Cytoplasmic Targeting of Mutant Poly(A)-Binding Protein Nuclear 1 Suppresses Protein Aggregation and Toxicity in Oculopharyngeal Muscular Dystrophy-Reference-Cited by-同舟云学术

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Cytoplasmic Targeting of Mutant Poly(A)-Binding Protein Nuclear 1 Suppresses Protein Aggregation and Toxicity in Oculopharyngeal Muscular Dystrophy

Published:2005-06-22 Issue:9 Volume:6 Page:766-779
ISSN:1398-9219
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language:en
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Author:

Abu-Baker Aida,Laganiere Simon,Fan Xueping,Laganiere Janet,Brais Bernard,Rouleau Guy A.

Publisher

Wiley

Subject

Cell Biology,Genetics,Molecular Biology,Biochemistry,Structural Biology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1600-0854.2005.00315.x/fullpdf

Reference65 articles.

1. Short GCG expansions in the PABP2 gene cause oculopharyngeal muscular dystrophy;Brais;Nat Genet,1998

2. Nuclear inclusions in oculopharyngeal dystrophy;Tome;Acta Neuropathol (Berl),1980

3. Altered growth and branching patterns in synpolydactyly caused by mutations in HOXD13;Muragaki;Science,1996

4. Mutations involving the transcription factor CBFA1 cause cleidocranial dysplasia;Mundlos;Cell,1997

5. Holoprosencephaly due to mutations in ZIC2, a homologue of Drosophila odd-paired;Brown;Nat Genet,1998

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1. Les agrégats nucléaires dans la dystrophie musculaire oculopharyngée;médecine/sciences;2022-12

2. Assessment of PABPN1 nuclear inclusions on a large cohort of patients and in a human xenograft model of oculopharyngeal muscular dystrophy;Acta Neuropathologica;2022-10-05

3. Nuclear poly(A) binding protein 1 (PABPN1) mediates zygotic genome activation-dependent maternal mRNA clearance during mouse early embryonic development;Nucleic Acids Research;2021-12-14

4. RNA-Based Therapy Utilizing Oculopharyngeal Muscular Dystrophy Transcript Knockdown and Replacement;Molecular Therapy - Nucleic Acids;2019-04

5. Dysfunctional transcripts are formed by alternative polyadenylation in OPMD;Oncotarget;2017-09-05

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