Lista de obras - José Luis Soto - Dominio Público Uruguay

A Label Free Disposable Device for Rapid Isolation of Rare Tumor Cells from Blood by Ultrasounds.

artículo científico publicado en 2018

Association Between Germline Mutations in BRF1, a Subunit of the RNA Polymerase III Transcription Complex, and Hereditary Colorectal Cancer.

artículo científico publicado en 2017

Biallelic MYH germline mutations as cause of Muir-Torre syndrome

artículo científico publicado en 2010

Characterization of a novel POLD1 missense founder mutation in a Spanish population

artículo científico publicado en 2017

Circulating tumour cell analysis as an early marker for relapse in stage II and III colorectal cancer patients: a pilot study

article

Clinical and Pathological Characterization of Lynch-Like Syndrome

scientific article published on 17 June 2019

Clinically important molecular features of Peruvian colorectal tumours: high prevalence of DNA mismatch repair deficiency and low incidence of KRAS mutations

artículo científico publicado en 2011

Co-occurrence of germline pathogenic variants for different hereditary cancer syndromes in patients with Lynch syndrome

artículo científico publicado en 2021

Comparative genomic hybridization and amplotyping by arbitrarily primed PCR in stage A B-CLL

artículo científico publicado en 2001

Comparison between universal molecular screening for Lynch syndrome and revised Bethesda guidelines in a large population-based cohort of patients with colorectal cancer

artículo científico publicado en 2011

Consensus document on the implementation of next generation sequencing in the genetic diagnosis of hereditary cancer.

artículo científico publicado en 2018

EPCAM germ line deletions as causes of Lynch syndrome in Spanish patients

artículo científico publicado en 2010

Functional significance of concomitant inactivation of hMLH1 and hMSH6 in tumor cells of the microsatellite mutator phenotype.

artículo científico publicado en 2001

GALNT12 is not a major contributor of familial colorectal cancer type X.

artículo científico publicado en 2013

Germline Mutations in FAN1 Cause Hereditary Colorectal Cancer by Impairing DNA Repair.

artículo científico publicado en 2015

HGUE-C-1 is an atypical and novel colon carcinoma cell line

artículo científico publicado en 2015

Hereditary Leiomyomatosis and Renal Cell Cancer Syndrome in Spain: Clinical and Genetic Characterization

artículo científico publicado en 2020

Highly sensitive MLH1 methylation analysis in blood identifies a cancer patient with low-level mosaic MLH1 epimutation

scientific article published on 28 November 2019

Histone deacetylase inhibitors induced caspase-independent apoptosis in human pancreatic adenocarcinoma cell lines.

artículo científico publicado en 2005

Identification of a founder EPCAM deletion in Spanish Lynch syndrome families.

artículo científico publicado en 2013

Imaging cytometry for counting circulating tumor cells: comparative analysis of the CellSearch vs ImageStream systems ⬇️

artículo científico publicado el 20 de marzo de 2013

Implementation of massive sequencing in the genetic diagnosis of hereditary cancer syndromes: diagnostic performance in the Hereditary Cancer Programme of the Valencia Community (FamCan-NGS)

scientific article published on 18 January 2019

Increased Risk of Colorectal Cancer in Patients With Multiple Serrated Polyps and Their First-Degree Relatives.

artículo científico publicado en 2017

KRAS and BRAF somatic mutations in colonic polyps and the risk of metachronous neoplasia.

artículo científico publicado en 2017

Lack of cytomegalovirus detection in human glioma.

artículo científico publicado en 2017

Methylation analysis of MLH1 improves the selection of patients for genetic testing in Lynch syndrome.

artículo científico publicado en 2010

Molecular biology of exocrine pancreatic cancer.

artículo científico publicado en 2006

Multidrug resistance-associated protein (MRP1) gene is strongly expressed in gastric carcinomas. Analysis by immunohistochemistry and real-time quantitative RT-PCR.

artículo científico publicado en 2005

New insights into POLE and POLD1 germline mutations in familial colorectal cancer and polyposis

artículo científico publicado en 2014

Notl-Msell methylation-sensitive amplied fragment length polymorhism for DNA methylation analysis of human cancers

artículo científico publicado en 2001

Novel Molecular Characterization of Colorectal Primary Tumors Based on miRNAs

scientific article published on 11 March 2019

POLE and POLD1 mutations in 529 kindred with familial colorectal cancer and/or polyposis: review of reported cases and recommendations for genetic testing and surveillance

artículo científico publicado en 2016

Post-transcriptional regulation of P-glycoprotein expression in cancer cell lines.

artículo científico publicado en 2007

Prevalence and characteristics of MUTYH-associated polyposis in patients with multiple adenomatous and serrated polyps.

artículo científico publicado en 2014

Prevalence of Lynch syndrome among patients with newly diagnosed endometrial cancers

artículo científico publicado en 2013

Prevalence of MLH1 constitutional epimutations as a cause of Lynch syndrome in unselected versus selected consecutive series of patients with colorectal cancer.

artículo científico publicado en 2015

Prevalence of germline MUTYH mutations among Lynch-like syndrome patients

artículo científico publicado en 2014

Primary constitutional MLH1 epimutations: a focal epigenetic event

artículo científico publicado en 2018

Real-time PCR with internal amplification control for detecting tuberculosis: method design and validation.

artículo científico publicado en 2009

Recurrent Testicular Germ Cell Tumors in a Family With MYH-Associated Polyposis

artículo científico publicado en 2012

Risk of cancer in cases of suspected lynch syndrome without germline mutation.

