PMC Links for GEO Profiles (Select 35264856) - PMC

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Items: 10

Select item 45873271.

Sequential Elution Interactome Analysis of the Mind Bomb 1 Ubiquitin Ligase Reveals a Novel Role in Dendritic Spine Outgrowth

Joseph Mertz, Haiyan Tan, Vishwajeeth Pagala, Bing Bai, Ping-Chung Chen, Yuxin Li, Ji-Hoon Cho, Timothy Shaw, Xusheng Wang, Junmin Peng

Mol Cell Proteomics. 2015 Jul; 14(7): 1898–1910. Published online 2015 Apr 30. doi: 10.1074/mcp.M114.045898

PMCID:: PMC4587327

Abstract Article PDF–2.6M

Select item 31780592.

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 28108553.

α1-Syntrophin Mutations Identified in Sudden Infant Death Syndrome Cause an Increase in Late Cardiac Sodium Current

Jianding Cheng, David W. Van Norstrand, Argelia Medeiros-Domingo, Carmen Valdivia, Bi-hua Tan, Bin Ye, Stacie Kroboth, Matteo Vatta, David J. Tester, Craig T. January, Jonathan C. Makielski, Michael J. Ackerman

Circ Arrhythm Electrophysiol. Author manuscript; available in PMC 2010 Dec 1.

Published in final edited form as: Circ Arrhythm Electrophysiol. 2009 Dec; 2(6): 667–676. doi: 10.1161/CIRCEP.109.891440

PMCID:: PMC2810855

Abstract Article PDF–1.3M

Select item 27267174.

α-1-Syntrophin Mutation and the Long-QT Syndrome: A Disease of Sodium Channel Disruption

Geru Wu, Tomohiko Ai, Jeffrey J. Kim, Bhagyalaxmi Mohapatra, Yutao Xi, Zhaohui Li, Shahrzad Abbasi, Enkhsaikhan Purevjav, Kaveh Samani, Michael J Ackerman, Ming Qi, Arthur J. Moss, Wataru Shimizu, Jeffrey A. Towbin, Jie Cheng, Matteo Vatta

Circ Arrhythm Electrophysiol. Author manuscript; available in PMC 2009 Aug 13.

Published in final edited form as: Circ Arrhythm Electrophysiol. 2008 Aug; 1(3): 193–201. doi: 10.1161/CIRCEP.108.769224

PMCID:: PMC2726717

Abstract Article PDF–2.2M

Select item 24421275.

Syntrophin mutation associated with long QT syndrome through activation of the nNOS–SCN5A macromolecular complex

Kazuo Ueda, Carmen Valdivia, Argelia Medeiros-Domingo, David J. Tester, Matteo Vatta, Gianrico Farrugia, Michael J. Ackerman, Jonathan C. Makielski

Proc Natl Acad Sci U S A. 2008 Jul 8; 105(27): 9355–9360. Published online 2008 Jun 30. doi: 10.1073/pnas.0801294105

PMCID:: PMC2442127

Abstract Article PDF–1.3M

Select item 21507016.

Absence of α-Syntrophin Leads to Structurally Aberrant Neuromuscular Synapses Deficient in Utrophin

Marvin E. Adams, Neal Kramarcy, Stuart P. Krall, Susana G. Rossi, Richard L. Rotundo, Robert Sealock, Stanley C. Froehner

J Cell Biol. 2000 Sep 18; 150(6): 1385–1398. doi: 10.1083/jcb.150.6.1385

PMCID:: PMC2150701

Abstract Article PDF–923K

Select item 20398577.

MLC1 is associated with the Dystrophin-Glycoprotein Complex at astrocytic endfeet

Ilja Boor, Machiel Nagtegaal, Wouter Kamphorst, Paul van der Valk, Jan C. Pronk, Jack van Horssen, Argirios Dinopoulos, Kevin E. Bove, Ignacio Pascual-Castroviejo, Francesco Muntoni, Raúl Estévez, Gert C. Scheper, Marjo S. van der Knaap

Acta Neuropathol. 2007 Oct; 114(4): 403–410. Published online 2007 Jul 13. doi: 10.1007/s00401-007-0247-0