Published in Nat Genet on July 01, 2004
Genome-wide analysis of conservation and divergence of microsatellites in rice. Mol Genet Genomics (2009) 0.84
Expression levels of DNA replication and repair genes predict regional somatic repeat instability in the brain but are not altered by polyglutamine disease protein expression or age. Hum Mol Genet (2013) 0.84
Divergent mitochondrial and endoplasmic reticulum association of DMPK splice isoforms depends on unique sequence arrangements in tail anchors. Mol Cell Biol (2005) 0.80
Chemotherapy induced microsatellite instability and loss of heterozygosity in chromosomes 2, 5, 10, and 17 in solid tumor patients. Cancer Cell Int (2014) 0.76
Somatic expansion behaviour of the (CTG)n repeat in myotonic dystrophy knock-in mice is differentially affected by Msh3 and Msh6 mismatch-repair proteins. Hum Mol Genet (2002) 2.48
Triplet-repeat oligonucleotide-mediated reversal of RNA toxicity in myotonic dystrophy. Proc Natl Acad Sci U S A (2009) 2.32
Molecular genetics of pseudoxanthoma elasticum: type and frequency of mutations in ABCC6. Hum Mutat (2005) 1.47
Contribution of mGluR and Fmr1 functional pathways to neurite morphogenesis, craniofacial development and fragile X syndrome. Hum Mol Genet (2006) 1.36
Common chromosomal fragile sites and cancer: focus on FRA16D. Cancer Lett (2005) 1.36
Huntingtin-deficient zebrafish exhibit defects in iron utilization and development. Hum Mol Genet (2007) 1.29
TRPM7 is required for breast tumor cell metastasis. Cancer Res (2012) 1.27
Increased OXPHOS activity precedes rise in glycolytic rate in H-RasV12/E1A transformed fibroblasts that develop a Warburg phenotype. Mol Cancer (2009) 1.20
Rab6 family proteins interact with the dynein light chain protein DYNLRB1. Cell Motil Cytoskeleton (2008) 1.16
Brain-type creatine kinase has a crucial role in osteoclast-mediated bone resorption. Nat Med (2008) 1.16
Transgenic overexpression of human DMPK accumulates into hypertrophic cardiomyopathy, myotonic myopathy and hypotension traits of myotonic dystrophy. Hum Mol Genet (2004) 1.14
Creatine kinase B-driven energy transfer in the brain is important for habituation and spatial learning behaviour, mossy fibre field size and determination of seizure susceptibility. Eur J Neurosci (2002) 1.13
ATP and FRET--a cautionary note. Nat Biotechnol (2007) 1.07
The pathogenic agent in Drosophila models of 'polyglutamine' diseases. Hum Mol Genet (2005) 1.06
Impaired intracellular energetic communication in muscles from creatine kinase and adenylate kinase (M-CK/AK1) double knock-out mice. J Biol Chem (2003) 1.05
Phosphotransfer dynamics in skeletal muscle from creatine kinase gene-deleted mice. Mol Cell Biochem (2004) 1.03
Modulation of cell motility by spatial repositioning of enzymatic ATP/ADP exchange capacity. J Biol Chem (2008) 1.03
A role for the Rab6B Bicaudal-D1 interaction in retrograde transport in neuronal cells. Exp Cell Res (2007) 1.02
Novel invadopodia components revealed by differential proteomic analysis. Eur J Cell Biol (2010) 1.01
Structural and behavioural consequences of double deficiency for creatine kinases BCK and UbCKmit. Behav Brain Res (2005) 1.00
Common chromosomal fragile site FRA16D mutation in cancer cells. Hum Mol Genet (2005) 1.00
Fen1 does not control somatic hypermutability of the (CTG)(n)*(CAG)(n) repeat in a knock-in mouse model for DM1. FEBS Lett (2006) 0.99
Creatine kinase-mediated ATP supply fuels actin-based events in phagocytosis. PLoS Biol (2008) 0.98
Drosophila orthologue of WWOX, the chromosomal fragile site FRA16D tumour suppressor gene, functions in aerobic metabolism and regulates reactive oxygen species. Hum Mol Genet (2010) 0.98
Mild impairment of motor nerve repair in mice lacking PTP-BL tyrosine phosphatase activity. Physiol Genomics (2004) 0.97
Common chromosomal fragile site FRA16D tumor suppressor WWOX gene expression and metabolic reprograming in cells. Genes Chromosomes Cancer (2013) 0.97
Cloning and characterization of mCRIP2, a mouse LIM-only protein that interacts with PDZ domain IV of PTP-BL. Genes Cells (2003) 0.96
Double-stranded RNA is pathogenic in Drosophila models of expanded repeat neurodegenerative diseases. Hum Mol Genet (2011) 0.94
31P saturation transfer spectroscopy predicts differential intracellular macromolecular association of ATP and ADP in skeletal muscle. J Biol Chem (2010) 0.94
Adenylate kinase 1 deficiency induces molecular and structural adaptations to support muscle energy metabolism. J Biol Chem (2003) 0.91
Perturbation of the Akt/Gsk3-β signalling pathway is common to Drosophila expressing expanded untranslated CAG, CUG and AUUCU repeat RNAs. Hum Mol Genet (2011) 0.90
Alternative splicing controls myotonic dystrophy protein kinase structure, enzymatic activity, and subcellular localization. Mol Cell Biol (2003) 0.90
Local ATP generation by brain-type creatine kinase (CK-B) facilitates cell motility. PLoS One (2009) 0.90
