Lista de obras - Daoud Sie - Dominio Público Uruguay

A barcode screen for epigenetic regulators reveals a role for the NuB4/HAT-B histone acetyltransferase complex in histone turnover

artículo científico publicado en 2011

Collembolan Transcriptomes Highlight Molecular Evolution of Hexapods and Provide Clues on the Adaptation to Terrestrial Life

artículo científico publicado en 2015

Combination of a six microRNA expression profile with four clinicopathological factors for response prediction of systemic treatment in patients with advanced colorectal cancer

artículo científico publicado en 2018

Condensin II mutation causes T-cell lymphoma through tissue-specific genome instability

artículo científico publicado en 2016

Copy number signatures and mutational processes in ovarian carcinoma

artículo científico publicado en 2018

DNA copy number analysis of fresh and formalin-fixed specimens by shallow whole-genome sequencing with identification and exclusion of problematic regions in the genome assembly

artículo científico publicado en 2014

Diagnosis of fanconi anemia: mutation analysis by next-generation sequencing

artículo científico publicado en 2012

EGFR mutation analysis in sputum of lung cancer patients: a multitechnique study

artículo científico publicado en 2013

Fetal fraction evaluation in non-invasive prenatal screening (NIPS)

scientific article published on 25 September 2018

Functional Screening Identifies Human miRNAs that Modulate Adenovirus Propagation in Prostate Cancer Cells.

artículo científico publicado en 2017

Genome-wide microRNA analysis of HPV-positive self-samples yields novel triage markers for early detection of cervical cancer.

artículo científico publicado en 2018

Genomic profiling of stage II and III colon cancers reveals APC mutations to be associated with survival in stage III colon cancer patients

artículo científico publicado en 2016

HELLP babies link a novel lincRNA to the trophoblast cell cycle

artículo científico publicado en 2012

High Prevalence and Clinical Relevance of Genes Affected by Chromosomal Breaks in Colorectal Cancer

artículo científico publicado en 2015

High-throughput semiquantitative analysis of insertional mutations in heterogeneous tumors.

artículo científico publicado en 2011

Insertional mutagenesis in mice deficient for p15Ink4b, p16Ink4a, p21Cip1, and p27Kip1 reveals cancer gene interactions and correlations with tumor phenotypes

artículo científico publicado en 2010

Landscape of chromosomal copy number aberrations in gangliogliomas and dysembryoplastic neuroepithelial tumours

artículo científico publicado en 2015

Large-scale mutagenesis in p19(ARF)- and p53-deficient mice identifies cancer genes and their collaborative networks

artículo científico publicado en 2008

MiR expression profiles of paired primary colorectal cancer and metastases by next-generation sequencing

artículo científico publicado en 2015

MicroRNA sequence and expression analysis in breast tumors by deep sequencing

artículo científico publicado en 2011

Molecular heterogeneity in human papillomavirus-dependent and -independent vulvar carcinogenesis.

artículo científico publicado en 2018

No evidence for active human papillomavirus (HPV) in fields surrounding HPV-positive oropharyngeal tumors

artículo científico publicado en 2013

Non-classic EGFR mutations in a cohort of Dutch EGFR-mutated NSCLC patients and outcomes following EGFR-TKI treatment.

artículo científico publicado en 2016

Nontemplated nucleotide additions distinguish the small RNA composition in cells from exosomes

artículo científico publicado en 2014

Novel cases of D-2-hydroxyglutaric aciduria with IDH1 or IDH2 mosaic mutations identified by amplicon deep sequencing

artículo científico publicado en 2013

One naive T cell, multiple fates in CD8+ T cell differentiation.

artículo científico publicado en 2010

Performance of amplicon-based next generation DNA sequencing for diagnostic gene mutation profiling in oncopathology

artículo científico publicado en 2014

Proper genomic profiling of (BRCA1-mutated) basal-like breast carcinomas requires prior removal of tumor infiltrating lymphocytes.

artículo científico publicado en 2015

Recruitment of antigen-specific CD8+ T cells in response to infection is markedly efficient

artículo científico publicado en 2009

Search for a gene expression signature of breast cancer local recurrence in young women

artículo científico publicado en 2012

ShrinkBayes: a versatile R-package for analysis of count-based sequencing data in complex study designs

artículo científico publicado en 2014

Somatic mutation in PIK3CA is a late event in cervical carcinogenesis

artículo científico publicado en 2015

Somatic mutations found in the healthy blood compartment of a 115-yr-old woman demonstrate oligoclonal hematopoiesis

artículo científico publicado en 2014

Spatial and temporal evolution of distal 10q deletion, a prognostically unfavorable event in diffuse low-grade gliomas

artículo científico publicado en 2014

Targeted sequencing by proximity ligation for comprehensive variant detection and local haplotyping.

