Published in J Nephrol on January 22, 2013
The cleaved cytoplasmic tail of polycystin-1 regulates Src-dependent STAT3 activation. J Am Soc Nephrol (2014) 0.83
A Single Nucleotide Variant in HNF-1β is Associated with Maturity-Onset Diabetes of the Young in a Large Chinese Family. Iran J Public Health (2016) 0.75
Comparative Genome of GK and Wistar Rats Reveals Genetic Basis of Type 2 Diabetes. PLoS One (2015) 0.75
A phase 3 study of deferasirox (ICL670), a once-daily oral iron chelator, in patients with beta-thalassemia. Blood (2005) 6.07
Febrile urinary tract infections in young children: recommendations for the diagnosis, treatment and follow-up. Acta Paediatr (2012) 2.34
Mutations in ANKRD26 are responsible for a frequent form of inherited thrombocytopenia: analysis of 78 patients from 21 families. Blood (2011) 2.29
North Star Ambulatory Assessment, 6-minute walk test and timed items in ambulant boys with Duchenne muscular dystrophy. Neuromuscul Disord (2010) 2.14
Mutations affecting the secretory COPII coat component SEC23B cause congenital dyserythropoietic anemia type II. Nat Genet (2009) 2.12
An infant with hypercalcemia: questions. Pediatr Nephrol (2013) 2.03
Cognitive reserve and cortical atrophy in multiple sclerosis: a longitudinal study. Neurology (2013) 1.72
Brain metabolic changes suggestive of axonal damage in radiologically isolated syndrome. Neurology (2013) 1.61
Mutational spectrum in congenital dyserythropoietic anemia type II: identification of 19 novel variants in SEC23B gene. Am J Hematol (2010) 1.60
Rituximab for the treatment of refractory autoimmune hemolytic anemia in children. Blood (2003) 1.58
A multicenter retrospective clinical study of CD5/CD10-negative chronic B cell leukemias. Am J Hematol (2008) 1.57
Long-term evolution of renal damage associated with unilateral vesicoureteral reflux. J Urol (2007) 1.52
Enhancement of the core near-band-edge emission induced by an amorphous shell in coaxial one-dimensional nanostructure: the case of SiC/SiO2 core/shell self-organized nanowires. Nanotechnology (2010) 1.50
Treatment with short-term, high-dose cyclosporin A in children with refractory chronic idiopathic thrombocytopenic purpura. Br J Haematol (2003) 1.42
Importance of Shank3 protein in regulating metabotropic glutamate receptor 5 (mGluR5) expression and signaling at synapses. J Biol Chem (2011) 1.40
Molecular basis of angiogenesis and cancer. Oncogene (2003) 1.38
Mutations in the 5' UTR of ANKRD26, the ankirin repeat domain 26 gene, cause an autosomal-dominant form of inherited thrombocytopenia, THC2. Am J Hum Genet (2011) 1.37
24 month longitudinal data in ambulant boys with Duchenne muscular dystrophy. PLoS One (2013) 1.34
p27Kip1 metabolism: a fascinating labyrinth. Cell Cycle (2007) 1.34
Von Hippel-Lindau-dependent polycythemia is endemic on the island of Ischia: identification of a novel cluster. Blood (2005) 1.26
Resveratrol: from basic science to the clinic. Cell Cycle (2007) 1.23
Iron chelation with deferasirox in adult and pediatric patients with thalassemia major: efficacy and safety during 5 years' follow-up. Blood (2011) 1.23
Photothermally-induced disordered patterns of corneal collagen revealed by SHG imaging. Opt Express (2009) 1.20
Tonic endovanilloid facilitation of glutamate release in brainstem descending antinociceptive pathways. J Neurosci (2007) 1.20
Molecular analysis of 42 patients with congenital dyserythropoietic anemia type II: new mutations in the SEC23B gene and a search for a genotype-phenotype relationship. Haematologica (2009) 1.20
Red blood cell membrane defects. Rev Clin Exp Hematol (2003) 1.19
Genetic basis of congenital erythrocytosis: mutation update and online databases. Hum Mutat (2013) 1.18
Ex vivo expansion of mesenchymal stromal cells. Best Pract Res Clin Haematol (2011) 1.18
Mutational scanning of potassium, sodium and chloride ion channels in malignant migrating partial seizures in infancy. Brain Dev (2005) 1.16
