Lista de obras - Antonio Amoroso - Dominio Público Uruguay

A Reliable Screening Procedure for Coeliac Disease in Clinical Practice

artículo científico publicado en 2002

A SPRY2 mutation leading to MAPK/ERK pathway inhibition is associated with an autosomal dominant form of IgA nephropathy

artículo científico publicado en 2015

A new polymorphism, g119A>G, in the integrin alpha 7 (ITGA7) gene

article

A novel defect in mitochondrial p53 accumulation following DNA damage confers apoptosis resistance in Ataxia Telangiectasia and Nijmegen Breakage Syndrome T-cells.

artículo científico publicado en 2010

A rapid and quantitative mass spectrometry method for determining the concentration of acylcarnitines and aminoacids in amniotic fluid.

artículo científico publicado en 2001

A rapid flow cytometry test based on histone H2AX phosphorylation for the sensitive and specific diagnosis of ataxia telangiectasia.

artículo científico publicado en 2008

A single-nucleotide polymorphism in the human beta-defensin 1 gene is associated with HIV-1 infection in Italian children

artículo científico publicado en 2004

A study of host defence peptide beta-defensin 3 in primates

artículo científico publicado en 2003

A xenogeneic monoclonal antibody recognizing specificities controlled by HLA-A and B alleles

artículo científico publicado en 1981

ALS with variable phenotypes in a six-generation family caused by leu144phe mutation in the SOD1 gene

artículo científico publicado en 2001

Allelism of MCKD, FJHN and GCKD caused by impairment of uromodulin export dynamics

article

An in vitro model of T cell receptor revision in mature human CD8+ T cells.

artículo científico publicado en 2007

Antibodies to anionic phospholipids and anti-beta2-GPI: association with thrombosis and thrombocytopenia in systemic lupus erythematosus

artículo científico publicado en 2003

Association of interferon-gamma +874A polymorphism with reduced long-term inflammatory response in haemodialysis patients.

artículo científico publicado en 2006

Autosomal dominant Alport syndrome: molecular analysis of the COL4A4 gene and clinical outcome.

artículo científico publicado en 2009

Autosomal dominant medullary cystic disease: a disorder with variable clinical pictures and exclusion of linkage with the NPH1 locus

scientific article published on 01 October 1998

B cell positive cross-match not due to anti-HLA Class I antibodies and first kidney graft outcome

artículo científico publicado en 2008

Beta-defensin 1 gene variability among non-human primates

artículo científico publicado en 2002

Brief report: Why did two patients who type for HLA-B13 have antibodies that react with all Bw4 antigens except HLA-B13?

artículo científico publicado en 2011

Centenarian Livers: Very Long-term Outcomes of Very Old Grafts.

artículo científico publicado en 2017

Changing trends in corneal graft surgery: a ten-year review.

artículo científico publicado en 2016

Clearance of polymeric IgA aggregates in humans

scientific article published on 01 November 1989

Combined prophylaxis decreases incidence of CMV-associated pneumonia after lung transplantation.

artículo científico publicado en 2009

Cytokine gene polymorphisms in hepatitis C virus-related oral lichen planus.

artículo científico publicado en 2007

Defective intracellular trafficking of uromodulin mutant isoforms

artículo científico publicado en 2006

Detection of Angiotensin II type I-receptor antibodies in transplant glomerulopathy

scientific article published on 22 November 2018

Diagnosis of triploidy in metaphases from uncultured amniocytes

artículo científico publicado en 2002

Discordant evolution of nephrotic syndrome in mono- and dizygotic twins

scientific article published on 29 December 2005

Discovery of new risk loci for IgA nephropathy implicates genes involved in immunity against intestinal pathogens

artículo científico publicado en 2014

Distribution of tumor necrosis factor alleles (NcoI RFLP) and their relationship to HLA haplotypes in an Italian population

scientific article published on 01 March 1993

Donor CYP3A5 genotype influences tacrolimus disposition on the first day after paediatric liver transplantation.

artículo científico publicado en 2017

Early reduced liver graft survival in hepatitis C recipients identified by two combined genetic markers

artículo científico publicado en 2016

Estimation of human leukocyte antigen class I and class II high-resolution allele and haplotype frequencies in the Italian population and comparison with other European populations

artículo científico publicado en 2012

Evaluation of different technical approaches for the research of human anti-Ia alloantisera

scientific article published on 01 May 1982

Evidence of a correlation between mannose binding lectin and celiac disease: a model for other autoimmune diseases

artículo científico publicado en 2005

Evolution of the mannose-binding lectin gene in primates.

