Lista de obras - Stefano Landi - Dominio Público Uruguay

A DATABASE OF SINGLE-NUCLEOTIDE POLYMORPHISMS AND A GENOTYPING MICROARRAY FOR GENETIC EPIDEMIOLOGY OF LUNG CANCER

artículo científico publicado en 2005

A TP53 polymorphism is associated with increased risk of colorectal cancer and with reduced levels of TP53 mRNA.

artículo científico publicado en 2004

A catalogue of polymorphisms related to xenobiotic metabolism and cancer susceptibility.

artículo científico publicado en 2002

A common polymorphism within MSLN affects miR-611 binding site and soluble mesothelin levels in healthy people.

artículo científico publicado en 2014

A novel similarity-measure for the analysis of genetic data in complex phenotypes

artículo científico publicado en 2009

A review of transcriptome studies combined with data mining reveals novel potential markers of malignant pleural mesothelioma

artículo científico publicado en 2011

ABO blood groups and pancreatic cancer risk and survival: results from the PANcreatic Disease ReseArch (PANDoRA) consortium.

artículo científico publicado en 2013

APEX DNA Microarray for the Identification of Pathogenic Fungi

scientific article published on 01 January 2013

Ala147Thr substitution in translocator protein is associated with adult separation anxiety in patients with depression

artículo científico publicado en 2009

Are baseline frequencies of SCEs, CAs, and MN in human lymphocytes related to hematological values?

scientific article published on 01 August 2000

Association between CYP2E1 polymorphisms and risk of differentiated thyroid carcinoma

artículo científico publicado en 2016

COMPASSS (COMplex PAttern of Sequence Search Software), a simple and effective tool for mining complex motifs in whole genomes

artículo científico publicado en 2010

Characterization of novel 3'untranslated regions and related polymorphisms of the gene NPPC, encoding for the C-type natriuretic peptide.

artículo científico publicado en 2013

Common variation at 2p13.3, 3q29, 7p13 and 17q25.1 associated with susceptibility to pancreatic cancer

artículo científico publicado en 2015

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

artículo científico publicado en 2012

DNA Repair and Cell Cycle Control Genes and the Risk of Young-Onset Lung Cancer

article

DNA microarray based on arrayed-primer extension technique for identification of pathogenic fungi responsible for invasive and superficial mycoses

artículo científico publicado en 2007

DeltaN133p53 expression levels in relation to haplotypes of the TP53 internal promoter region

artículo científico publicado en 2010

Detailed haplotype analysis at the TP53 locus in p.R337H mutation carriers in the population of Southern Brazil: evidence for a founder effect.

artículo científico publicado en 2010

Determining the effectiveness of High Resolution Melting analysis for SNP genotyping and mutation scanning at the TP53 locus

artículo científico publicado en 2009

Development of a sensitive and specific assay combining multiplex PCR and DNA microarray primer extension to detect high-risk mucosal human papillomavirus types

artículo científico publicado en 2006

Development of a sensitive and specific multiplex PCR method combined with DNA microarray primer extension to detect Betapapillomavirus types

artículo científico publicado en 2007

Development of lung cancer before the age of 50: the role of xenobiotic metabolizing genes.

artículo científico publicado en 2007

Dietary inflammatory index and inflammatory gene interactions in relation to colorectal cancer risk in the Bellvitge colorectal cancer case-control study

artículo científico publicado en 2014

EIF4G1 and RAN as Possible Drivers for Malignant Pleural Mesothelioma

artículo científico publicado en 2020

Effect of red cells and plasma blood in determining individual lymphocytes sensitivity to diepoxybutane assessed by in vitro induced sister chromatid exchanges

scientific article published on 01 November 1995

Erratum: 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

scholarly article published in Leukemia

Expression status of candidate genes in mesothelioma tissues and cell lines.

artículo científico publicado en 2014

GSTT1 and M1 polymorphisms in Hürthle thyroid cancer patients

artículo científico publicado en 2006

Generation of a DNA microarray for determination of E6 natural variants of human papillomavirus type 16.

