PMC Links for Protein (Select 391224457) - PMC

Select item 50210901.

PEX2 is the E3 ubiquitin ligase required for pexophagy during starvation

Graeme Sargent, Tim van Zutphen, Tatiana Shatseva, Ling Zhang, Valeria Di Giovanni, Robert Bandsma, Peter Kijun Kim

J Cell Biol. 2016 Sep 12; 214(6): 677–690. doi: 10.1083/jcb.201511034

PMCID:: PMC5021090

Select item 33662562.

Peroxisome deficiency-induced ER stress and SREBP-2 pathway activation in the liver of newborn PEX2 knock-out mice

Werner J. Kovacs, Khanichi N. Charles, Katharina M. Walter, Janis E. Shackelford, Thomas M. Wikander, Michael J. Richards, Steven J. Fliesler, Skaidrite K. Krisans, Phyllis L. Faust

Biochim Biophys Acta. Author manuscript; available in PMC 2013 Jun 1.

Published in final edited form as: Biochim Biophys Acta. 2012 Jun; 1821(6): 895–907. Published online 2012 Mar 13. doi: 10.1016/j.bbalip.2012.02.011

PMCID:: PMC3366256

Abstract Article PDF–2.2M

Select item 28196713.

Alpha-Synuclein Abnormalities in Mouse Models of Peroxisome Biogenesis Disorders

Eugenia Yakunin, Ann Moser, Virginie Loeb, Ann Saada Reisch, Phyllis Faust, Denis I. Crane, Myriam Baes, Ronit Sharon

J Neurosci Res. Author manuscript; available in PMC 2010 Mar 1.

Published in final edited form as: J Neurosci Res. 2010 Mar; 88(4): 866. doi: 10.1002/jnr.22246

PMCID:: PMC2819671

Abstract Article PDF–654K

Select item 26862524.

The Level of the Transcription Factor Pax6 Is Essential for Controlling the Balance between Neural Stem Cell Self-Renewal and Neurogenesis

Stephen N. Sansom, Dean S. Griffiths, Andrea Faedo, Dirk-Jan Kleinjan, Youlin Ruan, James Smith, Veronica van Heyningen, John L. Rubenstein, Frederick J. Livesey

PLoS Genet. 2009 Jun; 5(6): e1000511. Published online 2009 Jun 12. doi: 10.1371/journal.pgen.1000511

PMCID:: PMC2686252

Abstract Article PDF–4.5M

Select item 26523115.

Peroxisome Deficiency Causes a Complex Phenotype because of Hepatic SREBP/Insig Dysregulation Associated with Endoplasmic Reticulum Stress

Werner J. Kovacs, Khanichi N. Tape, Janis E. Shackelford, Thomas M. Wikander, Michael J. Richards, Steven J. Fliesler, Skaidrite K. Krisans, Phyllis L. Faust

J Biol Chem. 2009 Mar 13; 284(11): 7232–7245. doi: 10.1074/jbc.M809064200

PMCID:: PMC2652311

Abstract Article PDF–1.4M

Select item 21402006.

Targeted Deletion of the PEX2 Peroxisome Assembly Gene in Mice Provides a Model for Zellweger Syndrome, a Human Neuronal Migration Disorder

Phyllis L. Faust, Mary E. Hatten

J Cell Biol. 1997 Dec 1; 139(5): 1293–1305. doi: 10.1083/jcb.139.5.1293

PMCID:: PMC2140200

Abstract Article PDF–1.0M

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