulated clones were isolated in the first SSH: (1) Aminopeptidase N, (2) Homosapiens tumor translationally-controlled protein 1, (3) Human ATP synthetase A chain, (4) Signal recognition particle A10, (5) Mitochondrial ATP synthetase/ATPase subunit 6. Four upregulated clones were isolated in the second SSH: (1) Calcium-binding protein A10, (2) Keratin 6A, (3) 45 kD MIP repetitive element containing splicing factor and (4) poly(A)-binding protein. "
|5.||Muscular Diseases (Myopathy)
11/01/2001 - "To answer this question, we examined five patients with the clinical characteristics of oculopharyngodistal myopathy for GCG expansion in poly(A)-binding protein nuclear 1 gene (previously called poly(A)-binding protein 2), the causative gene defect for oculopharyngeal muscular dystrophy. "
11/21/2001 - "Oculopharyngeal muscular dystrophy (OPMD) is a rare myopathy caused by polyalanine triplet repeat expansion in the gene for poly(A) binding protein 2 (PABP2) and is found in isolated cohorts throughout the world. "
06/01/2000 - "Oculopharyngeal muscular dystrophy is a dominantly inherited myopathy caused by a GCG/polyalanine expansion in the gene encoding poly(A)-binding protein 2. Myotonic dystrophy is a clinically variable multisystem disease caused by a CTG expansion in the 3' untranslated region of the myotonin gene. "
|1.||A-Form DNA (A-DNA)
|2.||Poly(A)-Binding Protein II
|4.||Proteins (Proteins, Gene)
|5.||Peptide Initiation Factors (Initiation Factor)
|6.||Eukaryotic Initiation Factor-4G (Eukaryotic Initiation Factor 4G)
|7.||Messenger RNA (mRNA)
|8.||RNA (Ribonucleic Acid)
|10.||Eukaryotic Initiation Factor-4F (EIF4F)