PMC Links for GEO Profiles (Select 48574453) - PMC

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Items: 11

Select item 53972651.

Astrocytes induce proliferation of oligodendrocyte progenitor cells via connexin 47-mediated activation of the ERK/Id4 pathway

Zhaoyu Liu, Dan Xu, Shang Wang, Yi Chen, Zhen Li, Xiaoyan Gao, Lu Jiang, Yong Tang, Yan Peng

Cell Cycle. 2017; 16(7): 714–722. Published online 2017 Feb 22. doi: 10.1080/15384101.2017.1295183

PMCID:: PMC5397265

Abstract Article PDF–1.1M

Select item 40164932.

Extensive dysregulations of oligodendrocytic and astrocytic connexins are associated with disease progression in an amyotrophic lateral sclerosis mouse model

Yiwen Cui, Katsuhisa Masaki, Ryo Yamasaki, Shihoko Imamura, Satoshi O Suzuki, Shintaro Hayashi, Shinya Sato, Yuko Nagara, Mami F Kawamura, Jun-ichi Kira

J Neuroinflammation. 2014; 11: 42. Published online 2014 Mar 6. doi: 10.1186/1742-2094-11-42

PMCID:: PMC4016493

Abstract Article PDF–2.8M

Select item 36719133.

Functional Expression of the New Gap Junction Gene Connexin47 Transcribed in Mouse Brain and Spinal Cord Neurons

Barbara Teubner, Benjamin Odermatt, Martin Güldenagel, Goran Söhl, Joachim Degen, Feliksas F. Bukauskas, Jack Kronengold, Vytas K. Verselis, Yong Tae Jung, Christine A. Kozak, Karl Schilling, Klaus Willecke

J Neurosci. 2001 Feb 15; 21(4): 1117–1126. doi: 10.1523/JNEUROSCI.21-04-01117.2001

PMCID:: PMC3671913

Abstract Article PDF–574K

Select item 34434094.

Synaptic protein ubiquitination in rat brain revealed by antibody-based ubiquitome analysis

Chan-Hyun Na, Drew R. Jones, Yanling Yang, Xusheng Wang, Yanji Xu, Junmin Peng

J Proteome Res. Author manuscript; available in PMC 2013 Sep 7.

Published in final edited form as: J Proteome Res. 2012 Sep 7; 11(9): 4722–4732. Published online 2012 Aug 15. doi: 10.1021/pr300536k

PMCID:: PMC3443409

Abstract Article PDF–4.2M

Select item 31780595.

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 31312956.

Pathologic and Phenotypic Alterations in a Mouse Expressing a Connexin47 Missense Mutation That Causes Pelizaeus-Merzbacher–Like Disease in Humans

Oliver Tress, Marta Maglione, Armin Zlomuzica, Dennis May, Nikolai Dicke, Joachim Degen, Ekrem Dere, Helmut Kettenmann, Dieter Hartmann, Klaus Willecke

PLoS Genet. 2011 Jul; 7(7): e1002146. Published online 2011 Jul 7. doi: 10.1371/journal.pgen.1002146

PMCID:: PMC3131295

Abstract Article PDF–4.3M

Select item 30320647.

GJC2 Missense Mutations Cause Human Lymphedema

Robert E. Ferrell, Catherine J. Baty, Mark A. Kimak, Jenny M. Karlsson, Elizabeth C. Lawrence, Marlise Franke-Snyder, Stephen D. Meriney, Eleanor Feingold, David N. Finegold

Am J Hum Genet. 2010 Jun 11; 86(6): 943–948. doi: 10.1016/j.ajhg.2010.04.010

PMCID:: PMC3032064

Abstract Article PDF–1.0M

Select item 26402168.

Hereditary spastic paraplegia is a novel phenotype for GJA12/GJC2 mutations

Jennifer L. Orthmann-Murphy, Ettore Salsano, Charles K. Abrams, Alberto Bizzi, Graziella Uziel, Mona M. Freidin, Eleonora Lamantea, Massimo Zeviani, Steven S. Scherer, Davide Pareyson

Brain. 2009 Feb; 132(2): 426–438. Published online 2008 Dec 4. doi: 10.1093/brain/awn328

PMCID:: PMC2640216

Abstract Article PDF–894K

Select item 19370389.

Loss-of-function connexin47 mutations cause Pelizaeus-Merzbacher-like disease

Jennifer L. Orthmann-Murphy, Alan D. Enriquez, Charles K. Abrams, Steven S. Scherer

Mol Cell Neurosci. Author manuscript; available in PMC 2007 Aug 2.

Published in final edited form as: Mol Cell Neurosci. 2007 Apr; 34(4): 629–641. Published online 2007 Jan 25. doi: 10.1016/j.mcn.2007.01.010

PMCID:: PMC1937038

Abstract Article PDF–1.5M

Select item 155070410.

CONNEXIN-47 AND CONNEXIN-32 IN GAP JUNCTIONS OF OLIGODENDROCYTE SOMATA, MYELIN SHEATHS, PARANODAL LOOPS AND SCHMIDT-LANTERMAN INCISURES: IMPLICATIONS FOR IONIC HOMEOSTASIS AND POTASSIUM SIPHONING

N. KAMASAWA, A. SIK, M. MORITA, T. YASUMURA, K. G. V. DAVIDSON, J. I. NAGY, J. E. RASH

Neuroscience. Author manuscript; available in PMC 2006 Aug 18.

Published in final edited form as: Neuroscience. 2005; 136(1): 65–86. Published online 2005 Oct 3. doi: 10.1016/j.neuroscience.2005.08.027

Correction in:: volume 141 on page 545

PMCID:: PMC1550704

Abstract Article PDF–3.7M

Select item 121605911.

Mutations in the Gene Encoding Gap Junction Protein α12 (Connexin 46.6) Cause Pelizaeus-Merzbacher–Like Disease

Birgit Uhlenberg, Markus Schuelke, Franz Rüschendorf, Nico Ruf, Angela M. Kaindl, Marco Henneke, Holger Thiele, Gisela Stoltenburg-Didinger, Fuat Aksu, Haluk Topaloğlu, Peter Nürnberg, Christoph Hübner, Bernhard Weschke, Jutta Gärtner

Am J Hum Genet. 2004 Aug; 75(2): 251–260. Published online 2004 Jun 10. doi: 10.1086/422763