Lista de obras - Søren Vang - Dominio Público Uruguay

A Rare Case of Embryonal Carcinoma in a Patient with Turner Syndrome without Y Chromosomal Material but Mutations in KIT, AKT1, and ZNF358 Demonstrated Using Exome Sequencing.

artículo científico publicado en 2017

Actin mutations in hypertrophic and dilated cardiomyopathy cause inefficient protein folding and perturbed filament formation

artículo científico publicado en 2005

Analysis of Plasma Cell-Free DNA by Ultradeep Sequencing in Patients With Stages I to III Colorectal Cancer

artículo científico publicado en 2019

Analysis of circulating tumour DNA to monitor disease burden following colorectal cancer surgery.

artículo científico publicado en 2015

Antioxidant dysfunction: potential risk for neurotoxicity in ethylmalonic aciduria

artículo científico publicado en 2010

Characterization of genetic intratumor heterogeneity in colorectal cancer and matching patient-derived spheroid cultures

artículo científico publicado en 2017

Circular RNA expression is abundant and correlated to aggressiveness in early-stage bladder cancer.

artículo científico publicado en 2017

Clinical Implications of Monitoring Circulating Tumor DNA in Patients with Colorectal Cancer

artículo científico publicado en 2017

Comprehensive Transcriptional Analysis of Early-Stage Urothelial Carcinoma.

artículo científico publicado en 2016

Comprehensive multiregional analysis of molecular heterogeneity in bladder cancer

artículo científico publicado en 2017

Correlation between Ka/Ks and Ks is related to substitution model and evolutionary lineage.

artículo científico publicado en 2009

Correlation between early dynamics in circulating tumour DNA and outcome from FOLFIRI treatment in metastatic colorectal cancer

scientific article published on 08 August 2019

DNA hypermethylation and differential gene expression associated with Klinefelter syndrome

scientific article published in Scientific Reports

Deleterious mis-splicing of STK11 caused by a novel single-nucleotide substitution in the 3' polypyrimidine tract of intron five

artículo científico publicado en 2020

Early Detection of Metastatic Relapse and Monitoring of Therapeutic Efficacy by Ultra-Deep Sequencing of Plasma Cell-Free DNA in Patients With Urothelial Bladder Carcinoma

artículo científico publicado en 2019

Enrichment of Genetic Variants in the Glucocorticoid Receptor Signalling Pathway in Autoimmune Hepatitis with Failure of Standard Treatment

artículo científico publicado en 2017

Exploring the transcriptome of hormone-naive multifocal prostate cancer and matched lymph node metastases

scientific article published on 19 November 2018

FGF: a web tool for Fishing Gene Family in a whole genome database

artículo científico publicado en 2007

Gene conversion in the rice genome.

artículos científicos

Genome-wide nucleosome map and cytosine methylation levels of an ancient human genome

artículo científico publicado en 2014

Genomic Alterations in Liquid Biopsies from Patients with Bladder Cancer

artículo científico publicado en 2016

High rate of chimeric gene origination by retroposition in plant genomes

artículo científico publicado en 2006

Identification of expressed and conserved human noncoding RNAs

artículo científico publicado en 2013

Large-scale evaluation of SLC18A2 in prostate cancer reveals diagnostic and prognostic biomarker potential at three molecular levels

artículo científico publicado en 2016

Measuring consequences of protein misfolding and cellular stress using OMICS techniques

artículo científico publicado en 2010

Mitochondrial proteomics on human fibroblasts for identification of metabolic imbalance and cellular stress

artículo científico publicado en 2009

Molecular-Subtype-Specific Biomarkers Improve Prediction of Prognosis in Colorectal Cancer

artículo científico

Mutational analysis of the active site of human insulin-regulated aminopeptidase

artículo científico publicado en 2001

Mutational context and diverse clonal development in early and late bladder cancer.

artículo científico publicado en 2014

Next-generation sequencing of RNA and DNA isolated from paired fresh-frozen and formalin-fixed paraffin-embedded samples of human cancer and normal tissue

artículo científico publicado en 2014

Optimized targeted sequencing of cell-free plasma DNA from bladder cancer patients.

artículo científico publicado en 2018

Paired Exome Analysis Reveals Clonal Evolution and Potential Therapeutic Targets in Urothelial Carcinoma

artículo científico publicado en 2016

Phenotypic and genotypic features of a large kindred with a germline AIP variant

artículo científico publicado en 2020

Protein misfolding and human disease

artículo científico publicado en 2006

Proteomics Reveals that Redox Regulation Is Disrupted in Patients with Ethylmalonic Encephalopathy

artículo científico publicado en 2011

Quantitative proteomics reveals cellular targets of celastrol

artículo científico publicado en 2011

SNHG16 is regulated by the Wnt pathway in colorectal cancer and affects genes involved in lipid metabolism

artículo científico publicado en 2016

SNHG5 promotes colorectal cancer cell survival by counteracting STAU1-mediated mRNA destabilization

artículo científico publicado en 2016

Snap: an integrated SNP annotation platform

artículo científico publicado en 2006

Spatial and temporal clonal evolution during development of metastatic urothelial carcinoma

