Work

Correction: A dual druggable genome-wide siRNA and compound library screening approach identifies modulators of parkin recruitment to mitochondria.

Year: 2020

Type: erratum

Abstract: VOLUME 295 (2020) PAGES 3285–3300 An incorrect graph was used in Fig. 5C. This error has now been corrected. Additionally, some of the statistics reported in the legend and text referring to Fig. 5C were incorrect. The F statistics for Fig. 5C should state Fken(3,16) = 7.454, p < 0.01; FCCCP(1,16) = 102.9, p < 0.0001; Finteraction(3,16) = 7.480, p < 0.01. This correction does not affect the results or conclusions of this work.

Source: Journal of Biological Chemistry

DOI: 10.1074/jbc.aac120.013668

Authors: Helen L. Scott, Nicola Buckner, Francesc Fernandez-Albert, Elisa Pedone, Lorena Postiglione, Gongyu Shi, Nicholas Allen, Liang-Fong Wong, Lorenzo Magini, Lucia Marucci, Gregory A. O'Sullivan, Sarah Cole, Justin Powell, Peter Maycox, James B. Uney

Language: English

Topic: Parkinson's Disease Mechanisms and Treatments

Subfield: Clinical Neurology

Field: Medicine

Domain: Health Sciences

SDG: Good health and well-being

Open Access status: hybrid

Estimated APC paid: $3,430

Funders: Medical Research Council, Engineering and Physical Sciences Research Council, Biotechnology and Biological Sciences Research Council

Awards: Functions of the SAFB family identified by iCLIP, Novel mechanisms controlling the cellular stress response, BrisSynBio: Bristol Centre for Synthetic Biology, Transplantation of genetically modified haematopoietic stem cells for Friedreich's Ataxia, AUTOMATIC CELL FATE ENGINEERING USING MICROFLUIDICS DEVICES, Unravelling the role of beta-catenin in ground state pluripotency

OpenAlex ID: W4251918366

Cites: 65

Cited by: 1

Related to: 10