PMC Links for GEO Profiles (Select 60461121) - PMC

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Items: 11

Select item 59867691.

COMP-prohibitin 2 interaction maintains mitochondrial homeostasis and controls smooth muscle cell identity

Yiting Jia, Meili Wang, Chenfeng Mao, Fang Yu, Yingbao Wang, Rui Xiao, Changtao Jiang, Lemin Zheng, Qingbo Xu, Ming Zheng, Yi Fu, Qinghua Hu, Wei Kong

Cell Death Dis. 2018 Jun; 9(6): 676. Published online 2018 Jun 4. doi: 10.1038/s41419-018-0703-x

PMCID:: PMC5986769

Abstract Article PDF–6.0M

Select item 46380452.

Interacting Network of the Gap Junction (GJ) Protein Connexin43 (Cx43) is Modulated by Ischemia and Reperfusion in the Heart

Tania Martins-Marques, Sandra Isabel Anjo, Paulo Pereira, Bruno Manadas, Henrique Girão

Mol Cell Proteomics. 2015 Nov; 14(11): 3040–3055. Published online 2015 Aug 27. doi: 10.1074/mcp.M115.052894

PMCID:: PMC4638045

Abstract Article PDF–2.5M

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 29240544.

Identification of a Substrate-binding Site in a Peroxisomal β-Oxidation Enzyme by Photoaffinity Labeling with a Novel Palmitoyl Derivative

Yoshinori Kashiwayama, Takenori Tomohiro, Kotomi Narita, Miyuki Suzumura, Tuomo Glumoff, J. Kalervo Hiltunen, Paul P. Van Veldhoven, Yasumaru Hatanaka, Tsuneo Imanaka

J Biol Chem. 2010 Aug 20; 285(34): 26315–26325. Published online 2010 Jun 21. doi: 10.1074/jbc.M110.104547

PMCID:: PMC2924054

Abstract Article PDF–1.5M

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 17160236.

D-3-hydroxyacyl-CoA dehydratase/D-3-hydroxyacyl-CoA dehydrogenase bifunctional protein deficiency: a newly identified peroxisomal disorder.

Y Suzuki, L L Jiang, M Souri, S Miyazawa, S Fukuda, Z Zhang, M Une, N Shimozawa, N Kondo, T Orii, T Hashimoto

Am J Hum Genet. 1997 Nov; 61(5): 1153–1162. doi: 10.1086/301599

PMCID:: PMC1716023

Summary Page Browse PDF–2.2M

Select item 13802087.

Mutational Spectrum of d-Bifunctional Protein Deficiency and Structure-Based Genotype-Phenotype Analysis

Sacha Ferdinandusse, Mari S. Ylianttila, Jolein Gloerich, M. Kristian Koski, Wendy Oostheim, Hans R. Waterham, J. Kalervo Hiltunen, Ronald J. A. Wanders, Tuomo Glumoff

Am J Hum Genet. 2006 Jan; 78(1): 112–124. Published online 2005 Nov 15. doi: 10.1086/498880

PMCID:: PMC1380208

Abstract Article PDF–1.4M

Select item 11360198.

Molecular cloning of a novel widely expressed human 80 kDa 17 beta-hydroxysteroid dehydrogenase IV.

J Adamski, T Normand, F Leenders, D Monté, A Begue, D Stéhelin, P W Jungblut, Y de Launoit

Biochem J. 1995 Oct 15; 311(Pt 2): 437–443. doi: 10.1042/bj3110437

PMCID:: PMC1136019

Summary Page Browse PDF–1.8M

Select item 1663439.

Pex13 Inactivation in the Mouse Disrupts Peroxisome Biogenesis and Leads to a Zellweger Syndrome Phenotype

Megan Maxwell, Jonas Bjorkman, Tam Nguyen, Peter Sharp, John Finnie, Carol Paterson, Ian Tonks, Barbara C. Paton, Graham F. Kay, Denis I. Crane

Mol Cell Biol. 2003 Aug; 23(16): 5947–5957. doi: 10.1128/MCB.23.16.5947-5957.2003

PMCID:: PMC166343

Abstract Article PDF–704K

Select item 13924110.

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

Select item 1927211.

Peroxisomal d-hydroxyacyl-CoA dehydrogenase deficiency: Resolution of the enzyme defect and its molecular basis in bifunctional protein deficiency

Elisabeth G. van Grunsven, Emanuel van Berkel, Lodewijk Ijlst, Peter Vreken, Johannis B. C. de Klerk, Jerzy Adamski, Hugh Lemonde, Peter T. Clayton, Dean A. Cuebas, Ronald J. A. Wanders

Proc Natl Acad Sci U S A. 1998 Mar 3; 95(5): 2128–2133. doi: 10.1073/pnas.95.5.2128