Published in Crit Rev Clin Lab Sci on December 21, 2011
Removal of immunoglobulin-like domains from titin's spring segment alters titin splicing in mouse skeletal muscle and causes myopathy. J Gen Physiol (2014) 0.96
Structurally distinct polycyclic aromatic hydrocarbons induce differential transcriptional responses in developing zebrafish. Toxicol Appl Pharmacol (2013) 0.86
Crosstalk between NSL histone acetyltransferase and MLL/SET complexes: NSL complex functions in promoting histone H3K4 di-methylation activity by MLL/SET complexes. PLoS Genet (2013) 0.86
Identification of a conserved set of upregulated genes in mouse skeletal muscle hypertrophy and regrowth. J Appl Physiol (1985) (2014) 0.84
Probing muscle ankyrin-repeat protein (MARP) structure and function. Anat Rec (Hoboken) (2014) 0.84
Poxviral ankyrin proteins. Viruses (2015) 0.82
Human skeletal muscle type 1 fibre distribution and response of stress-sensing proteins along the titin molecule after submaximal exhaustive exercise. Histochem Cell Biol (2017) 0.81
Mineralocorticoid receptors are present in skeletal muscle and represent a potential therapeutic target. FASEB J (2015) 0.80
Profiling of skeletal muscle Ankrd2 protein in human cardiac tissue and neonatal rat cardiomyocytes. Histochem Cell Biol (2015) 0.78
Cytosolic CARP promotes angiotensin II- or pressure overload-induced cardiomyocyte hypertrophy through calcineurin accumulation. PLoS One (2014) 0.78
Maternal nutrition induces gene expression changes in fetal muscle and adipose tissues in sheep. BMC Genomics (2014) 0.78
Differential expression and localization of Ankrd2 isoforms in human skeletal and cardiac muscles. Histochem Cell Biol (2016) 0.77
Distinct Skeletal Muscle Gene Regulation from Active Contraction, Passive Vibration, and Whole Body Heat Stress in Humans. PLoS One (2016) 0.77
Global deletion of Ankrd1 results in a wound-healing phenotype associated with dermal fibroblast dysfunction. Am J Pathol (2014) 0.77
Canonical Wnt signalling regulates nuclear export of Setdb1 during skeletal muscle terminal differentiation. Cell Discov (2016) 0.76
Effects of aging, exercise, and disease on force transfer in skeletal muscle. Am J Physiol Endocrinol Metab (2015) 0.76
CARP, a myostatin-downregulated gene in CFM Cells, is a novel essential positive regulator of myogenesis. Int J Biol Sci (2014) 0.76
Targeting Mechanotransduction at the Transcriptional Level: YAP and BRD4 Are Novel Therapeutic Targets for the Reversal of Liver Fibrosis. Front Pharmacol (2016) 0.75
Comparative transcriptome analysis of muscular dystrophy models Large(myd), Dmd(mdx)/Large(myd) and Dmd(mdx): what makes them different? Eur J Hum Genet (2016) 0.75
RepeatsDB 2.0: improved annotation, classification, search and visualization of repeat protein structures. Nucleic Acids Res (2016) 0.75
Muscle contraction is required to maintain the pool of muscle progenitors via YAP and NOTCH during fetal myogenesis. Elife (2016) 0.75
MLP and CARP are linked to chronic PKCα signalling in dilated cardiomyopathy. Nat Commun (2016) 0.75
Characterization of muscle ankyrin repeat proteins in human skeletal muscle. Am J Physiol Cell Physiol (2017) 0.75
Mutations in Cypher/ZASP in patients with dilated cardiomyopathy and left ventricular non-compaction. J Am Coll Cardiol (2003) 3.20
Mutations in the amiloride-sensitive epithelial sodium channel in patients with cystic fibrosis-like disease. Hum Mutat (2009) 1.71
The Ankrd2 protein, a link between the sarcomere and the nucleus in skeletal muscle. J Mol Biol (2004) 1.38
Genes that determine immunology and inflammation modify the basic defect of impaired ion conductance in cystic fibrosis epithelia. J Med Genet (2010) 1.26
A mutation in telethonin alters Nav1.5 function. J Biol Chem (2008) 1.20
