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The Journal of Biological Chemistry|August 26, 2006
Age-specific CUGBP1-eIF2 complex increases translation of CCAAT/enhancer-binding protein beta in old liverLubov T Timchenko, Elizabeth Salisbury, Guo-Li Wang, et al.
Biomedical Science|January 1, 1991
Rat DNA sequence associated with a complex form of DNA polymerase alpha in nonregenerating liver interacts with a ubiquitous transcription/replication factor Oct-1N A Timchenko, O P Zhuchenko, L T Timchenko, et al.
Biochimie|January 1, 1995
The mouse Kin-17 gene codes for a new protein involved in DNA transactions and is akin to the bacterial RecA proteinA Tissier, P Kannouche, D S Biard, et al.
Experimental Cell Research|June 24, 2008
Ectopic expression of cyclin D3 corrects differentiation of DM1 myoblasts through activation of RNA CUG-binding protein, CUGBP1Elizabeth Salisbury, Keiko Sakai, Benedikt Schoser, et al.
The Journal of Clinical Investigation|November 20, 2012
GSK3β mediates muscle pathology in myotonic dystrophyKarlie Jones, Christina Wei, Polina Iakova, et al.
Nucleic Acids Research|November 15, 1996
Identification of a (CUG)n triplet repeat RNA-binding protein and its expression in myotonic dystrophyL T Timchenko, J W Miller, N A Timchenko, et al.
The American Journal of Pathology|July 11, 2009
Expression of RNA CCUG repeats dysregulates translation and degradation of proteins in myotonic dystrophy 2 patientsElizabeth Salisbury, Benedikt Schoser, Christiane Schneider-Gold, et al.
Cell Death & Disease|October 21, 2016
Functional KCa1.1 channels are crucial for regulating the proliferation, migration and differentiation of human primary skeletal myoblastsRajeev B Tajhya, Xueyou Hu, Mark R Tanner, et al.
Neuromuscular Disorders : NMD|December 17, 2013
Most expression and splicing changes in myotonic dystrophy type 1 and type 2 skeletal muscle are shared with other muscular dystrophiesLinda L Bachinski, Keith A Baggerly, Valerie L Neubauer, et al.
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