Nature Search

Author Correction: Deubiquitinase Usp12 functions noncatalytically to induce autophagy and confer neuroprotection in models of Huntington’s disease

Rebecca Aron
Pasquale Pellegrini
Steven Finkbeiner
Amendments and CorrectionsOpen Access21 Feb 2020
Nature Communications

Volume: 11, P: 1
Correction: Corrigendum: Identifying polyglutamine protein species in situ that best predict neurodegeneration

Jason Miller
Montserrat Arrasate
Steven Finkbeiner
Amendments and Corrections15 Feb 2012
Nature Chemical Biology

Volume: 8, P: 318
Publisher Correction: Deubiquitinase Usp12 functions noncatalytically to induce autophagy and confer neuroprotection in models of Huntington’s disease

Rebecca Aron
Pasquale Pellegrini
Steven Finkbeiner
Amendments and CorrectionsOpen Access07 May 2020
Nature Communications

Volume: 11, P: 1
A genomic screen in yeast implicates kynurenine 3-monooxygenase as a therapeutic target for Huntington disease

Flaviano Giorgini
Paolo Guidetti
Paul J Muchowski
Research03 Apr 2005
Nature Genetics

Volume: 37, P: 526-531
Modulation of neurodegeneration by molecular chaperones

Paul J. Muchowski
Jennifer L. Wacker
Reviews01 Jan 2005
Nature Reviews Neuroscience

Volume: 6, P: 11-22
Kynurenines in the mammalian brain: when physiology meets pathology

Tryptophan metabolism along the kynurenine pathway generates several neuroactive metabolites. Schwarcz and colleagues discuss the regulation of this pathway in the normal brain and in neurological and psychiatric disorders, and consider the potential therapeutic opportunities of targeting this pathway.

Robert Schwarcz
John P. Bruno
Hui-Qiu Wu
Reviews08 Jun 2012
Nature Reviews Neuroscience

Volume: 13, P: 465-477
Hsp70 and Hsp40 attenuate formation of spherical and annular polyglutamine oligomers by partitioning monomer

Jennifer L Wacker
M Hadi Zareie
Paul J Muchowski
Research14 Nov 2004
Nature Structural & Molecular Biology

Volume: 11, P: 1215-1222
Deubiquitinase Usp12 functions noncatalytically to induce autophagy and confer neuroprotection in models of Huntington’s disease

Abnormal accumulations of toxic proteins are often found in degenerating neurons. Here, Aron and colleagues show that non-enzymatic function of deubiquitinase Usp12 can mitigate neuronal cell death caused by mutant Huntingtin by inducing neuronal autophagic function.

Rebecca Aron
Pasquale Pellegrini
Steven Finkbeiner
ResearchOpen Access28 Sept 2018
Nature Communications

Volume: 9, P: 1-14
Identifying polyglutamine protein species in situ that best predict neurodegeneration

Conformation-specific antibodies and longitudinal tracking of individual neurons in situ identifies a toxic monomer species linked to Huntington's disease.

Jason Miller
Montserrat Arrasate
Steven Finkbeiner
Research30 Oct 2011
Nature Chemical Biology

Volume: 7, P: 925-934
The International Bathymetric Chart of the Arctic Ocean Version 5.0

Martin Jakobsson
Rezwan Mohammad
Larry Mayer
ResearchOpen Access21 Dec 2024
Scientific Data

Volume: 11, P: 1-22
Tracking protein aggregation and mislocalization in cells with flow cytometry

Protein localization changes in cells are monitored at high-throughput applying pulse-shape analysis to flow-cytometry data. The authors use the technique in combination with tetracysteine-based oligomer sensors to monitor toxic protein aggregation in a cellular model of Huntington's disease.

Yasmin M Ramdzan
Saskia Polling
Danny M Hatters
Research18 Mar 2012
Nature Methods

Volume: 9, P: 467-470
Forensic microbiology reveals that Neisseria animaloris infections in harbour porpoises follow traumatic injuries by grey seals

Geoffrey Foster
Adrian M. Whatmore
Lonneke L. IJsseldijk
ResearchOpen Access11 Oct 2019
Scientific Reports

Volume: 9, P: 1-8
NLRs at the intersection of cell death and immunity

In this Review, Jenny Ting and colleagues discuss the role of the NLR (nucleotide-binding domain, leucine-rich repeat containing) family proteins in various forms of cell death, including two newly recognized types of cell death — pyroptosis and pyronecrosis.

Jenny P.-Y. Ting
Stephen B. Willingham
Daniel T. Bergstralh
Reviews01 May 2008
Nature Reviews Immunology

Volume: 8, P: 372-379

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Author Correction: Deubiquitinase Usp12 functions noncatalytically to induce autophagy and confer neuroprotection in models of Huntington’s disease

Correction: Corrigendum: Identifying polyglutamine protein species in situ that best predict neurodegeneration

Publisher Correction: Deubiquitinase Usp12 functions noncatalytically to induce autophagy and confer neuroprotection in models of Huntington’s disease

A genomic screen in yeast implicates kynurenine 3-monooxygenase as a therapeutic target for Huntington disease

Modulation of neurodegeneration by molecular chaperones

Kynurenines in the mammalian brain: when physiology meets pathology

Hsp70 and Hsp40 attenuate formation of spherical and annular polyglutamine oligomers by partitioning monomer

Deubiquitinase Usp12 functions noncatalytically to induce autophagy and confer neuroprotection in models of Huntington’s disease

Identifying polyglutamine protein species in situ that best predict neurodegeneration

The International Bathymetric Chart of the Arctic Ocean Version 5.0

Tracking protein aggregation and mislocalization in cells with flow cytometry

Forensic microbiology reveals that Neisseria animaloris infections in harbour porpoises follow traumatic injuries by grey seals

NLRs at the intersection of cell death and immunity

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