Disease Phenotypes in a Mouse Model of RNA Toxicity Are Independent of Protein Kinase Cα and Protein Kinase Cβ

Targeting PKCθ in skeletal muscle and muscle diseases: good or bad?: Table 1

(2014) Valeria Marrocco et al.   BIOCHEMICAL SOCIETY TRANSACTIONS

Protein kinase C theta (PKCθ) modulates the ClC-1 chloride channel activity and skeletal muscle phenotype: a biophysical and gene expression study in mouse models lacking the PKCθ

(2014) Giulia Maria Camerino et al.   PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY

Development of an AP-FRET Based Analysis for Characterizing RNA-Protein Interactions in Myotonic Dystrophy (DM1)

(2014) Shagufta Rehman et al.   PLoS One

Suppression of protein kinase C theta contributes to enhanced myogenesis In vitro via IRS1 and ERK1/2 phosphorylation

(2013) Joseph S Marino et al.   BMC CELL BIOLOGY

Compound loss of muscleblind-like function in myotonic dystrophy

(2013) Kuang-Yung Lee et al.   EMBO Molecular Medicine

Progressive impairment of muscle regeneration in muscleblind-like 3 isoform knockout mice

(2013) Michael G. Poulos et al.   HUMAN MOLECULAR GENETICS

Evaluating the effects of CELF1 deficiency in a mouse model of RNA toxicity

(2013) Yun Kyoung Kim et al.   HUMAN MOLECULAR GENETICS

High-content screening identifies small molecules that remove nuclear foci, affect MBNL distribution and CELF1 protein levels via a PKC-independent pathway in myotonic dystrophy cell lines

(2013) Ami Ketley et al.   HUMAN MOLECULAR GENETICS

GSK3β mediates muscle pathology in myotonic dystrophy

(2012) Karlie Jones et al.   JOURNAL OF CLINICAL INVESTIGATION

PKC Theta Ablation Improves Healing in a Mouse Model of Muscular Dystrophy

(2012) Luca Madaro et al.   PLoS One

Zebrafish deficient for Muscleblind-like 2 exhibit features of myotonic dystrophy

(2011) L. E. Machuca-Tzili et al.   Disease Models & Mechanisms

PKCθ signaling is required for myoblast fusion by regulating the expression of caveolin-3 and β1D integrin upstream focal adhesion kinase

(2011) Luca Madaro et al.   MOLECULAR BIOLOGY OF THE CELL

Expansion of CUG RNA repeats causes stress and inhibition of translation in myotonic dystrophy 1 (DM1) cells

(2010) Claudia Huichalaf et al.   FASEB JOURNAL

CUGBP1 overexpression in mouse skeletal muscle reproduces features of myotonic dystrophy type 1

(2010) Amanda J. Ward et al.   HUMAN MOLECULAR GENETICS

Knockout of the predominant conventional PKC isoform, PKCα, in mouse skeletal muscle does not affect contraction-stimulated glucose uptake

(2009) Thomas E. Jensen et al.   AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM

PKC inhibition ameliorates the cardiac phenotype in a mouse model of myotonic dystrophy type 1

(2009) Guey-Shin Wang et al.   JOURNAL OF CLINICAL INVESTIGATION

Muscleblind-like 2 (Mbnl2) -deficient mice as a model for myotonic dystrophy

(2008) Minqi Hao et al.   DEVELOPMENTAL DYNAMICS

Ectopic expression of cyclin D3 corrects differentiation of DM1 myoblasts through activation of RNA CUG-binding protein, CUGBP1

(2008) Elizabeth Salisbury et al.   EXPERIMENTAL CELL RESEARCH