PMC Links for GEO Profiles (Select 46615394) - PMC

Select item 68318511.

Rewiring of the Human Mitochondrial Interactome during Neuronal Reprogramming Reveals Regulators of the Respirasome and Neurogenesis

Mohamed Taha Moutaoufik, Ramy Malty, Shahreen Amin, Qingzhou Zhang, Sadhna Phanse, Alla Gagarinova, Mara Zilocchi, Larissa Hoell, Zoran Minic, Maria Gagarinova, Hiroyuki Aoki, Jocelyn Stockwell, Matthew Jessulat, Florian Goebels, Kirsten Broderick, Nichollas E. Scott, James Vlasblom, Gabriel Musso, Bhanu Prasad, Eleonora Lamantea, Barbara Garavaglia, Alex Rajput, Kei Murayama, Yasushi Okazaki, Leonard J. Foster, Gary D. Bader, Francisco S. Cayabyab, Mohan Babu

iScience. 2019 Sep 27; 19: 1114–1132. Published online 2019 Sep 4. doi: 10.1016/j.isci.2019.08.057

PMCID:: PMC6831851

Abstract Article PDF–9.8M

Select item 31906942.

d-Amino Acid Oxidase Activity Is Inhibited by an Interaction with Bassoon Protein at the Presynaptic Active Zone

Michael Popiolek, John F. Ross, Erik Charych, Pranab Chanda, Eckart D. Gundelfinger, Stephen J. Moss, Nicholas J. Brandon, Mark H. Pausch

J Biol Chem. 2011 Aug 19; 286(33): 28867–28875. Published online 2011 Jun 23. doi: 10.1074/jbc.M111.262063

PMCID:: PMC3190694

Abstract Article PDF–1.0M

Select item 31780593.

Phylogenetic-based propagation of functional annotations within the Gene Ontology consortium

Pascale Gaudet, Michael S. Livstone, Suzanna E. Lewis, Paul D. Thomas

Brief Bioinform. 2011 Sep; 12(5): 449–462. Published online 2011 Aug 27. doi: 10.1093/bib/bbr042

PMCID:: PMC3178059

Abstract Article PDF–1.0M

Select item 28210604.

Late-onset Leigh syndrome in a patient with mitochondrial complex I NDUFS8 mutations

Vincent Procaccio, Douglas C. Wallace

Neurology. Author manuscript; available in PMC 2010 Feb 12.

Published in final edited form as: Neurology. 2004 May 25; 62(10): 1899. doi: 10.1212/01.wnl.0000125251.56131.65

PMCID:: PMC2821060

Abstract Article PDF–442K

Select item 27788445.

A mitochondrial protein compendium elucidates complex I disease biology

David J. Pagliarini, Sarah E. Calvo, Betty Chang, Sunil A. Sheth, Scott B. Vafai, Shao-En Ong, Geoffrey A. Walford, Canny Sugiana, Avihu Boneh, William K. Chen, David E. Hill, Marc Vidal, James G. Evans, David R. Thorburn, Steven A. Carr, Vamsi K. Mootha

Cell. Author manuscript; available in PMC 2009 Nov 18.

Published in final edited form as: Cell. 2008 Jul 11; 134(1): 112–123. doi: 10.1016/j.cell.2008.06.016

PMCID:: PMC2778844

Abstract Article PDF–1.2M

Select item 13776316.

The first nuclear-encoded complex I mutation in a patient with Leigh syndrome.

J Loeffen, J Smeitink, R Triepels, R Smeets, M Schuelke, R Sengers, F Trijbels, B Hamel, R Mullaart, L van den Heuvel

Am J Hum Genet. 1998 Dec; 63(6): 1598–1608. doi: 10.1086/302154

PMCID:: PMC1377631

Summary PDF–435K

Select item 1392417.

Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences

Mammalian Gene Collection (MGC) Program Team

Proc Natl Acad Sci U S A. 2002 Dec 24; 99(26): 16899–16903. Published online 2002 Dec 11. doi: 10.1073/pnas.242603899

PMCID:: PMC139241

Abstract Article PDF–118K

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