artículo científico publicado en 2014

The T7-primer is a source of experimental bias and introduces variability between microarray platforms

artículo científico publicado en 2008

To DNA or not to DNA? That is the question, when it comes to molecular subtyping for the clinic!

artículo científico publicado en 2011

Volatile anesthetics modulate gene expression in breast and brain tumor cells.

artículo científico publicado en 2010

Lista de obras de Daoud Sie

A barcode screen for epigenetic regulators reveals a role for the NuB4/HAT-B histone acetyltransferase complex in histone turnover

Collembolan Transcriptomes Highlight Molecular Evolution of Hexapods and Provide Clues on the Adaptation to Terrestrial Life

Combination of a six microRNA expression profile with four clinicopathological factors for response prediction of systemic treatment in patients with advanced colorectal cancer

Condensin II mutation causes T-cell lymphoma through tissue-specific genome instability

Copy number signatures and mutational processes in ovarian carcinoma

DNA copy number analysis of fresh and formalin-fixed specimens by shallow whole-genome sequencing with identification and exclusion of problematic regions in the genome assembly

Diagnosis of fanconi anemia: mutation analysis by next-generation sequencing

EGFR mutation analysis in sputum of lung cancer patients: a multitechnique study

Fetal fraction evaluation in non-invasive prenatal screening (NIPS)

Functional Screening Identifies Human miRNAs that Modulate Adenovirus Propagation in Prostate Cancer Cells.

Genome-wide microRNA analysis of HPV-positive self-samples yields novel triage markers for early detection of cervical cancer.

Genomic profiling of stage II and III colon cancers reveals APC mutations to be associated with survival in stage III colon cancer patients

HELLP babies link a novel lincRNA to the trophoblast cell cycle

High Prevalence and Clinical Relevance of Genes Affected by Chromosomal Breaks in Colorectal Cancer

High-throughput semiquantitative analysis of insertional mutations in heterogeneous tumors.

Insertional mutagenesis in mice deficient for p15Ink4b, p16Ink4a, p21Cip1, and p27Kip1 reveals cancer gene interactions and correlations with tumor phenotypes

Landscape of chromosomal copy number aberrations in gangliogliomas and dysembryoplastic neuroepithelial tumours

Large-scale mutagenesis in p19(ARF)- and p53-deficient mice identifies cancer genes and their collaborative networks

MiR expression profiles of paired primary colorectal cancer and metastases by next-generation sequencing

MicroRNA sequence and expression analysis in breast tumors by deep sequencing

Molecular heterogeneity in human papillomavirus-dependent and -independent vulvar carcinogenesis.

No evidence for active human papillomavirus (HPV) in fields surrounding HPV-positive oropharyngeal tumors

Non-classic EGFR mutations in a cohort of Dutch EGFR-mutated NSCLC patients and outcomes following EGFR-TKI treatment.

Nontemplated nucleotide additions distinguish the small RNA composition in cells from exosomes

Novel cases of D-2-hydroxyglutaric aciduria with IDH1 or IDH2 mosaic mutations identified by amplicon deep sequencing

One naive T cell, multiple fates in CD8+ T cell differentiation.

Performance of amplicon-based next generation DNA sequencing for diagnostic gene mutation profiling in oncopathology

Proper genomic profiling of (BRCA1-mutated) basal-like breast carcinomas requires prior removal of tumor infiltrating lymphocytes.

Recruitment of antigen-specific CD8+ T cells in response to infection is markedly efficient

Search for a gene expression signature of breast cancer local recurrence in young women

ShrinkBayes: a versatile R-package for analysis of count-based sequencing data in complex study designs

Somatic mutation in PIK3CA is a late event in cervical carcinogenesis

Somatic mutations found in the healthy blood compartment of a 115-yr-old woman demonstrate oligoclonal hematopoiesis

Spatial and temporal evolution of distal 10q deletion, a prognostically unfavorable event in diffuse low-grade gliomas

Targeted sequencing by proximity ligation for comprehensive variant detection and local haplotyping.

The T7-primer is a source of experimental bias and introduces variability between microarray platforms

To DNA or not to DNA? That is the question, when it comes to molecular subtyping for the clinic!

Volatile anesthetics modulate gene expression in breast and brain tumor cells.