PMC Links for Nucleotide (Select 1647814482) - PMC

Select item 55064011.

Autophagy compensates impaired energy metabolism in CLPXP‐deficient Podospora anserina strains and extends healthspan

Laura Knuppertz, Heinz D. Osiewacz

Aging Cell. 2017 Aug; 16(4): 704–715. Published online 2017 Apr 27. doi: 10.1111/acel.12600

PMCID:: PMC5506401

Article PDF–1.5M

Select item 51980082.

A Novel Missense Mutation in the CLPP Gene Causing Perrault Syndrome Type 3 in a Turkish Family

Fatma Dursun, Hussein Sheikh Ali Mohamoud, Noreen Karim, Muhammad Naeem, Musharraf Jelani, Heves Kırmızıbekmez

J Clin Res Pediatr Endocrinol. 2016 Dec; 8(4): 472–477. Published online 2016 Dec 1. doi: 10.4274/jcrpe.2717

PMCID:: PMC5198008

Article PDF–424K

Select item 49367143.

The Mitochondrial Unfoldase-Peptidase Complex ClpXP Controls Bioenergetics Stress and Metastasis

Jae Ho Seo, Dayana B. Rivadeneira, M. Cecilia Caino, Young Chan Chae, David W. Speicher, Hsin-Yao Tang, Valentina Vaira, Silvano Bosari, Alessandro Palleschi, Paolo Rampini, Andrew V. Kossenkov, Lucia R. Languino, Dario C. Altieri

PLoS Biol. 2016 Jul; 14(7): e1002507. Published online 2016 Jul 7. doi: 10.1371/journal.pbio.1002507

PMCID:: PMC4936714

Article PDF–11M

Select item 49315574.

Loss of CLPP alleviates mitochondrial cardiomyopathy without affecting the mammalian UPR^mt

Dominic Seiferling, Karolina Szczepanowska, Christina Becker, Katharina Senft, Steffen Hermans, Priyanka Maiti, Tim König, Alexandra Kukat, Aleksandra Trifunovic

EMBO Rep. 2016 Jul; 17(7): 953–964. Published online 2016 May 6. doi: 10.15252/embr.201642077

PMCID:: PMC4931557

Article PDF–2.2M

Select item 12193535.

A human homologue of Escherichia coli ClpP caseinolytic protease: recombinant expression, intracellular processing and subcellular localization.

T J Corydon, P Bross, H U Holst, S Neve, K Kristiansen, N Gregersen, L Bolund

Biochem J. 1998 Apr 1; 331(Pt 1): 309–316. doi: 10.1042/bj3310309

PMCID:: PMC1219353

Summary PDF–373K

Select item 52169716.

LACE1 interacts with p53 and mediates its mitochondrial translocation and apoptosis

Jana Cesnekova, Jana Spacilova, Hana Hansikova, Josef Houstek, Jiri Zeman, Lukas Stiburek

Oncotarget. 2016 Jul 26; 7(30): 47687–47698. Published online 2016 Jun 13. doi: 10.18632/oncotarget.9959

PMCID:: PMC5216971

Article PDF–6.3M

Select item 51105157.

Specific MRI Abnormalities Reveal Severe Perrault Syndrome due to CLPP Defects

Tom E. J. Theunissen, Radek Szklarczyk, Mike Gerards, Debby M. E. I. Hellebrekers, Elvira N. M. Mulder-Den Hartog, Jo Vanoevelen, Rick Kamps, Bart de Koning, S. Lane Rutledge, Thomas Schmitt-Mechelke, Carola G. M. van Berkel, Marjo S. van der Knaap, Irenaeus F. M. de Coo, Hubert J. M. Smeets

Front Neurol. 2016; 7: 203. Published online 2016 Nov 16. doi: 10.3389/fneur.2016.00203

PMCID:: PMC5110515

Article PDF–1.4M

Select item 49825218.

DNA Microarray Highlights Nrf2-Mediated Neuron Protection Targeted by Wasabi-Derived Isothiocyanates in IMR-32 Cells

Phoebe Zapanta Trio, Satoru Fujisaki, Shunsuke Tanigawa, Ayami Hisanaga, Kozue Sakao, De-Xing Hou

Gene Regul Syst Bio. 2016; 10: 73–83. Published online 2016 Aug 11. doi: 10.4137/GRSB.S39440

PMCID:: PMC4982521

Article PDF–1.6M

Select item 36173819.

Perrault Syndrome Is Caused by Recessive Mutations in CLPP, Encoding a Mitochondrial ATP-Dependent Chambered Protease

Emma M. Jenkinson, Atteeq U. Rehman, Tom Walsh, Jill Clayton-Smith, Kwanghyuk Lee, Robert J. Morell, Meghan C. Drummond, Shaheen N. Khan, Muhammad Asif Naeem, Bushra Rauf, Neil Billington, Julie M. Schultz, Jill E. Urquhart, Ming K. Lee, Andrew Berry, Neil A. Hanley, Sarju Mehta, Deirdre Cilliers, Peter E. Clayton, Helen Kingston, Miriam J. Smith, Thomas T. Warner, University of Washington Center for Mendelian Genomics, Graeme C. Black, Dorothy Trump, Julian R.E. Davis, Wasim Ahmad, Suzanne M. Leal, Sheikh Riazuddin, Mary-Claire King, Thomas B. Friedman, William G. Newman

Am J Hum Genet. 2013 Apr 4; 92(4): 605–613. doi: 10.1016/j.ajhg.2013.02.013

PMCID:: PMC3617381

Article PDF–1.1M

Select item 250488710.

BACH1 Is a Specific Repressor of HMOX1 That Is Inactivated by Arsenite

John F. Reichard, Maureen A. Sartor, Alvaro Puga

J Biol Chem. 2008 Aug 15; 283(33): 22363–22370. doi: 10.1074/jbc.M801784200

PMCID:: PMC2504887

Article PDF–342K

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