artículo científico publicado en 2004

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 outcome in multiple myeloma patients receiving high-dose melphalan.

artículo científico publicado en 2009

Genetic signature of differentiated thyroid carcinoma susceptibility: a machine learning approach

artículo científico publicado en 2022

Genetic susceptibility to malignant mesothelioma and exposure to asbestos: the influence of the familial factor.

artículo científico publicado en 2007

Genetic susceptibility to malignant pleural mesothelioma and other asbestos-associated diseases

artículo científico publicado en 2008

Genetic susceptibility to pancreatic cancer and its functional characterisation: the PANcreatic Disease ReseArch (PANDoRA) consortium

artículo científico publicado en 2012

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

artículo científico

Genome-wide association study identifies multiple susceptibility loci for pancreatic cancer

artículo científico publicado en 2014

Genome-wide association study on differentiated thyroid cancer

scientific journal article

Genotype and haplotype analysis of cell cycle genes in sporadic colorectal cancer in the Czech Republic.

artículo científico publicado en 2009

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

In silico and in vitro analysis of rare germline allelic variants of RET oncogene associated with medullary thyroid cancer.

artículo científico publicado en 2011

Induction of DNA strand breaks by trihalomethanes in primary human lung epithelial cells.

artículo científico publicado en 2003

Induction of genetic damage in human lymphocytes and mutations in Salmonella by trihalomethanes: role of red blood cells and GSTT1-1 polymorphism

artículo científico publicado en 1999

Induction of sister chromatid exchanges in human peripheral blood lymphocytes by bromoform: investigation of the role of GSTT1-1 polymorphism.

artículo científico publicado en 1999

Interleukin-4 and interleukin-4 receptor polymorphisms and colorectal cancer risk

artículo científico publicado en 2007

Lack of Replication of Seven Pancreatic Cancer Susceptibility Loci Identified in Two Asian Populations

article

Laparoscopic nerve-sparing complete excision of deep endometriosis: is it feasible?

article by Stefano Landi et al published March 2006 in Human Reproduction

MAP3K7 and GSTZ1 are associated with human longevity: a two-stage case-control study using a multilocus genotyping

artículo científico publicado en 2012

MSLN gene silencing has an anti-malignant effect on cell lines overexpressing mesothelin deriving from malignant pleural mesothelioma.

artículo científico publicado en 2014

Medullary thyroid carcinoma (MTC) and RET proto-oncogene: mutation spectrum in the familial cases and a meta-analysis of studies on the sporadic form

artículo científico

MicroRNA binding site polymorphisms as biomarkers in cancer management and research.

artículo científico publicado en 2014

Modulating factors of individual sensitivity to diepoxybutane: chromosome aberrations induced in vitro in human lymphocytes

artículo científico publicado en 1997

Modulating factors of individual sensitivity to diepoxybutane: sister chromatid exchanges induced in vitro in human lymphocytes.

artículo científico publicado en 1996

Mutation spectra in Salmonella TA98, TA100, and TA104 of two phenylbenzotriazole mutagens (PBTA-1 and PBTA-2) detected in the Nishitakase River in Kyoto, Japan

artículo científico publicado en 1999

Mutation spectra in Salmonella of analogues of MX: implications of chemical structure for mutational mechanisms

artículo científico publicado en 2000

Mutation spectra of the drinking water mutagen 3-chloro-4-methyl-5-hydroxy-2(5H)-furanone (MCF) in Salmonella TA100 and TA104: comparison to MX.

artículo científico publicado en 2000

NBN 657del5 heterozygous mutations and colorectal cancer risk in the Czech Republic.

