Lista de obras - Juan Sainz - Dominio Público Uruguay

A common variant within the HNF1B gene is associated with overall survival of multiple myeloma patients: results from the IMMEnSE consortium and meta-analysis.

artículo científico publicado en 2016

A comprehensive investigation on common polymorphisms in the MDR1/ABCB1 transporter gene and susceptibility to colorectal cancer

artículo científico publicado en 2012

Antioxidant enzymes and effects of tempol on the development of hypertension induced by nitric oxide inhibition.

artículo científico publicado en 2005

Association between genetic polymorphism in the promotor region of CD209 and propensity to develop invasive pulmonary aspergillosis

artículo científico publicado en 2010

Common Genetic Polymorphisms within NFκB-Related Genes and the Risk of Developing Invasive Aspergillosis

artículo científico publicado en 2016

Common gene variants within 3'-untranslated regions as modulators of multiple myeloma risk and survival

scientific article published on 05 November 2020

Comprehensive investigation of genetic variation in the 8q24 region and multiple myeloma risk in the IMMEnSE consortium

artículo científico publicado en 2012

Contribution of endothelium-derived relaxing factors to P2Y-purinoceptor-induced vasodilation in the isolated rat kidney

artículo científico publicado en 2000

Correction: Polymorphisms at phase I-metabolizing enzyme and hormone receptor loci influence the response to anti-TNF therapy in rheumatoid arthritis patients

scientific article published on 01 December 2019

Corrigendum: Genome-wide association study identifies variants at 16p13 associated with survival in multiple myeloma patients

artículo científico publicado en 2015

Dectin-1 and DC-SIGN polymorphisms associated with invasive pulmonary Aspergillosis infection

artículo científico publicado en 2012

Do myeloproliferative neoplasms and multiple myeloma share the same genetic susceptibility loci?

artículo científico publicado en 2020

Early mortality in multiple myeloma: the time-dependent impact of comorbidity: A population-based study in 621 real-life patients

artículo científico publicado en 2016

Effect of type 2 diabetes predisposing genetic variants on colorectal cancer risk

artículo científico publicado en 2012

Effects of deoxycorticosterone on renal vascular reactivity and flow-pressure curve in spontaneously hypertensive rats.

artículo científico publicado en 2004

Exome sequencing identifies germline variants in DIS3 in familial multiple myeloma.

artículo científico publicado en 2019

GWAS-identified common variants for obesity are not associated with the risk of developing colorectal cancer

artículo científico publicado en 2014

Gender difference in the role of endothelium-derived relaxing factors modulating renal vascular reactivity

scientific article published on 01 February 2004

Gender-specific effects of genetic variants within Th1 and Th17 cell-mediated immune response genes on the risk of developing rheumatoid arthritis

artículo científico publicado en 2013

Genetic Variants and Multiple Myeloma Risk: IMMEnSE Validation of the Best Reported Associations--An Extensive Replication of the Associations from the Candidate Gene Era

article

Genetic polymorphisms associated with telomere length and risk of developing myeloproliferative neoplasms

artículo científico publicado en 2020

Genetic polymorphisms in genes of class switch recombination and multiple myeloma risk and survival: an IMMEnSE study

article

Genetic variants of IL6 gene promoter influence on C-reactive protein levels but are not associated with susceptibility to invasive pulmonary aspergillosis in haematological patients

scientific article published on 11 January 2008

Genetic variants within immune-modulating genes influence the risk of developing rheumatoid arthritis and anti-TNF drug response: a two-stage case-control study.

artículo científico publicado en 2015

Genetic variants within the TNFRSF1B gene and susceptibility to rheumatoid arthritis and response to anti-TNF drugs

article

Genetics and molecular epidemiology of multiple myeloma: the rationale for the IMMEnSE consortium (review).

artículo científico

Genome-wide association study identifies variants at 16p13 associated with survival in multiple myeloma patients.

artículo científico publicado en 2015

Genome-wide gene expression analysis in mouse embryonic stem cells.

artículo científico publicado en 2011

Host immune genetic variations influence the risk of developing acute myeloid leukaemia: results from the NuCLEAR consortium

artículo científico publicado en 2020

IL-10 overexpression predisposes to invasive aspergillosis by suppressing antifungal immunity

artículo científico publicado en 2017

IL1 gene cluster polymorphisms and its haplotypes may predict the risk to develop invasive pulmonary aspergillosis and modulate C-reactive protein level.

artículo científico publicado en 2008

Identification of miRSNPs associated with the risk of multiple myeloma.