artículo científico publicado en 2004

Ex vivo lung perfusion increases the pool of lung grafts: analysis of its potential and real impact on a lung transplant program

artículo científico publicado en 2013

Exome sequencing in children of women with skewed X-inactivation identifies atypical cases and complex phenotypes.

artículo científico publicado en 2016

Fc-receptor function of the mononuclear phagocyte system in glomerulonephritis secondary to some multisystem diseases

scientific article published on 01 January 1987

Fragile X syndrome, mental retardation and macroorchidism

scientific article published on 01 October 1998

Frequency of the HFE gene mutations in five Italian populations.

artículo científico publicado en 2002

Frequency of the new HLA-B*2709 allele in ankylosing spondylitis patients and healthy individuals

artículo científico publicado en 1995

Genetic factors in mother-to-child transmission of HCV infection

artículo científico publicado en 2009

Genetic heterogeneity in Italian families with IgA nephropathy: suggestive linkage for two novel IgA nephropathy loci

artículo científico publicado en 2006

Genome-Wide Association Study Identifies Risk Variants for Lichen Planus in Patients With Hepatitis C Virus Infection

artículo científico publicado en 2017

Genome-Wide Study Updates in the International Genetics and Translational Research in Transplantation Network (iGeneTRAiN)

artículo científico publicado en 2019

Genome-wide association study identifies susceptibility loci for IgA nephropathy

artículo científico publicado en 2011

Genomic Mismatch at LIMS1 Locus and Kidney Allograft Rejection

scientific article published on 01 May 2019

Geographic differences in genetic susceptibility to IgA nephropathy: GWAS replication study and geospatial risk analysis

artículo científico publicado en 2012

HLA-C/KIR genotypes in oral lichen planus patients infected or non-infected with hepatitis C virus.

artículo científico publicado en 2010

HLA-DR antigens in HBsAg-positive chronic active liver disease with and without associated delta infection

scientific article published on 01 November 1984

Hepatic uptake of organic anions affects the plasma bilirubin level in subjects with Gilbert's syndrome mutations in UGT1A1

scientific article published on 01 March 2001

Human Liver Stem Cells Suppress T-Cell Proliferation, NK Activity, and Dendritic Cell Differentiation

artículo científico publicado en 2016

Human mesenchymal stem cell-derived microvesicles modulate T cell response to islet antigen glutamic acid decarboxylase in patients with type 1 diabetes

article

Human mesenchymal stem cells modulate cellular immune response to islet antigen glutamic acid decarboxylase in type 1 diabetes

artículo científico publicado en 2010

Identification of a new allele, HLA-DRB5*0113, through three different molecular biology techniques.

artículo científico publicado en 2006

IgA Nephropathy: The Presence of Familial Disease Does Not Confer an Increased Risk for Progression

artículo científico publicado en 2006

Immune function assay (immunknow) drop over first 6 months after renal transplant: a predictor of opportunistic viral infections?

artículo científico publicado en 2014

Impact of viral eradication with sofosbuvir-based therapy on the outcome of post-transplant hepatitis C with severe fibrosis.

artículo científico publicado en 2016

Interleukin-4RA gene polymorphism is associated with oral mucous membrane pemphigoid

artículo científico publicado en 2013

Intrahepatic Administration of Human Liver Stem Cells in Infants with Inherited Neonatal-Onset Hyperammonemia: A Phase I Study

scientific article published on 01 February 2020

Involvement of HLA class I alleles in natural killer (NK) cell-specific functions: expression of HLA-Cw3 confers selective protection from lysis by alloreactive NK clones displaying a defined specificity (specificity 2) ⬇️

artículo científico publicado el 1 de octubre de 1992

Linkage and linkage disequilibrium analysis of X-STRs in Italian families.

artículo científico publicado en 2010

Liver transplantation in defects of cholesterol biosynthesis: the case of lathosterolosis

artículo científico publicado en 2014

Long-Term Outcomes and Discard Rate of Kidneys by Decade of Extended Criteria Donor Age.

artículo científico publicado en 2016

MBL2 and MASP2 gene polymorphisms in patients with hepatocellular carcinoma.