artículo científico publicado en 2009

No association between increased levels of high-frequency sister chromatid exchange cells (HFCs) and the risk of cancer in healthy individuals

artículo científico publicado en 2004

Novel genetic variants in differentiated thyroid cancer and assessment of the cumulative risk

artículo científico publicado en 2015

Novel genome-wide association study-based candidate loci for differentiated thyroid cancer risk

artículo científico publicado en 2014

Obesity and the risk of papillary thyroid cancer: a pooled analysis of three case-control studies

artículo científico publicado en 2014

Oxytocin receptor polymorphisms and adult attachment style in patients with depression

artículo científico publicado en 2009

Persistence of 4-nitroquinoline-1-oxide induced lesions in human lymphocytes

artículo científico publicado en 1996

Polymorphisms in Genes of Nucleotide and Base Excision Repair: Risk and Prognosis of Colorectal Cancer

article

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 of genes coding for insulin-like growth factor 1 and its major binding proteins, circulating levels of IGF-I and IGFBP-3 and breast cancer risk: results from the EPIC study

artículo científico publicado en 2006

Polymorphisms of glutathione-S-transferase M1 and manganese superoxide dismutase are associated with the risk of malignant pleural mesothelioma.

artículo científico publicado en 2007

Polymorphisms of the dopamine receptor gene DRD2 and colorectal cancer risk

artículo científico publicado en 2005

Polymorphisms within inflammatory genes and colorectal cancer.

artículo científico publicado en 2006

Pooled analysis of NAT2 genotypes as risk factors for asbestos-related malignant mesothelioma

article

Pregnancy outcomes and deliveries after laparoscopic myomectomy

scientific article published on 01 May 2003

Preoperative double-contrast barium enema in patients with suspected intestinal endometriosis

artículo científico publicado en 2004

Repeated analysis of sister chromatid exchange induction by diepoxybutane in cultured human lymphocytes: effect of glutathione S-transferase T1 and M1 genotype

scientific article published on 01 March 1996

Risk of malignant pleural mesothelioma and polymorphisms in genes involved in the genome stability and xenobiotics metabolism

article

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

artículo científico publicado en 2014

Sequence Variants in Cell Cycle Control Pathway, X-ray Exposure, and Lung Cancer Risk: A Multicenter Case-Control Study in Central Europe

Single tube genotyping of GSTM1, GSTT1 and TP53 polymorphisms by multiplex PCR

scientific article published on 01 October 2006

Sister chromatid exchange and micronucleus frequency in human lymphocytes of 1,650 subjects in an Italian population: I. Contribution of methodological factors

artículo científico publicado en 1998

Sister chromatid exchange and micronucleus frequency in human lymphocytes of 1,650 subjects in an Italian population: II. Contribution of sex, age, and lifestyle

artículo científico publicado en 1998

Sperm-FISH analysis and human monitoring: a study on workers occupationally exposed to styrene.

artículo científico publicado en 2003

Spontaneous sister chromatid exchange and chromosome aberration frequency in humans: the familial effect

artículo científico publicado en 1999

TERT gene harbors multiple variants associated with pancreatic cancer susceptibility

artículo científico publicado en 2015

TPO genetic variants and risk of differentiated thyroid carcinoma in two European populations.

artículo científico publicado en 2013

The nature of high frequency sister chromatid exchange cells (HFCs).

artículo científico publicado en 1997

The role of microRNA-binding site polymorphisms in DNA repair genes as risk factors for bladder cancer and breast cancer and their impact on radiotherapy outcomes ⬇️

artículo científico publicado en 2011

Transversus abdominis plane block associated with locoregional anesthesia with a laparotenser for gynecologic surgery in an awake state

artículo científico publicado en 2013

Two novel polymorphisms in 5' flanking region of the mesothelin gene are associated with soluble mesothelin-related peptide (SMRP) levels

artículo científico publicado en 2011

Use of three-way differential staining and liquid holding for the assessment of individual repair capacity

scientific article published on 01 February 1995

Uterine rupture in a nulliparous woman with septate uterus of the second trimester pregnancy and review in literature

artículo científico publicado en 2012

Variation within 3'-UTRs of base excision repair genes and response to therapy in colorectal cancer patients: A potential modulation of microRNAs binding

artículo científico publicado en 2013

Lista de obras de Stefano Landi

A DATABASE OF SINGLE-NUCLEOTIDE POLYMORPHISMS AND A GENOTYPING MICROARRAY FOR GENETIC EPIDEMIOLOGY OF LUNG CANCER

A TP53 polymorphism is associated with increased risk of colorectal cancer and with reduced levels of TP53 mRNA.

