about
Human aldolase A natural mutants: relationship between flexibility of the C-terminal region and enzyme functionFunctional analysis of the promoter of the mitochondrial phosphate carrier human gene: identification of activator and repressor elements and their transcription factorsA new human species of aldolase A mRNA from fibroblasts.Beta catenin and cytokine pathway dysregulation in patients with manifestations of the "PTEN hamartoma tumor syndrome"Differential expression and cellular localization of ZNF224 and ZNF255, two isoforms of the Krüppel-like zinc-finger protein family.Genetics, diagnosis and management of colorectal cancer (Review).KRAB-Zinc Finger Proteins: A Repressor Family Displaying Multiple Biological Functions.Synergistic effect of interleukin-10-receptor variants in a case of early-onset ulcerative colitis.ZNF224: Structure and role of a multifunctional KRAB-ZFP protein.WT1-mediated repression of the proapoptotic transcription factor ZNF224 is triggered by the BCR-ABL oncogeneRole of WT1-ZNF224 interaction in the expression of apoptosis-regulating genes.Biochemical and functional interaction between ZNF224 and ZNF255, two members of the Kruppel-like zinc-finger protein family and WT1 protein isoforms.The Kruppel-like zinc finger protein ZNF224 recruits the arginine methyltransferase PRMT5 on the transcriptional repressor complex of the aldolase A gene.The Italian external quality control program for familial adenomatous polyposis of the colon: five years of experience.Alternative splicing and nonsense-mediated mRNA decay in the regulation of a new adenomatous polyposis coli transcript.The Krüppel-like zinc-finger protein ZNF224 represses aldolase A gene transcription by interacting with the KAP-1 co-repressor protein.Characterization of a silencer that modulates transcription of the human distal aldolase A promoter.Growth-arrested dependence of aldolase A L-type mRNA expression in rodent cell lines.Contribution of large genomic rearrangements in Italian Lynch syndrome patients: characterization of a novel alu-mediated deletion.Differential expression of PTEN gene correlates with phenotypic heterogeneity in three cases of patients showing clinical manifestations of PTEN hamartoma tumour syndrome.Cis-acting elements in the promoter region of the human aldolase C gene.PKC-dependent phosphorylation of the p97 repressor regulates the transcription of aldolase A L-type promoter.Negative regulation of the mouse aldolase A gene. A cell cycle-dependent DNA binding activity functions as a silencer of gene transcription.Role of the cold shock domain protein A in the transcriptional regulation of HBG expression.Alu-mediated genomic deletion of the serine/threonine protein kinase 11 (STK11) gene in Peutz-Jeghers syndrome.Increased mucosal nitric oxide production in ulcerative colitis is mediated in part by the enteroglial-derived S100B protein.Defective mRNA levels are responsible for a beta-thalassemia phenotype associated with Hb Federico II, a novel hemoglobin variant [beta-106 (G8) Leu->Val].Purification and properties of several transfer RNA methyltransferases from S. typhimurium.Delayed decline of gamma-globin expression in infant age associated with the presence of Ggamma-158 (C-->T) polymorphism.Three submicroscopic deletions at the APC locus and their rapid detection by quantitative-PCR analysis.Multivariate analysis as a method for evaluating the pathogenicity of novel genetic MLH1 variants in patients with colorectal cancer and microsatellite instability.Implication of adenomatous polyposis coli and MUTYH mutations in familial colorectal polyposis.Wnt pathway, angiogenetic and hormonal markers in sporadic and familial adenomatous polyposis-associated juvenile nasopharyngeal angiofibromas (JNA).WT1 protein is a transcriptional activator of the antiapoptotic bag3 gene.Real-time PCR quantification of human DKC1 expression in colorectal cancer.Three novel germline mutations in the adenomatous polyposis coli gene.Identification and molecular characterization of the --CAMPANIA deletion, a novel alpha (0) -thalassemic defect, in two unrelated Italian families [corrected].Multiple Control Elements Regulate Transcription from the Most Distal Promoter of Human Aldolase A GeneIn vivo activity of the most proximal promoter of the human aldolase A ene and analysis of transcriptional control elementsPrenatal diagnosis of haemoglobinopathies: our experience of 523 cases
P50
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P50
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hulumtuese
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հետազոտող
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Paola Izzo
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Paola Izzo
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Paola Izzo
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Paola Izzo
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Paola Izzo
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Paola Izzo
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Paola Izzo
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Paola Izzo
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Paola Izzo
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Paola Izzo
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Paola Izzo
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Paola Izzo
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Paola Izzo
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Paola Izzo
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Paola Izzo
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P106
P1153
7007028917
P21
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P496
0000-0003-1549-0615