Lista de obras - Daniel Rueda - Dominio Público Uruguay

A sensitive and scalable microsatellite instability assay to diagnose constitutional mismatch repair deficiency by sequencing of peripheral blood leukocytes

scientific article published on 06 March 2019

Age at onset should be a major criterion for subclassification of colorectal cancer.

artículo científico publicado en 2013

An alternative approach to establishing unbiased colorectal cancer risk estimation in Lynch syndrome

scientific article published on 17 June 2019

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

artículo científico publicado en 2017

Association of Polyps with Early-Onset Colorectal Cancer and Throughout Surveillance: Novel Clinical and Molecular Implications

scientific article published on 29 November 2019

Classifying early-onset colorectal cancer according to tumor location: new potential subcategories to explore

artículo científico publicado en 2015

Clinical and Molecular Comparative Study of Colorectal Cancer Based on Age-of-onset and Tumor Location: Two Main Criteria for Subclassifying Colorectal Cancer

artículo científico publicado en 2019

Comment on 'Distinct clinical outcomes of two CIMP-positive colorectal cancer subtypes based on a revised CIMP classification system'.

artículo científico publicado en 2018

Comment on 'Wild-type APC prediction of poor prognosis in microsatellite-stable proximal colorectal cancer differs according to the age of onset'.

artículo científico publicado en 2016

DNA copy number profiling reveals different patterns of chromosomal instability within colorectal cancer according to the age of onset

artículo científico publicado en 2015

Detailed characterization of MLH1 p.D41H and p.N710D variants coexisting in a Lynch syndrome family with conserved MLH1 expression tumors.

artículo científico publicado en 2014

Differential clinicopathological and molecular features within late-onset colorectal cancer according to tumor location.

artículo científico publicado en 2018

Differential expression of JAK2 and Src kinase genes in response to hydroxyurea treatment in polycythemia vera and essential thrombocythemia.

artículo científico publicado en 2011

Early-onset colorectal cancer is an easy and effective tool to identify retrospectively Lynch syndrome.

artículo científico publicado en 2011

Early-onset colorectal cancer: a separate subset of colorectal cancer

artículo científico publicado en 2014

Frequency and impact of KRAS mutation in early onset colorectal cancer

artículo científico publicado en 2016

Genome-wide linkage analysis and tumoral characterization reveal heterogeneity in familial colorectal cancer type X.

artículo científico publicado en 2014

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

artículo científico publicado en 2015

High-sensitivity microsatellite instability assessment for the detection of mismatch repair defects in normal tissue of biallelic germline mismatch repair mutation carriers

artículo científico publicado en 2019

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

artículo científico publicado en 2013

Inhibition of glioma growth in vivo by selective activation of the CB(2) cannabinoid receptor.

artículo científico publicado en 2001

Involvement of the cAMP/protein kinase A pathway and of mitogen-activated protein kinase in the anti-proliferative effects of anandamide in human breast cancer cells

artículo científico publicado en 1999

Mechanism of extracellular signal-regulated kinase activation by the CB(1) cannabinoid receptor.

artículo científico publicado en 2002

NOMO-1 gene is deleted in early-onset colorectal cancer.

artículo científico publicado en 2017

New Perspectives in Multiple Primary Colorectal Cancer: A Surgical Approach.

artículo científico publicado en 2016

No Overt Clinical Immunodeficiency Despite Immune Biological Abnormalities in Patients With Constitutional Mismatch Repair Deficiency.

artículo científico publicado en 2018

Primary constitutional MLH1 epimutations: a focal epigenetic event

artículo científico publicado en 2018

Prospective Clinical Integration of an Amplicon-Based Next-Generation Sequencing Method to Select Advanced Non-Small-Cell Lung Cancer Patients for Genotype-Tailored Treatments

artículo científico publicado en 2017

Redefining synchronous colorectal cancers based on tumor clonality

scientific article published on 16 October 2018

Role of GALNT12 in the genetic predisposition to attenuated adenomatous polyposis syndrome.

artículo científico publicado en 2017

Somatic Embryonic FGFR2 Mutations in Keratinocytic Epidermal Nevi.

artículo científico publicado en 2016

The endocannabinoid anandamide inhibits neuronal progenitor cell differentiation through attenuation of the Rap1/B-Raf/ERK pathway.

artículo científico publicado en 2002

Toward a Molecular Classification of Synchronous Colorectal Cancer: Clinical and Molecular Characterization.

