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Lista de obras de Paola Borgiani

3020insC mutation within the NOD2 gene in Crohn's disease: frequency and association with clinical pattern in an Italian population

article

A European Spectrum of Pharmacogenomic Biomarkers: Implications for Clinical Pharmacogenomics

artículo científico publicado en 2016

A family study of asymptomatic small bowel Crohn's disease

artículo científico publicado en 2013

A multilocus genetic study in a cohort of Italian SLE patients confirms the association with STAT4 gene and describes a new association with HCP5 gene

artículo científico publicado en 2014

A pharmacogenetics study in Mozambican patients treated with nevirapine: full resequencing of TRAF3IP2 gene shows a novel association with SJS/TEN susceptibility

artículo científico publicado en 2015

ABCC10 rs2125739 polymorphism and nevirapine-induced hepatotoxicity: lack of association in a population from Mozambique

artículo científico publicado en 2013

ACP1 and human adaptability. 1. Association with common diseases: a case-control study.

artículo científico publicado en 1995

ATG16L1 Ala197Thr Is Not Associated With Susceptibility to Crohn’s Disease or With Phenotype in an Italian Population

article

Age-related macular degeneration: insights into inflammatory genes

artículo científico publicado en 2014

Allelic variants in the CYP2C9 and VKORC1 loci and interindividual variability in the anticoagulant dose effect of warfarin in Italians.

artículo científico publicado en 2007

Association between CYP2B6 polymorphisms and Nevirapine-induced SJS/TEN: a pharmacogenetics study

artículo científico publicado en 2013

Autophagy and inflammatory bowel disease: Association between variants of the autophagy-related IRGM gene and susceptibility to Crohn's disease

artículo científico publicado en 2015

Both maternal and foetal genetic factors contribute to macrosomia of diabetic pregnancy

artículo científico publicado en 1994

CYP4F2 genetic variant (rs2108622) significantly contributes to warfarin dosing variability in the Italian population.

artículo científico publicado en 2009

Characterization of a novel CYP2C9 gene mutation and structural bioinformatic protein analysis in a warfarin hypersensitive patient

artículo científico publicado en 2011

Characterization of a single nucleotide polymorphism in the ZNF9 gene and analysis of association with myotonic dystrophy type II (DM2) in the Italian population.

artículo científico publicado en 2004

Common polymorphisms in MIR146a, MIR128a and MIR27a genes contribute to neuropathy susceptibility in type 2 diabetes

article

Comparative analysis between saliva and buccal swabs as source of DNA: lesson from HLA-B*57:01 testing.

artículo científico publicado en 2015

Correction: A European Spectrum of Pharmacogenomic Biomarkers: Implications for Clinical Pharmacogenomics

artículo científico publicado en 2017

Could MicroRNA polymorphisms influence warfarin dosing? A pharmacogenetics study on mir133 genes

artículo científico publicado en 2015

Crohn's disease, the mycobacterium paratuberculosis and the genetic bond: An unexpected trio

artículo científico publicado en 2015

Direct PCR: a new pharmacogenetic approach for the inexpensive testing of HLA-B*57:01.

artículo científico publicado en 2014

EPHX1 Polymorphisms Are Not Associated With Warfarin Response in an Italian Population

article

Erythrocyte acid phosphatase (ACP1) activity. In vitro modulation by adenosine and inosine and effects of adenosine deaminase (ADA) polymorphism

scientific article published on 01 January 1989

FLG (filaggrin) null mutations and sunlight exposure: Evidence of a correlation.

artículo científico publicado en 2015

Folic acid and methionine in the prevention of teratogen-induced congenital defects in mice.

artículo científico publicado en 2008

Further evidence that polymorphisms of the OLR1 gene are associated with susceptibility to coronary artery disease and myocardial infarction

article

Genetic control of serum IgE levels: a study of low molecular weight protein tyrosine phosphatase

artículo científico publicado el 1 de marzo de 2003

Genetic interactions and the environment: a study of ADA and ACP1 systems in the Sardinian population.

artículo científico publicado en 1995

Genotypes of cytosolic low-molecular-weight protein-tyrosine-phosphatase correlate with age at onset of type 1 diabetes in a sex-specific manner.

artículo científico publicado en 2002

Genotyping OLR1 Gene: A Genomic Biomarker for Cardiovascular Diseases

article

HCP5 genetic variant (RS3099844) contributes to Nevirapine-induced Stevens Johnsons Syndrome/Toxic Epidermal Necrolysis susceptibility in a population from Mozambique.

artículo científico publicado en 2013

Haplotypes in IL-8 Gene Are Associated to Age-Related Macular Degeneration: A Case-Control Study.

artículo científico publicado en 2013

Haptoglobin development in newborn infants from diabetic mothers

artículo científico publicado en 1994

High warfarin sensitivity in carriers of CYP2C9*35 is determined by the impaired interaction with P450 oxidoreductase.

artículo científico publicado en 2013

IL-4 receptor alpha chain genetic polymorphism and total IgE levels in the English population: two-locus haplotypes are more informative than individual SNPs

scientific article published on 01 April 2002

Impact of the CYP4F2 p.V433M polymorphism on coumarin dose requirement: systematic review and meta-analysis

artículo científico publicado en 2012

Interaction between ABO blood groups and ADA genetic polymorphism during intrauterine life. A comparative analysis of couples with habitual abortion and normal puerperae delivering a live-born infant

artículo científico publicado en 1995

Interleukin-23R Arg381Gln is associated with susceptibility to Crohn's disease but not with phenotype in an Italian population

artículo científico publicado en 2007

Intrauterine development and MNSs blood groups in repeated spontaneous abortion.

artículo científico publicado en 2003

MicroRNA genetic variations: association with type 2 diabetes

artículo científico publicado en 2013

Neonatal screening, clinical features and genetic testing for galactosemia

artículo científico publicado en 2005

Nevirapine-induced hepatotoxicity and pharmacogenetics: a retrospective study in a population from Mozambique

artículo científico publicado en 2010

OLR1 gene and coronary artery disease/acute myocardial infarction: replication in an independently collected sample

article

Phosphotyrosine protein phosphatases and diabetic pregnancy: an association between low molecular weight acid phosphatase and degree of glycemic control.

artículo científico publicado en 1996

Psoriatic arthritis and CARD15 gene polymorphisms: no evidence for association in the Italian population.

artículo científico publicado en 2004

Role of genetics in prevention of coronary atherosclerosis.

artículo científico publicado en 2003

TCF7L2 gene polymorphisms and type 2 diabetes: association with diabetic retinopathy and cardiovascular autonomic neuropathy

article

TRAF3IP2 gene is associated with cutaneous extraintestinal manifestations in inflammatory bowel disease.

artículo científico publicado en 2012

Type 2 diabetes and the genetics of signal transduction: a study of interaction between adenosine deaminase and acid phosphatase locus 1 polymorphisms.

artículo científico publicado en 2004