artículo científico publicado en 2016

The ACADS gene variation spectrum in 114 patients with short-chain acyl-CoA dehydrogenase (SCAD) deficiency is dominated by missense variations leading to protein misfolding at the cellular level

artículo científico publicado en 2008

Toxic response caused by a misfolding variant of the mitochondrial protein short-chain acyl-CoA dehydrogenase

artículo científico publicado en 2010

Transcriptomic and proteomic intra-tumor heterogeneity of colorectal cancer varies depending on tumor location within the colorectum

artículo científico publicado en 2020

TreeFam: 2008 Update

artículo científico publicado en 2008

Tumor-specific usage of alternative transcription start sites in colorectal cancer identified by genome-wide exon array analysis

artículo científico publicado en 2011

Widespread DNA hypomethylation and differential gene expression in Turner syndrome

artículo científico publicado en 2016

Lista de obras de Søren Vang

A Rare Case of Embryonal Carcinoma in a Patient with Turner Syndrome without Y Chromosomal Material but Mutations in KIT, AKT1, and ZNF358 Demonstrated Using Exome Sequencing.

Actin mutations in hypertrophic and dilated cardiomyopathy cause inefficient protein folding and perturbed filament formation

Analysis of Plasma Cell-Free DNA by Ultradeep Sequencing in Patients With Stages I to III Colorectal Cancer

Analysis of circulating tumour DNA to monitor disease burden following colorectal cancer surgery.

Antioxidant dysfunction: potential risk for neurotoxicity in ethylmalonic aciduria

Characterization of genetic intratumor heterogeneity in colorectal cancer and matching patient-derived spheroid cultures

Circular RNA expression is abundant and correlated to aggressiveness in early-stage bladder cancer.

Clinical Implications of Monitoring Circulating Tumor DNA in Patients with Colorectal Cancer

Comprehensive Transcriptional Analysis of Early-Stage Urothelial Carcinoma.

Comprehensive multiregional analysis of molecular heterogeneity in bladder cancer

Correlation between Ka/Ks and Ks is related to substitution model and evolutionary lineage.

Correlation between early dynamics in circulating tumour DNA and outcome from FOLFIRI treatment in metastatic colorectal cancer

DNA hypermethylation and differential gene expression associated with Klinefelter syndrome

Deleterious mis-splicing of STK11 caused by a novel single-nucleotide substitution in the 3' polypyrimidine tract of intron five

Early Detection of Metastatic Relapse and Monitoring of Therapeutic Efficacy by Ultra-Deep Sequencing of Plasma Cell-Free DNA in Patients With Urothelial Bladder Carcinoma

Enrichment of Genetic Variants in the Glucocorticoid Receptor Signalling Pathway in Autoimmune Hepatitis with Failure of Standard Treatment

Exploring the transcriptome of hormone-naive multifocal prostate cancer and matched lymph node metastases

FGF: a web tool for Fishing Gene Family in a whole genome database

Gene conversion in the rice genome.

Genome-wide nucleosome map and cytosine methylation levels of an ancient human genome

Genomic Alterations in Liquid Biopsies from Patients with Bladder Cancer

High rate of chimeric gene origination by retroposition in plant genomes

Identification of expressed and conserved human noncoding RNAs

Large-scale evaluation of SLC18A2 in prostate cancer reveals diagnostic and prognostic biomarker potential at three molecular levels

Measuring consequences of protein misfolding and cellular stress using OMICS techniques

Mitochondrial proteomics on human fibroblasts for identification of metabolic imbalance and cellular stress

Molecular-Subtype-Specific Biomarkers Improve Prediction of Prognosis in Colorectal Cancer

Mutational analysis of the active site of human insulin-regulated aminopeptidase

Mutational context and diverse clonal development in early and late bladder cancer.

Next-generation sequencing of RNA and DNA isolated from paired fresh-frozen and formalin-fixed paraffin-embedded samples of human cancer and normal tissue

Optimized targeted sequencing of cell-free plasma DNA from bladder cancer patients.

Paired Exome Analysis Reveals Clonal Evolution and Potential Therapeutic Targets in Urothelial Carcinoma

Phenotypic and genotypic features of a large kindred with a germline AIP variant

Protein misfolding and human disease

Proteomics Reveals that Redox Regulation Is Disrupted in Patients with Ethylmalonic Encephalopathy

Quantitative proteomics reveals cellular targets of celastrol

SNHG16 is regulated by the Wnt pathway in colorectal cancer and affects genes involved in lipid metabolism

SNHG5 promotes colorectal cancer cell survival by counteracting STAU1-mediated mRNA destabilization

Snap: an integrated SNP annotation platform

Spatial and temporal clonal evolution during development of metastatic urothelial carcinoma

The ACADS gene variation spectrum in 114 patients with short-chain acyl-CoA dehydrogenase (SCAD) deficiency is dominated by missense variations leading to protein misfolding at the cellular level

Toxic response caused by a misfolding variant of the mitochondrial protein short-chain acyl-CoA dehydrogenase

Transcriptomic and proteomic intra-tumor heterogeneity of colorectal cancer varies depending on tumor location within the colorectum

TreeFam: 2008 Update

Tumor-specific usage of alternative transcription start sites in colorectal cancer identified by genome-wide exon array analysis

Widespread DNA hypomethylation and differential gene expression in Turner syndrome