A class III PDZ binding motif in the myotilin and FATZ families binds enigma family proteins: a common link for Z-disc myopathies. Mol Cell Biol (2008) 1.17
The Z-disc proteins myotilin and FATZ-1 interact with each other and are connected to the sarcolemma via muscle-specific filamins. J Cell Sci (2005) 1.08
Telethonin deficiency is associated with maladaptation to biomechanical stress in the mammalian heart. Circ Res (2011) 1.07
The TNFalpha receptor TNFRSF1A and genes encoding the amiloride-sensitive sodium channel ENaC as modulators in cystic fibrosis. Hum Genet (2006) 1.05
A novel role for cardiac ankyrin repeat protein Ankrd1/CARP as a co-activator of the p53 tumor suppressor protein. Arch Biochem Biophys (2010) 1.02
Muscle Research and Gene Ontology: New standards for improved data integration. BMC Med Genomics (2009) 1.01
Targeted deletion of the muscular dystrophy gene myotilin does not perturb muscle structure or function in mice. Mol Cell Biol (2006) 1.00
Solution structure of ZASP PDZ domain; implications for sarcomere ultrastructure and enigma family redundancy. Structure (2004) 0.99
Reconstructing the population history of European Romani from genome-wide data. Curr Biol (2012) 0.98
A1ATVar: a relational database of human SERPINA1 gene variants leading to alpha1-antitrypsin deficiency and application of the VariVis software. Hum Mutat (2009) 0.97
Telethonin protein expression in neuromuscular disorders. Biochim Biophys Acta (2002) 0.95
Loss of function of hNav1.5 by a ZASP1 mutation associated with intraventricular conduction disturbances in left ventricular noncompaction. Circ Arrhythm Electrophysiol (2012) 0.94
High frequency of the R75Q CFTR variation in patients with chronic obstructive pulmonary disease. J Cyst Fibros (2004) 0.92
Differential involvement of sarcomeric proteins in myofibrillar myopathies: a morphological and immunohistochemical study. Acta Neuropathol (2009) 0.91
Post-transcriptional silencing of the Drosophila homolog of human ZASP: a molecular and functional analysis. Cell Tissue Res (2009) 0.91
The effects of Ankrd2 alteration indicate its involvement in cell cycle regulation during muscle differentiation. Biochim Biophys Acta (2008) 0.89
The use of D-dimer with new cutoff can be useful in diagnosis of venous thromboembolism in pregnancy. Eur J Obstet Gynecol Reprod Biol (2010) 0.88
Multi-tasking role of the mechanosensing protein Ankrd2 in the signaling network of striated muscle. PLoS One (2011) 0.87
Alpha-1-antitrypsin in pathogenesis of hepatocellular carcinoma. Hepat Mon (2012) 0.86
Type and location of venous thromboembolism in carriers of Factor V Leiden or prothrombin G20210A mutation versus patients with no mutation. Clin Appl Thromb Hemost (2008) 0.86
Novel ORC4L gene mutation in B-cell lymphoproliferative disorders. Am J Med Sci (2009) 0.85
Alpha-1-antitrypsin deficiency in Serbian adults with lung diseases. Genet Test Mol Biomarkers (2012) 0.85
Procarboxypeptidase U (TAFI) contributes to the risk of thrombosis in patients with hereditary thrombophilia. Thromb Res (2009) 0.84
BPAG1 isoform-b: complex distribution pattern in striated and heart muscle and association with plectin and alpha-actinin. Exp Cell Res (2009) 0.83
The CFTR M470V gene variant as a potential modifier of COPD severity: study of Serbian population. Genet Test (2008) 0.82
A ZASP missense mutation, S196L, leads to cytoskeletal and electrical abnormalities in a mouse model of cardiomyopathy. Circ Arrhythm Electrophysiol (2010) 0.82
Non-invasive prenatal testing for aneuploidy and beyond: challenges of responsible innovation in prenatal screening. Eur J Hum Genet (2015) 0.80
Genetic risk factors for arterial ischemic stroke in children: a possible MTHFR and eNOS gene-gene interplay? J Child Neurol (2009) 0.80
Matrix metalloproteinases gene variants in idiopathic disseminated bronchiectasis. J Investig Med (2009) 0.79
