Nuclear inclusions

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NHMRC Senior Research Fellow Department of Biochemistry and Molecular Biology | Faculty of Medicine, Dentistry and Health Sciences Level 2 South, Bio21 Molecular Science and Biotechnology Institute, 30 Flemington Road The University of Melbourne, Victoria 3010 Australia (1)
NHMRC Senior Research Fellow Department of Biochemistry and Molecular Biology | Faculty of Medicine, Dentistry and Health Sciences Level 2 South, Bio21 Molecular Science and Biotechnology Institute, 30 Flemington Road The University of Melbourne, Victoria 3010 Australia T: +61 3 8344 2530 | E: dhatters@unimelb.edu.au (1)
Principal Scientist, CSIR- Centre for Cellular and Molecular Biology, Hyderabad, India (1)
University of Geneva, Faculty of Medicine, 1211 Geneva, Switzerland (1)
University of Zurich Department of Quantitative Biomedicine (1)
Zbynek Zdrahal, Research group Proteomics, CEITEC-MU, Masaryk University, Kamenice 5, 625 00, Brno, Czech Republic (1)

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Depletion of p62 reduces nuclear inclusions and paradoxically ameliorates disease phenotypes in Huntington's model mice

Huntington's disease (HD) is a dominantly inherited genetic disease caused by mutant huntingtin (htt) protein with expanded polyglutamine tracts. A neuropathological hallmark of HD is the presence of neuronal inclusions of mutant htt. p62 is an important regulatory protein in selective autophagy, ...

ORGANISM(S): Mus musculus

2014-10-10 | E-GEOD-62210 | biostudies-arrayexpress

SILAC proteomics on MG132-induced nuclear aggregates

H1299 cells were labelled either with light (Lys0/Arg0) or heavy (Lys8/Arg10) amino acids and were either unstressed (light), stressed (heavy) with MG132 (15hrs) or stressed with MG132 and allowed to recover for 8hrs (light). Equal number of unstressed and MG132 stressed cells or MG132 stressed cell...

ORGANISM(S): Homo sapiens (Human)

2025-05-07 | PXD054637 | Pride

Depletion of p62 reduces nuclear inclusions and paradoxically ameliorates disease phenotypes in Huntington’s model mice

Huntington’s disease (HD) is a dominantly inherited genetic disease caused by mutant huntingtin (htt) protein with expanded polyglutamine tracts. A neuropathological hallmark of HD is the presence of neuronal inclusions of mutant htt. p62 is an important regulatory protein in selective autophagy, a ...

ORGANISM(S): Mus musculus

2014-10-10 | GSE62210 | GEO

A nuclear protein quality control system for elimination of nucleolus-related inclusions.

Not available

S-EPMC11791210 | biostudies-literature

Rapid flow cytometric measurement of protein inclusions and nuclear trafficking.

Not available

S-EPMC4981889 | biostudies-literature

RBM45 associates with nuclear stress bodies and forms nuclear inclusions during chronic cellular stress and in neurodegenerative diseases.

Not available

S-EPMC7318465 | biostudies-literature

Heterogeneous nuclear ribonucleoproteins R and Q accumulate in pathological inclusions in FTLD-FUS.