artículo científico publicado en 2016

Unsupervised Analysis of Array Comparative Genomic Hybridization Data from Early-Onset Colorectal Cancer Reveals Equivalence with Molecular Classification and Phenotypes.

artículo científico publicado en 2016

Use of Sorafenib as an effective treatment in an AML patient carrying a new point mutation affecting the Juxtamembrane domain of FLT3.

artículo científico publicado en 2012

Use of exome sequencing to determine the full profile of genetic variants in the fluoropyrimidine pathway in colorectal cancer patients affected by severe toxicity

artículo científico publicado en 2017

[Surgical options for familial adenomatous polyposis depending on genetic factors]

artículo científico publicado en 2014

Lista de obras de Daniel Rueda

A sensitive and scalable microsatellite instability assay to diagnose constitutional mismatch repair deficiency by sequencing of peripheral blood leukocytes

Age at onset should be a major criterion for subclassification of colorectal cancer.

An alternative approach to establishing unbiased colorectal cancer risk estimation in Lynch syndrome

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

Association of Polyps with Early-Onset Colorectal Cancer and Throughout Surveillance: Novel Clinical and Molecular Implications

Classifying early-onset colorectal cancer according to tumor location: new potential subcategories to explore

Clinical and Molecular Comparative Study of Colorectal Cancer Based on Age-of-onset and Tumor Location: Two Main Criteria for Subclassifying Colorectal Cancer

Comment on 'Distinct clinical outcomes of two CIMP-positive colorectal cancer subtypes based on a revised CIMP classification system'.

Comment on 'Wild-type APC prediction of poor prognosis in microsatellite-stable proximal colorectal cancer differs according to the age of onset'.

DNA copy number profiling reveals different patterns of chromosomal instability within colorectal cancer according to the age of onset

Detailed characterization of MLH1 p.D41H and p.N710D variants coexisting in a Lynch syndrome family with conserved MLH1 expression tumors.

Differential clinicopathological and molecular features within late-onset colorectal cancer according to tumor location.

Differential expression of JAK2 and Src kinase genes in response to hydroxyurea treatment in polycythemia vera and essential thrombocythemia.

Early-onset colorectal cancer is an easy and effective tool to identify retrospectively Lynch syndrome.

Early-onset colorectal cancer: a separate subset of colorectal cancer

Frequency and impact of KRAS mutation in early onset colorectal cancer

Genome-wide linkage analysis and tumoral characterization reveal heterogeneity in familial colorectal cancer type X.

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

High-sensitivity microsatellite instability assessment for the detection of mismatch repair defects in normal tissue of biallelic germline mismatch repair mutation carriers

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

Inhibition of glioma growth in vivo by selective activation of the CB(2) cannabinoid receptor.

Involvement of the cAMP/protein kinase A pathway and of mitogen-activated protein kinase in the anti-proliferative effects of anandamide in human breast cancer cells

Mechanism of extracellular signal-regulated kinase activation by the CB(1) cannabinoid receptor.

NOMO-1 gene is deleted in early-onset colorectal cancer.

New Perspectives in Multiple Primary Colorectal Cancer: A Surgical Approach.

No Overt Clinical Immunodeficiency Despite Immune Biological Abnormalities in Patients With Constitutional Mismatch Repair Deficiency.

Primary constitutional MLH1 epimutations: a focal epigenetic event

Prospective Clinical Integration of an Amplicon-Based Next-Generation Sequencing Method to Select Advanced Non-Small-Cell Lung Cancer Patients for Genotype-Tailored Treatments

Redefining synchronous colorectal cancers based on tumor clonality

Role of GALNT12 in the genetic predisposition to attenuated adenomatous polyposis syndrome.

Somatic Embryonic FGFR2 Mutations in Keratinocytic Epidermal Nevi.

The endocannabinoid anandamide inhibits neuronal progenitor cell differentiation through attenuation of the Rap1/B-Raf/ERK pathway.

Toward a Molecular Classification of Synchronous Colorectal Cancer: Clinical and Molecular Characterization.

Unsupervised Analysis of Array Comparative Genomic Hybridization Data from Early-Onset Colorectal Cancer Reveals Equivalence with Molecular Classification and Phenotypes.

Use of Sorafenib as an effective treatment in an AML patient carrying a new point mutation affecting the Juxtamembrane domain of FLT3.

Use of exome sequencing to determine the full profile of genetic variants in the fluoropyrimidine pathway in colorectal cancer patients affected by severe toxicity

[Surgical options for familial adenomatous polyposis depending on genetic factors]