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Cell Death and Differentiation (2)
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Showing 1–8 of 8 results

Advanced filters: Author: Warunee Dansithong Clear advanced filters

Staufen1 links RNA stress granules and autophagy in a model of neurodegeneration

Spinocerebellar ataxia type 2 (SCA2) is caused by polyglutamine repeats in the ATXN2 protein. Here the authors demonstrate that Staufen1, known to be an RNA-binding protein, interacts with ATXN2 and contributes to pathology in a mouse model of SCA2.

Sharan Paul
Warunee Dansithong
Stefan M. Pulst
ResearchOpen Access07 Sept 2018
Nature Communications

Volume: 9, P: 1-14
Correction: Staufen 1 amplifies proapoptotic activation of the unfolded protein response

Mandi Gandelman
Warunee Dansithong
Stefan M. Pulst
Amendments and Corrections19 Jan 2021
Cell Death & Differentiation

Volume: 28, P: 3374
Targeting STAU1 prevents p53 apoptotic signaling in neurodegeneration

Mandi Gandelman
Sharan Paul
Stefan M. Pulst
ResearchOpen Access27 Oct 2025
Cell Death & Disease

Volume: 16, P: 1-12
Muscleblind-like 3 deficit results in a spectrum of age-associated pathologies observed in myotonic dystrophy

Jongkyu Choi
Donald M. Dixon
Sita Reddy
ResearchOpen Access03 Aug 2016
Scientific Reports

Volume: 6, P: 1-10
Antisense oligonucleotide therapy for spinocerebellar ataxia type 2

Antisense oligonucleotides against ATXN2 improved motor neuron function and restored firing frequency in cerebellar Purkinje cells in mouse models of spinocerebellar ataxia type 2.

Daniel R. Scoles
Pratap Meera
Stefan M. Pulst
Research12 Apr 2017
Nature

Volume: 544, P: 362-366
Methods and feasibility study for exome sequencing as a universal second-tier test in newborn screening

Nicole Ruiz-Schultz
David Sant
Andreas Rohrwasser
Research13 Jan 2021
Genetics in Medicine

Volume: 23, P: 767-776
Staufen 1 amplifies proapoptotic activation of the unfolded protein response

Mandi Gandelman
Warunee Dansithong
Stefan M. Pulst
ResearchOpen Access15 May 2020
Cell Death & Differentiation

Volume: 27, P: 2942-2951
Toward newborn screening of metachromatic leukodystrophy: results from analysis of over 27,000 newborn dried blood spots

Xinying Hong
Jessica Daiker
Michael H. Gelb
Research20 Nov 2020
Genetics in Medicine

Volume: 23, P: 555-561