Oculopharyngeal muscular dystrophy-like nuclear inclusions are present in normal magnocellular neurosecretory neurons of the hypothalamus
Author:
Publisher
Oxford University Press (OUP)
Subject
Genetics(clinical),Genetics,Molecular Biology,General Medicine
Link
http://academic.oup.com/hmg/article-pdf/13/8/829/6948782/ddh101.pdf
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1. Emerging and established biomarkers of oculopharyngeal muscular dystrophy;Neuromuscular Disorders;2023-11
2. Pharyngeal pathology in a mouse model of oculopharyngeal muscular dystrophy is associated with impaired basal autophagy in myoblasts;Frontiers in Cell and Developmental Biology;2022-10-14
3. Proteomic analysis reveals that wildtype and alanine-expanded nuclear poly(A)-binding protein exhibit differential interactions in skeletal muscle;Journal of Biological Chemistry;2019-05
4. Post-transcriptional regulation of Pabpn1 by the RNA binding protein HuR;Nucleic Acids Research;2018-06-25
5. Novel mouse models of oculopharyngeal muscular dystrophy (OPMD) reveal early onset mitochondrial defects and suggest loss of PABPN1 may contribute to pathology;Human Molecular Genetics;2017-05-29
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