artículo científico publicado en 2008

MBL2 polymorphisms are involved in HIV-1 infection in Brazilian perinatally infected children

artículo científico publicado en 2003

Melusin gene (ITGB1BP2) nucleotide variations study in hypertensive and cardiopathic patients

artículo científico publicado en 2009

Molecular analysis of hyperoxaluria type 1 in Italian patients reveals eight new mutations in the alanine: glyoxylate aminotransferase gene

artículo científico publicado en 1999

Molecular aspects of a novel HLA-A02 allele (A0297): the first HLA class I allele mutated at codon 232

artículo científico publicado en 2007

Multicenter study on hepatitis C virus-related cryoglobulinemic glomerulonephritis.

artículo científico publicado en 2007

NADPH oxidase (NOX2) activity is a modifier of survival in ALS.

artículo científico publicado en 2014

NADPH oxidase 2 (NOX2) enzyme activation in patients with chronic inflammatory demyelinating polyneuropathy

artículo científico publicado en 2016

OMiR: Identification of associations between OMIM diseases and microRNAs

artículo científico publicado en 2010

Osteopontin gene haplotypes correlate with multiple sclerosis development and progression

scientific article published on 25 April 2005

Peptide-specific CTL in tumor infiltrating lymphocytes from metastatic melanomas expressing MART-1/Melan-A, gp100 and Tyrosinase genes: a study in an unselected group of HLA-A2.1-positive patients.

artículo científico publicado en 1995

Phosphorylated alpha-enolase induces autoantibodies in HLA-DR8 pancreatic cancer patients and triggers HLA-DR8 restricted T-cell activation

artículo científico publicado en 2015

Physical and functional independency of p70 and p58 natural killer (NK) cell receptors for HLA class I: their role in the definition of different groups of alloreactive NK cell clones.

scientific article published on February 1996

Polymorphism at codon 54 of mannose-binding protein gene influences AIDS progression but not HIV infection in exposed children

article

Primary hyperoxaluria type 1: update and additional mutation analysis of the AGXT gene.

artículo científico publicado en 2009

Prognostic value of the stromal cell-derived factor 1 3'A mutation in pediatric human immunodeficiency virus type 1 infection

artículo científico publicado en 2002

Prognostic values of soluble CD30 and CD30 gene polymorphisms in heart transplantation

artículo científico publicado en 2006

Quantitation of HBV cccDNA in anti-HBc-positive liver donors by droplet digital PCR: a new tool to detect occult infection.

artículo científico publicado en 2018

Rare Functional Variants in Complement Genes and Anti-FH Autoantibodies-Associated aHUS

article

Relationship among C1q-fixing de novo donor specific antibodies, C4d deposition and renal outcome in transplant glomerulopathy.

artículo científico

Role of interferon-gamma gene polymorphisms in susceptibility to IgA nephropathy: a family-based association study

artículo científico publicado en 2006

Role of non-HLA genetic polymorphisms in graft-versus-host disease after haematopoietic stem cell transplantation

scientific article published on 01 October 2006

Search for genetic association between IgA nephropathy and candidate genes selected by function or by gene mapping at loci IGAN2 and IGAN3

article

Secreted protein acidic and rich in cysteine (SPARC) gene polymorphism association with hepatocellular carcinoma in Italian patients

artículo científico publicado en 2009

Severe course of primary hyperoxaluria and renal failure after domino hepatic transplantation.

artículo científico publicado en 2005

Successful Urgent Liver Retransplantation for Donor-Transmitted Hepatocellular Carcinoma

artículo científico publicado en 2016

T cell neoepitope discovery in colorectal cancer by high throughput profiling of somatic mutations in expressed genes

artículo científico publicado en 2015

The IgA nephropathy Biobank. An important starting point for the genetic dissection of a complex trait.

artículo científico publicado en 2005

The cyclin-dependent kinase inhibitor 5, 6-dichloro-1-beta-D-ribofuranosylbenzimidazole induces nongenotoxic, DNA replication-independent apoptosis of normal and leukemic cells, regardless of their p53 status

artículo científico publicado en 2009

The distribution of KIR-HLA functional blocks is different from north to south of Italy

artículo científico publicado en 2014

The genetic architecture of membranous nephropathy and its potential to improve non-invasive diagnosis

artículo científico publicado en 2020

The rediscovery of uromodulin (Tamm-Horsfall protein): from tubulointerstitial nephropathy to chronic kidney disease.

