Lista de obras - Martin Kerick - Dominio Público Uruguay

A new dominant peroxiredoxin allele identified by whole-genome re-sequencing of random mutagenized yeast causes oxidant-resistance and premature aging

artículo científico publicado en 2010

Admixture mapping analysis reveals differential genetic ancestry associated with Chagas disease susceptibility in the Colombian population

artículo científico publicado en 2021

Allele frequencies of BRAFV600 mutations in primary melanomas and matched metastases and their relevance for BRAF inhibitor therapy in metastatic melanoma

artículo científico publicado en 2015

Alterations of pre-mRNA splicing in human inflammatory bowel disease

article

Campylobacter jejuni impairs sodium transport and epithelial barrier function via cytokine release in human colon

artículo científico publicado en 2017

Campylobacter jejuni impairs sodium transport and epithelial barrier function via cytokine release in human colon.

artículo científico publicado en 2017

Classic bladder exstrophy: Frequent 22q11.21 duplications and definition of a 414 kb phenocritical region

article

ENaC Dysregulation Through Activation of MEK1/2 Contributes to Impaired Na+ Absorption in Lymphocytic Colitis

artículo científico publicado en 2015

Epigenome-Wide Comparative Study Reveals Key Differences Between Mixed Connective Tissue Disease and Related Systemic Autoimmune Diseases

Epigenomic profiling of non-small cell lung cancer xenografts uncover LRP12 DNA methylation as predictive biomarker for carboplatin resistance

artículo científico publicado en 2018

Epithelial barrier dysfunction in lymphocytic colitis through cytokine-dependent internalization of claudin-5 and -8.

artículo científico publicado en 2017

Exome sequencing identifies potential novel candidate genes in patients with unexplained colorectal adenomatous polyposis

artículo científico publicado en 2016

GWAS for systemic sclerosis identifies multiple risk loci and highlights fibrotic and vasculopathy pathways

scientific article published on 31 October 2019

GWAS loci associated with Chagas cardiomyopathy influences DNA methylation levels

artículo científico publicado en 2021

Genetic control of global gene expression levels in the intestinal mucosa: a human twin study

artículo científico publicado en 2009

Genome-wide DNA methylation events in TMPRSS2-ERG fusion-negative prostate cancers implicate an EZH2-dependent mechanism with miR-26a hypermethylation

artículo científico publicado en 2012

Genome-wide whole blood transcriptome profiling in a large European cohort of systemic sclerosis patients

scientific article published on 19 June 2020

Genomic Risk Score impact on susceptibility to systemic sclerosis

scientific article published on 01 October 2020

Genomic and phenotypic insights from an atlas of genetic effects on DNA methylation

artículo científico publicado en 2021

Genomic and transcriptomic heterogeneity of colorectal tumors arising in Lynch Syndrome

artículo científico

HLA class I loss and PD-L1 expression in lung cancer: impact on T-cell infiltration and immune escape.

artículo científico publicado en 2017

High-throughput miRNA and mRNA sequencing of paired colorectal normal, tumor and metastasis tissues and bioinformatic modeling of miRNA-1 therapeutic applications

artículo científico publicado en 2013

Hsp90 inhibition differentially destabilises MAP kinase and TGF-beta signalling components in cancer cells revealed by kinase-targeted chemoproteomics

artículo científico publicado en 2012

Identity-by-descent filtering of exome sequence data identifies PIGV mutations in hyperphosphatasia mental retardation syndrome

artículo científico publicado en 2010

Integrative epigenomics in Sjögren´s syndrome reveals novel pathways and a strong interaction between the HLA, autoantibodies and the interferon signature

artículo científico publicado en 2021

LSD1 modulates the non-canonical integrin β3 signaling pathway in non-small cell lung carcinoma cells.

artículo científico publicado en 2017

Low-level APC mutational mosaicism is the underlying cause in a substantial fraction of unexplained colorectal adenomatous polyposis cases

artículo científico publicado en 2015

Microarray analysis of tumor necrosis factor alpha induced gene expression in U373 human glioblastoma cells

artículo científico publicado en 2003

Somatic mutation profiles of MSI and MSS colorectal cancer identified by whole exome next generation sequencing and bioinformatics analysis

artículo científico publicado en 2010

TET2- and TDG-mediated changes are required for the acquisition of distinct histone modifications in divergent terminal differentiation of myeloid cells.

artículo científico publicado en 2017

Targeted high throughput sequencing in clinical cancer settings: formaldehyde fixed-paraffin embedded (FFPE) tumor tissues, input amount and tumor heterogeneity

artículo científico publicado en 2011

The bromodomain protein BRD4 regulates splicing during heat shock

artículo científico publicado en 2016

The bromodomain protein BRD4 regulates the KEAP1/NRF2-dependent oxidative stress response.