artículo científico publicado en 2013

SEOM clinical guideline on hereditary colorectal cancer (2019)

artículo científico publicado en 2020

Streptococcus gallolyticus infection in colorectal cancer and association with biological and clinical factors.

artículo científico publicado en 2017

TGFB1andTGFBR1polymorphic variants in relationship to bladder cancer risk and prognosis

artículo científico publicado en 2009

TGFBR1 intralocus epistatic interaction as a risk factor for colorectal cancer.

artículo científico publicado en 2012

The TGFBR1*6A allele is not associated with susceptibility to colorectal cancer in a Spanish population: a case-control study.

artículo científico publicado en 2009

The heritability and patterns of DNA methylation in normal human colorectum

artículo científico publicado en 2016

Tumour cells resistance in cancer therapy.

artículo científico publicado en 2007

Lista de obras de José Luis Soto

A Label Free Disposable Device for Rapid Isolation of Rare Tumor Cells from Blood by Ultrasounds.

Association Between Germline Mutations in BRF1, a Subunit of the RNA Polymerase III Transcription Complex, and Hereditary Colorectal Cancer.

Biallelic MYH germline mutations as cause of Muir-Torre syndrome

Characterization of a novel POLD1 missense founder mutation in a Spanish population

Circulating tumour cell analysis as an early marker for relapse in stage II and III colorectal cancer patients: a pilot study

Clinical and Pathological Characterization of Lynch-Like Syndrome

Clinically important molecular features of Peruvian colorectal tumours: high prevalence of DNA mismatch repair deficiency and low incidence of KRAS mutations

Co-occurrence of germline pathogenic variants for different hereditary cancer syndromes in patients with Lynch syndrome

Comparative genomic hybridization and amplotyping by arbitrarily primed PCR in stage A B-CLL

Comparison between universal molecular screening for Lynch syndrome and revised Bethesda guidelines in a large population-based cohort of patients with colorectal cancer

Consensus document on the implementation of next generation sequencing in the genetic diagnosis of hereditary cancer.

EPCAM germ line deletions as causes of Lynch syndrome in Spanish patients

Functional significance of concomitant inactivation of hMLH1 and hMSH6 in tumor cells of the microsatellite mutator phenotype.

GALNT12 is not a major contributor of familial colorectal cancer type X.

Germline Mutations in FAN1 Cause Hereditary Colorectal Cancer by Impairing DNA Repair.

HGUE-C-1 is an atypical and novel colon carcinoma cell line

Hereditary Leiomyomatosis and Renal Cell Cancer Syndrome in Spain: Clinical and Genetic Characterization

Highly sensitive MLH1 methylation analysis in blood identifies a cancer patient with low-level mosaic MLH1 epimutation

Histone deacetylase inhibitors induced caspase-independent apoptosis in human pancreatic adenocarcinoma cell lines.

Identification of a founder EPCAM deletion in Spanish Lynch syndrome families.

Imaging cytometry for counting circulating tumor cells: comparative analysis of the CellSearch vs ImageStream systems ⬇️

Implementation of massive sequencing in the genetic diagnosis of hereditary cancer syndromes: diagnostic performance in the Hereditary Cancer Programme of the Valencia Community (FamCan-NGS)

Increased Risk of Colorectal Cancer in Patients With Multiple Serrated Polyps and Their First-Degree Relatives.

KRAS and BRAF somatic mutations in colonic polyps and the risk of metachronous neoplasia.

Lack of cytomegalovirus detection in human glioma.

Methylation analysis of MLH1 improves the selection of patients for genetic testing in Lynch syndrome.

Molecular biology of exocrine pancreatic cancer.

Multidrug resistance-associated protein (MRP1) gene is strongly expressed in gastric carcinomas. Analysis by immunohistochemistry and real-time quantitative RT-PCR.

New insights into POLE and POLD1 germline mutations in familial colorectal cancer and polyposis

Notl-Msell methylation-sensitive amplied fragment length polymorhism for DNA methylation analysis of human cancers

Novel Molecular Characterization of Colorectal Primary Tumors Based on miRNAs

POLE and POLD1 mutations in 529 kindred with familial colorectal cancer and/or polyposis: review of reported cases and recommendations for genetic testing and surveillance

Post-transcriptional regulation of P-glycoprotein expression in cancer cell lines.

Prevalence and characteristics of MUTYH-associated polyposis in patients with multiple adenomatous and serrated polyps.

Prevalence of Lynch syndrome among patients with newly diagnosed endometrial cancers

Prevalence of MLH1 constitutional epimutations as a cause of Lynch syndrome in unselected versus selected consecutive series of patients with colorectal cancer.

Prevalence of germline MUTYH mutations among Lynch-like syndrome patients

Primary constitutional MLH1 epimutations: a focal epigenetic event

Real-time PCR with internal amplification control for detecting tuberculosis: method design and validation.

Recurrent Testicular Germ Cell Tumors in a Family With MYH-Associated Polyposis

Risk of cancer in cases of suspected lynch syndrome without germline mutation.

SEOM clinical guideline on hereditary colorectal cancer (2019)

Streptococcus gallolyticus infection in colorectal cancer and association with biological and clinical factors.

TGFB1andTGFBR1polymorphic variants in relationship to bladder cancer risk and prognosis

TGFBR1 intralocus epistatic interaction as a risk factor for colorectal cancer.

The TGFBR1*6A allele is not associated with susceptibility to colorectal cancer in a Spanish population: a case-control study.

The heritability and patterns of DNA methylation in normal human colorectum

Tumour cells resistance in cancer therapy.