A catalogue of polymorphisms related to xenobiotic metabolism and cancer susceptibility.

A common polymorphism within MSLN affects miR-611 binding site and soluble mesothelin levels in healthy people.

A novel similarity-measure for the analysis of genetic data in complex phenotypes

A review of transcriptome studies combined with data mining reveals novel potential markers of malignant pleural mesothelioma

ABO blood groups and pancreatic cancer risk and survival: results from the PANcreatic Disease ReseArch (PANDoRA) consortium.

APEX DNA Microarray for the Identification of Pathogenic Fungi

Ala147Thr substitution in translocator protein is associated with adult separation anxiety in patients with depression

Are baseline frequencies of SCEs, CAs, and MN in human lymphocytes related to hematological values?

Association between CYP2E1 polymorphisms and risk of differentiated thyroid carcinoma

COMPASSS (COMplex PAttern of Sequence Search Software), a simple and effective tool for mining complex motifs in whole genomes

Characterization of novel 3'untranslated regions and related polymorphisms of the gene NPPC, encoding for the C-type natriuretic peptide.

Common variation at 2p13.3, 3q29, 7p13 and 17q25.1 associated with susceptibility to pancreatic cancer

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

DNA Repair and Cell Cycle Control Genes and the Risk of Young-Onset Lung Cancer

DNA microarray based on arrayed-primer extension technique for identification of pathogenic fungi responsible for invasive and superficial mycoses

DeltaN133p53 expression levels in relation to haplotypes of the TP53 internal promoter region

Detailed haplotype analysis at the TP53 locus in p.R337H mutation carriers in the population of Southern Brazil: evidence for a founder effect.

Determining the effectiveness of High Resolution Melting analysis for SNP genotyping and mutation scanning at the TP53 locus

Development of a sensitive and specific assay combining multiplex PCR and DNA microarray primer extension to detect high-risk mucosal human papillomavirus types

Development of a sensitive and specific multiplex PCR method combined with DNA microarray primer extension to detect Betapapillomavirus types

Development of lung cancer before the age of 50: the role of xenobiotic metabolizing genes.

Dietary inflammatory index and inflammatory gene interactions in relation to colorectal cancer risk in the Bellvitge colorectal cancer case-control study

EIF4G1 and RAN as Possible Drivers for Malignant Pleural Mesothelioma

Effect of red cells and plasma blood in determining individual lymphocytes sensitivity to diepoxybutane assessed by in vitro induced sister chromatid exchanges

Erratum: 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

Expression status of candidate genes in mesothelioma tissues and cell lines.

GSTT1 and M1 polymorphisms in Hürthle thyroid cancer patients

Generation of a DNA microarray for determination of E6 natural variants of human papillomavirus type 16.

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 outcome in multiple myeloma patients receiving high-dose melphalan.

Genetic signature of differentiated thyroid carcinoma susceptibility: a machine learning approach

Genetic susceptibility to malignant mesothelioma and exposure to asbestos: the influence of the familial factor.

Genetic susceptibility to malignant pleural mesothelioma and other asbestos-associated diseases

Genetic susceptibility to pancreatic cancer and its functional characterisation: the PANcreatic Disease ReseArch (PANDoRA) consortium

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

Genome-wide association study identifies multiple susceptibility loci for pancreatic cancer

Genome-wide association study on differentiated thyroid cancer

Genotype and haplotype analysis of cell cycle genes in sporadic colorectal cancer in the Czech Republic.

