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Links from Protein

Items: 6

1.
FE65 and FE65L1 share common synaptic functions and genetically interact with the APP family in neuromuscular junction formation
Paul Strecker, Susann Ludewig, Marco Rust, Tabea A. Mundinger, Andreas Görlich, Elisa G. Krächan, Christina Mehrfeld, Joachim Herz, Martin Korte, Suzanne Y. Guénette, Stefan Kins
Sci Rep. 2016; 6: 25652. Published online 2016 May 11. doi: 10.1038/srep25652
PMCID:
PMC4899880
AbstractArticlePDF–2.1M
2.
Mutations in DCHS1 Cause Mitral Valve Prolapse
Ronen Durst, Kimberly Sauls, David S Peal, Annemarieke deVlaming, Katelynn Toomer, Maire Leyne, Monica Salani, Michael E. Talkowski, Harrison Brand, Maëlle Perrocheau, Charles Simpson, Christopher Jett, Matthew R. Stone, Florie Charles, Colby Chiang, Stacey N. Lynch, Nabila Bouatia-Naji, Francesca N. Delling, Lisa A. Freed, Christophe Tribouilloy, Thierry Le Tourneau, Hervé LeMarec, Leticia Fernandez-Friera, Jorge Solis, Daniel Trujillano, Stephan Ossowski, Xavier Estivill, Christian Dina, Patrick Bruneval, Adrian Chester, Jean-Jacques Schott, Kenneth D. Irvine, Yaopan Mao, Andy Wessels, Tahirali Motiwala, Michel Puceat, Yoshikazu Tsukasaki, Donald R. Menick, Harinath Kasiganesan, Xingju Nie, Ann-Marie Broome, Katherine Williams, Amanda Johnson, Roger R. Markwald, Xavier Jeunemaitre, Albert Hagege, Robert A. Levine, David J. Milan, Russell A. Norris, Susan A. Slaugenhaupt
Nature. Author manuscript; available in PMC 2016 Mar 3.
Published in final edited form as: Nature. 2015 Sep 3; 525(7567): 109–113. Published online 2015 Aug 10. doi: 10.1038/nature14670
PMCID:
PMC4720389
AbstractArticlePDF–3.6M
3.
An epigenomic role of Fe65 in the cellular response to DNA damage
Seungjin Ryu, Francesca Teles, Giuseppina Minopoli, Tommaso Russo, Michael G. Rosenfeld, Yousin Suh
Mutat Res. Author manuscript; available in PMC 2016 Jun 1.
Published in final edited form as: Mutat Res. 2015 Jun; 776: 40–47. Published online 2015 Jan 28. doi: 10.1016/j.mrfmmm.2015.01.006
PMCID:
PMC4531264
AbstractArticlePDF–1.6M
4.
FE65 and FE65L1 amyloid precursor protein–binding protein compound null mice display adult-onset cataract and muscle weakness
Jaehong Suh, Juliet A. Moncaster, Lirong Wang, Imran Hafeez, Joachim Herz, Rudolph E. Tanzi, Lee E. Goldstein, Suzanne Y. Guénette
FASEB J. 2015 Jun; 29(6): 2628–2639. Published online 2015 Mar 10. doi: 10.1096/fj.14-261453
PMCID:
PMC4447227
AbstractArticle
5.
Evidence of oxidative stress and in vivo neurotoxicity of beta-amyloid in a transgenic mouse model of Alzheimer's disease: a chronic oxidative paradigm for testing antioxidant therapies in vivo.
M. A. Pappolla, Y. J. Chyan, R. A. Omar, K. Hsiao, G. Perry, M. A. Smith, P. Bozner
Am J Pathol. 1998 Apr; 152(4): 871–877.
PMCID:
PMC1858256
SummaryPage BrowsePDF–2.9M
6.
Genetic Mapping of 262 Loci Derived from Expressed Sequences in a Murine Interspecific Cross Using Single-Strand Conformational Polymorphism Analysis
Kevin P. Brady, Lucy B. Rowe, Helen Her, Tamara J. Stevens, Janan Eppig, Daniel J. Sussman, James Sikela, David R. Beier
Genome Res. 1997 Nov; 7(11): 1085–1093. doi: 10.1101/gr.7.11.1085
PMCID:
PMC310685
AbstractArticlePDF–334K

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