scientific article published on 08 June 2011

Tracking of the origin of recurrent mutations of the BRCA1 and BRCA2 genes in the North-East of Italy and improved mutation analysis strategy

artículo científico publicado en 2016

Treatment with plasmapheresis, immunoglobulins and rituximab for chronic-active antibody-mediated rejection in kidney transplantation: Clinical, immunological and pathological results

artículo científico publicado en 2018

Two-tier analysis of histone H2AX phosphorylation allows the identification of Ataxia Telangiectasia heterozygotes

scientific article published on 23 January 2009

Updated genetic testing of Italian patients referred with a clinical diagnosis of primary hyperoxaluria

article

Urinary secretion and extracellular aggregation of mutant uromodulin isoforms.

artículo científico publicado en 2012

Uromodulin storage diseases: clinical aspects and mechanisms

artículo científico publicado en 2004

Variant mannose-binding lectin alleles are associated with celiac disease

artículo científico publicado en 2002

YouTube®: An ally or an enemy in the promotion of living donor kidney transplantation?

artículo científico publicado en 2016

Lista de obras de Antonio Amoroso

A Reliable Screening Procedure for Coeliac Disease in Clinical Practice

A SPRY2 mutation leading to MAPK/ERK pathway inhibition is associated with an autosomal dominant form of IgA nephropathy

A new polymorphism, g119A>G, in the integrin alpha 7 (ITGA7) gene

A novel defect in mitochondrial p53 accumulation following DNA damage confers apoptosis resistance in Ataxia Telangiectasia and Nijmegen Breakage Syndrome T-cells.

A rapid and quantitative mass spectrometry method for determining the concentration of acylcarnitines and aminoacids in amniotic fluid.

A rapid flow cytometry test based on histone H2AX phosphorylation for the sensitive and specific diagnosis of ataxia telangiectasia.

A single-nucleotide polymorphism in the human beta-defensin 1 gene is associated with HIV-1 infection in Italian children

A study of host defence peptide beta-defensin 3 in primates

A xenogeneic monoclonal antibody recognizing specificities controlled by HLA-A and B alleles

ALS with variable phenotypes in a six-generation family caused by leu144phe mutation in the SOD1 gene

Allelism of MCKD, FJHN and GCKD caused by impairment of uromodulin export dynamics

An in vitro model of T cell receptor revision in mature human CD8+ T cells.

Antibodies to anionic phospholipids and anti-beta2-GPI: association with thrombosis and thrombocytopenia in systemic lupus erythematosus

Association of interferon-gamma +874A polymorphism with reduced long-term inflammatory response in haemodialysis patients.

Autosomal dominant Alport syndrome: molecular analysis of the COL4A4 gene and clinical outcome.

Autosomal dominant medullary cystic disease: a disorder with variable clinical pictures and exclusion of linkage with the NPH1 locus

B cell positive cross-match not due to anti-HLA Class I antibodies and first kidney graft outcome

Beta-defensin 1 gene variability among non-human primates

Brief report: Why did two patients who type for HLA-B13 have antibodies that react with all Bw4 antigens except HLA-B13?

Centenarian Livers: Very Long-term Outcomes of Very Old Grafts.

Changing trends in corneal graft surgery: a ten-year review.

Clearance of polymeric IgA aggregates in humans

Combined prophylaxis decreases incidence of CMV-associated pneumonia after lung transplantation.

Cytokine gene polymorphisms in hepatitis C virus-related oral lichen planus.

Defective intracellular trafficking of uromodulin mutant isoforms

Detection of Angiotensin II type I-receptor antibodies in transplant glomerulopathy

Diagnosis of triploidy in metaphases from uncultured amniocytes

Discordant evolution of nephrotic syndrome in mono- and dizygotic twins

Discovery of new risk loci for IgA nephropathy implicates genes involved in immunity against intestinal pathogens

Distribution of tumor necrosis factor alleles (NcoI RFLP) and their relationship to HLA haplotypes in an Italian population

Donor CYP3A5 genotype influences tacrolimus disposition on the first day after paediatric liver transplantation.

Early reduced liver graft survival in hepatitis C recipients identified by two combined genetic markers

Estimation of human leukocyte antigen class I and class II high-resolution allele and haplotype frequencies in the Italian population and comparison with other European populations

Evaluation of different technical approaches for the research of human anti-Ia alloantisera

Evidence of a correlation between mannose binding lectin and celiac disease: a model for other autoimmune diseases

Evolution of the mannose-binding lectin gene in primates.

Ex vivo lung perfusion increases the pool of lung grafts: analysis of its potential and real impact on a lung transplant program

Exome sequencing in children of women with skewed X-inactivation identifies atypical cases and complex phenotypes.