Intracellular NAD(H) levels control motility and invasion of glioma cells. Cell Mol Life Sci (2013) 0.90
Molecular therapy in myotonic dystrophy: focus on RNA gain-of-function. Hum Mol Genet (2010) 0.87
Selective neuronal requirement for huntingtin in the developing zebrafish. Hum Mol Genet (2009) 0.87
Mice lacking brain-type creatine kinase activity show defective thermoregulation. Physiol Behav (2009) 0.87
Metabolism of circulating ADP in the bloodstream is mediated via integrated actions of soluble adenylate kinase-1 and NTPDase1/CD39 activities. FASEB J (2012) 0.87
Mice lacking the UbCKmit isoform of creatine kinase reveal slower spatial learning acquisition, diminished exploration and habituation, and reduced acoustic startle reflex responses. Mol Cell Biochem (2004) 0.86
Neuroprotective mechanisms of creatine occur in the absence of mitochondrial creatine kinase. Neurobiol Dis (2004) 0.86
Somatic CTG*CAG repeat instability in a mouse model for myotonic dystrophy type 1 is associated with changes in cell nuclearity and DNA ploidy. BMC Mol Biol (2007) 0.86
Design and analysis of effects of triplet repeat oligonucleotides in cell models for myotonic dystrophy. Mol Ther Nucleic Acids (2013) 0.85
Cancer cell metabolism regulates extracellular matrix degradation by invadopodia. Eur J Cell Biol (2013) 0.84
Comparative toxicity of polyglutamine, polyalanine and polyleucine tracts in Drosophila models of expanded repeat disease. Hum Mol Genet (2011) 0.84
Two structurally distinct and spatially compartmentalized adenylate kinases are expressed from the AK1 gene in mouse brain. Mol Cell Biochem (2004) 0.83
MR spectroscopy of muscle and brain in guanidinoacetate methyltransferase (GAMT)-deficient mice: validation of an animal model to study creatine deficiency. Magn Reson Med (2003) 0.83
Creatine kinase B deficient neurons exhibit an increased fraction of motile mitochondria. BMC Neurosci (2008) 0.83
FRA16D common chromosomal fragile site oxido-reductase (FOR/WWOX) protects against the effects of ionizing radiation in Drosophila. Oncogene (2005) 0.82
DMPK protein isoforms are differentially expressed in myogenic and neural cell lineages. Muscle Nerve (2009) 0.82
The DMWD protein from the myotonic dystrophy (DM1) gene region is developmentally regulated and is present most prominently in synapse-dense brain areas. Brain Res (2003) 0.81
A tail-anchored myotonic dystrophy protein kinase isoform induces perinuclear clustering of mitochondria, autophagy, and apoptosis. PLoS One (2009) 0.81
In vivo magnetic resonance spectroscopy of transgenic mouse models with altered high-energy phosphoryl transfer metabolism. NMR Biomed (2007) 0.80
Know thy fly. Trends Genet (2007) 0.80
Divergent mitochondrial and endoplasmic reticulum association of DMPK splice isoforms depends on unique sequence arrangements in tail anchors. Mol Cell Biol (2005) 0.80
Adenylate kinase 1 knockout mice have normal thiamine triphosphate levels. Biochim Biophys Acta (2002) 0.80
Ubiquitous expression of CUG or CAG trinucleotide repeat RNA causes common morphological defects in a Drosophila model of RNA-mediated pathology. PLoS One (2012) 0.78
Distinct roles for Toll and autophagy pathways in double-stranded RNA toxicity in a Drosophila model of expanded repeat neurodegenerative diseases. Hum Mol Genet (2013) 0.78
Dynamic mutations: where are they now? Adv Exp Med Biol (2012) 0.77
Gated dynamic 31P MRS shows reduced contractile phosphocreatine breakdown in mice deficient in cytosolic creatine kinase and adenylate kinase. NMR Biomed (2009) 0.77
Abnormal actomyosin assembly in proliferating and differentiating myoblasts upon expression of a cytosolic DMPK isoform. Biochim Biophys Acta (2011) 0.77
In vivo magnetic resonance spectroscopy of transgenic mice with altered expression of guanidinoacetate methyltransferase and creatine kinase isoenzymes. Subcell Biochem (2007) 0.76
Complete brain-type creatine kinase deficiency in mice blocks seizure activity and affects intracellular calcium kinetics. Epilepsia (2009) 0.76
Gene duplication and conversion events shaped three homologous, differentially expressed myosin regulatory light chain (MLC2) genes. Eur J Cell Biol (2012) 0.76
Phosphorylation target site specificity for AGC kinases DMPK E and Lats2. J Cell Biochem (2012) 0.75
Adenylate kinase I does not affect cellular growth characteristics under normal and metabolic stress conditions. Exp Cell Res (2004) 0.75
2010 Marigold therapeutic strategies for myotonic dystrophy. Neuromuscul Disord (2011) 0.75
Coiled-coil interactions modulate multimerization, mitochondrial binding and kinase activity of myotonic dystrophy protein kinase splice isoforms. FEBS J (2006) 0.75
Magnetization transfer effect on the creatine methyl resonance studied by CW off-resonance irradiation in human skeletal muscle on a clinical MR system. Magn Reson Med (2003) 0.75