Lista de obras - Sevtap Savas - Dominio Público Uruguay

A Survival Association Study of 102 Polymorphisms Previously Associated with Survival Outcomes in Colorectal Cancer

artículo científico publicado en 2015

A comprehensive catalogue of functional genetic variations in the EGFR pathway: protein-protein interaction analysis reveals novel genes and polymorphisms important for cancer research

artículo científico publicado en 2009

A curated database of genetic markers from the angiogenesis/VEGF pathway and their relation to clinical outcome in human cancers ⬇️

artículo científico publicado el 12 de diciembre de 2011

A whole-genome SNP association study of NCI60 cell line panel indicates a role of Ca2+ signaling in selenium resistance

artículo científico publicado en 2010

ABCC2 polymorphisms and survival in the Princess Margaret cohort study and the NCIC clinical trials group BR.24 trial of platinum-treated advanced stage non-small cell lung cancer patients.

artículo científico publicado en 2016

Bioinformatic analyses identifies novel protein-coding pharmacogenomic markers associated with paclitaxel sensitivity in NCI60 cancer cell lines.

artículo científico publicado en 2011

Biological implications of SNPs in signal peptide domains of human proteins

artículo científico publicado en 2008

Candidate nsSNPs that can affect the functions and interactions of cell cycle proteins

scientific article published on 01 February 2005

Discovery of genetic profiles impacting response to chemotherapy: application to gemcitabine.

artículo científico publicado en 2008

Functional nonsynonymous single nucleotide polymorphisms from the TGF-beta protein interaction network

artículo científico publicado en 2006

Genetic sequence variants and the development of secondary primary cancers in patients with head and neck cancers

article

Genetic variations as cancer prognostic markers: review and update

artículo científico publicado en 2009

Germline INDELs and CNVs in a cohort of colorectal cancer patients: their characteristics, associations with relapse-free survival time, and potential time-varying effects on the risk of relapse

artículo científico publicado en 2017

Hereditary haemorrhagic telangiectasia: mutation detection, test sensitivity and novel mutations.

artículo científico publicado en 2006

Human non-synonymous single nucleotide polymorphisms can influence ubiquitin-mediated protein degradation.

artículo científico publicado en 2007

Influence of pre-diagnostic cigarette smoking on colorectal cancer survival: overall and by tumour molecular phenotype.

artículo científico publicado en 2014

MTHFR Glu429Ala and ERCC5 His46His polymorphisms are associated with prognosis in colorectal cancer patients: analysis of two independent cohorts from Newfoundland.

artículo científico publicado en 2013

Missense variants of uncertain significance (VUS) altering the phosphorylation patterns of BRCA1 and BRCA2.

artículo científico publicado en 2013

NCI60 cancer cell line panel data and RNAi analysis help identify EAF2 as a modulator of simvastatin and lovastatin response in HCT-116 cells.

artículo científico publicado en 2011

Phosphorylation states of cell cycle and DNA repair proteins can be altered by the nsSNPs

artículo científico publicado en 2005

Polymorphisms cMyc-N11S and p27-V109G and breast cancer risk and prognosis

artículo científico publicado en 2007

Prenatal prediction of childhood-onset spinal muscular atrophy (SMA) in Turkish families

artículo científico publicado en 2002

Special considerations in prognostic research in cancer involving genetic polymorphisms

artículo científico publicado en 2013

Structure, diversity, and evolution of the 45-bp VNTR in intron 5 of the USH1C gene.

artículo científico publicado en 2004

Studying genetic variations in cancer prognosis (and risk): a primer for clinicians

scientific article published on 06 July 2009

The USH1C 216G-->A mutation and the 9-repeat VNTR(t,t) allele are in complete linkage disequilibrium in the Acadian population.

artículo científico publicado en 2001

The long-term survival characteristics of a cohort of colorectal cancer patients and baseline variables associated with survival outcomes with or without time-varying effects

scientific article published on 29 July 2019

Two functional indel polymorphisms in the promoter region of the Brahma gene (BRM) and disease risk and progression-free survival in colorectal cancer.

artículo científico publicado en 2018

Useful genetic variation databases for oncologists investigating the genetic basis of variable treatment response and survival in cancer.