artículo científico publicado en 2016

Impact of polymorphic variation at 7p15.3, 3p22.1 and 2p23.3 loci on risk of multiple myeloma

Inherited variation in the xenobiotic transporter pathway and survival of multiple myeloma patients

artículo científico publicado en 2018

Interleukin-10 promoter polymorphism as risk factor to develop invasive pulmonary aspergillosis

artículo científico publicado en 2007

NFKB2 polymorphisms associate with the risk of developing rheumatoid arthritis and response to TNF inhibitors: Results from the REPAIR consortium

scientific article published on 09 March 2020

Polymorphisms in Host Immunity-Modulating Genes and Risk of Invasive Aspergillosis: Results from the AspBIOmics Consortium

artículo científico publicado en 2015

Polymorphisms in regulators of xenobiotic transport and metabolism genes PXR and CAR do not affect multiple myeloma risk: a case-control study in the context of the IMMEnSE consortium

artículo científico publicado en 2013

Polymorphisms in xenobiotic transporters ABCB1, ABCG2, ABCC2, ABCC1, ABCC3 and multiple myeloma risk: a case–control study in the context of the International Multiple Myeloma rESEarch (IMMEnSE) consortium

artículo científico publicado en 2011

Polymorphisms within the <i>TNFSF4</i> and <i>MAPKAPK2</i> Loci Influence the Risk of Developing Invasive Aspergillosis: A Two-Stage Case Control Study in the Context of the aspBIOmics Consortium

artículo científico publicado en 2020

Repeat polymorphisms in ESR2 and AR and colorectal cancer risk and prognosis: results from a German population-based case-control study

artículo científico publicado en 2014

Risk of multiple myeloma is associated with polymorphisms within telomerase genes and telomere length.

artículo científico publicado en 2014

Role of endothelium-derived relaxing factors in adrenomedullin-induced vasodilation in the rat kidney

artículo científico publicado en 2002

Role of endothelium-derived relaxing factors in the renal response to vasoactive agents in hypothyroid rats.

artículo científico publicado en 2003

Steroid hormone-related polymorphisms associate with the development of bone erosions in rheumatoid arthritis and help to predict disease progression: Results from the REPAIR consortium

artículo científico publicado en 2019

TNFR1 mRNA expression level and TNFR1 gene polymorphisms are predictive markers for susceptibility to develop invasive pulmonary aspergillosis.

artículo científico publicado en 2010

TRAF1/C5 but not PTPRC variants are potential predictors of rheumatoid arthritis response to anti-tumor necrosis factor therapy.

artículo científico publicado en 2015

Transplantation-Associated Thrombotic Microangiopathy in Patients Treated With Sirolimus and Cyclosporine as Salvage Therapy for Graft-Versus-Host Disease

artículo científico publicado en 2015

Type 2 diabetes-related variants influence the risk of developing multiple myeloma: results from the IMMEnSE consortium

artículo científico publicado en 2015

Variable number of tandem repeats of TNF receptor type 2 promoter as genetic biomarker of susceptibility to develop invasive pulmonary aspergillosis

artículo científico publicado en 2006

Lista de obras de Juan Sainz

A common variant within the HNF1B gene is associated with overall survival of multiple myeloma patients: results from the IMMEnSE consortium and meta-analysis.

A comprehensive investigation on common polymorphisms in the MDR1/ABCB1 transporter gene and susceptibility to colorectal cancer

Antioxidant enzymes and effects of tempol on the development of hypertension induced by nitric oxide inhibition.

Association between genetic polymorphism in the promotor region of CD209 and propensity to develop invasive pulmonary aspergillosis

Common Genetic Polymorphisms within NFκB-Related Genes and the Risk of Developing Invasive Aspergillosis

Common gene variants within 3'-untranslated regions as modulators of multiple myeloma risk and survival

Comprehensive investigation of genetic variation in the 8q24 region and multiple myeloma risk in the IMMEnSE consortium

Contribution of endothelium-derived relaxing factors to P2Y-purinoceptor-induced vasodilation in the isolated rat kidney

Correction: Polymorphisms at phase I-metabolizing enzyme and hormone receptor loci influence the response to anti-TNF therapy in rheumatoid arthritis patients

Corrigendum: Genome-wide association study identifies variants at 16p13 associated with survival in multiple myeloma patients

Dectin-1 and DC-SIGN polymorphisms associated with invasive pulmonary Aspergillosis infection

Do myeloproliferative neoplasms and multiple myeloma share the same genetic susceptibility loci?

