Lista de obras -

Altered gating properties of functional Cx26 mutants associated with recessive non-syndromic hearing loss.

artículo científico publicado en 2004

Analysis of 13 cell types reveals evidence for the expression of numerous novel primate- and tissue-specific microRNAs

artículo científico publicado en 2015

Argonaute CLIP-Seq reveals miRNA targetome diversity across tissue types

artículo científico publicado en 2014

Assessment of isomiR Discrimination Using Commercial qPCR Methods.

artículo científico publicado en 2017

Autosomal recessive congenital ichthyosis: Genomic landscape and phenotypic spectrum in a cohort of 125 consanguineous families

scientific article published on 16 January 2019

Beyond the one-locus-one-miRNA paradigm: microRNA isoforms enable deeper insights into breast cancer heterogeneity.

artículo científico publicado en 2015

CRISPR Knockout of the HuR Gene Causes a Xenograft Lethal Phenotype

artículo científico publicado en 2017

Chordin, FGF signaling, and mesodermal factors cooperate in zebrafish neural induction

artículo científico publicado en 2005

Clinical exome performance for reporting secondary genetic findings

artículo científico publicado en 2014

Clinical genomics: when whole genome sequencing is like a whole-body CT scan.

artículo científico publicado en 2014

CoAIMs: a cost-effective panel of ancestry informative markers for determining continental origins.

artículo científico publicado en 2010

Donor splice-site mutation in CUL4B is likely cause of X-linked intellectual disability

artículo científico publicado en 2014

Evaluation of Post-transcriptional Gene Regulation in Pancreatic Cancer Cells: Studying RNA Binding Proteins and Their mRNA Targets

article

GPRC5A is a potential oncogene in pancreatic ductal adenocarcinoma cells that is upregulated by gemcitabine with help from HuR.

artículo científico publicado en 2016

High Concentration Capture Probes Enhance Massively Parallel Sequencing Assays.

artículo científico publicado en 2016

Host IDO2 Gene Status Influences Tumor Progression and Radiotherapy Response in KRAS-Driven Sporadic Pancreatic Cancers

scientific article published on 28 September 2018

HuR is a post-transcriptional regulator of core metabolic enzymes in pancreatic cancer ⬇️

artículo científico publicado el 13 de junio de 2013

HuR posttranscriptionally regulates WEE1: implications for the DNA damage response in pancreatic cancer cells

artículo científico publicado en 2014

HuR's post-transcriptional regulation of Death Receptor 5 in pancreatic cancer cells.

artículo científico publicado en 2012

IsomiRs and tRNA-derived fragments are associated with metastasis and patient survival in uveal melanoma

scientific article published on 16 August 2019

Knowledge about the presence or absence of miRNA isoforms (isomiRs) can successfully discriminate amongst 32 TCGA cancer types

artículo científico publicado en 2017

MINTbase v2.0: a comprehensive database for tRNA-derived fragments that includes nuclear and mitochondrial fragments from all The Cancer Genome Atlas projects

artículo científico publicado en 2017

Murine -linked hydrocephalus is caused by hyperpermeability of the choroid plexus

artículo científico publicado en 2019

Next generation sequencing in cancer: opportunities and challenges for precision cancer medicine.

artículo científico publicado en 2016

Performance of exome sequencing for pharmacogenomics.

artículo científico publicado en 2014

Post-transcriptional Regulation of BRCA2 through Interactions with miR-19a and miR-19b

artículo científico publicado en 2016

Posttranscriptional Regulation of PARG mRNA by HuR Facilitates DNA Repair and Resistance to PARP Inhibitors.

artículo científico publicado en 2017

Posttranscriptional Upregulation of IDH1 by HuR Establishes a Powerful Survival Phenotype in Pancreatic Cancer Cells.

artículo científico publicado en 2017

Profiles of miRNA Isoforms and tRNA Fragments in Prostate Cancer.

artículo científico publicado en 2018

Recessive mutation in tetraspanin CD151 causes Kindler syndrome-like epidermolysis bullosa with multi-systemic manifestations including nephropathy.

artículo científico publicado en 2017

Reply to Backes and Keller: Identification of novel tissue-specific and primate-specific human microRNAs

artículo científico publicado en 2015

Short RNA regulators: the past, the present, the future, and implications for precision medicine and health disparities

scientific article published on 16 July 2019

Single-Cell Genomics

scientific article published on 14 March 2019

Small RNA Sequencing across Diverse Biofluids Identifies Optimal Methods for exRNA Isolation

scientific article published on 01 April 2019

TRNA-derived fragments as sex-dependent circulating candidate biomarkers for Parkinson's disease

scientific article published on 25 May 2019

The Sustained Induction of c-MYC Drives Nab-Paclitaxel Resistance in Primary Pancreatic Ductal Carcinoma Cells

artículo científico publicado en 2019

The human platelet: strong transcriptome correlations among individuals associate weakly with the platelet proteome.

artículo científico publicado en 2014

The mRNA-binding protein HuR promotes hypoxia-induced chemoresistance through posttranscriptional regulation of the proto-oncogene PIM1 in pancreatic cancer cells.

artículo científico publicado en 2015

The microRNAs within the DLK1-DIO3 genomic region: involvement in disease pathogenesis

artículo científico publicado en 2013

Threshold-seq: a tool for determining the threshold in short RNA-seq datasets.

