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Epidemiology of haemolytic uremic syndrome in children. Data from the North Italian HUS network.Correction of defective CFTR/ENaC function and tightness of cystic fibrosis airway epithelium by amniotic mesenchymal stromal (stem) cells.Genetics of leptin and obesity: a HuGE review.Use of parthenogenetic activation of human oocytes as an experimental model for evaluation of polar body based PGD assay performance.Towards Plant Species Identification in Complex Samples: A Bioinformatics Pipeline for the Identification of Novel Nuclear Barcode Candidates.Role of simian virus 40 in cancer incidence in solid organ transplant patients.Human amnion-derived cells: prospects for the treatment of lung diseases.Molecular characterization of an unauthorized genetically modified Bacillus subtilis production strain identified in a vitamin B2 feed additive.Amniotic mesenchymal stem cells: a new source for hepatocyte-like cells and induction of CFTR expression by coculture with cystic fibrosis airway epithelial cellsNovel nuclear barcode regions for the identification of flatfish species.A common CYP1B1 polymorphism is associated with 2-OHE1/16-OHE1 urinary estrone ratio.Pleural malignant mesothelioma, genetic susceptibility and asbestos exposure.GSTM1 [corrected] deletion modifies the levels of polycyclic aromatic hydrocarbon-DNA adducts in human sperm.MTHFR C677T polymorphism, GSTM1 deletion and male infertility: a possible suggestion of a gene-gene interaction?Borderline sweat test: Utility and limits of genetic analysis for the diagnosis of cystic fibrosis.Molecular and clinical features associated with CFTR gene rearrangements in Italian population: identification of a new duplication and recurrent deletions.Effects of metabolic genotypes on intermediary biomarkers in subjects exposed to PAHS: Results from the EXPAH studyA novel donor splice site characterized by CFTR mRNA analysis induces a new pseudo-exon in CF patientsFine Characterization of the Recurrent c.1584+18672A>G Deep-Intronic Mutation in the Cystic Fibrosis Transmembrane Conductance Regulator GeneA wide methodological approach to identify a large duplication in CFTR gene in a CF patient uncharacterised by sequencing analysis
P50
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P50
description
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Valentina Paracchini
@ast
Valentina Paracchini
@en
Valentina Paracchini
@es
Valentina Paracchini
@nl
type
label
Valentina Paracchini
@ast
Valentina Paracchini
@en
Valentina Paracchini
@es
Valentina Paracchini
@nl
prefLabel
Valentina Paracchini
@ast
Valentina Paracchini
@en
Valentina Paracchini
@es
Valentina Paracchini
@nl
P106
P31
P496
0000-0002-4847-9992