Early mortality in multiple myeloma: the time-dependent impact of comorbidity: A population-based study in 621 real-life patients

Effect of type 2 diabetes predisposing genetic variants on colorectal cancer risk

Effects of deoxycorticosterone on renal vascular reactivity and flow-pressure curve in spontaneously hypertensive rats.

Exome sequencing identifies germline variants in DIS3 in familial multiple myeloma.

GWAS-identified common variants for obesity are not associated with the risk of developing colorectal cancer

Gender difference in the role of endothelium-derived relaxing factors modulating renal vascular reactivity

Gender-specific effects of genetic variants within Th1 and Th17 cell-mediated immune response genes on the risk of developing rheumatoid arthritis

Genetic Variants and Multiple Myeloma Risk: IMMEnSE Validation of the Best Reported Associations--An Extensive Replication of the Associations from the Candidate Gene Era

Genetic polymorphisms associated with telomere length and risk of developing myeloproliferative neoplasms

Genetic polymorphisms in genes of class switch recombination and multiple myeloma risk and survival: an IMMEnSE study

Genetic variants of IL6 gene promoter influence on C-reactive protein levels but are not associated with susceptibility to invasive pulmonary aspergillosis in haematological patients

Genetic variants within immune-modulating genes influence the risk of developing rheumatoid arthritis and anti-TNF drug response: a two-stage case-control study.

Genetic variants within the TNFRSF1B gene and susceptibility to rheumatoid arthritis and response to anti-TNF drugs

Genetics and molecular epidemiology of multiple myeloma: the rationale for the IMMEnSE consortium (review).

Genome-wide association study identifies variants at 16p13 associated with survival in multiple myeloma patients.

Genome-wide gene expression analysis in mouse embryonic stem cells.

Host immune genetic variations influence the risk of developing acute myeloid leukaemia: results from the NuCLEAR consortium

IL-10 overexpression predisposes to invasive aspergillosis by suppressing antifungal immunity

IL1 gene cluster polymorphisms and its haplotypes may predict the risk to develop invasive pulmonary aspergillosis and modulate C-reactive protein level.

Identification of miRSNPs associated with the risk of multiple myeloma.

Impact of polymorphic variation at 7p15.3, 3p22.1 and 2p23.3 loci on risk of multiple myeloma

Inherited variation in the xenobiotic transporter pathway and survival of multiple myeloma patients

Interleukin-10 promoter polymorphism as risk factor to develop invasive pulmonary aspergillosis

NFKB2 polymorphisms associate with the risk of developing rheumatoid arthritis and response to TNF inhibitors: Results from the REPAIR consortium

Polymorphisms in Host Immunity-Modulating Genes and Risk of Invasive Aspergillosis: Results from the AspBIOmics Consortium

Polymorphisms in regulators of xenobiotic transport and metabolism genes PXR and CAR do not affect multiple myeloma risk: a case-control study in the context of the IMMEnSE consortium

Polymorphisms in xenobiotic transporters ABCB1, ABCG2, ABCC2, ABCC1, ABCC3 and multiple myeloma risk: a case–control study in the context of the International Multiple Myeloma rESEarch (IMMEnSE) consortium

Polymorphisms within the <i>TNFSF4</i> and <i>MAPKAPK2</i> Loci Influence the Risk of Developing Invasive Aspergillosis: A Two-Stage Case Control Study in the Context of the aspBIOmics Consortium

Repeat polymorphisms in ESR2 and AR and colorectal cancer risk and prognosis: results from a German population-based case-control study

Risk of multiple myeloma is associated with polymorphisms within telomerase genes and telomere length.

Role of endothelium-derived relaxing factors in adrenomedullin-induced vasodilation in the rat kidney

Role of endothelium-derived relaxing factors in the renal response to vasoactive agents in hypothyroid rats.

Steroid hormone-related polymorphisms associate with the development of bone erosions in rheumatoid arthritis and help to predict disease progression: Results from the REPAIR consortium

TNFR1 mRNA expression level and TNFR1 gene polymorphisms are predictive markers for susceptibility to develop invasive pulmonary aspergillosis.

TRAF1/C5 but not PTPRC variants are potential predictors of rheumatoid arthritis response to anti-tumor necrosis factor therapy.

Transplantation-Associated Thrombotic Microangiopathy in Patients Treated With Sirolimus and Cyclosporine as Salvage Therapy for Graft-Versus-Host Disease

Type 2 diabetes-related variants influence the risk of developing multiple myeloma: results from the IMMEnSE consortium

Variable number of tandem repeats of TNF receptor type 2 promoter as genetic biomarker of susceptibility to develop invasive pulmonary aspergillosis