Lista de obras - Isabel Barragan - Dominio Público Uruguay

A novel genetic study of Chinese families with autosomal recessive retinitis pigmentosa

scientific article published on 29 November 2006

CYP2W1 polymorphism: functional aspects and relation to risk for colorectal cancer.

artículo científico publicado en 2013

CYP3A5 is unlikely to mediate anticancer drug resistance in hepatocellular carcinoma

artículo científico publicado en 2019

Copy-Number Variations inEYS:A Significant Event in the Appearance of arRP ⬇️

artículo científico publicado el 29 de julio de 2011

Cytostatic Effect of Repeated Exposure to Simvastatin: A Mechanism for Chronic Myotoxicity Revealed by the Use of Mesodermal Progenitors Derived from Human Pluripotent Stem Cells.

artículo científico publicado en 2015

EDIL3 promotes epithelial-mesenchymal transition and paclitaxel resistance through its interaction with integrin αVβ3 in cancer cells

scientific article published on 16 September 2020

EYS is a major gene for rod-cone dystrophies in France.

artículo científico publicado en 2010

Effects of incorporated drugs on degradation of novel 2,2'-bis(2-oxazoline) linked poly(lactic acid) films.

artículo científico publicado en 2006

Epigenetic mechanisms of importance for drug treatment.

artículo científico publicado en 2014

Epigenetic prediction of response to anti-PD-1 treatment in non-small-cell lung cancer: a multicentre, retrospective analysis

artículo científico publicado en 2018

Exclusion of four candidate genes, KHDRBS2, PTP4A1, KIAA1411 and OGFRL1, as causative of autosomal recessive retinitis pigmentosa.

artículo científico publicado en 2005

Genetic and epigenetic regulation of gene expression in fetal and adult human livers

artículo científico publicado en 2014

Identification of novel mutations in the ortholog of Drosophila eyes shut gene (EYS) causing autosomal recessive retinitis pigmentosa.

artículo científico publicado en 2010

Linkage validation of RP25 Using the 10K genechip array and further refinement of the locus by new linked families.

artículo científico publicado en 2007

Long-term chronic toxicity testing using human pluripotent stem cell-derived hepatocytes

artículo científico publicado en 2014

Microarray-based mutation analysis of 183 Spanish families with Usher syndrome.

artículo científico publicado en 2009

Molecular genetic analysis of two functional candidate genes in the autosomal recessive retinitis pigmentosa, RP25, locus

artículo científico publicado en 2005

Mutation spectrum of EYS in Spanish patients with autosomal recessive retinitis pigmentosa

artículo científico publicado en 2010

Ontogeny, distribution and potential roles of 5-hydroxymethylcytosine in human liver function

artículo científico publicado en 2013

Pharmacoepigenetics and Toxicoepigenetics: Novel Mechanistic Insights and Therapeutic Opportunities

artículo científico publicado en 2017

Single base resolution analysis of 5-hydroxymethylcytosine in 188 human genes: implications for hepatic gene expression

artículo científico publicado en 2016

Strong effects of environmental factors on prevalence and course of major depressive disorder are not moderated by 5-HTTLPR polymorphisms in a large Dutch sample

artículo científico publicado en 2012

Lista de obras de Isabel Barragan

A novel genetic study of Chinese families with autosomal recessive retinitis pigmentosa

CYP2W1 polymorphism: functional aspects and relation to risk for colorectal cancer.

CYP3A5 is unlikely to mediate anticancer drug resistance in hepatocellular carcinoma

Copy-Number Variations inEYS:A Significant Event in the Appearance of arRP ⬇️

Cytostatic Effect of Repeated Exposure to Simvastatin: A Mechanism for Chronic Myotoxicity Revealed by the Use of Mesodermal Progenitors Derived from Human Pluripotent Stem Cells.

EDIL3 promotes epithelial-mesenchymal transition and paclitaxel resistance through its interaction with integrin αVβ3 in cancer cells

EYS is a major gene for rod-cone dystrophies in France.

Effects of incorporated drugs on degradation of novel 2,2'-bis(2-oxazoline) linked poly(lactic acid) films.

Epigenetic mechanisms of importance for drug treatment.

Epigenetic prediction of response to anti-PD-1 treatment in non-small-cell lung cancer: a multicentre, retrospective analysis

Exclusion of four candidate genes, KHDRBS2, PTP4A1, KIAA1411 and OGFRL1, as causative of autosomal recessive retinitis pigmentosa.

Genetic and epigenetic regulation of gene expression in fetal and adult human livers

Identification of novel mutations in the ortholog of Drosophila eyes shut gene (EYS) causing autosomal recessive retinitis pigmentosa.

Linkage validation of RP25 Using the 10K genechip array and further refinement of the locus by new linked families.

Long-term chronic toxicity testing using human pluripotent stem cell-derived hepatocytes

Microarray-based mutation analysis of 183 Spanish families with Usher syndrome.

Molecular genetic analysis of two functional candidate genes in the autosomal recessive retinitis pigmentosa, RP25, locus

Mutation spectrum of EYS in Spanish patients with autosomal recessive retinitis pigmentosa

Ontogeny, distribution and potential roles of 5-hydroxymethylcytosine in human liver function

Pharmacoepigenetics and Toxicoepigenetics: Novel Mechanistic Insights and Therapeutic Opportunities

Single base resolution analysis of 5-hydroxymethylcytosine in 188 human genes: implications for hepatic gene expression

Strong effects of environmental factors on prevalence and course of major depressive disorder are not moderated by 5-HTTLPR polymorphisms in a large Dutch sample