Fc-receptor function of the mononuclear phagocyte system in glomerulonephritis secondary to some multisystem diseases

Fragile X syndrome, mental retardation and macroorchidism

Frequency of the HFE gene mutations in five Italian populations.

Frequency of the new HLA-B*2709 allele in ankylosing spondylitis patients and healthy individuals

Genetic factors in mother-to-child transmission of HCV infection

Genetic heterogeneity in Italian families with IgA nephropathy: suggestive linkage for two novel IgA nephropathy loci

Genome-Wide Association Study Identifies Risk Variants for Lichen Planus in Patients With Hepatitis C Virus Infection

Genome-Wide Study Updates in the International Genetics and Translational Research in Transplantation Network (iGeneTRAiN)

Genome-wide association study identifies susceptibility loci for IgA nephropathy

Genomic Mismatch at LIMS1 Locus and Kidney Allograft Rejection

Geographic differences in genetic susceptibility to IgA nephropathy: GWAS replication study and geospatial risk analysis

HLA-C/KIR genotypes in oral lichen planus patients infected or non-infected with hepatitis C virus.

HLA-DR antigens in HBsAg-positive chronic active liver disease with and without associated delta infection

Hepatic uptake of organic anions affects the plasma bilirubin level in subjects with Gilbert's syndrome mutations in UGT1A1

Human Liver Stem Cells Suppress T-Cell Proliferation, NK Activity, and Dendritic Cell Differentiation

Human mesenchymal stem cell-derived microvesicles modulate T cell response to islet antigen glutamic acid decarboxylase in patients with type 1 diabetes

Human mesenchymal stem cells modulate cellular immune response to islet antigen glutamic acid decarboxylase in type 1 diabetes

Identification of a new allele, HLA-DRB5*0113, through three different molecular biology techniques.

IgA Nephropathy: The Presence of Familial Disease Does Not Confer an Increased Risk for Progression

Immune function assay (immunknow) drop over first 6 months after renal transplant: a predictor of opportunistic viral infections?

Impact of viral eradication with sofosbuvir-based therapy on the outcome of post-transplant hepatitis C with severe fibrosis.

Interleukin-4RA gene polymorphism is associated with oral mucous membrane pemphigoid

Intrahepatic Administration of Human Liver Stem Cells in Infants with Inherited Neonatal-Onset Hyperammonemia: A Phase I Study

Involvement of HLA class I alleles in natural killer (NK) cell-specific functions: expression of HLA-Cw3 confers selective protection from lysis by alloreactive NK clones displaying a defined specificity (specificity 2) ⬇️

Linkage and linkage disequilibrium analysis of X-STRs in Italian families.

Liver transplantation in defects of cholesterol biosynthesis: the case of lathosterolosis

Long-Term Outcomes and Discard Rate of Kidneys by Decade of Extended Criteria Donor Age.

MBL2 and MASP2 gene polymorphisms in patients with hepatocellular carcinoma.

MBL2 polymorphisms are involved in HIV-1 infection in Brazilian perinatally infected children

Melusin gene (ITGB1BP2) nucleotide variations study in hypertensive and cardiopathic patients

Molecular analysis of hyperoxaluria type 1 in Italian patients reveals eight new mutations in the alanine: glyoxylate aminotransferase gene

Molecular aspects of a novel HLA-A*02 allele (A*0297): the first HLA class I allele mutated at codon 232

Multicenter study on hepatitis C virus-related cryoglobulinemic glomerulonephritis.

NADPH oxidase (NOX2) activity is a modifier of survival in ALS.

NADPH oxidase 2 (NOX2) enzyme activation in patients with chronic inflammatory demyelinating polyneuropathy

OMiR: Identification of associations between OMIM diseases and microRNAs

Osteopontin gene haplotypes correlate with multiple sclerosis development and progression

Peptide-specific CTL in tumor infiltrating lymphocytes from metastatic melanomas expressing MART-1/Melan-A, gp100 and Tyrosinase genes: a study in an unselected group of HLA-A2.1-positive patients.

Phosphorylated alpha-enolase induces autoantibodies in HLA-DR8 pancreatic cancer patients and triggers HLA-DR8 restricted T-cell activation

Physical and functional independency of p70 and p58 natural killer (NK) cell receptors for HLA class I: their role in the definition of different groups of alloreactive NK cell clones.

Polymorphism at codon 54 of mannose-binding protein gene influences AIDS progression but not HIV infection in exposed children

Molecular aspects of a novel HLA-A02 allele (A0297): the first HLA class I allele mutated at codon 232