Anti-CD20 monoclonal antibody (Rituximab) for life-threatening autoimmune haemolytic anaemia in a patient with systemic lupus erythematosus. Br J Haematol (2002) 1.15
p57(Kip2) and cancer: time for a critical appraisal. Mol Cancer Res (2011) 1.13
Thrombocytopenia-associated mutations in the ANKRD26 regulatory region induce MAPK hyperactivation. J Clin Invest (2014) 1.13
Platelet activation induces cell-surface immunoreactive tissue factor expression, which is modulated differently by antiplatelet drugs. Arterioscler Thromb Vasc Biol (2003) 1.12
Organism-sediment interactions govern post-hypoxia recovery of ecosystem functioning. PLoS One (2012) 1.11
A novel hyperekplexia-causing mutation in the pre-transmembrane segment 1 of the human glycine receptor alpha1 subunit reduces membrane expression and impairs gating by agonists. J Biol Chem (2004) 1.09
Chalcones: a valid scaffold for monoamine oxidases inhibitors. J Med Chem (2009) 1.07
Targeting p27Kip1 protein: its relevance in the therapy of human cancer. Expert Opin Ther Targets (2011) 1.07
Prevalence and risk factors for pulmonary arterial hypertension in a large group of β-thalassemia patients using right heart catheterization: a Webthal study. Circulation (2013) 1.06
Occult hepatitis B and infliximab-induced HBV reactivation. Inflamm Bowel Dis (2007) 1.06
Locoregionally advanced carcinoma of the oropharynx: conventional radiotherapy vs. accelerated hyperfractionated radiotherapy vs. concomitant radiotherapy and chemotherapy--a multicenter randomized trial. Int J Radiat Oncol Biol Phys (2003) 1.06
Improving the characterization of radiologically isolated syndrome suggestive of multiple sclerosis. PLoS One (2011) 1.05
Synthesis, molecular modeling studies and selective inhibitory activity against MAO of N1-propanoyl-3,5-diphenyl-4,5-dihydro-(1H)-pyrazole derivatives. Eur J Med Chem (2008) 1.03
Preserved antibody levels and loss of memory B cells against pneumococcus and tetanus after splenectomy: tailoring better vaccination strategies. Eur J Immunol (2013) 1.02
The N-terminal 11 amino acids of human erythrocyte band 3 are critical for aldolase binding and protein phosphorylation: implications for band 3 function. Blood (2005) 1.02
Clinical and laboratory features of 103 patients from 42 Italian families with inherited thrombocytopenia derived from the monoallelic Ala156Val mutation of GPIbα (Bolzano mutation). Haematologica (2011) 1.02
The endovanilloid/endocannabinoid system: a new potential target for osteoporosis therapy. Bone (2011) 1.01
CD26 expression in mature B-cell neoplasia: its possible role as a new prognostic marker in B-CLL. Hematol Oncol (2009) 1.01
Association of breast cancer and polymorphisms of interleukin-10 and tumor necrosis factor-alpha genes. Clin Chem (2003) 1.00
Retinoic acid induces p27Kip1 nuclear accumulation by modulating its phosphorylation. Cancer Res (2006) 0.99
ROBO2 gene variants are associated with familial vesicoureteral reflux. J Am Soc Nephrol (2008) 0.98
Interaction between vanilloid and glutamate receptors in the central modulation of nociception. Eur J Pharmacol (2002) 0.97
Synthesis and biological evaluation of N-substituted-3,5-diphenyl-2-pyrazoline derivatives as cyclooxygenase (COX-2) inhibitors. Eur J Med Chem (2010) 0.97
PTPepsilon has a critical role in signaling transduction pathways and phosphoprotein network topology in red cells. Proteomics (2008) 0.96
Assessment of outcome predictors in first-episode acute myelitis: a retrospective study of 53 cases. Arch Neurol (2010) 0.96
Palmitoylethanolamide reduces formalin-induced neuropathic-like behaviour through spinal glial/microglial phenotypical changes in mice. CNS Neurol Disord Drug Targets (2013) 0.96
Periaqueductal gray metabotropic glutamate receptor subtype 7 and 8 mediate opposite effects on amino acid release, rostral ventromedial medulla cell activities, and thermal nociception. J Neurophysiol (2007) 0.95