artículo científico publicado en 2010

Validation of genetic sequence variants as prognostic factors in early-stage head and neck squamous cell cancer survival

artículo científico publicado en 2011

Variable distribution of TFF2 (Spasmolysin) alleles in Europeans does not indicate predisposition to gastric cancer

artículo científico publicado en 1999

Vascular endothelial growth factor pathway polymorphisms as prognostic and pharmacogenetic factors in cancer: a systematic review and meta-analysis

artículo científico

dbCPCO: a database of genetic markers tested for their predictive and prognostic value in colorectal cancer

artículo científico publicado en 2010

Lista de obras de Sevtap Savas

A Survival Association Study of 102 Polymorphisms Previously Associated with Survival Outcomes in Colorectal Cancer

A comprehensive catalogue of functional genetic variations in the EGFR pathway: protein-protein interaction analysis reveals novel genes and polymorphisms important for cancer research

A curated database of genetic markers from the angiogenesis/VEGF pathway and their relation to clinical outcome in human cancers ⬇️

A whole-genome SNP association study of NCI60 cell line panel indicates a role of Ca2+ signaling in selenium resistance

ABCC2 polymorphisms and survival in the Princess Margaret cohort study and the NCIC clinical trials group BR.24 trial of platinum-treated advanced stage non-small cell lung cancer patients.

Bioinformatic analyses identifies novel protein-coding pharmacogenomic markers associated with paclitaxel sensitivity in NCI60 cancer cell lines.

Biological implications of SNPs in signal peptide domains of human proteins

Candidate nsSNPs that can affect the functions and interactions of cell cycle proteins

Discovery of genetic profiles impacting response to chemotherapy: application to gemcitabine.

Functional nonsynonymous single nucleotide polymorphisms from the TGF-beta protein interaction network

Genetic sequence variants and the development of secondary primary cancers in patients with head and neck cancers

Genetic variations as cancer prognostic markers: review and update

Germline INDELs and CNVs in a cohort of colorectal cancer patients: their characteristics, associations with relapse-free survival time, and potential time-varying effects on the risk of relapse

Hereditary haemorrhagic telangiectasia: mutation detection, test sensitivity and novel mutations.

Human non-synonymous single nucleotide polymorphisms can influence ubiquitin-mediated protein degradation.

Influence of pre-diagnostic cigarette smoking on colorectal cancer survival: overall and by tumour molecular phenotype.

MTHFR Glu429Ala and ERCC5 His46His polymorphisms are associated with prognosis in colorectal cancer patients: analysis of two independent cohorts from Newfoundland.

Missense variants of uncertain significance (VUS) altering the phosphorylation patterns of BRCA1 and BRCA2.

NCI60 cancer cell line panel data and RNAi analysis help identify EAF2 as a modulator of simvastatin and lovastatin response in HCT-116 cells.

Phosphorylation states of cell cycle and DNA repair proteins can be altered by the nsSNPs

Polymorphisms cMyc-N11S and p27-V109G and breast cancer risk and prognosis

Prenatal prediction of childhood-onset spinal muscular atrophy (SMA) in Turkish families

Special considerations in prognostic research in cancer involving genetic polymorphisms

Structure, diversity, and evolution of the 45-bp VNTR in intron 5 of the USH1C gene.

Studying genetic variations in cancer prognosis (and risk): a primer for clinicians

The USH1C 216G-->A mutation and the 9-repeat VNTR(t,t) allele are in complete linkage disequilibrium in the Acadian population.

The long-term survival characteristics of a cohort of colorectal cancer patients and baseline variables associated with survival outcomes with or without time-varying effects

Two functional indel polymorphisms in the promoter region of the Brahma gene (BRM) and disease risk and progression-free survival in colorectal cancer.

Useful genetic variation databases for oncologists investigating the genetic basis of variable treatment response and survival in cancer.

Validation of genetic sequence variants as prognostic factors in early-stage head and neck squamous cell cancer survival

Variable distribution of TFF2 (Spasmolysin) alleles in Europeans does not indicate predisposition to gastric cancer

Vascular endothelial growth factor pathway polymorphisms as prognostic and pharmacogenetic factors in cancer: a systematic review and meta-analysis

dbCPCO: a database of genetic markers tested for their predictive and prognostic value in colorectal cancer