artículo científico publicado en 2014

The metabolic growth limitations of petite cells lacking the mitochondrial genome

artículo científico publicado en 2021

The pentose phosphate pathway is a metabolic redox sensor and regulates transcription during the antioxidant response

artículo científico publicado en 2011

The power of NGS technologies to delineate the genome organization in cancer: from mutations to structural variations and epigenetic alterations.

scientific article published on June 2011

Transcriptional signature induced by a metastasis-promoting c-Src mutant in a human breast cell line

artículo científico publicado en 2016

Using the canary genome to decipher the evolution of hormone-sensitive gene regulation in seasonal singing birds

artículo científico publicado en 2015

[High-throughput sequencing of frozen and paraffin-embedded tumor and normal tissue]

scientific article published on 01 October 2010

Lista de obras de Martin Kerick

A new dominant peroxiredoxin allele identified by whole-genome re-sequencing of random mutagenized yeast causes oxidant-resistance and premature aging

Admixture mapping analysis reveals differential genetic ancestry associated with Chagas disease susceptibility in the Colombian population

Allele frequencies of BRAFV600 mutations in primary melanomas and matched metastases and their relevance for BRAF inhibitor therapy in metastatic melanoma

Alterations of pre-mRNA splicing in human inflammatory bowel disease

Campylobacter jejuni impairs sodium transport and epithelial barrier function via cytokine release in human colon

Campylobacter jejuni impairs sodium transport and epithelial barrier function via cytokine release in human colon.

Classic bladder exstrophy: Frequent 22q11.21 duplications and definition of a 414 kb phenocritical region

ENaC Dysregulation Through Activation of MEK1/2 Contributes to Impaired Na+ Absorption in Lymphocytic Colitis

Epigenome-Wide Comparative Study Reveals Key Differences Between Mixed Connective Tissue Disease and Related Systemic Autoimmune Diseases

Epigenomic profiling of non-small cell lung cancer xenografts uncover LRP12 DNA methylation as predictive biomarker for carboplatin resistance

Epithelial barrier dysfunction in lymphocytic colitis through cytokine-dependent internalization of claudin-5 and -8.

Exome sequencing identifies potential novel candidate genes in patients with unexplained colorectal adenomatous polyposis

GWAS for systemic sclerosis identifies multiple risk loci and highlights fibrotic and vasculopathy pathways

GWAS loci associated with Chagas cardiomyopathy influences DNA methylation levels

Genetic control of global gene expression levels in the intestinal mucosa: a human twin study

Genome-wide DNA methylation events in TMPRSS2-ERG fusion-negative prostate cancers implicate an EZH2-dependent mechanism with miR-26a hypermethylation

Genome-wide whole blood transcriptome profiling in a large European cohort of systemic sclerosis patients

Genomic Risk Score impact on susceptibility to systemic sclerosis

Genomic and phenotypic insights from an atlas of genetic effects on DNA methylation

Genomic and transcriptomic heterogeneity of colorectal tumors arising in Lynch Syndrome

HLA class I loss and PD-L1 expression in lung cancer: impact on T-cell infiltration and immune escape.

High-throughput miRNA and mRNA sequencing of paired colorectal normal, tumor and metastasis tissues and bioinformatic modeling of miRNA-1 therapeutic applications

Hsp90 inhibition differentially destabilises MAP kinase and TGF-beta signalling components in cancer cells revealed by kinase-targeted chemoproteomics

Identity-by-descent filtering of exome sequence data identifies PIGV mutations in hyperphosphatasia mental retardation syndrome

Integrative epigenomics in Sjögren´s syndrome reveals novel pathways and a strong interaction between the HLA, autoantibodies and the interferon signature

LSD1 modulates the non-canonical integrin β3 signaling pathway in non-small cell lung carcinoma cells.

Low-level APC mutational mosaicism is the underlying cause in a substantial fraction of unexplained colorectal adenomatous polyposis cases

Microarray analysis of tumor necrosis factor alpha induced gene expression in U373 human glioblastoma cells

Somatic mutation profiles of MSI and MSS colorectal cancer identified by whole exome next generation sequencing and bioinformatics analysis

TET2- and TDG-mediated changes are required for the acquisition of distinct histone modifications in divergent terminal differentiation of myeloid cells.

Targeted high throughput sequencing in clinical cancer settings: formaldehyde fixed-paraffin embedded (FFPE) tumor tissues, input amount and tumor heterogeneity

The bromodomain protein BRD4 regulates splicing during heat shock

The bromodomain protein BRD4 regulates the KEAP1/NRF2-dependent oxidative stress response.

The metabolic growth limitations of petite cells lacking the mitochondrial genome

The pentose phosphate pathway is a metabolic redox sensor and regulates transcription during the antioxidant response

The power of NGS technologies to delineate the genome organization in cancer: from mutations to structural variations and epigenetic alterations.

Transcriptional signature induced by a metastasis-promoting c-Src mutant in a human breast cell line

Using the canary genome to decipher the evolution of hormone-sensitive gene regulation in seasonal singing birds

[High-throughput sequencing of frozen and paraffin-embedded tumor and normal tissue]