Resveratrol: from basic studies to bedside. Cancer Treat Res (2014) 0.94
Frequency of congenital dyserythropoietic anemias in Europe. Eur J Haematol (2010) 0.94
No clear evidence of ACEi efficacy on the progression of chronic kidney disease in children with hypodysplastic nephropathy--report from the ItalKid Project database. Nephrol Dial Transplant (2007) 0.94
B lymphocyte reconstitution after hematopoietic stem cell transplantation: functional immaturity and slow recovery of memory CD27+ B cells. Exp Hematol (2005) 0.94
Distribution, characterization and significance of polyomavirus genomic sequences in tumors of the brain and its covering. J Med Virol (2005) 0.92
Molecular mechanisms of dendritic spine development and maintenance. Acta Neurobiol Exp (Wars) (2008) 0.92
TRPV1-dependent and -independent alterations in the limbic cortex of neuropathic mice: impact on glial caspases and pain perception. Cereb Cortex (2011) 0.91
InAs/InSb nanowire heterostructures grown by chemical beam epitaxy. Nanotechnology (2009) 0.91
The analgesic effect of N-arachidonoyl-serotonin, a FAAH inhibitor and TRPV1 receptor antagonist, associated with changes in rostral ventromedial medulla and locus coeruleus cell activity in rats. Neuropharmacology (2008) 0.91
Permanent renal parenchymal defects after febrile UTI are closely associated with vesicoureteric reflux. Pediatr Nephrol (2006) 0.90
Decreased subunit stability as a novel mechanism for potassium current impairment by a KCNQ2 C terminus mutation causing benign familial neonatal convulsions. J Biol Chem (2005) 0.90
Membrane association of peroxiredoxin-2 in red cells is mediated by the N-terminal cytoplasmic domain of band 3. Free Radic Biol Med (2012) 0.90
A genome search for primary vesicoureteral reflux shows further evidence for genetic heterogeneity. Pediatr Nephrol (2008) 0.90
Reliability of EMA binding test in the diagnosis of hereditary spherocytosis in Italian patients. Acta Haematol (2010) 0.90
Polynucleotide phosphorylase hinders mRNA degradation upon ribosomal protein S1 overexpression in Escherichia coli. RNA (2008) 0.90
Cannabinoid receptor type 2 functional variant influences liver damage in children with non-alcoholic fatty liver disease. PLoS One (2012) 0.89
A novel KCNQ3 mutation in familial epilepsy with focal seizures and intellectual disability. Epilepsia (2014) 0.89
Riboflavin and ultraviolet A collagen crosslinking: in vivo thermographic analysis of the corneal surface. J Cataract Refract Surg (2007) 0.89
Effects of intra-ventrolateral periaqueductal grey palmitoylethanolamide on thermoceptive threshold and rostral ventromedial medulla cell activity. Eur J Pharmacol (2011) 0.89
Congenital nephrotic syndrome of the Finnish type in Italy: a molecular approach. J Nephrol (2002) 0.89
CNR2 functional variant (Q63R) influences childhood immune thrombocytopenic purpura. Haematologica (2011) 0.89
Congenital dyserythropoietic anemia type II: exclusion of seven candidate genes. Blood Cells Mol Dis (2003) 0.88
In vivo effect of the natural antioxidant hydroxytyrosol on cyclosporine nephrotoxicity in rats. Nephrol Dial Transplant (2007) 0.88
Renal hypoplasia without optic coloboma associated with PAX2 gene deletion. Nephrol Dial Transplant (2007) 0.88
Spectrum of FANCA mutations in Italian Fanconi anemia patients: identification of six novel alleles and phenotypic characterization of the S858R variant. Hum Mutat (2003) 0.88
Central/diffuse abdominal perception of urological pain in children. Acta Paediatr (2006) 0.88
P27Kip1 serine 10 phosphorylation determines its metabolism and interaction with cyclin-dependent kinases. Cell Cycle (2014) 0.88
Retinoic acid inhibits the growth of bone marrow mesenchymal stem cells and induces p27Kip1 and p16INK4A up-regulation. Mol Cell Biochem (2003) 0.88