Gender-related reference intervals of urinary 8-oxo-7,8-dihydro-2'-deoxyguanosine determined by liquid chromatography-tandem mass spectrometry in Serbian population. Clin Biochem (2012) 0.79
Profiling of skeletal muscle Ankrd2 protein in human cardiac tissue and neonatal rat cardiomyocytes. Histochem Cell Biol (2015) 0.78
Genetic alterations in SMAD4 and K-ras in Serbian patients with endometrial carcinoma. Int J Gynecol Cancer (2012) 0.78
Alpha-1-antitrypsin phenotypes and neutrophil elastase gene promoter polymorphisms in lung cancer. Pathol Oncol Res (2010) 0.78
Isoelectric focusing phenotyping and denaturing gradient gel electrophoresis genotyping: a comparison of two methods in detection of alpha-1-antitrypsin variants. Transl Res (2008) 0.77
MTHFR C677T polymorphism in chronic pancreatitis and pancreatic adenocarcinoma. Cell Biochem Funct (2008) 0.77
Angiotensin-converting enzyme gene insertion/deletion polymorphism in patients with chronic pancreatitis and pancreatic cancer. Dig Surg (2011) 0.77
Proteomics identification of differentially expressed proteins in the muscle of dysferlin myopathy patients. Proteomics Clin Appl (2009) 0.77
Prothrombotic genetic risk factors in stroke: a possible different role in pediatric and adult patients. Clin Appl Thromb Hemost (2012) 0.77
Analysis of CFTR Gene Variants in Idiopathic Bronchiectasis in Serbian Children. Pediatr Allergy Immunol Pulmonol (2013) 0.76
Cytoskeletal basis of ion channel function in cardiac muscle. Future Cardiol (2006) 0.76
Healthcare in Serbia in transition period. EPMA J (2010) 0.76
Remodeling of dystrophin and sarcomeric Z-band occurs in pediatric cardiomyopathies: a unifying mechanism for force transmission defect. J Cardiovasc Med (Hagerstown) (2009) 0.76
Structural and functional analysis of SMAD4 gene promoter in malignant pancreatic and colorectal tissues: detection of two novel polymorphic nucleotide repeats. Cancer Epidemiol (2010) 0.76
Is an integrative laboratory algorithm more effective in detecting alpha-1-antitrypsin deficiency in patients with premature chronic obstructive pulmonary disease than AAT concentration based screening approach? Biochem Med (Zagreb) (2014) 0.75
Identification of a rare p.G320R alpha-1-antitrypsin variant in emphysema and lung cancer patients. Genet Mol Biol (2010) 0.75
Screening of alpha-1-antitrypsin gene by denaturing gradient gel electrophoresis (DGGE). J Biochem Biophys Methods (2006) 0.75
Functional analysis of novel alpha-1 antitrypsin variants G320R and V321F. Mol Biol Rep (2014) 0.75
Clopidogrel High On-Treatment Platelet Reactivity in Patients with Carotid Artery Stenosis Undergoing Endarterectomy. A Pilot Study. Curr Vasc Pharmacol (2016) 0.75
Prothrombin 3'end gene variants in isolated pulmonary embolism--the first report of FIIc.*64_*66del and FIIc.*303T>C variants. Acta Cardiol (2015) 0.75
Cell-free DNA as biomarker and source for mutation detection in primary colorectal cancer. J BUON (2017) 0.75
Combined thrombophilic risk factors and essential thrombocythemia in patient with recurrent venous thromboembolic episodes-thirty-three-year follow-up. J Thromb Thrombolysis (2005) 0.75
Determination of transgene copy number in stably transfected mammalian cells by PCR-capillary electrophoresis assay. Biochem Genet (2013) 0.75
FV Leiden mutation and risk of recurrent venous thromboembolism in Serbian population. J Thromb Thrombolysis (2007) 0.75
Does anticoagulant therapy improve pregnancy outcome equally, regardless of specific thrombophilia type? Clin Appl Thromb Hemost (2012) 0.75
+1040 C/T polymorphism in coding region of thrombin-activatable fibrinolysis inhibitor gene and the risk of idiopathic recurrent fetal loss. Blood Coagul Fibrinolysis (2010) 0.75
Polymorphisms of beta2-adrenergic receptor gene in serbian asthmatic adults: effects on response to Beta-agonists. Mol Diagn Ther (2014) 0.75