artículo científico publicado en 2017

Unraveling the role of microRNA/isomiR network in multiple primary melanoma pathogenesis

artículo científico publicado en 2021

What is translational bioinformatics?

artículo científico publicado en 2015

Whole exome sequencing identifies a germline MET mutation in two siblings with hereditary wild-type RET medullary thyroid cancer.

artículo científico publicado en 2017

Whole-exome sequencing of DNA from peripheral blood mononuclear cells (PBMC) and EBV-transformed lymphocytes from the same donor

artículo científico publicado en 2011

tRNA Fragments Show Intertwining with mRNAs of Specific Repeat Content and Have Links to Disparities

scientific article published on 17 April 2019

Lista de obras de

Altered gating properties of functional Cx26 mutants associated with recessive non-syndromic hearing loss.

Analysis of 13 cell types reveals evidence for the expression of numerous novel primate- and tissue-specific microRNAs

Argonaute CLIP-Seq reveals miRNA targetome diversity across tissue types

Assessment of isomiR Discrimination Using Commercial qPCR Methods.

Autosomal recessive congenital ichthyosis: Genomic landscape and phenotypic spectrum in a cohort of 125 consanguineous families

Beyond the one-locus-one-miRNA paradigm: microRNA isoforms enable deeper insights into breast cancer heterogeneity.

CRISPR Knockout of the HuR Gene Causes a Xenograft Lethal Phenotype

Chordin, FGF signaling, and mesodermal factors cooperate in zebrafish neural induction

Clinical exome performance for reporting secondary genetic findings

Clinical genomics: when whole genome sequencing is like a whole-body CT scan.

CoAIMs: a cost-effective panel of ancestry informative markers for determining continental origins.

Donor splice-site mutation in CUL4B is likely cause of X-linked intellectual disability

Evaluation of Post-transcriptional Gene Regulation in Pancreatic Cancer Cells: Studying RNA Binding Proteins and Their mRNA Targets

GPRC5A is a potential oncogene in pancreatic ductal adenocarcinoma cells that is upregulated by gemcitabine with help from HuR.

High Concentration Capture Probes Enhance Massively Parallel Sequencing Assays.

Host IDO2 Gene Status Influences Tumor Progression and Radiotherapy Response in KRAS-Driven Sporadic Pancreatic Cancers

HuR is a post-transcriptional regulator of core metabolic enzymes in pancreatic cancer ⬇️

HuR posttranscriptionally regulates WEE1: implications for the DNA damage response in pancreatic cancer cells

HuR's post-transcriptional regulation of Death Receptor 5 in pancreatic cancer cells.

IsomiRs and tRNA-derived fragments are associated with metastasis and patient survival in uveal melanoma

Knowledge about the presence or absence of miRNA isoforms (isomiRs) can successfully discriminate amongst 32 TCGA cancer types

MINTbase v2.0: a comprehensive database for tRNA-derived fragments that includes nuclear and mitochondrial fragments from all The Cancer Genome Atlas projects

Murine -linked hydrocephalus is caused by hyperpermeability of the choroid plexus

Next generation sequencing in cancer: opportunities and challenges for precision cancer medicine.

Performance of exome sequencing for pharmacogenomics.

Post-transcriptional Regulation of BRCA2 through Interactions with miR-19a and miR-19b

Posttranscriptional Regulation of PARG mRNA by HuR Facilitates DNA Repair and Resistance to PARP Inhibitors.

Posttranscriptional Upregulation of IDH1 by HuR Establishes a Powerful Survival Phenotype in Pancreatic Cancer Cells.

Profiles of miRNA Isoforms and tRNA Fragments in Prostate Cancer.

Recessive mutation in tetraspanin CD151 causes Kindler syndrome-like epidermolysis bullosa with multi-systemic manifestations including nephropathy.

Reply to Backes and Keller: Identification of novel tissue-specific and primate-specific human microRNAs

Short RNA regulators: the past, the present, the future, and implications for precision medicine and health disparities

Single-Cell Genomics

Small RNA Sequencing across Diverse Biofluids Identifies Optimal Methods for exRNA Isolation

TRNA-derived fragments as sex-dependent circulating candidate biomarkers for Parkinson's disease

The Sustained Induction of c-MYC Drives Nab-Paclitaxel Resistance in Primary Pancreatic Ductal Carcinoma Cells

The human platelet: strong transcriptome correlations among individuals associate weakly with the platelet proteome.

The mRNA-binding protein HuR promotes hypoxia-induced chemoresistance through posttranscriptional regulation of the proto-oncogene PIM1 in pancreatic cancer cells.

The microRNAs within the DLK1-DIO3 genomic region: involvement in disease pathogenesis

Threshold-seq: a tool for determining the threshold in short RNA-seq datasets.

Unraveling the role of microRNA/isomiR network in multiple primary melanoma pathogenesis

What is translational bioinformatics?

Whole exome sequencing identifies a germline MET mutation in two siblings with hereditary wild-type RET medullary thyroid cancer.

Whole-exome sequencing of DNA from peripheral blood mononuclear cells (PBMC) and EBV-transformed lymphocytes from the same donor

tRNA Fragments Show Intertwining with mRNAs of Specific Repeat Content and Have Links to Disparities