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

In silico and in vitro analysis of rare germline allelic variants of RET oncogene associated with medullary thyroid cancer.

Induction of DNA strand breaks by trihalomethanes in primary human lung epithelial cells.

Induction of genetic damage in human lymphocytes and mutations in Salmonella by trihalomethanes: role of red blood cells and GSTT1-1 polymorphism

Induction of sister chromatid exchanges in human peripheral blood lymphocytes by bromoform: investigation of the role of GSTT1-1 polymorphism.

Interleukin-4 and interleukin-4 receptor polymorphisms and colorectal cancer risk

Lack of Replication of Seven Pancreatic Cancer Susceptibility Loci Identified in Two Asian Populations

Laparoscopic nerve-sparing complete excision of deep endometriosis: is it feasible?

MAP3K7 and GSTZ1 are associated with human longevity: a two-stage case-control study using a multilocus genotyping

MSLN gene silencing has an anti-malignant effect on cell lines overexpressing mesothelin deriving from malignant pleural mesothelioma.

Medullary thyroid carcinoma (MTC) and RET proto-oncogene: mutation spectrum in the familial cases and a meta-analysis of studies on the sporadic form

MicroRNA binding site polymorphisms as biomarkers in cancer management and research.

Modulating factors of individual sensitivity to diepoxybutane: chromosome aberrations induced in vitro in human lymphocytes

Modulating factors of individual sensitivity to diepoxybutane: sister chromatid exchanges induced in vitro in human lymphocytes.

Mutation spectra in Salmonella TA98, TA100, and TA104 of two phenylbenzotriazole mutagens (PBTA-1 and PBTA-2) detected in the Nishitakase River in Kyoto, Japan

Mutation spectra in Salmonella of analogues of MX: implications of chemical structure for mutational mechanisms

Mutation spectra of the drinking water mutagen 3-chloro-4-methyl-5-hydroxy-2(5H)-furanone (MCF) in Salmonella TA100 and TA104: comparison to MX.

NBN 657del5 heterozygous mutations and colorectal cancer risk in the Czech Republic.

No association between increased levels of high-frequency sister chromatid exchange cells (HFCs) and the risk of cancer in healthy individuals

Novel genetic variants in differentiated thyroid cancer and assessment of the cumulative risk

Novel genome-wide association study-based candidate loci for differentiated thyroid cancer risk

Obesity and the risk of papillary thyroid cancer: a pooled analysis of three case-control studies

Oxytocin receptor polymorphisms and adult attachment style in patients with depression

Persistence of 4-nitroquinoline-1-oxide induced lesions in human lymphocytes

Polymorphisms in Genes of Nucleotide and Base Excision Repair: Risk and Prognosis of Colorectal Cancer

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 of genes coding for insulin-like growth factor 1 and its major binding proteins, circulating levels of IGF-I and IGFBP-3 and breast cancer risk: results from the EPIC study

Polymorphisms of glutathione-S-transferase M1 and manganese superoxide dismutase are associated with the risk of malignant pleural mesothelioma.

Polymorphisms of the dopamine receptor gene DRD2 and colorectal cancer risk

Polymorphisms within inflammatory genes and colorectal cancer.

Pooled analysis of NAT2 genotypes as risk factors for asbestos-related malignant mesothelioma

Pregnancy outcomes and deliveries after laparoscopic myomectomy

Preoperative double-contrast barium enema in patients with suspected intestinal endometriosis

Repeated analysis of sister chromatid exchange induction by diepoxybutane in cultured human lymphocytes: effect of glutathione S-transferase T1 and M1 genotype

Risk of malignant pleural mesothelioma and polymorphisms in genes involved in the genome stability and xenobiotics metabolism

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

Sequence Variants in Cell Cycle Control Pathway, X-ray Exposure, and Lung Cancer Risk: A Multicenter Case-Control Study in Central Europe

Single tube genotyping of GSTM1, GSTT1 and TP53 polymorphisms by multiplex PCR