Zhao Y, Wang Y, Tulehalede A, Meng Z, Xu L, Bai H
Int J Mol Sci. 2025; 26(4).
PMID: 40003927
PMC: 11854990.
DOI: 10.3390/ijms26041459.
Atienzar-Aroca S, Kat M, Lopez-Castel A
Int J Mol Sci. 2024; 25(21).
PMID: 39519345
PMC: 11546515.
DOI: 10.3390/ijms252111794.
Mehmood H, Kasher P, Barrett-Jolley R, Walmsley G
BMC Vet Res. 2024; 20(1):477.
PMID: 39425123
PMC: 11488271.
DOI: 10.1186/s12917-024-04309-z.
Nait-Saidi R, Chartier A, Abgueguen E, Guedat P, Simonelig M
Open Biol. 2023; 13(4):230008.
PMID: 37042114
PMC: 10090878.
DOI: 10.1098/rsob.230008.
Ribot C, Soler C, Chartier A, Al Hayek S, Nait-Saidi R, Barbezier N
PLoS Genet. 2022; 18(1):e1010015.
PMID: 35025870
PMC: 8791501.
DOI: 10.1371/journal.pgen.1010015.
Nuclear poly(A) binding protein 1 (PABPN1) mediates zygotic genome activation-dependent maternal mRNA clearance during mouse early embryonic development.
Zhao L, Zhu Y, Wu Y, Pi S, Shen L, Fan H
Nucleic Acids Res. 2021; 50(1):458-472.
PMID: 34904664
PMC: 8855302.
DOI: 10.1093/nar/gkab1213.
Similarities of developmental gene expression changes in the brain between human and experimental animals: rhesus monkey, mouse, Zebrafish, and Drosophila.
Nakajima R, Hagihara H, Miyakawa T
Mol Brain. 2021; 14(1):135.
PMID: 34493287
PMC: 8425040.
DOI: 10.1186/s13041-021-00840-4.
Anti-prion Drugs Targeting the Protein Folding Activity of the Ribosome Reduce PABPN1 Aggregation.
Bamia A, Sinane M, Nait-Saidi R, Dhiab J, Keruzore M, Nguyen P
Neurotherapeutics. 2021; 18(2):1137-1150.
PMID: 33533011
PMC: 8423950.
DOI: 10.1007/s13311-020-00992-6.
Bruno-3 regulates sarcomere component expression and contributes to muscle phenotypes of myotonic dystrophy type 1.
Picchio L, Legagneux V, Deschamps S, Renaud Y, Chauveau S, Paillard L
Dis Model Mech. 2018; 11(5).
PMID: 29716962
PMC: 5992612.
DOI: 10.1242/dmm.031849.
Novel mouse models of oculopharyngeal muscular dystrophy (OPMD) reveal early onset mitochondrial defects and suggest loss of PABPN1 may contribute to pathology.
Vest K, Phillips B, Banerjee A, Apponi L, Dammer E, Xu W
Hum Mol Genet. 2017; 26(17):3235-3252.
PMID: 28575395
PMC: 5886286.
DOI: 10.1093/hmg/ddx206.
PABPN1 gene therapy for oculopharyngeal muscular dystrophy.
Malerba A, Klein P, Bachtarzi H, Jarmin S, Cordova G, Ferry A
Nat Commun. 2017; 8:14848.
PMID: 28361972
PMC: 5380963.
DOI: 10.1038/ncomms14848.
An Antibody to Detect Alanine-Expanded PABPN1: A New Tool to Study Oculopharyngeal Muscular Dystrophy.
Vest K, Apponi L, Banerjee A, Pavlath G, Corbett A
J Neuromuscul Dis. 2016; 2(4):439-446.
PMID: 27858752
PMC: 5207656.
DOI: 10.3233/JND-150111.
Protein quality control in the nucleus.
Jones R, Gardner R
Curr Opin Cell Biol. 2016; 40:81-89.
PMID: 27015023
PMC: 4887289.
DOI: 10.1016/j.ceb.2016.03.002.
Transgenic Drosophila for Investigating DUX4 and FRG1, Two Genes Associated with Facioscapulohumeral Muscular Dystrophy (FSHD).
Jones T, Parilla M, Jones P
PLoS One. 2016; 11(3):e0150938.
PMID: 26942723
PMC: 4778869.
DOI: 10.1371/journal.pone.0150938.
Regulated Intron Retention and Nuclear Pre-mRNA Decay Contribute to PABPN1 Autoregulation.
Bergeron D, Pal G, Beaulieu Y, Chabot B, Bachand F
Mol Cell Biol. 2015; 35(14):2503-17.
PMID: 25963658
PMC: 4475927.
DOI: 10.1128/MCB.00070-15.
RAN translation at CGG repeats induces ubiquitin proteasome system impairment in models of fragile X-associated tremor ataxia syndrome.
Oh S, He F, Krans A, Frazer M, Taylor J, Paulson H
Hum Mol Genet. 2015; 24(15):4317-26.
PMID: 25954027
PMC: 4492395.
DOI: 10.1093/hmg/ddv165.
Model organisms in the fight against muscular dystrophy: lessons from drosophila and Zebrafish.
Plantie E, Migocka-Patrzalek M, Daczewska M, Jagla K
Molecules. 2015; 20(4):6237-53.
PMID: 25859781
PMC: 6272363.
DOI: 10.3390/molecules20046237.
Mitochondrial dysfunction reveals the role of mRNA poly(A) tail regulation in oculopharyngeal muscular dystrophy pathogenesis.
Chartier A, Klein P, Pierson S, Barbezier N, Gidaro T, Casas F
PLoS Genet. 2015; 11(3):e1005092.
PMID: 25816335
PMC: 4376527.
DOI: 10.1371/journal.pgen.1005092.
RNA-binding protein misregulation in microsatellite expansion disorders.
Goodwin M, Swanson M
Adv Exp Med Biol. 2014; 825:353-88.
PMID: 25201111
PMC: 4483269.
DOI: 10.1007/978-1-4939-1221-6_10.
Getting folded: chaperone proteins in muscle development, maintenance and disease.
Smith D, Carland C, Guo Y, Bernstein S
Anat Rec (Hoboken). 2014; 297(9):1637-49.
PMID: 25125177
PMC: 4135391.
DOI: 10.1002/ar.22980.